Practice Standards Scheme Manual
CONTENTS
1 Staff ................................................................................................................................... 7
2 Clinical Governance and Communication ................................................................................ 15
3 Out-of-Hours Patient Care ..................................................................................................... 18
4 Premises and Out-patient Facilities ........................................................................................ 20
5 In-patient Facilities .............................................................................................................. 29
6 Diagnostic Equipment and Facilities ...................................................................................... 44
7 Laboratory and Post-Mortem Facilities .................................................................................... 53
8 Medicinal Products .............................................................................................................. 56
9 Safety Procedures ................................................................................................................ 67
10 Small Animal Emergency Service Clinics (ESC) ....................................................................... 79
Appendix 1 – Veterinary Nursing Training Practice – Additional Resources
RCVS Practice Standards Scheme
The Practice Standards have been developed by the Practice Standards Group which included representatives
from the British Veterinary Association (BVA); the British Small Animal Veterinary Association (BSAVA); the British
Veterinary Hospitals Association (BVHA); the British Equine Veterinary Association (BEVA); British Cattle Veterinary
Association (BCVA); RCVS Council; the Society of Practising Veterinary Surgeons (SPVS); the Veterinary Practice
Management Association (VPMA); the British Association of Veterinary Emergency Clinics (BAVEC); Veterinary Nurses
Council and the British Veterinary Nurses Association (BVNA) and were approved in principle by RCVS Council on
5 November 2009.
CORE STANDARDS - These standards are relevant to all veterinary practices and reflect mainly legal
requirements which must be met in running a veterinary practice.
GENERAL PRACTICE – The following categories are recognised:-
Small Animal, Equine, Farm Animal and Small Animal Emergency Service Clinic
For Small Animal and Equine practices the standards reflect the requirements of a primary care practice which
aims to facilitate the achievement of high standards of clinical care, and encompass many of the facilities
required for veterinary nurse training (TP) standards.
Appendix 1 gives guidance on additional resources to be provided by a General Practice wishing to apply for
accreditation as a Veterinary Nursing Training Practice. Please note that inspection of these resources and
assessment of the training capabilities of the practice will be carried out by a Veterinary Nursing Approved
Centre (VNAC).
For Farm Animal practices, the standards reflect both the requirements of a primary care practice which
promotes the achievement of high standards of clinical care, and also a proactive approach to management,
through the use of health planning, client training and communication.
For Small Animal Emergency Service Clinics, the standards reflect the requirements of a designated out-of-
hours provider. A Small Animal Emergency Service Clinic must fulfil the requirements for a Small Animal
General Practice and the additional requirements set out in section 10.
A General Practice must meet all Core Standards as well as General Practice standards.
VETERINARY HOSPITAL - the following categories are recognised:-
Small Animal and Equine
For Small Animal and Equine Veterinary Hospitals, the standards reflect the requirements of a General Practice
(above) allied with additional facilities and protocols for the investigation and treatment of more complex cases.
A Veterinary Hospital must meet all Core Standards and General Practice Standards, as well as specific Hospital
Standards.
KEY TO ABBREVIATIONS
C = Core Standards
GP = General Practice
VH = Veterinary Hospital
SA = Small Animal
FA = Farm Animal
EQ = Equine
ESC = Emergency Service Clinic
L = Legislative Requirement
++(FA) = Where this symbol appears the Standard is to be met by GP/FA, if applicable
Production of documentary evidence is required
,
Guidance notes are highlighted in yellow text
7
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
1 STAFF
1.1 All the veterinary surgeons and veterinary nurses working for the
practice must be registered with the RCVS and covered by Professional
Indemnity Insurance. Suitably Qualified Persons (SQPs) must provide
evidence of registration with the Animal Medicines Training Regulatory
Authority (AMTRA) appropriate for the product range supplied
(L)
The practice must provide the RCVS registration numbers of all veterinary surgeons
and veterinary nurses working for the practice in any capacity, as well as a copy of
current Professional Indemnity Insurance (covering all vets and veterinary nurses,
including locums and veterinary surgeons from overseas).
1.2 The practice must provide a written statement of the main terms of
employment for all employees (L)
C / ALL
RCVS registration numbers are listed in The
RCVS Directory of Veterinary Practices or can
be obtained direct from the Royal College of
Veterinary Surgeons, Belgravia House,
62-64 Horseferry Road, London SW1P 2AF
T 020 7222 2001 or E [email protected]
and at www.rcvs.org.uk/checkregister.
Registration numbers for RVNs/LVNs can be
found at www.rcvs.org.uk/vnlist.
A “Veterinary Nurse” means a person whose
name is entered in the List of Veterinary Nurses
(which incorporates the Register of Veterinary
Nurses) maintained by the RCVS. Types of SQP
and colour-coding for current IDs can be found on
the AMTRA website www.amtra.org.uk/SQP_types.
html.
All employers are legally obliged to give their
employees a written statement relating to the
terms and conditions of their employment
within two months of starting work. This may be
provided in the form of a letter of engagement
and/or written contract.
The law allows the employer to issue the
written statement in instalments but certain
key information should be included in a single
principal document. These are:
• Names of employer and employee;
• Date when employment began;
• Scale or rate of pay;
Continued on following page...
C / ALL
,
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
8
1.2 The practice must provide a written statement of the main terms of
employment for all employees (L)
C / ALL
,
Continued...
• Pay intervals;
• Hours of work – taking into account the
Working Time Regulations;
• Holiday entitlement, including Public
Holidays;
• Job title;
• Job location.
Instalments added to the principal statement
should include:
• Sickness and injury rules;
• Details of pension arrangements. There
must be provision for a Stakeholder Pension
scheme where there are more than five
employees;
• Length of notice on both sides;
• Disciplinary rules;
• Grievance procedure.
The inspector will ask to see written statements/
contracts for veterinary surgeons, veterinary
nurses and all categories of support staff, but will
respect their confidentiality.
(Please note that the inspector will not be able
to comment on the legal correctness of the
contracts/written statements.)
The BVA provides sample contracts for its
members only. They are freely available to
download in PDF format from their website:
www.bva.co.uk, or contact the Technical
Development Officer at BVA: 7 Mansfield Street,
London W1G 9NQ T 020 7636 6541
F 020 7637 0053.
Continued on following page...
9
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
1.2 The practice must provide a written statement of the main terms of
employment for all employees (L)
1.3 The practice must provide written job descriptions for all veterinary
surgeons, veterinary nursing and other support staff (L)
C / ALL
,
Continued...
SPVS has a manual of forms available, including
contracts and terms and conditions.
A Self Help Guide to Producing a Written
Statement is available from ACAS – the Advisory,
Conciliation & Arbitration Service – by contacting
the National Helpline 0845 7474747 or via
www.acas.org.uk or via Head Office - address:
ACAS, Brandon House, 180 Borough High Street,
London SE1 1LW.
An Advisory Booklet Written statement of
employment particulars (PL 700) is available
from most offices of the Employment Service and
Job Centres.
Additional assistance is available from the
Department for Business, Enterprise and
Regulatory Reform T 020 7215 5000;
E enquiries@berr.gsi.gov.uk.
Please note: as requirements may change,
practices should check with individual
organisations that forms/samples supplied are up
to date.
C / ALL
,
The inspector will ask to see examples of each
type of job description within the practice and
that they are reviewed annually. A job description
exists to define the role of the employee within
the practice, their areas of responsibility and a
clear understanding of their day-to-day duties.
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
10
1.4 The practice must have an equal opportunities policy that is known to
all staff (L)
1.5 The practice must have a non-discrimination policy that is known to
all staff (L)
1.6 The practice must have written requirements for a professional
standard of behaviour, personal hygiene and appearance to be
maintained by all members of the practice at all times. A biosecurity
policy must also be available
C / ALL
,
A written policy is required which may be part of
the Terms and Conditions of Employment.
,
C / ALL
A written policy is required.
,
C / ALL
The inspector will ask to see the written policy
relating to veterinary surgeons, veterinary nurses
and all categories of support staff. This may be
part of Terms and Conditions of employment,
job contracts or a separate Standard Operating
Procedure (SOP). This policy is to help portray a
professional image and comply with Health and
Safety advice.
The practice biosecurity policy should include
disinfection of personal protective equipment and
clothing and cleanliness of vehicles.
11
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
1.7 The practice must have protocols, known to all relevant staff, for
dealing with members of the public
Written protocols required.
The hospital must employ at least one Registered/Listed veterinary nurse, with respon-
GP / ALL
,
The inspector will ask to see written protocols for
staff dealing with members of the public.
The inspector will ask to see guidelines where
appropriate for such things as:
• Staff induction procedure;
• Client confidentiality;
• Answering the telephone/greeting clients;
• Appointment procedures and recognition of
emergencies;
• Practice policy for home, farm, stable, and
yard visits;
• Complaints procedure;
• Practice arrangements for out-of-hours cover,
referrals and second opinions;
• Practice arrangements for acceptance of
incoming referrals;
• Vaccination, parasite control and neutering
policies (where applicable);
• Prescribing – dispensing policy;
• Systems/training for those assisting a
veterinary surgeon;
• PETS passports, TB testing, exports and other
OV activities.
Where veterinary nurses are carrying out work
under Schedule 3 of the Veterinary Surgeons
Act 1966, the inspector will require evidence
of suitable training. Where suppport staff are
required to assist with clinical activities, the
inspector will ask to see evidence of suitable
training. Evidence may be provided verbally, with
the inspector speaking to a cross-section of staff.
The aim for the future is that the requirement
for employment of Registered/Listed VNs will be
extended to GPs. Also, that SA/EQ Hospitals will
be required to increase the number of Registered
/Listed VNs employed by them.
VH / SA
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
12
sibilty for nursing in the hospital.
The hospital must employ at least one Registered/Listed equine veterinary nurse.
1.8 Veterinary surgeons and veterinary nurses must undertake Continuing
Professional Development (CPD)
CPD records must be provided for all veterinary surgeons and veterinary nurses in the
practice team to satisfy the RCVS requirements as a minimum.
A written policy encouraging CPD for all veterinary surgeons, veterinary nurses and
VH / EQ
The inspector will ask to see the CPD records of
all the veterinary surgeons and veterinary nurses
showing the details of CPD undertaken. This
must provide evidence that at least the minimum
CPD recommended by the RCVS is being
undertaken. (It is required that Listed Veterinary
Nurses will undertake the same requirements as
Registered Veterinary Nurses.)
For veterinary surgeons, the minimum
requirement is 105 hours over three years (an
average of 35 hours per year). For Registered
veterinary nurses the requirement is 45 hours
over three years. The practice team includes full-
time and part-time employees, as well as locums
and others supplying veterinary services on a
regular or ‘ad hoc’ basis.
C / ALL
,
GP / ALL
,
The inspector will ask to see a written policy
encouraging CPD for all veterinary surgeons,
veterinary nurses and clinical support staff.
Up-to-date reference material may be provided
from a range of sources (eg books / e-library)
provided that they are demonstrable to the
Inspector.
While there are no restrictions on the areas of
CPD undertaken by individuals it is expected that
a significant proportion of CPD will be relevant to
the overall types of work undertaken by the both
the individual and the practice as a whole.
13
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
clinical support staff is required, as well as CPD records for all qualified staff.
Suitable up-to-date reference material must be freely available and accessible to all
staff.
The hospital must have at least two certificate holders (one with a component covering
equine surgery) on the veterinary team. Other certificates may be in any discipline
that has an equine component.
A one-year CPD plan must be provided for the hospital team.
,
It is recognised that where a certificate holder
leaves a practice, some time may be required
for obtaining a replacement. Evidence should
however be provided of the steps taken to ensure
continuity in compliance with this standard.
The aim for the future (2015) is that VH/EQs
will have one Diplomate in Equine surgery to
replace the current Certificate holder; and that
VH/SAs will have at least one Certificate holder
in a discipline appropriate for the workload of the
practice.
VH / EQ
VH / ALL
,
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
14
1.9 The practice must have in place an annual performance review system
for all clinical staff to monitor and plan development
,
C / ALL
This would include:
• PDP for newly-graduated veterinary surgeons;
• Developing Schedule 3 skills for veterinary
nurses (if appropriate);
• Developing skills for current and new
equipment and technology.
It is expected that this would inform training
needs and direct future CPD both for individuals
and to meet the overall needs of the practice.
It is expected that members of staff will explain
to the inspector how developmental needs have
been discussed and any issues addressed.
15
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
2 CLINICAL GOVERNANCE & COMMUNICATION
2.1 The practice must have a system in place for monitoring and
discussing the clinical outcome of cases and for acting on the results
The inspector will ask to see some system for monitoring and discussing the clinical
outcome of some common procedures. This may vary from clinical audit reports to
notes of clinical discussion meetings but inevitably starts with some form of record
keeping.
Regular Morbidity and Mortality meetings should be held to discuss the outcome
of clinical cases. Hospitals must be able to produce records of such meetings and
demonstrate any changes in procedures as a consequence of any resultant action list.
Continued monitoring to assess the effectiveness of any changes must be undertaken.
GP / ALL
,
For all practices:- this is a developing area and
practices should avail themselves of the skills
and information available through individual
organisations such as the BCVA, BVHA, BSAVA,
BEVA, SPVS, VPMA, BVA.
A recommended starting point would be rates of
post-surgical infection and actions taken/ discus-
sion of significant events and resultant action.
Significant events could, for example, include
unexpected reactions/critical incidents/peri-
anaesthetic deaths, but could equally include
positive outcomes.
For FA practices, a starting point might be a
record of outcomes of operations, unexpected
deaths and actions taken.
Auditing of the standard of hospital procedures
is encouraged and may become mandatory in the
future (VHs).
VH / ALL
,
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
16
2.2 The practice must access and use animal health data from the farms
under their care
Evidence must be available of pro-active farm health management. The inspector will
expect to see the use of farm data.
2.3 The practice must have an effective means of communication with its
clients
The practice will need to demonstrate how it communicates with all, or the majority,
of its clients.
The practice must provide evidence of pro-active communication with clients
• Client training or general meetings to be held at least twice a year;
• Newsletters to clients at least quarterly.
The practice must ensure that the public are aware of the identity of the individuals
involved in the care of their animals.
,
GP / FA
This may take the form of access to Herd
Companion, Interherd, CIS (Cattle Information
Service) records as well as ready access to farm
records, farm-specific advisory notes for some or
all of the practice clients.
C / ALL
,
This could be by means of waiting room notices,
newsletters/brochures, invoice messaging, general
mailings, emails, websites or client meetings
and will include at least opening hours/services
provided/contact numbers.
,
GP / FA
It is acceptable for client training/general
meetings to be held jointly with another
practice(s). The inspector will expect to see
evidence of the meetings/training, for example,
the contents of meetings, issues focused upon,
as well as a record of the key points discussed.
GP / ALL
It would be acceptable for clients to be made
aware of the identity of individuals by such
means as badges/picture boards/websites/
newsletters. The inspector will check that only
Registered and Listed veterinary nurses are
identified as ‘veterinary nurses’.
17
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
2.4 The practice must have a means of monitoring client perceptions and
feedback
The practice must have a means of recording and considering client complaints.
The practice must have a written complaints policy and must keep a record of
complaints received and the responses made.
The practice must have a means of encouraging feedback from clients and acting
upon the results of feedback.
C / ALL
,
GP / ALL
VH / ALL
,
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
18
3 OUT-OF-HOURS PATIENT CARE
3.1 The practice must take steps to provide 24-hour emergency cover for
the care of animals of those species treated by the practice during
normal working hours
A veterinary surgeon must, if in practice, take steps to provide 24-hour emergency
cover for those species treated by the practice during normal working hours, including
attending away from the practice premises on the rare occasions when in the
veterinary surgeon’s professional judgement it is deemed necessary.
The inspector will ask to see the written duty rota or formal written arrangement with
an alternative veterinary surgeon/practice and by what means the practice informs
clients of the out-of-hours arrangements. It is acceptable for clients’ initial contact to
be with an automated or remote device such as an answering machine used to give a
duty telephone number.
24-hour emergency cover must be provided by a veterinary surgeon suitably trained in
farm animal practice. A protocol must be available to ensure that back-up is available
if required.
The inspector will ask to see what arrangements are made for surgical emergencies
to ascertain that a suitably trained person would be available to assist in the
administration of a general anaesthetic. (It is recognised that this may not be relevant
for FA practices where the use of general anaesthesia would not be commonplace.)
Initial direct contact with a mobile telephone is not acceptable, unless a back-up
C / ALL
Please refer to the Code of Professional Conduct
and Guidance note 3. While no acceptable
time or distance is specified, as each will be
influenced by local conditions, when making
arrangements for the provision of 24-hour
emergency cover, practices should give
consideration to these factors. Practices should
check carefully that their written contract/
agreement with another practice or Accredited
Emergency Service Centre (ESC) establishes
clearly who is responsible for out-of-hours home
visits, on the rare occasions that such visits may
be necessary.
,
,
GP / FA
Back-up may be by telephone/by personal
attendance, as appropriate.
Reliance by a practice on individuals
predominantly working in other disciplines would
not be considered as meeting the requirement
without evidence of ongoing training/levels of
training attained.
,
GP / ALL
VH / ALL
19
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
landline is used as well. This would mean that incoming calls to the mobile telephone
must be diverted to a landline if the mobile telephone is not answered.
Out-patients
The hospital must make arrangements for the provision of 24-hour emergency cover
either:
By making a veterinary surgeon available 24 hours a day to attend animals on site;
or
In the case of a SA Hospital, by outsourcing the provision of 24-hour emergency cover
to another SA Hospital or to a designated Small Animal Emergency Service Clinic.
(ESC) (See Section 10).
The inspector will require to see the formal written arrangement entered into between
the SA Hospital and the SA Hospital/ESC.
4 PREMISES AND OUT-PATIENT FACILITIES
VH / ALL
For a practice to provide out-of-hours emergency
cover to a Small Animal Hospital, it must either
be another SA Hospital or an accredited ESC
under the Practice Standards Scheme (ie it must
fulfill all of the GP requirements as well as the
additional requirements set out in Section 10 of
the Manual). All Hospitals must continue to care
for their own in-patients. Accredited ESC status
requires at least one on-duty veterinary surgeon
to “be on the clinic’s premises at all times during
all of the hours of operation of the clinic.” This
does not preclude a veterinary surgeon attending
off-site in the rare circumstances that this may
be necessary. Practices should therefore check
carefully that their contract with an ESC estab-
lishes clearly who is responsible for out-of-hours
home visits, on the rare occasions that such visits
may be necessary on clinical or welfare grounds.
VH / SA
,
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
20
4.1 The practice premises must be accessible, well maintained and kept
clean (L/BP)
The premises must be in good decorative order, clean and well maintained so as to
create an atmosphere of clinical cleanliness and efficiency. The premises must be free
of offensive odours, and be kept in an orderly condition. Cleaning Schedules must be
produced on a regular basis and be routinely audited. All parts of the premises must
be adequately lit and ventilated. Adequate storage facilities must be provided. The
area immediately surrounding the premises must be maintained in a clean and tidy
state.
The buildings must be constructed of brick, stonework, or other substantive materials.
The internal walls and floors of in-patient areas must be impervious so as to permit
thorough cleansing and disinfection. The join between the floor and the wall must
have a curved finish to aid cleaning, with the coving being carried at least 75mm up
the wall. All joints in the flooring material or coving must be impervious and finished
flush with the surface. Stick-on coving is not acceptable.
Emergency lighting must be provided to allow the hospital to continue to function in
NOTE: GP requirements set out in sections 4.1/4.2/4.4/4.5/4.7 MARKED ++ (FA)
WILL ALSO APPLY TO GP/FA where practice premises (other than administrative
offices or drugs and other equipment storage facilities) are provided.
C / ALL
The premises must be suitable and adequate for
its intended purpose. Buildings must be heated
to fulfill minimum legal requirements (ordinarily
16ºC), as appropriate.
In the event that this Standard is not met, it is
recommended that a list of decorative shortcom-
ings be written down at the time of inspection.
GP / SA &
.EQ ++ (FA)
,
The Standards currently only require coving in
“in-patient areas” so that coving in waiting areas,
and consulting rooms is not to be insisted on.
VH / ALL
VH / ALL
Both emergency background lighting to
enable safe evacuation of the premises and
an uninterruptable source of light/power for
completing surgery, in the event of a power
failure, are required.
If powered lifts are used in equine practices it is
essential that emergency power or an alternative
mechanical means of lifting is available to
ensure the ability to lift/move the patient upon
completion of all procedures.
,
21
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
the event of a power cut or electrical failure. Additional emergency power/lighting, to
permit the completion of essential tasks such as operative surgery, must be provided
by a back-up generator, portable rechargeable lighting units, uninterruptable power
supplies or similar devices. Simple torches are not sufficient as emergency back-up in
operating areas.
Adequate temperature regulation must be available for efficient functioning of the
hospital staff and equipment.
Heating may be required so that the ambient temperature can be maintained above
18 degrees Celsius in the working area of the building. In addition, cooling may be
required to avoid working temperatures exceeding 26 degrees Celsius. Maximum/
minimum thermometers must be provided and records kept.
There should be adequate back-up power supply to enable intraoperative radiography
to be performed.
4.2 The practice must provide a waiting room or reception area of
adequate size, with sufficient seating, for the normal caseload of the
practice. Staff must have access to appropriate staff amenities (L/BP)
Office and reception facilities must be provided which are easily accessible to clients
VH / EQ
C / ALL
The inspector may ask to see the appointment
diary or enquire about the busiest times to assess
if the waiting room or reception area is adequate.
Appropriate staff amenities should include toilets
and handwashing facilities.
Staff refreshments must not be prepared in
clinical areas.
GP / SA &
.EQ ++ (FA)
It is acceptable for these to be available “on
request” on an ad hoc basis. No general signpost-
ing is required.
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
22
and staff as appropriate. Sufficient telephone capacity and reception staff must be
provided to meet the workload of the practice.
Toilet and washroom facilities must be available to staff and clients and maintained in
a clean and orderly manner. These do not need to be separate facilities.
The inspector will require to be satisfied that arrangements are in place suitable for
the workload of the practice for clients to contact the practice, book appointments
and arrange visits.
The waiting area must be designed to encourage reasonable separation of dogs, cats
and other predator/prey species, and nervous animals.
4.3 Any other commercial businesses run from the practice must be of an
acceptable professional nature
The display of commercially retailed merchandise within the veterinary premises shall
be permissible, provided the display is of an acceptably professional nature and of
relevant goods. Medicines must not be available for self-service except those with a
category AVM-GSL.
There must be separate accommodation for hospital patients and animals being
groomed. Any boarding or grooming business must be separate from hospital facilities.
Public areas (waiting room, reception, public toilets) and staff facilities (rest-room,
toilets, offices) may be shared.
4.4 Where consultations are carried out at the premises, the practice must
have one or more consulting areas, which provide a clean, hygienic
environment for consultations in private
The consulting area may be used for other purposes, provided that hygiene is not
compromised.
A stretcher or trolley must be provided for the safe transportation of heavy animals.
GP / FA
VH / SA
Where absolute separation cannot be achieved,
a protocol for achieving separation as necessary
should be available.
C / ALL
VH / SA
C / ALL
C / SA
23
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
There must be an adequate number of examination rooms. The size and number of
examination rooms must be sufficient for the normal workload of the practice. There
must be sufficient space for the veterinary surgeon, nurse, patients and client(s).
Privacy must be ensured by adequate soundproofing, and must allow complete closure
from the public (ie doors and windows that close, windows with blinds).
The area used for unloading, loading and examination of large animal patients must
be able to be secured to prevent escape of the patient.
There must be appropriately designed facilities in which detailed examinations of
horses, as well as diagnostic procedures such as diagnostic analgesia, radiography,
ultrasonography and endoscopy can be performed. An area suitable for trotting and
lunging horses must also be available.
An appropriate area out of sight of the general public must be available for the safe
euthanasia of horses.
A facility for the unloading of emergency cases close to the examination/induction
area is essential. A loading ramp must be available in a quiet secure area for non-
emergency cases.
A covered area suitable for farriery must be available at the practice.
A trot up area, which must be dedicated, level, firm and 25 metres long, and a firm
area for lunging horses, must be available on site. An all-weather exercise area must
also be available on site.
4.5 The floor area and table in the consulting area must be made of
GP / SA ++
.(FA)
“Consultation Area” for Farm Animal Practices
could, in certain circumstances be the “back of a
truck”. However, if animals are being off-loaded
(and not examined on-trailer) - the area must be
secure. It would be acceptable to tailgate into a
building so long as the vehicle was driven right
up to the building. If unloading takes place into
an open car park, there must be a gate to close
off the car park.
GP / EQ ++
(FA)
GP / EQ
Please note: for GP/EQs the area for trotting and
lunging need not be on the pratice premises so
long as it is available.
VH / EQ
C / ALL
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
24
materials suitable for thorough cleaning and there must be adequate
washing and disinfection facilities
The floor finish must be such as to reduce the risk of the patient slipping and/or
falling. Every examination area must have a hand basin available for use by staff and
clients either within or immediately adjacent to the consulting area. Procedures must
be in place to minimise cross-infection in clinical areas. Particular attention should
be paid to high contact areas such as phones/door-handles/keyboards and clinical
equipment used. Each room must have facilities for safe disposal or sharps, hazardous
and non-hazardous waste.
There must be a hand basin within each consulting area available for use by staff and
clients.
4.6 Basic diagnostic and surgical equipment, appropriate to the practice,
must be readily available in the consulting area(s) (BP)
A minimum of a stethoscope, thermometer, ophthalmoscope and auroscope must be
available in the practice, which may be shared between consulting areas.
At least the following must:
a. be present in each vehicle: stethoscope, thermometer, foot-trimming equipment,
basic obstetric equipment, flutter valve and basic surgical equipment, waterproof
boots and outer clothing and a means of disinfection after each visit.
b. be otherwise available: sterile operating kits appropriate for the species and
procedures generally encountered and in date equipment for the collection and
storage of laboratory specimens.
Stomach tubes and shoe removing/hoof kit must be available, as well as sterile
operating kits for procedures generally encountered and in-date equipment for the
collection and storage of laboratory specimans.
Minor surgical instruments such as scissors and forceps must also be available. An
X-ray viewer must be easily available within the out-patient area.
Equipment for the measurement of systolic blood pressure must also be available.
This may be measured by oscillometric or Doppler methods.
GP / SA &
.EQ ++
VH / SA
C / ALL
C / FA
It is accepted that equipment in each vehicle
may vary depending on the species treatment, so
that, for example, the needs of a poultry practice
will differ from a cattle practice. Equipment must
be appropriate for the range of species treated by
the practice.
GP / EQ
GP / SA ++
(FA)
VH / ALL
25
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
Equipment for the measurement of intraocular pressure must be available. This may
be measured by Schiotz tonometer or by electronic methods.
Suitably constructed stocks for the restraint of patients are required.
4.7 There must be adequate ventilation and lighting in the consulting
area, as appropriate to the work undertaken
At least one examination area must be able to be darkened.
4.8 The practice must have a means of estimating the weight of species
routinely treated
Charts must be available.
Weigh tapes/bands or scales must be provided.
Scales must be provided to allow accurate weighing of the full range of species
routinely treated. The weight of all patients to be anaesthetised must be routinely
recorded.
4.9 Likely charges must be discussed with clients and updated as
necessary
Discussion should take place with the client covering a range of treatment options and
prognoses, and the likely charges (including ancillary or associated charges and likely
post-operative care) so as to ensure that the client is in a position to give informed
consent. The practice must be able to provide written estimates on request.
4.10 Itemised invoices must be available at the request of the client
VH / SA
VH / EQ
C / ALL
GP / SA &
.EQ ++
C / ALL
For example, standard weight tables.
GP / EQ
VH / EQ
GP / SA &
C / ALL
,
The inspector will ask to see how fee estimates
are generated and what procedures are in place
to update and inform clients of ongoing costs.
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
26
Itemised invoices may be produced by computer or manually and must include a
breakdown of services, drugs and consumables, VAT and any surcharges.
4.11 The practice must maintain an efficient system of documenting and
filing clinical records and comply with the Data Protection Act
(L)
Where appropriate, records must be maintained for each animal or herd. There must
be adequate back-up for computerised records.
An efficient system of recording, filing, and locating records must be in operation.
C / ALL
The Data Protection Act 1998 (as amended) sets
out eight enforceable principles of good practice
with which all organisations processing personal
data, even if exempt from notification, must
comply. These require data to be:
• fairly and lawfully processed;
• processed for limited purposes;
• adequate, relevant and not excessive;
• accurate;
• not kept longer than necessary;
• processed in accordance with individual’s
rights;
• kept secure;
• not transferred to other countries without
adequate protection.
Practices may be exempt from notification if
they are processing data only for the following
purposes of their own business:
• accounts and records;
• staff administration;
• contacting own clients.
Evidence of registration under the provisions of
the Data Protection Act (if appropriate) should be
provided.
C / ALL
,
C / ALL
Different organisations (eg Veterinary Defence
Society/Veterinary Medicines Directorate/
HM Revenue and Customs) will have different
requirements for the length of time records
should be kept. Practices should check
directly with these organisations for up-to-date
information.
27
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
Records must be maintained so that any veterinary surgeon coming into the practice
may, by reading the records, be able to proceed with the continuity of care of the
patient.
Complete records must contain the following information, where applicable:
• Owner identification - name, address, contact telephone numbers;
• Patient identification - name, species, breed, colour, age, sex, radio frequency
identification device or tattoo number and weight (re FA – individual animal
identification may be useful and held by the practice but is not compulsory);
• Dates - of all examinations, investigations, and treatments;
• Clinical information – history and details of clinical examination, investigations,
provisional diagnosis and treatments;
• Vaccinations - batch numbers and dates (re FA – All treatments – batch numbers
and dates)
• Special considerations – abnormal drug reactions by patient or client, concurrent
clinical conditions;
• Repeat prescriptions – authorisation and review date;
• External communications – referrals, lab reports;
• Consent forms and estimates.
There must be facility for easy referral of patients from a branch surgery to the full
facilities available at a hospital. The clinical records system must be capable of
passing patient records between branches and the hospital.
Records must also include therapeutic and nursing plans.
4.12 Vehicles routinely used for practice must be clean and well maintained
GP / ALL
VH / ALL
C / ALL
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
28
and equipped sufficiently to enable basic procedures to be performed
at the client’s premises
The contents must be organised in such a way to give the appearance of
professionalism and enable the medicines carried to be stored according to the
manufacturers’ recommendations.
There must be clear segregation of clean and contaminated items and protective
clothing and safe storage and transport of waste materials, including sharps.
The inspector will view as many vehicles as practicable to be reasonably sure that this
Standard is met.
29
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
5 IN-PATIENT FACILITIES
5.1 When animals are admitted for any diagnostic or surgical procedures,
informed consent must be sought
The inspector will require to see evidence that informed consent is sought for all
procedures.
Signed consent forms are required for all procedures when a patient is admitted to
the care of a veterinary surgeon. This will include: diagnostics, medical treatments,
surgery and euthanasia.
5.2 In-patient facilities must be secure, in good condition and sufficient
for the workload of the practice
Any in-patient facilities must be of a suitable size, securable, sturdy, escape-proof,
without potentially injurious faults and easily cleanable. A range of bedding, feed
stuffs and clean fresh water must be available.
Washing and disinfectant facilities must be provided for staff in the kennels annd
cattery.
Dirt trays, absorbent litter and adequate cage space are required for feline in-patients.
Sanitary facilities for ambulatory canine in-patients must be provided. These may be
outside and precautions must be taken to prevent the escape of animals.
Feeding equipment must be disposable or regularly disinfected.
NOTE: ALL GP requirements set out in sections 5.1/5.2/5.3/5.7/5.8 and marked
++(FA) WILL ALSO APPLY TO GP / FA PRACTICES if inpatient facilities are provided).
C / ALL
For further information, see Code of Professional
Conduct and Guidance note 11 and the
Veterinary Defence Society website:
www.veterinarydefencesociety.co.uk
,
GP / SA &
.EQ ++ (FA)
“Admitted” means where an animal is in the
care of the veterinary surgeon and is outwith the
presence of the owner.
C / ALL
C / SA
The expectation is that each ward area will have
its own sink located in the ward. Where this is
impossible, and the nearest sink is located in
an adjacent room, then consideration must be
given as to whether the room in which the sink
is located is in a ‘clean’ or a ‘dirty’ environment.
As ‘dirty’ procedures are done in the ward area,
it would generally be unsuitable for the sink
or access to it to be via a clean environment.
Additionally, consideration must be given to the
touching of the door handles; it would not be
acceptable for staff to use their hands to open a
door to access a sink in the adjacent room.
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
30
There must be the ability for hospitalisation of the full range of species routinely
admitted.
There must be a range of accommodation of a suitable size for the number and
species routinely treated. There must be adequate heating, lighting and ventilation of
this area. A suitable range of bedding materials, feeding utensils and sanitary facilities
must be provided. There must be suitable provision for the storage and preparation of
food. A range of diets must be available to meet the needs of in-patients and stored
appropriately.
The inspector will ask to see the daily surgery log and appointment list to correlate
with in-patient facilities available.
Washing, disinfection and food storage facilities that are separate from those in the
clinical areas, must be provided for staff.
Equipment that will be in contact with the patients must be chosen to minimise the
risk of cross-contamination or exacerbation of any clinical condition.
There must be a positive means of identifying the patient while on the premises. This
may involve tagging the patient and/or well-identified accommodation.
Facilities to maintain body temperature (eg heat pads) must be available.
Facilities to provide supplementary oxygen must be available.
Re: GP/SA - Suitable cages must be available for
day hospitalisation. It is acceptable for patients
requiring overnight hospitalisation to be trans-
ferred elsewhere, where it is in the interests of
the patient.
Re: GP/EQ – At least one stable suitable for
accommodating horses overnight must be
available.
GP / SA &
.EQ ++ (FA)
GP / SA &
.EQ ++ (FA)
,
GP / SA ++
(FA)
31
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
There must be a minimum of six kennels or cages for the hospitalisation of patients.
Towels, blankets, or acrylic bedding materials must be provided. The kennels or cages,
and their fittings, must be made of non-permeable materials so as to be easily cleaned
and disinfected. Where dogs are treated there must be at least one large kennel
suitable for a giant breed of dog together with a good range of smaller kennels and
cages. At least one cage must be of the walk-in type. There must be no overcrowding.
Newspaper alone is not considered a suitable bedding material for overnight stay
patients.
There must be the ability to cater for the full range of species treated and species
segregation where appropriate. In particular, consideration must be given to separation
of prey and predator species.
Facilities must be provided for the bathing, grooming, and drying of in-patients.
Heat pads must be available for in-patients. Sanitary facilities for ambulatory canine
patients must be provided indoors, under cover or outside within the site boundary.
Suitable facilities for neonatal care must be provided.
There must be provision for the cooking of fresh food for in-patients. Refrigeration is
necessary for storage of fresh foods.
There must be a minimum of six stables. Stables must be made of non-permeable,
durable material to allow easy cleaning. There must be a stable of suitable size to
accommodate a mare and foal.
There must be facilities for adequate, hygienic, safe storage and disposal of bedding.
Ready access to an exercise yard or paddock of suitable size must be provided with
safe and well-maintained fencing.
Facilities must be provided for the routine washing, grooming and handling of
patients.
VH / SA
VH / EQ
See section 4.4 GP / EQ – the lunging area
referred to may double as the exercise paddock.
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
32
5.3 The practice must provide facilities and adequate nursing staff for the
care of any in-patients
The practice must have a written policy for the overnight care of in-patients detailing
who is responsible, frequency of checks etc. The owners must be informed of the level
of overnight supervision during an overnight stay.
All hospitalised animals (other than short/routine surgical procedures admitted as day
cases) must have in-patient sheets recording basic husbandry parameters, with timed
and initialled entries:
• Temperature;
• Pulse;
• Respiration;
• Treatments;
• Food and water intake;
• Urine and faeces output;
• Clinical signs;
,
C / ALL
The inspector will ask to see what arrangements
are made for the care of in-patients (if
applicable) including information given to
clients regarding the level of care given. This
may include a written duty rota for a nurse or
veterinary surgeon on call to regularly attend the
practice or for the transfer of in-patients to a
more appropriate practice.
Practices are encouraged to use Registered/Listed
VNs to provide the nursing care of in-patients
whenever possible.
The inspector will wish to be satisfied that all
post-op cases are being monitored until dis-
charged from the premises.
GP / SA &
.EQ ++ (FA)
33
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
A person directly responsible for the nursing care of in-patients must be within the
curtilage of the site at all times. There must be a minimum of daily examination of all
in-patients by a veterinary surgeon, which should be recorded on the hospital records.
There must be residential accommodation or other arrangements so that a veterinary
surgeon, veterinary nurse or an adequately trained member of lay staff is present on
the premises 24 hours a day, every day of the year. There must be reasonable and
secure night-time access from the residential accommodation to the hospital facilities
(it is not acceptable for staff members to have to step on to a public highway); 24-
hour continual nursing attention must be available, if needed, for in-patients, and a
veterinary surgeon must be available 24 hours a day to attend in-patients.
5.4 The practice must provide separate accommodation for the isolation of
infectious and zoonotic cases or have a written policy for dealing with
such cases that is known to all members of staff
The inspector will expect to see a Standard Operating Procedure (SOP), which details
the procedure for isolation and care of infectious cases. Either separate isolation
facilities must be provided along with the SOP, or, if such facilities are not available,
there must be a detailed SOP for isolation of infectious cases, including barrier-
nursing requirements.
Staff must be trained to implement the SOP, which must include:
• Details of waste disposal;
• Protective clothing to be worn;
• Disinfection of all utensils/equipment and accommodation;
• Designated persons to be responsible;
• Reference to COSHH and Health and Safety information pertaining to the risks of
dangerous pathogens and zoonoses;
• Clear information regarding the demarkation of the isolation area.
Evidence of the monitoring and up-to-date
hospital records will be looked at.
For hospitals, a veterinary surgeon or other
responsible person (not necessarily, but prefer-
ably a Listed/Registered VN or enrolled student
VN) should be on the premises 24/7 in order to
meet public expectations for a hospital. It is not
acceptable only to have a presence on the
occasions when there are in-patients already in
the building.
VH / ALL
C / ALL
,
Where truly separate and self-contained isolation
facilities are not available, there must be a
detailed SOP setting out how infectious cases are
to be dealt with or referred elsewhere. Sending
patients home is insufficient.
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
34
A hospital must have the ability to isolate an infectious animal from all other patients.
Isolation facilities must have:
• Hand-washing facilities;
• Separate air space;
• Ventilation that produces a negative air pressure in the facility to reduce the risk of
cross-infection;
• Separate drains to avoid cross-infection.
Isolation facilities can mean either a special area to which access is limited or a
separate ward. It is recommended that there is a written policy, which details the
procedure for isolation and care of cases including barrier-nursing requirements. The
written policy must be available to relevant staff who must be fully conversant with its
contents.
Isolation facilities must be provided.
5.5 The practice must provide a range of intravenous fluids, suitable
administration sets and catheters for those species routinely treated
Intravenous fluids must include blood volume expanders and crystalloids. There must
be the ability to deliver controlled small qualities of intravenous fluids (eg Burettes).
There must be the ability to provide close control of fluid replacement by an infusion
pump or syringe driver suitable for infusion of high volumes rapidly or low volumes
slowly. Facilities for blood transfusion must be available.
Provision must be made for continuous administration of intravenous fluids at an
appropriate rate.
VH / SA
In ward areas, ventilation could be arranged for
air to be drawn from cleaner areas to isolation or
contaminated areas and thence extracted from
the building. The underlying principle is that the
risk of any cross-infection should be minimised,
therefore airflow should be from “clean” to
“dirty” areas, rather than “dirty” to “clean”.
,
VH / EQ
The isolation box should be separate from the
general-use boxes, and must not be a stable
within an American barn set up where the air
space is shared. It could possibly be on the
end of a row of externally-opening stables but
it should open in the opposite direction to the
others. It must not share air space with the other
boxes (ie walls must extend to the ceiling all
round), must not drain into a common area and
must be accessible for all purposes (treatment,
feeding, mucking out etc) without crossing the
general stable or treatment area. There should be
separate PPE, tack and mucking-out equipment
and access to the box must be restricted to
limited personnel who must wear protective
clothing. There should ideally be separate
handwashing facilities.
GP / SA
VH / SA
VH / EQ
35
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
5.6 Area used for the conduct of surgical procedures
This area must have easily cleanable surfaces and a good source of illumination.
The operating theatre must be available for the conduct of sterile surgery at all times
– it must not double up as a consulting room. It must only contain equipment for use
in surgical procedures and X-ray equipment. There must be a written procedure for
the maintenance of a surgically clean environment. A separate preparation area for the
clipping of patients must be provided. There must be an adjustable-height operating
table. Scrub facilities must be separate from ward washing facilities. Lighting
suitable for the accurate illumination of surgical sites on the patient must be provided
in the theatre.
A means for displaying radiographs must be available in the theatre.
The induction of, and recovery from, general anaesthesia are high risk for both
patient and handler. If undertaken, there must be an area that is appropriate for
the procedures to be undertaken, bearing in mind patient and handler safety. The
induction area can also be the operating area providing surgical cleanliness/sterility is
not compromised and is appropriate for the procedure undertaken.
A suitable and safe system of transporting horses between the operating area and the
induction/recovery area (if different) must be available.
C / ALL
,
A separate area for clipping does not mean that
a practice has to have a separate room used
exclusively for preparation purposes. The clipping
area may be situated in a room that has another
function; it cannot, however, be in the operating
theatre.
An autoclave can be placed in an operating
theatre, provided that there is a suitable SOP for
maintaining asepsis.
Endotracheal tubes should not be stored on the
wall of the operating theatre. Anaesthetic circuits
are permissible.
GP / SA
A laptop or mobile X-ray viewer or digital display
screen would be acceptable.
GP / SA ++
.(FA)
GP / SA ++
.(FA)
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
36
A preparation room must be provided, separate from the operating theatre, for the pre-
operative preparation of surgical patients. Scrubbing-up facilities must be provided,
with suitable elbow, foot, or electric-eye operated taps. The scrubbing-up facilities
must be separate from those provided for cleansing and disinfection and adequately
screened from the operating table(s).
At least one operating theatre of adequate size must be provided and used only for
the conduct of surgical operations. Such operating theatres shall not be used for the
pre-operative preparation of patients, or for any purpose which could compromise their
use for aseptic surgery.
The operating theatre must be a closed room with no through traffic. There must
be no clear view of the interior of the theatre by the general public from outside the
premises. Doorways must be sufficiently wide for access into the theatre by trolleys.
Where possible, all fittings in the theatre must be flush with the walls and ceilings.
Orthopaedic operations must be performed as the only procedure in the theatre (at any
one time).
Electrosurgery and suction must be available for surgical use. There must be a high
standard of surgical asepsis (eg surgical gloves must be worn during all aseptic
procedures). All personnel must wear scrub suits and hats in the theatre and no
outdoor shoes or clothing are allowed. Consideration must be given to the order in
which procedures are undertaken, with those most likely to introduce contamination
being done last.
A clock with a sweep second hand must be visible from within the operating theatre.
Lighting suitable for the accurate illumination of surgical sites on the patient must be
provided in the theatre. This lighting must continue to function in the event of loss of
power. An operating lamp must be supplied by an uninterruptable power supply or a
generator sufficient to complete a surgical procedure.
There must be a provision for performing aseptic intra-operative radiography.
VH / ALL
The inspector may want to observe a surgical
procedure.
A written protocol for maintenance of asepsis
should be produced.
,
VH / EQ
Continuous lighting which is suitable to complete
operative surgery must illuminate automatically
in the event of power failure.
37
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
An operating table of adjustable height, and capable of holding the patient in a tilted
position, must be provided in the operating theatre.
Provision must be made to remove a horse from the operating table in case of winch
failure.
5.7 The practice must have equipment for the administration of oxygen
and the safe maintenance of anaesthesia
Equipment for the administration of oxygen and the safe maintenance of anaesthesia
and resuscitation must be appropriate for the species treated.
There must be adequate facilities for the induction and maintenance of general
anaesthesia in the full range of species routinely treated. Equipment must be
available for the maintenance of body temperature during anaesthesia and recovery.
A range of endotracheal tubes must be available. Anaesthetic circuits suitable for
the range of patients routinely treated must be provided. Circuits must include a
circuit suitable for small patients such as a T-piece, a circuit suitable for medium-
sized patients, such as a Lack or a Bain, and a circuit suitable for a giant breed of
dog such as a circle unit, or a high flow rate mechanism for a non-rebreathing unit.
There must be a source of oxygen and emergency oxygen flush with reducing valve,
rotameter and vaporiser. Temperature-compensated vaporisers must be used. The use
of uncompensated vaporisers is not permitted except when used in-circuit such as in
the Stephen’s machine.
There must be suitable means of resuscitation. A resuscitation pack must always
be maintained and be readily available for instant use, and checked to ensure the
contents are in date.
VH / SA
A tilting table is advised but not compulsory at
this stage, as long as other means of tilting are
available.
VH / EQ
C / ALL
GP / SA &
.EQ ++ (FA)
GP / SA ++
(FA)
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
38
A range of induction and maintenance agents must be stocked to permit anaesthesia
of all patients treated including the high risk patient. There must be adequate primary
and reserve supplies of oxygen.
There must be adequate means of supportive therapy under anaesthesia. Facilities for
lengthy intermittent positive pressure ventilation must be provided.
5.8 The practice must provide suitable monitoring for anaesthetised
patients
A veterinary surgeon should administer general anaesthesia if the induction dose is
either incremental or to effect.
A member of staff adequately trained in monitoring patients under general anaesthetic
must be present throughout the procedure.
A trained member of staff, other than the surgeon, must be present to monitor
the patient throughout the general anaesthetic. Evidence of suitable training must
be provided if the member of staff is not a Listed/Registered veterinary nurse.
Anaesthetic charts must be filled in for each patient (except in emergency or for very
short procedures (eg cat castrate).These charts must form part of the clinical records.
Also:
• at least one other monitoring device must be available eg oesophageal
stethoscope, pulse oximeter, capnograph, ECG.
• The charts must include:
* Date;
* Personnel involved;
* Induction agent;
* Maintenance agent;
* Duration of anaesthetic;
* Surgical procedure;
* Any anaesthetic complications;
* Vital signs.
Mechanical ventilation is required for EQ
Hospitals. It is not, however, a requirement for
SA Hospitals. These must be able to provide IPPV
for as long as is necessary and must be able to
demonstrate to inspectors how this is undertaken
safely, whether mechanically or manually.
VH / ALL
C / ALL
GP / SA
,
In-house training is acceptable, but must be
evidenced to the inspector. The inspector will
wish to speak to those put forward as having
competency in anaesthestic monitoring.
39
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
All general anaesthesia must be induced and maintained by an MRCVS. Anaesthetics
lasting more than an hour must be adequately monitored by a veterinary surgeon and
must include monitoring by direct arterial blood pressure measurement and ECG.
Monitoring must be available including pulse oximetry and capnography, blood
pressure measurement facility, and oesophageal stethoscope. Records of vital signs
and agents employed must be retained. Evidence of staff training in the use of
monitoring facilities must be provided.
There must be adequate post-anaesthetic monitoring. An anaesthetic monitoring
room or area must be available and records must be maintained until the animal
has recovered. Proper ventilation must be provided to limit staff exposure to exhaled
gases.
5.9 There must be a programme of regular care and maintenance of
anaesthetic equipment (L/BP)
Anaesthetic equipment must be subject to professional maintenance according to the
manufacturers’ recommendations. Regular service records must be produced for all
anaesthetic equipment.
5.10 The practice must provide facilities for the scavenging of anaesthetic
gases (L)
Scavenging must comply with current health and safety laws.
Facilities for scavenging include any device or ducting system for the removal of waste
gases from the operating area:
• Passive scavenging – by duct to the open air;
• Charcoal absorbers – eg Aldosorb;
• Active scavenging – via a pump and air break device.
GP / EQ
VH / SA
The criteria should not be interpreted to imply
that every piece of monitoring equipment is
required for every operation. What is required
should be based on a risk assessment and will
depend on the number and nature of operations
performed – practices should ensure that
equipment provided is adequate for the work
actually undertaken.
VH / ALL
,
C / ALL
The inspector will ask staff how equipment is
checked before use on a daily basis.
C / ALL
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
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5.11 The practice must carry out monitoring of anaesthetic pollutants in
operating areas and maintain written records of this (L)
Written evidence of measurement of personal exposure to anaesthetic monitoring is
required. Monitoring must be carried out on an annual basis, or if the nature of the
anaesthetic equipment and circuitry is changed.
Inspectors will check that the readings recorded fall within the current Workplace
Exposure Limits for the agent(s) used. These are currently:
10ppm Halothane
50ppm Isoflurane
60ppm Sevoflurane
100ppm Nitrous oxide
All these values are subject to review and are calculated on an eight-hour Time
Weighted Average (TWA) basis.
If a sophisticated active scavenging system is in operation, it must be serviced
annually. An inspection certificate must be available and is an acceptable alternative
to personal dosimetry.
5.12 The practice must have disinfection and/or sterilisation facilities
suitable for the work undertaken
There must be adequate facilities for sterilisation, and a recognised method of
sterilisation must be employed.
The practice must provide an autoclave, vacuum or non-vacuum or other recognised
sterilisation systems, for the effective sterilisation of instruments and equipment.
Sterile gloves and gowns must be available and used where appropriate.
Appropriate external and internal sterility indicators for the system employed must be
used to monitor the efficiency of the technique.
,
,
C / ALL
External sterility indicators should be employed
in all instances; internal and external indicators
are necessary in wrapped/bulky packs. (Internal
indicators are not required for single instruments/
non-bulky packs).
GP / ALL
41
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
Sterile packs must be provided in sufficient quantity to meet the workload of the
practice.
Sterile packs must have the sterilisation date marked on them, and there must be a
written practice policy on when re-sterilisation will be required.
Vacuum autoclaves are compulsory.
Vacuum autoclaves are compulsory for wrapped packs/drapes.
5.13 The practice must provide a range of suitable surgical instruments and
suture materials for the work undertaken
Sterile packs for emergency surgery must be available at all times.
Surgical instruments must be provided for the following types of procedures:
• General;
• Dental;
• Ophthalmic.
Orthopaedic surgery, including facilities for the repair of fractures.
Orthopaedic instrumentation must include arthroscopic and internal fixation
equipment.
5.14 There must be a Written Scheme of Examination for all autoclaves
within the practice, as required under Pressure Systems Safety
Regulations (2000). A current certificate of inspection must also be
available (L)
For autoclaves and dental compressors greater than 250 bar litres, a separate Written
Scheme of Examination and Certificate of Inspection are required.
GP / ALL
,
VH / EQ
VH / SA
C / ALL
GP / ALL
VH / ALL
VH / SA
VH / EQ
C / ALL
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A Written Scheme of Examination must be titled as such, and must specify how and
when the autoclave(s) must be inspected. Practices must also have a Certificate of
Inspection under the regulations. It will be titled Certificate of Inspection under the
Pressure Systems Safety Regulations (2000).
5.15 Provision of dental equipment
If the dental machine has a compressor greater than 250 bar litres it requires a
written Scheme of Examination.
A selection of hand scalers, curettes, periodontal probes, elevators and/or luxators
must be available suitable for the range of species to be treated.
The instruments must be sharp and evidence of training of staff in the proper use,
sharpening and instrument care must be available. Personal protective equipment
should include aprons, face masks, goggles and disposable gloves.
A range of angled and straight hand held rasps and a gag must be available.
Facilities must be available to mechanically scale and polish teeth.
Facilities must be available to mechanically section teeth and perform surgical
extractions. Suitable cooling water must be available at the operative site. High speed
air driven dental hand pieces are recommended. Electrically driven hand pieces may
be used.
Suitable facilities for performing rabbit dentistry should be available (Including
suitable gags, anaesthesia, rasps). Rabbit incisor teeth should be mechanically
trimmed. Clipping the teeth would not be considered acceptable.
,
Only pressure vessels over 250 bar litres
are covered by the Pressure Systems Safety
Regulations (2000). All autoclaves would come
into this category and each would require both a
written Scheme of Examination and Certificate of
Inspection. Dental machines are unlikely to work
at such high pressure and so are usually exempt
from the provisions.
NB - A service is not necessarily an inspection
under the regulations, and a note of the last
service is not a written Scheme of Examination.
A Written Scheme may be obtainable from the
manufacturers.
C / ALL
C / ALL
C / EQ
GP / SA
43
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
Proper dental records and treatment charts must be maintained. Suitable summaries
must be made on the patient main record.
Measures must be employed to reduce aerosol contamination of other areas, especially
the sterile operating theatre.
Dentistry must never be performed in surgical theatres. Suitably-powered air extractors
in the dental area will be of assistance.
The use of sterilised dental packs for each procedure is expected.
Suitable facilities to obtain dental radiographs must be available. This will require the
use of intra-oral and non-screen films or digital facilities.
Motorised dental equipment and evidence of training in their use must be available.
,
GP / SA
Specific measures to prevent contamination
beyond the immediate dental area must be taken.
These might include use of suction tips close to
the operating head of scalers and dental hand
pieces, an extraction fan close to the operating
site or ideally a dedicated dental procedure room
with negative pressure ventilation.
VH / SA
VH / EQ
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6 DIAGNOSTIC EQUIPMENT AND FACILITIES
6.1 The practice must:
Provide ultrasonographic equipment capable of acquiring good quality images of the
flexor tendons of the distal limbs, superficial structures and per rectum images of the
ovaries and uterus.
Provide (or demonstrate an ability to access where necessary) ultrasonic equipment for
the full range of species treated.
Provide an ultrasound system capable of providing diagnostic quality images of the
full range of species treated.
Provide electrocardiography equipment producing a recordable trace suitable for
taking measurements.
Electrocardiography Recordings (ECG) must be suitably filed and stored. Use of a
remote diagnostic facility is acceptable.
Facilities must be available for bone marrow aspiration.
Endoscopes must be provided to allow diagnostic investigation of the upper and lower
digestive tract and upper airway/trachea of appropriate species.
A pair of biopsy forceps must be available.
GP / EQ
Evidence must be provided of training or CPD for
staff in use of the equipment. Reference material
must be available.
GP / SA
,
VH / SA
,
VH / ALL
Evidence must be provided of training or CPD for
staff. Reference material must be available.
It is recognised that there are few courses for
endoscopy. “In-house” training could be provided
by one individual in a practice to another. In
this case the approach accepted would be that
competency should not be purely taken on trust
and that more will be expected in the inspection
process. The inspector will wish to speak to those
put forward as having competency in endoscope
use, and depending upon the responses given, for
the inspector to decide upon what (if any) further
issues might be raised (eg look at what reference
material is available, look at evidence of use by
reference to clinical cases).
,
VH / SA
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C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
L Legislative Requirement ++(FA) The Standard is to be met by GP/FA, if applicable
Diagnostic ultrasound will require sector and linear transducers with a frequency range
of 2.5 to 7.5 MHz. A recording system for images must be available.
Endoscope(s) of an appropriate quality suitable for the workload of the hospital must
be provided. A pair of biopsy forceps must be available.
6.2 X-ray facilities
Evidence must be provided of diagnostic quality radiographs of all parts of the range
of species treated. There must be sufficient provision for the non-human physical
restraint of SA patients during radiography and regular inspection of safety equipment
must be recorded. Sufficient means of mechanical restraint must be provided for the
range of species treated. Core SA/EQ practices must be able to demonstrate what
system/procedure/protocol is in place if a patient requires an X-ray and this facility is
not available within the practice.
There must be X-ray facilities suitable for the range of species routinely treated.
Equine practices must have equipment to X-ray distal limbs.
Radiographic facilities must be suitable and adequate for the needs of the hospital
and be readily available at all times.
It must be possible to obtain diagnostic radiographs in adult horses of the head, the
cervical and thoracic spine, the chest, the fore and hind limbs including shoulder,
pelvis and stifle.
VH / EQ
C / SA / EQ
For an individual premises (branch or main
practice) to be accredited as a GP there must be
X-ray facilities actually available on site in those
premises.
GP / SA
The equipment and a competent radiographer
must be readily available at the practice at
all times; it cannot be available intermittently
through, for example, an external provider.
GP / EQ
VH / ALL
VH / EQ
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6.3 A suitable and sufficient assessment of the risks of ionising radiation
must be made for the purpose of identifying the measures to restrict
exposures to employees and other persons (L)
The risk assessment must be sufficient to demonstrate that:
• All hazards with a potential to cause a radiation accident have been identified;
• The nature and magnitude of the risks have been evaluated.
Where the risk assessment shows the existence of a risk of a reasonably foreseeable
radiation accident, the radiation employer shall take all reasonable steps to:
• Prevent any such accident;
• Limit the consequences of any such accident;
• Provide employees with such instruction and training as is necessary to restrict
their exposure.
6.4 The practice must appoint a radiation protection adviser (RPA) who
possesses appropriate knowledge and experience relevant to veterinary
practice (L)
The inspector will ask to see an agreement with an RPA, including the scope of the
activities upon which advice is required. RPAs previously appointed under IRR85
must be reappointed in writing. The inspector will ask to see a copy of the last RPA
report, together with evidence that any recommendations have been complied with.
C / ALL
,
The precise frequency of visits by an RPA will be
discussed and agreed between the RPA and the
practice. Material changes in eg equipment or
workload must be notified to the RPA, who will
decide if a visit is required.
Practices should note that a Certificate of
Competency issued to an RPA does not
automatically denote experience of veterinary
practice and suitable enquiries should be made.
A list of the RPA 2000 Certificate holders is
available from
http://www.rpa2000.org.uk/lists-of-certificate-
holders-and-available-consultants
C / ALL
47
C Core Standards GP General Practice VH Veterinary Hospital SA Small Animal FA Farm Animal EQ Equine ESC Emergency Service Clinic
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6.5 The practice must appoint a Radiation Protection Supervisor (RPS) in
writing (L)
The RPS must command sufficient authority to supervise the work so that it is
performed in accordance with the local rules and have an adequate understanding
of the requirement of the Ionising Radiation Regulations. They must also know what
to do in an emergency. The inspector will ask to see a written appointment of one or
more suitable RPSs.
6.6 The practice must notify the Health and Safety Executive (HSE) of
their use of ionising radiations (L)
Veterinary use of ionising radiations requires prior notification to the HSE at least 28
days before commencing such work for the first time. Where any subsequent changes
are made to the work with ionising radiations, which would affect the particulars given
in the notification, the changes must be notified to the HSE immediately.
C / ALL
,
,
In the absence of a copy of the letter sent by the
practice to HSE (and for practices in business
for a number of years and without any formal
documents) the practice should send a fax or
email ([email protected].uk) to the HSE and retain
a copy of the notification for their records.
There is no specific form for notifying HSE but
notification must be in writing to the local HSE
office and the inspector will require to see a copy.
Notification should include:
• Name and address of Radiation Employer;
• Address of premises where the work is carried
out;
• Nature of the business of the employer;
• Category of the source of the ionising
radiations;
• Whether or not any source is to be used at
premises other than the address of the work
premises;
• Dates of notification and commencement of
the work activity.
C / ALL
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6.7 A copy of Guidance Notes for the Safe Use of Ionising Radiations in
Veterinary Practice (IRR 1999) must be available to all members of
the practice
These guidance notes do not seek to give detailed and comprehensive advice on all
aspects of the use of ionising radiations in the veterinary profession and the practice
must have consulted a RPA.
6.8 There must be a system of personal dose monitoring for all persons
entering the controlled area as agreed with the appointed RPA.
Records must be maintained of the doses received for at least two
years (L)
The arrangements for personal dose monitoring must be made in consultation with the
RPA.
6.9 Written local rules must be approved by the RPA and clearly displayed
to all staff (L)
Local rules must be displayed in the X-ray room and MUST contain:
• Name of RPS;
• Controlled area – when and where it exists;
• Dose investigation level;
• Contingency plan;
• Written arrangements;
• Name, address and telephone number of RPA;
• Duties of RPS;
• How entry to controlled area is restricted;
• Arrangements for maintenance of equipment
• Dosimetry arrangements;
• Use, storage and inspection of Personal Protective Equipment (PPE).
,
C / ALL
Copies are available from the BVA.
,
C / ALL
Any personal dose meters should normally be
worn on the trunk. They must not be left inside
a controlled area when not being worn and
must be stored away from sources of ionising
radiationsand extremes of temperature. They
must only be worn by the person to whom they
are issued.
,
C / ALL
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Clinical staff involved with radiography must sign to indicate that they have read
and understood the local rules. Separate local rules must be agreed with the RPA in
respect of any separate dental X-ray equipment.
6.10 A controlled area must be designated in accordance with advice from
the RPA. It must also be adequately described in the local rules,
physically demarcated where practical and provided with suitable and
sufficient signs and warnings, all in accordance with the RPAs advice
(L)
A specified room must be provided for radiography. It is desirable but not essential
that the room is used solely for radiography. The controlled area should be designated
according to the RPAs advice and usually requires a red warning light at each
entrance to the X-ray room, which should be wired so as to illuminate automatically
while the X-ray machine is in use.
6.11 The X-ray machine must be serviced annually and there must be
written evidence of a satisfactory report (L)
6.12 The X-ray machine must have a functional light beam diaphragm
The X-ray beam must be collimated so as to leave a margin of unexposed film on all
edges of the radiograph.
,
C / ALL
C / ALL
,
C / ALL
The inspector will ask to see the X-ray machine’s
service records.
C / ALL
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6.13 Sufficient personal protective equipment must be provided and
examined at regular intervals (L)
When necessary, the practice must provide at least one protective apron with a lead
equivalence throughout of not less than 0.25mm, and, if animals are ever held,
must provide hand and forearm protectors with a lead equivalence of not less than
0.5mm, sufficient for all personnel involved. When not in use, aprons should be hung
over large diameter bars to avoid damage. All protective clothing must be thoroughly
examined on an annual basis.
6.14 Suitable cassettes and positioning aids must be provided (L/BP)
A range of foot blocks and cassette-holding devices must be available and be used so
as to ensure that no part of any person is exposed to the primary beam.
No animal should be held unless there are clinical reasons why they cannot be
restrained by other means. Suitable drugs and equipment for anaesthesia or sedation
must be available. Positioning aids such as sand bags, cradles, wedges and ties must
be suitable for the range of species routinely treated.
A good quality grid must be available. A suitable range of cassettes, screens or digital
alternatives must be available.
Screen film combinations or digital systems to minimise exposure while providing
the necessary level of detail must be used. Screens must be kept clean. Measuring
callipers, or other suitable devices, must be available to determine accurately the
depth of the part being radiographed.
The hospital must be able to perform a range of contrast examinations and a suitable
range of contrast material must be available.
Personal protective equipment may not be
required where a practice confirms that:
• Animals are never held; and
• There are no circumstances where staff enter
the controlled area when the x-ray machine is
switched on; and
• The isolation switch for the machine is
located out with the controlled area; and
• The practice provides written confirmation
from their RPA that the situation is
acceptable.
C / ALL
C / EQ
C / SA
GP / SA
A range of grids suitable for species routinely
treated should be available. This should include
a grid and cassette of at least 30cm x 40cm. The
underlying principle is that x-rays of a large dog’s
chest may be taken in one picture to avoid errors
in two frames.
VH / ALL
51
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6.15 A chart of commonly used exposures must be available
6.16 A record of all X-ray exposures, which contains a chronological record
of the patient details, date, region radiographed, exposure factors and
personnel involved must be available/easily retrievable (L/BP)
This must provide a permanent record of all X-ray exposures and records and identify
the persons involved. Suitable back-up must be provided for the electronic files
produced by digital radiography.
The detailed record of X-ray exposures must contain:
• Patient identification;
• Breed;
• Area exposed/view;
• Exposure factors;
• Type of film/grid/screen;
• Date;
• Quality of the resultant radiograph;
• Names of any personnel present.
Original x-ray plates should be retained or scanned and kept in computerised form.
The sole use of self-adhesive labels for the identification of radiographs is not
acceptable. Radiographs should be identified at the time of the exposure.
6.17 There must be suitable film processing facilities (used and maintained
in accordance with the manufacturer’s instructions to avoid wasted
exposures). The film processing area must be ventilated (L/BP)
Good film processing techniques are essential to avoid unnecessary exposures.
In particular, the development time, temperature and replenishment must be in
accordance with the manufacturers instructions.
A chart of commonly used exposures is more
accessible than an X-ray logbook and helps to
reduce the number of incorrect exposures.
,
C / ALL
GP / ALL
VH / ALL
C / ALL
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Unless digital radiography is in use, automatic processors with automatic
replenishment must be employed to develop radiographs instead of manual methods.
6.18 All X-ray chemicals must be stored safely and disposed of in an
appropriate manner (L)
Advice of relevant local water authorities must be obtained and recorded unless all
material is disposed of by a registered contractor.
VH / ALL
C / ALL
,
Silver traps may be used in accordance with
guidance/approval from the relevant local water
authority.
53
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7 LABORATORY AND POST-MORTEM FACILITIES
7.1 Provision of laboratory facilities and/or referral of samples to an
external organisation (L/BP)
Where pathological samples are sent to external organisations, a suitable range of
containers, envelopes and forms must be available. There must be an SOP for the
post and packaging of pathological samples which complies with current packaging
regulations.
There must be a clinical microscope, and facilities to assess packed cell volume,
prepare blood smears, and to measure blood glucose, blood urea concentrations and
urine specific gravity.
There must be a clinical microscope and facilities to assess packed cell volume and
total protein.
Laboratory facilities for routine diagnostic tests must be available at all times. Where
laboratory facilities are not provided on site, suitable arrangements must be made to
enable laboratory investigations on emergency cases.
Suitable arrangements must be made for the following detailed investigations:
• Biochemistry;
• Haematology;
• Parasitology;
• Bacteriology.
The following equipment must be provided on the premises:
• Binocular microscope with mechanical stage, electric light source and oil
immersion facility;
• Centrifuge suitable for PCV, blood separation and urine sedimentation;
• Urinary refractometer;
• Biochemistry analyser to include Creatinine, Urea, Glucose, Total Protein and
Calcium;
• Electrolyte analyser.
Laboratory facilities for biochemistry, haematology, parasitology, and bacteriology must
be available on the premises at all times.
C / ALL
,
GP / SA
It is acceptable for BUN testing to be done
off site. In that situation we would expect the
inspector to be provided with details of the
arrangements in place for obtaining results within
a reasonable time (reasonable to be considered in
light of the clinical necessities of the individual
practice under consideration).
GP / EQ
The reason for requesting these facilities is to
ensure that the practice is able to perform basic
diagnostic procedures at all times.
VH / SA
There must be the ability to look at smears on
site. Evidence must be provided of training or
CPD for staff in use of all equipment and in the
interpretation of results. Reference materials
must be provided.
VH / EQ
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54
7.2 The laboratory procedures must be performed in a clean and tidy
designated area used specifically for that purpose
The laboratory bench shall be made of impervious materials to permit proper cleaning.
There must be adequate facilities for washing of hands. There must be adequate
facilities for storage of specimens and reagents, including refrigeration, and disposal
of waste materials.
7.3 All laboratory procedures must be undertaken by designated persons
who are suitably trained in the tasks performed by them
A list of persons trained in handling laboratory specimens and in the risks of
laboratory work must be kept.
If bacteriology is undertaken on site, adequately qualified staff must be available. The
accurate interpretation of bacteriology plates requires staff qualified to HNC in
Applied Biology or equivalent standard.
If bacteriology is undertaken on site, adequately qualified staff must be available.
The accurate interpretation of bacteriology plates requires staff qualified to HNC in
Applied Biology or equivalent standard. There must be a nominated person in overall
charge of the laboratory facilities.
7.4 The results of all laboratory tests must be stored so as to permit easy
retrieval
Data must be stored safely in an easily retrievable form.
A complete recording system must be maintained of all tests undertaken in the
practice or by any outside laboratory. A system must be in place to track samples
referred to an outside laboratory to ensure results are obtained and communicated
promptly to the client.
The designated area does not have to be a
separate room and may, for example, be part of
the dispensary or the preparation area. However,
the designated area/bench must be clearly used
only for laboratory purposes.
C / ALL
C / ALL
,
GP / EQ
,
VH / ALL
,
The inspector will expect to see evidence of
storage of results.
C / ALL
GP / ALL
,
55
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7.5 There must be suitable arrangements for quality control (QC) and
assurance of automated practice laboratory tests
In addition to internal QC procedures, quality assurance by reference of internal
samples to external laboratories or internal analysis of external samples must be
routinely undertaken and results documented.
7.6 Adequate post-mortem facilities must be available or other
arrangements made
Post-mortem examinations on site must be performed in an area not concurrently
used for clinical work. This may be achieved by performing the examination after
clinical work has ceased or an external laboratory may provide facilities, in which
case, adequate licensed arrangements must be in place for the transport of carcases
for diagnostic quality examination to be performed. Adequate Health and Safety
procedures must be in place if post-mortem examinations are conducted on site.
When conducting post-mortem examinations full consideration must be given to the
health and safety issues associated with primates, birds and reptiles. Adequate risk
assessment and protocols need to be undertaken and consideration must be given
to the use of active filtered air extraction and the provision of suitable additional
adequate protective clothing, and the use of glove boxes or similar, to guard against
zoonoses.
GP / ALL
The inspector will expect to see results of the
external qualilty assurance.
The frequency of external quality assurance
testing should be related to the number of tests
undertaken. It is expected that this will be at
least quarterly.
,
When making arrangements for a post-mortem
examination the practice must ensure that clients
are made aware of the level of procedure being
undertaken, ie whether or not it will involve a full
pathological examination, as well as the costs
involved.
C / ALL
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56
8 MEDICINAL PRODUCTS
8.1 All medicinal products must be stored in a clean and tidy location in
accordance with manufacturers’ recommendations and appropriate
records kept (L)
A record of premises and other places where medicines are stored or kept must be
available.
All medicines should be stored in accordance with manufacturers’ recommendations
whether in the practice or in a vehicle. If it is stipulated that a medicine be used
within a specific time period, it must be labelled with the opening date, once
broached.
Accurate records of POM-V and POM-VPS medicines received and supplied must be
kept.
Records of medicines administered to food-producing animals must include batch
numbers; in the case of a product for a non-food-producing animal, this need only be
recorded either on the date of receipt of the batch or the date a veterinary medicinal
product from the batch is first supplied.
,
Under the Veterinary Medicines Regulations
(VMRs), it is necessary for a record to be kept at
a practice’s main premises of all premises and
other places where medicines are stored. This
could, for example, be homes where medicines
are kept for on-call purposes and practice cars.
The Record may be in any form, provided that it
is accessible to the inspector.
C / ALL
Premises should have Veterinary Medicinal
Product (VMP) storage areas clearly separated
from food / drink for human consumption and
toilet and washing areas
VMPs should be stored in areas that are not
accessible to the public. Medication should
be placed out of sight in closed cupboards
(not glass-fronted) or drawers but there is no
requirement for cupboards to be locked. It is
acceptable for small quantities of drugs to be
in consulting rooms for use during consultation.
These should be kept to a minimum and should
be in drawers/cupboards.
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There should be additional records of medicines administered to food producing
animals under the Cascade as detailed in Part 3 of the VMRs.
The pharmacy must be operated in accordance with the rules laid out in the
current BVA Code of Practice or alternative appropriate publication. Monitoring of
temperatures wherever medicines are stored must be undertaken (including consulting
rooms and prep rooms).There must be proper monitoring and recording of maximum
and minimum temperatures in the refrigerator and pharmacy, and where temperatures
have been recorded outwith the appropriate ranges, there must be evidence of
an action plan to remedy such deviations, and to deal with affected medicines.
Consideration should be given to the use of alarms to indicate when temperatures
stray out of set parameters. An adequate supply of medicines and materials used in
the treatment of patients must be readily available.
At least one member of staff must have completed an appropriate pharmacy course,
(for example, BSAVA Dispensing Course or Glasgow University dispensing course)
within the last five years.
8.2 There must be an efficient stock control and stock rotation system in
operation. Out-of-date medicines must be disposed of according to
current legislation (L)
There must be an efficient stock control system to ensure a continuous supply of
all medicines and removal of out-of-date medicines. At least once a year a detailed
audit should be carried out and incoming and outgoing medicines reconciled with
medicines held in stock and any discrepancies recorded.
A practice must be able to demonstrate to the inspector the ability to carry out a
detailed audit as clarified by the VMD; in addition, the inspector will ask to see a full
audit and reconciliation of all Schedule 2 controlled drugs (ie the Register - see 8.3
below – and the balance of drugs in stock).
Medicines should be disposed of in accordance with the relevant regulations.
,
If maximum and minimum temperature
recordings are being taken wherever medicines
are stored it is not necessary to take additional
recordings of ambient temperatures.
Data loggers and maximum/minimum
thermometers will provide constant monitoring.
However, for those without an alarm to warn
of temperature deviations, and for maximum/
minimum thermometers, checks are required to
be made daily and the inspector will ask to see
written records, produced on a weekly basis,
showing the results for the week.
,
VH / ALL
,
See VMD’s clarification note on record keeping
www.vmd.gov.uk/General/VMR/VMG07notes.htm.
This indicates that a system linking incoming
and outgoing transactions with stock held, for
example, may provide an ongoing running total
which, with the addition of a periodic physical
stock count to verify the stock held, may meet
the audit requirement.
Where an annual or more frequent stock take,
which includes the main features set out above,
is carried out for any reason such as, for example,
tax purposes, the VMD would consider that the
“detailed audit” requirement is being met.
C / ALL
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8.3 If Controlled Drugs are kept, these must be stored and recorded
according to current legislation (L)
Schedule 2 Controlled Drugs must be kept in a secure, lockable and immovable
receptacle that can only be opened by a veterinary surgeon or a person authorised
by him or her. A register of such drugs obtained, supplied and used must be kept in
accordance with the Misuse of Drugs Act 1971 (and the Misuse of Drugs Regulations
2001, as amended).
Controlled drugs are regulated by the Misuse of Drugs Act 1971 and the Misuse of
Drugs Regulations 2001 as amended. These regulations classify such drugs into 5
schedules, numbered in decreasing order of severity of control.
C / ALL
For information on the requirements on a CD
Register, see the BVA Code of Practice on
Medicines/The BSAVA Guide to Medicines.
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Schedule 1: Includes LSD, cannabis, and other hallucinogenic drugs, which are not
used medicinally. Possession and supply are prohibited except in accordance with
Home Office Authority.
Schedule 2: Includes etorphine, fentanyl, morphine, papaveretum, pethidine,
diamorphine (heroin), cocaine and amphetamine. Record all purchases and each
individual supply (within 24 hours). Registers must be kept for two calendar years
after the last entry. Drugs must be kept under safe custody (locked secure cabinet),
except quinalbarbitone. Drugs may not be destroyed except in the presence of a
person authorised by the Secretary of State. Failure to comply with this Act can lead
to prosecution.
Schedule 3: Includes butorphanol, buprenorphine, pentazocine, the barbiturates (eg
pentobaritone and phenobarbitone but not quinalbarbitone - now Schedule 2) and
others. Subject to certain exemptions, Schedule 3 drugs must be kept under safe
custody (locked secured cabinet), buprenorphine, diethylpropion and temazepam must
be kept under safe custody (locked secure cabinet); it is advisable that all Schedule 3
drugs are locked away. Retention of invoices for five years is necessary.
Schedule 4: Includes most of the benzodiazepines (temazepam is now in Schedule 3)
and androgenic and anabolic steroids (eg clenbuterol).
Schedule 5: Includes preparations (such as several codeine products) which, because
of their strength, are exempt from virtually all Controlled Drug requirements other than
the retention of invoices for five years.
Ketamine may be the subject of misuse and, therefore, must be stored in the
controlled drugs cabinet and its use recorded in an informal register.
,
The inspector will ask to see the Controlled
Drugs cabinet and registers (a register should be
kept for each controlled drug) and prescriptions
against which supplies of Controlled Drugs of
Schedule 2 and 3 have been made, to confirm in
particular that:
• Appropriate records are kept;
• That any out-of-date Controlled Drugs have
been destroyed by an authorised person;
• For supplies of Controlled Drugs of Schedules
2 and 3, against other veterinary surgeon’s
prescriptions;
* The prescriptions have been retained at
least two years;
* The date on which the supply was made is
marked on the retained prescriptions;
* The supply of Controlled Drugs was made
within 28 days of the appropriate date
on the prescription (also for supplies of
Controlled Drugs of Schedule 4);
* The name of the person who collected
the controlled drugs is recorded in the
Controlled Drugs Register (for Controlled
drugs of Schedule 2 only).
C / ALL
,
The requirements for entries for the informal
ketamine register are the same as for the Register
(though the entries need not be signed). It is
expected that running totals will be kept and
checks against stock carried out at least weekly.
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8.4 Medicines must be prescribed and supplied according to current
guidelines (L)
POM-V and POM-VPS medicines may be prescribed and supplied by a veterinary
surgeon. Alternatively, medicines may be prescribed and a prescription written
by a veterinary surgeon and the supply made by another veterinary surgeon (or a
pharmacist) on the authority of that prescription.
PRESCRIBING GENERALLY
• A veterinary surgeon who prescribes a POM-V medicine must first carry out a
clinical assessment of the animal and the animal must be under his or her care
(See Code of Professional Conduct and Guidance note 4).
• A veterinary surgeon who prescribes a POM-V or POM-VPS medicine must be
satisfied that the person who will use the product will do so safely, and intends to
use it for the purpose for which it is authorised.
PRESCRIBING WITHOUT SUPPLYING
If a veterinary surgeon prescribes by written prescription (for supply by another
veterinary surgeon or a pharmacist), in addition to the requirements for prescribing
generally, he, or she must:
• Each time he or she prescribes the medicine advise on its safe administration and
as necessary on any warnings or contra-indications on the label or package leaflet;
• Not prescribe more than the minimum amount required for the treatment
(see exemptions in Schedule 3 paragraph 7 of the VMRs).
PRESCRIBING WITH SUPPLY
If a veterinary surgeon supplies a POM-V or POM-VPS medicine, in addition to the
requirements for prescribing generally they must:
• Advise on its safe administration and, as necessary, on any warnings or contra-
indications on the label, package leaflet;
• Not supply more than the minimum amount required for the treatment
(see exemptions in Schedule 3 paragraph 7 of the VMRs).
C / ALL
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[A Suitably Qualified Person (SQP) under the Veterinary Medicines Regulations is
under similar requirements for the prescription and supply of POM-VPS medicines.]
SUPPLY IN THE ABSENCE OF THE VETERINARY SURGEON
Having prescribed a POM-V or POM-VPS medicines, if the veterinary surgeon is not
present when the medicine is handed over, they must:
• Authorise each transaction individually before the medicine is supplied;
• Be satisfied that the person handing it over is competent so to do.
SUPPLY OF NFA-VPS MEDICINES BY A VETERINARY SURGEON OR SQP
If a veterinary surgeon or SQP supplies an NFA-VPS they must:
• Be satisfied that the person who will use the medicine will do so safely, and
intends to use it for the purpose for which it is authorised;
• Each time the medicine is supplied, advise on its safe administration and on any
warnings or contra-indications on the label, package leaflet;
• Not supply more than the minimum amount required for the treatment (see
exemptions in Schedule 3, paragraph 7 of the VMRs).
SHEEP DIP
In the case of supply of sheep dips, the customer/user must provide a certificate of
competence in the safe use of sheep dips and must be provided with two pairs of
gloves with every product prescribed and supplied, as well as a laminated notice.
A veterinary surgeon could meet the requirement
to authorise each transaction by:
• Handing over a medicine personally following
a consultation, or instructing a fellow member
of staff to supply the medicine;
• Making a note on a client’s records that
repeat prescriptions could be supplied to the
client;
• A member of staff taking a call from a
client and putting a medicine aside for the
veterinary surgeon to authorise before being
supplied;
• In the case of a client unexpectedly coming
into the practice, by a phone call to the
veterinary surgeon to authorise the supply.
C / ALL
,
The inspector will ask to see appropriate
protocols, certificate records and/or a random
sample of clinical records for evidence of
compliance with all these requirements. Re
SQPs, the inspector will ask to see SOP for
procedures for supplying POM-VPS/NFA-VPS.
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Sheep dip certificate numbers must be retained for at least three years.
8.5 All containers and outer packs must be dispensed by the practice
legibly and indelibly labelled with the following information (L/BP)
MEDICINES OTHER THAN POM-Vs
All such medicines supplied by the practice must be labelled in accordance with the
VMRs. Generally, such medicines must be supplied in a container (with labelling)
specified in the marketing authorisation for the medicine. It is advised that, in
addition, such medicines are labelled with the name and address of the practice
supplying the medicine.
For supply under the Cascade see below.
POM-V
All POM-V medicines supplied by the practice must be labelled with the following
information:
• The name and address of the animal owner;
• The name and address of the veterinary practice supplying the medicine;
• The date of supply;
• The words “keep out of the reach of children”;
• The words “for animal treatment only” unless the package or container is too small
for it to be practicable to do so;
• The words “for external use only” for topical preparations;
• The name and quantity of the product, its strength and directions for use.
MEDICINE SUPPLIED FOR USE UNDER THE CASCADE
Medicines for supply under the Cascade, must include the following additional
information:
• Identification of the animal or group of animals;
• Name of the veterinary surgeon who has prescribed the product.
And, unless already specified on the manufacturer’s packaging:
• Any special precautions;
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• The expiry date;
• Any necessary warnings for the user, target species, administration or disposal of
the product.
The inspector will ask to see a practice label produced and evidence that medicines
for supply are labelled appropriately.
Child-resistant containers must be used unless otherwise requested. Paper or
plastic envelopes are unacceptable as the sole container for dispensing of medicinal
products.
Tablets and capsules must be dispensed in crush-proof and moisture-proof containers.
Sachets and manufacturers’ strip or blister pack medicines should be dispensed in
paperboard cartons or wallets, or paper envelopes.
All labels must be mechanically or machine produced. Handwritten labels are not
acceptable.
8.6 Practices must make clients aware that they can request a prescription
(L)
Veterinary surgeons must:
• Ensure clients are able to obtain prescriptions, as appropriate (a veterinary surgeon
may prescribe a medicine of category Prescription Only Medicine, Veterinarian,
[POM-V] only following a clinical assessment of an animal under his or her care;
a prescription may not be appropriate if the animal is an in-patient or immediate
treatment is necessary);
• Subject to any legal restrictions, ensure there is adequate provision on information
on medicine prices, including the current prices for the ten relevant veterinary
medicinal products most commonly prescribed during a recent and typical three-
month period, to provide clients with a fair and representative illustration of the
practice’s medicines prices;
• Provide the price of any relevant veterinary medicinal product stocked or sold, to
clients or other legitimate enquirers making reasonable requests;
• If requested, inform clients of the price of any medicine to be prescribed or
dispensed;
• Where possible and relevant, inform clients of the frequency and charges regarding
,
C / ALL
VH / ALL
,
The inspector will ask to see evidence that the
practice complies with this guidance and that the
correct code of practice for prescription writing is
available for veterinary surgeons.
C / ALL
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further examinations of animals requiring repeat prescriptions;
• Provide clients with an invoice that distinguishes the price of relevant veterinary
• Medicinal products from other charges and, where practicable, provide clients with
an invoice that distinguishes the price of individual relevant veterinary medicinal
products;
• Advise clients, by means of a large and prominently displayed sign or signs (in the
waiting room or other appropriate area), with reference to the following:
* “Prescriptions are available from this practice.
* “You may obtain Prescription Only Medicines, Category V, (POM-Vs) from your
veterinary surgeon OR ask for a prescription and obtain these medicines from
another veterinary surgeon or a pharmacy.
* “Your veterinary surgeon may prescribe POM-Vs only for animals under their
care.
* “A prescription may not be appropriate if your animal is an in-patient or
immediate treatment is necessary.
* “You will be informed, on request, of the price of any medicine that may be
dispensed for your animal.
* “The general policy of this practice is to re-assess an animal requiring
repeat prescriptions every [xx] months, but this may vary with individual
circumstances. The standard charge for a re-examination is £[xx].
* “The current prices for the ten POM-Vs most commonly prescribed or supplied
during [xx] (a typical three-month period were:
* “[The ten drugs and prices listed];
* “Further information on the prices of medicines is available on request.”
• Provide new clients with a written version of the information set out in the sign or
signs referred to above, which may be set out in a practice leaflet or client letter or
terms of business document.
• On a continuing basis, take reasonable steps to ensure that all clients are provided
with a written version of the information set out in the sign or signs referred to
above, which may be set out in a practice leaflet or client letter
C / ALL
Precise wording need not be followed, but all
points should be covered in the sign.
The Prescription Notice/List of Top Ten Drugs
must be placed in a prominent position. The
Inspector will expect that any notice will be at
least A4 size, and clearly visible.
Reasonable steps may include a combination of
practice leaflets, client letters, information on
practice websites
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8.7 Medicines must be used in accordance with the legislation commonly
referred to as “the Cascade” (L)
The prescribing Cascade is contained in the Medicines (Restrictions on the
Administration of Veterinary Medicinal Products) Regulations 2004. If there is
no suitable authorised veterinary medicinal product in the United Kingdom for a
condition in a particular species, in order to avoid unacceptable suffering veterinary
surgeons may exercise their clinical judgement according to the “Cascade”, whereby
they select in the following order:
• A veterinary medicinal product authorised in the United Kingdom for use with
another animal species, or for another condition in the same species;
• If, and only if, there is no such product that is suitable, either:
* A medicinal product authorised in the United Kingdom for human use or
* A veterinary medicinal product not authorised in the United Kingdom but
authorised in another European Member State for use with any animal species
(in the case of a food-producing animal, it must be a food-producing species)
(see Special Import Certificate VMD Guidance Note 7);
• If, and only if, there is no such product that is suitable, a veterinary medicinal
product prepared extemporaneously by a pharmacist, a veterinary surgeon or a
person holding a manufacturing authorisation authorising the manufacture of that
type of product;
• If a veterinary surgeon considers that there is not a suitable veterinary medicinal
product authorised in the UK or another EU Members state to treat a condition
then it is possible to apply for a Special Treatment Certificate (STC) to import a
suitable authorised product from outside the UK. A STC will not be issued if a
suitable product is authorised and available in the UK or in another EU Member
State.
,
The inspector will wish to see evidence that off-
label medicines are clearly identified to owners
who give informed consent for their use. Written
forms for signature are expected. Human generic
preparations must not be used other than under
Veterinary Medicines Guidance Note 15 (VMG15)
which allows for the welfare of animals to be a
primary consideration in the choice of treatment.
It is not acceptable to use an all embracing
“general” lifelong consent for any and all off-
label products that might be given to any animal,
though it would be acceptable where there is
a specific ongoing condition requiring off-label
drugs for a lifelong consent form to be used.
Similarly in the case of eg exotics where there
are no licensed products available, this would
be acceptable. The inspector will ask to see
completed off-label forms – not just that a stock
of blank forms is held.
Records of products administered to food-
producing animals under the cascade should
contain the following information, going back five
years:
• The date the veterinary surgeon
examined the animals;
• The name and address of the owner;
• The identification and the number of animals
treated;
• The result of the veterinary surgeon’s clinical
assessment;
• The trade name of the product if there is one;
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8.8 The practice must have access to advice from a service providing
veterinary specific advice on management of poisons .
Evidence of a current contract should be provided or an SOP must show how to access
the information in an emergency.
8.9 A practice must be able to access SARSS report forms (L)
Adverse reactions in humans or animals to medicinal products must be reported
promptly to the Veterinary Medicines Directorate and/or to the manufacturer. A
protocol is required that recognises when the use of SARSS forms is necessary.
Completed copies should be retained and form part of the clinical records.
8.10 The practice must have a Wholesale Dealers Authorisation (WDA) if
over 5% of the Veterinary Medicinal Products annual turnover is from
wholesale trade
• The manufacturer’s batch number; shown on
the product, if there is one;
• The name and quantity of the active
substances;
• The doses administered or supplied;
• The duration of treatment; and,
• The withdrawal period.
Where a whole herd/flock is treated with a
medicine, it may be acceptable to record ‘whole
herd’ or ‘whole flock’ and not every individual
animal’s number.
,
GP / ALL
It is not necessary to have a formal annual
contract. An SOP to show how information is
being assessed, for example, via websites on a
‘pay-as-you-go’ basis would be acceptable.
,
The inspector will ask to see the protocol so as
to be satisfied that the practice will be able to
recognise any adverse reactions and also ask the
practice about the frequency of reporting. If there
have been any such reports, the inspector will ask
to see copies.
C / ALL
The inspector will ask to see a copy of any WDA
and evidence that Veterinary Medicinal Products
are supplied only to approved businesses (WDA
holder, veterinary surgeon, SQP, pharmacist).
,
C / ALL
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9 SAFETY PROCEDURES
9.1 The practice must set out its policy for Health and Safety (L)
Under the Health & Safety at Work Act 1974, employers are required to have a policy
setting out how they ensure that risks to Health & Safety to employees, contractors
and customers are kept as low as is reasonably practical.
Where five or more people are employed (even if this is only temporarily) this policy
must be set down in writing. Such a written policy must include:
• A statement of general policy;
• Delegated responsibilities for dealing with specific areas
(eg equipment, substances, training, first aid, fire, reporting of accidents etc);
• General instructions to staff arising out of the significant findings of the risk
assessments.
Such a document must aim to be concise, pointing the reader to more detailed
guidance where necessary.
9.2 The practice must undertake Health & Safety risk assessments (L)
The Management of Health & Safety at Work Regulations 1999 requires employers
and the self-employed to identify:
• The hazards arising from their work;
• Who could be affected by those hazards;
• The measures to control the risk of those hazards causing harm.
,
The law applies when people are at work so will
also apply to farm/equine practitioners working
mainly from vehicles but also from home, and
where locums are used. Employers have duties to
ensure the health and safety of their employees
and this includes situations where work is carried
out at, or from, home.
Veterinary surgeons who are self-employed also
have duties towards their own health and safety
and that of third parties (eg their family/locum)
therefore, health and safety requirements do
apply in this situation (it would be unacceptable
for a home-based veterinary surgeon, for example,
to store veterinary drugs in a domestic cabinet
with other medication intended for the family:
suitable storage would be required). Equipment
used at home for work purposes also needs to
comply with health and safety regulations and
would be subject to maintenance and testing.
C / ALL
C / ALL
This includes employees, part-time staff,
trainees, clients, contractors and others who may
be affected by work activities.
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The measures identified by the risk assessment will include the need to comply
with other regulations (eg Ionising Radiations) as well as those to deal with specific
hazards not covered by regulations (eg the hazardous behaviour of animals). They
must, in order of priority, seek to:
• Eliminate the hazard (eg substitute a disinfectant containing glutaraldehyde with a
less hazardous one);
• Physically control access to the hazard (eg prevent entry into areas where ionising
radiations are being used);
• Provide information, instruction, training and supervision to ensure people work in
a safe manner (eg SOPs, safety signs, local rules, proper training);
• Consider if personal protective equipment needs to be provided (eg face masks or
goggles).
Where five or more people are employed, these significant findings of the risk
assessment must be recorded (often as an attachment to the Health & Safety policy).
Risks from the activities of work areas commonly found in veterinary work should be
assessed, and local rules formulated.
Activities/work areas to be considered would include both physical and psychological
health, for example:
• Cleanliness/tidiness;
• Disinfection;
• Handling and restraint of animals (including the use of on farm facilities);
• Manual handling and lifting of weights (with particular reference to aids for moving
heavy/paraplegic animals);
• Slips/trips/falls;
• Veterinary medicines/pharmaceuticals;
• Anaesthetic gases;
• Injection procedures (risk of self-injection);
• Risk to pregnant workers;
• Risk of work related stress;
• Proper use of work equipment:
* Display screen equipment;
* Office electrical equipment;
* Portable electrical appliances;
* Autoclave;
C / ALL
Risk assessments must still be undertaken and
policies formulated even where a practice has
five or less employees, but these do not have to
be in written form, although this is encouraged
in all cases. Where a practice with five or fewer
employees has no written risk assessment,
it should be able to explain the assessments
undertaken to the inspector.
,
,
Please note: these are examples only and
practices should refer to the HSE for further
information/consideration to be given to specific
matters that may affect their individual practices.
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* Dental machine;
* X-ray machine;
Anaesthetic equipment;
* Laboratory equipment;
• Laboratory procedures;
• Dental procedures using mechanical scaling;
• Security of staff, including provisions for lone/night working;
• Dealing with members of the public;
• Personal protective equipment;
• First aid, recording and reporting of accidents;
• Disposal of sharps, clinical, pharmaceutical, chemical and other waste (including
safe handling of spillages/leakages, broken and unwanted containers);
• Infectious disease/biological agents;
• Zoonoses; (eg fungal - ringworm; bacterial - salmonella; viral - birdflu)
• Working at height;
• Water supplies/air-conditioning maintenance;
• Transport and storage and use of gas cylinders;
• Vehicles and driving for work
• Risk assessments for the employment of young persons (under 18 years of age) are
required;
• A Risk Assessment assessing whether the practice premises does, or is liable to,
contain asbestos, any risk arising therefrom and action taken to manage risk, may
be required (Control of Asbestos at Work Regulations 2002 & 2006).
These rules must be displayed or have been drawn to the attention of all members of
staff and regularly reviewed.
C / ALL
Proper safety precautions must be taken for staff
on duty at night. An appropriate protocol for
dealing with night-time callers must be in place.
Suitable means must be available to enable staff
to call for immediate assistance when necessary.
In addition to undertaking risk assessments for
storage and transport of drugs and firearms, other
veterinary aspects of working out of a vehicle,
such as bio-security and waste disposal also need
to be considered.
Other considerations should include: is the
person a competent driver/appropriately licensed
for the vehicle they will drive? Are they aware of
the employer’s policy on work-related road safety?
This list is not exhaustive and would equally
apply to small animal practices providing vehicles
to staff members.
Under the 2006 Regulations, owners and
tenants with leases that include responsibility for
building maintenance must carry out a survey to
locate asbestos containing materials and record
their condition, which can then be used to assess
risks and decide what action is required. (See
HSE leaflet INOG223 (rev 3).)
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9.3 The practice must make arrangements to consult with staff on matters
of Health & Safety (L)
Employers have a legal duty to consult with their employees regarding Health &
Safety. This should include:
• The regular circulation of the Health & Safety policy amongst staff, including the
significant findings of risk assessments;
• The regular circulation of the results of any monitoring of Health & Safety
standards in the work place and action for their improvement;
• Not only giving information to employees but also listening and taking into account
what they say before making any health and safety decisions.
The inspector will ask to see evidence that staff have free access to the practice
Health & Safety policy, risk assessments and its regular updates. This evidence will
require staff to sign and date policies and reviews to confirm they have been read.
Updates may be annual or more frequently if hazards/risks change.
C / ALL
Consulting employees on health and safety
matters is a legal requirement and is more than
simply having health and safety documents on
site for staff to refer to and is very important
in creating and maintaining a safe and healthy
working environment. Through consultation, an
employer should motivate staff and make them
aware of health and safety issues. This helps to
improve efficiency and reduce the number of
accidents and work-related illnesses.
Consultation with employees must be carried out
on matters to do with their health and safety at
work including:
• Any change which may substantially
affect their health and safety at work ie in
procedures, equipment or ways of working;
• Changes to an employer’s arrangements for
getting competent people to help him or her
satisfy health and safety laws;
• Information must be given to employees on
the likely dangers arising from their work,
measures to reduce or eliminate these risks
and how they should deal with these risks;
and,
• Information on planned health and
safety training and any health and safety
consequences in introducing new technology.
,
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9.4 The practice must have a completed Health & Safety law poster, which
is displayed for all staff to see (L)
9.5 The practice must have appointed, in writing, a Safety Officer/Health
& Safety Representative amongst the staff (L)
9.6 The practice must have undertaken a thorough assessment of the risks
arising from the use of veterinary medicines substances hazardous to
health within the practice (L)
The risk to Health & Safety from veterinary medicines and other substances has to
be assessed under the Control Of Substances Hazardous to Health Regulations 2002
(COSHH). There is wide variation in risk – many are low to medium risk but there are
some substances in veterinary practice, which pose a very serious risk to health.
Implementing measures to control the exposure to low or medium risk substances
can be adequately achieved when they are assessed by their therapeutic group/type/
route of administration etc. The practice can set out standard measures to control
exposures, for example:
• Injectable anaesthetics;
• Pour-on anthelmintics;
• Steroidal compounds;
• Antibiotics.
,
Practices should note that an updated poster was
introduced with effect from April 2009. However,
the ‘old’ version issued in 1999 remains valid
until April 2014. As an alternative to a poster a
practice may give its workers a pocket card (as
approved by HSE). (The ‘old’ leaflet also remains
valid until April 2014.)
C / ALL
,
As part of the practice arrangements for
communicating with employees about issues
that may affect their Health & Safety, a Safety
Officer/Health & Safety Representative must be
appointed and have drawn up a written list of
duties.
C / ALL
C / ALL
,
Safety data-sheets are not legally required
for veterinary medicines and many medicine
companies do not produce them. Practices
should therefore ensure that they have access
to the current version of either the Summary of
Products Characteristics (SPC) or a data-sheet
for each authorised medicine used or stored
in the practice. Copies of the current NOAH
Compendium of Data Sheets are acceptable
to fulfill this requirement for those medicine
companies that participate. See www.vmd.gov.
uk/ProductInformationDatabase/Default.aspx (for
veterinary SPC) and www.emc.medicines.org.uk
(for non-veterinary SPCs).
It should be noted that the lists mentioned are
not exhaustive and practices should consider
their own individual medicine/substance usage.
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Within these groups, practices must identify any specific medicines or substances that
could have longer-term health risks, such as allergies eg Penicillin, or sensitivities eg
latex.
Specific and detailed assessments and the resulting measures to control exposure
must be made for high-risk substances such as:
• Any hormones;
• Oil-based vaccines;
• Cytotoxic drugs;
• Gluteraldehyde disinfectants;
• Micotil (tilmicosin);
• Large animal Immobilon (etorphine);
• Zoonoses
9.7 The practice must have appointed, in writing, a Fire Officer, and
drawn up a written list of the practice Fire Officer’s duties. A Fire Risk
Assessment must have been drawn up (L)
The inspector will ask to see a list of the practice Fire Officer’s duties and the Fire
Risk Assessment, including procedures for raising the alarm and evacuation. Where
gas/oxygen cylinders are being transported in practice vehicles, a 2kg dry powder
fire extinguisher is required in the vehicle. Evidence should be provided of suitable
hazard training.
C / ALL
The responsible person (eg employer, owner,
occupier) must carry out a fire safety risk
assessment and implement appropriate fire
precautionary and protection measures, and
maintain a fire management plan. For guidance,
see: www.communities.gov.uk/fire/firesafety/
firesafetylaw/aboutguides.
Hazard Training is any suitable instructions given
to the user. A risk assesment by a competent
person, with instructions on this given to any
staff carrying cylinders would be sufficient.
,
C / ALL
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Stored pressurised gas cylinders must be kept securely outside the building unless
authorised by a fire officer. Stocks of explosives or inflammable agents must be stored
in locked metal cupboards.
Smoke detectors, which provide a warning in the residential accommodation, must be
installed in the kennel area.
9.8 There must be evidence of the annual servicing of fire extinguishers
and alarms (L)
The inspector will ask to see annual service records.
Best practice is to store cylinders of oxygen
and flammable gases outside in the open air,
which allows vapours to be dispersed effectively.
Storage outside should be secure.
If storage has to be located within a building, an
adequate level of ventilation should be provided
either by mechanical ventilation or the presence
of a sufficient size and number of permanent
openings. Flammable gases, such as LPG, if
stored inside, may only be stored in purpose-built
compartments or buildings with fire-resistant
walls and explosion relief. Only limited quantities
should be stored and should not be placed under
stairs, near waiting rooms or compressors.
Risk assessments should be undertaken to take
into account compatibility of substances stored
and the suitability of the arrangements made.
Smoke detectors must be placed in the
residential accommodation.
VH / SA
C / ALL
,
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9.9 The practice must have an accident book, and all staff must know
where it is located (L)
An accident book is required by law and must meet the requirements of the Data
Protection Act. It must record the following:
• Date and time of accident or occurrence;
• Full name and address of the person involved and the injury or condition suffered;
• Where the accident or occurrence happened;
• A brief description of the circumstances;
• In the case of a reportable disease, the date of diagnosis, the occupation of the
person concerned and the name or nature of the disease.
Records should be removed and stored securely and information kept for at least three
years.
9.10 The practice must have a procedure for the Reporting of Injuries,
Diseases and Dangerous Occurrences as required by RIDDOR
regulations 1995 (L)
Any injury, accident or work-related illness which keeps an employee off work or
unable to do their normal job for more than three days must be reported to the
Incident Contact Centre (ICC) within 10 days. The Incident Contact Centre is the
single point of contact for all incidents in the UK.
C / ALL
,
The duty to report falls on employers and the
self-employed and those on control of premises,
and covers everyone at work and non-workers
such as visitors, members of the public.
Examples of what should be reported include:
death; major injuries such as broken arm/leg,
poisoning, electrical shock, amputation injury;
any injury where a person is away from work and
unable to do their normal job for more than three
days; certain cases of work related disease.
C / ALL
,
Incidents can be reported by:
T 0845 3009923
F 0845 3009924
Post to ICC, Caerphilly Business Park, Caerphilly
CF83 3GG (HSE) or via the internet at
www.riddor.gov.uk.
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9.11 There must be a suitably stocked first-aid box, as required under
the Health and Safety (First Aid) Regulations 1981, and a person or
persons must have been appointed to take charge should someone fall
ill or be injured, and to restock the first-aid box as required (L)
There must be an appointed person to take charge should someone fall ill or be
injured, and to restock the first-aid box. A second person must be appointed to take
charge if the first appointee is off duty.
A first aid box is required for each practice vehicle.
There is no standard list of items to be included in the first-aid box, although there is
a suggested minimum:
• A leaflet giving general guidance on first-aid;
• 20 individually wrapped sterile adhesive dressings (plasters);
• Two sterile eye pads;
• Four individually wrapped triangular bandages;
• Six safety pins;
• Medium-sized individually wrapped sterile unmedicated wound dressings;
• Two large sterile individually wrapped unmedicated wound dressings;
• One pair of disposable gloves;
• Tablets or medicines should not be kept in the first-aid box.
The inspector will ask to see the first-aid box, the
list of contents and will check that the contents
are in date and checked regularly.
An ‘Appointed Person’ is an individual nominated
by their employer to take charge when someone
is injured or falls ill. Their responsibilities
include looking after the first aid equipment,
eg restocking the first aid box and calling an
ambulance. Appointed persons should not
administer first aid unless trained to do so.
Note: Nomination of an appointed person is a
minimum requirement, but practices should
consider if an appointment of more than one
person is necessary or if a first aider should be
appointed. (A first aider is someone who has
undergone a training course in administering
first aid and holds a current first aid at work
certificate (these are time-limited to three years).
A first aider can undertake the duties of an
appointed person.)
For further guidance, see HSE leaflet INDG214
(rev 1).
C / ALL
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9.12 The practice must have Employers’ Liability Insurance. The certificate
must be displayed for all members of staff to see (L)
9.13 The practice must have Public Liability Insurance (L)
9.14 There must be a written programme of formal visual inspection of
electrical equipment within the practice, as required under the
Electricity at Work Regulations 1989 and provision for safe installation
and maintenance of gas appliances (Gas Safety Installation & Use)
Regulations 1998 (L)
The practice must have a written programme for the inspection and testing of all its
electrical equipment. For the electrical installation in the building, the frequency
of the inspection (by a competent person) should be as directed by that competent
person. A formal visual inspection of portable appliances, cables and leads, should be
carried out at least annually, with a combined inspection and test recommended every
two years. Advice should, however, be sought from a competent person regarding the
appropriate frequency for combined inspection and test as this will depend upon the
individual circumstances of a practice. Equipment should be labelled with the date
of inspection, failed equipment must not be used and repaired equipment must be
tested before use. Residual Current Devices are required for any equipment used in
wet conditions.
All gas appliances require to be maintained in a safe condition. Advice should
be sought from a suitably qualified person regarding an ongoing programme of
examination.
,
C / ALL
The inspector will check that the certificate is
suitably displayed.
,
C / ALL
The inspector will ask to see the insurance
certificate or policy.
,
The inspector will ask to see:
• The PAT testing & visual inspection records
• Evidence of inspection of the electrical
installation by a competent person
• Gas safety certificates
Practices are referred also to their own insurers
for any requirements imposed by them.
C / ALL
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9.15 Hazardous (special*) waste must be appropriately segregated, safely
stored and disposed of by a suitably permitted waste contractor
The inspector will ask to see evidence of:
• A contract with a permitted waste contractor(s);
• Policies and practice to segregate waste into appropriate streams and to store it
hygienically;
• Consignment notes for hazardous waste disposal, which form the basis of a
hazardous waste register for those practices in England and Wales;
• Hazardous waste registration for those premises in England and Wales that
produce more than 500kg of hazardous waste per annum.
*hazardous waste is referred to as special waste in Scotland
9.16 Non-hazardous (non-special*) waste must be appropriately
segregated, safely stored and disposed of by a suitably permitted
waste contractor
The inspector will ask to see evidence of:
• A contract with a permitted waste contractor(s);
• Polices and practice to segregate waste into appropriate streams;
• Waste transfer notes for non-hazardous waste disposal.
*Non-hazardous waste is referred to as non-special waste in Scotland
,
For both hazardous and non-hazardous waste,
practices may wish to refer to the BVA Good
Practice Guide to Handling Veterinary Waste
for guidance. However, local variations exist
and practices should consult the Environmental
Agency or their own local waste management
authority for information.
The inspector will ask to see:
• The PAT testing & visual inspection records
• Evidence of inspection of the electrical
installation by a competent person
• Gas safety certificates
C / ALL
,
C / ALL
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9.17 The practice must be aware of The Lifting Operations & Lifting
Equipment Regulations 1998 and must carry out the necessary
examination/testing of any equipment covered by the Regulations prior
to use and thereafter have the equipment inspected regularly (L)
9.18 The practice must pass inspection by a Duty Firearms Officer in
respect of any firearms/tranquillizer and dart guns held at the practice
for the purpose of euthanasia/tranquillization of animals. Individual
veterinary surgeons must have been issued with the relevant firearms
certificate (L)
C / ALL
The Regulations require that lifting equipment is:
• Sufficiently strong, stable and suitable for its
intended use;
• Positioned or installed to prevent risk of
injury;
• Visibly marked with appropriate information
for safe use;
and that lifting operations are planned and
supervised and carried out by competent
operators.
Lifting equipment should be examined prior
to first use and thereafter inspected regularly
in accordance with recommendations of a
competent person who shall issue a certificate of
inspection and report of any action required.
An example of equipment covered by the
Regulations is overhead gantry cranes for lifting
anaesthetised horses. It is unlikely that height-
adjustable operating tables for use with small
animals where no ‘lifting’ as such takes place,
will be covered.
The inspector will ask to see the original firearms
certificate(s).
C / ALL
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10 EMERGENCY SERVICE CLINICS
10.1 Staff
All clinical staff must be provided with guidance notes on emergency practice policies
before commencement of work. There must be formal evidence of induction of staff at
the outset of their employment.
A one-year CPD plan must be provided for the ESC team.
A full-time veterinary surgeon must be employed by each ESC premises who shall
have overall responsibility for all professional matters within the clinic.
A full-time Registered/Listed veterinary nurse must be employed by each ESC
premises, whose primary role is the responsibility for the nursing and clinical care of
the clinic’s patients and who shall be directly involved in such care.
At least one on-duty veterinary surgeon, directly responsible for the care of in-patients
and any new admissions or out-of-hours appointments must be on the clinic’s
premises at all times during all of the hours of operation of the clinic.
In addition to the veterinary surgeon, at least one other on-duty member of staff whose
role is the active involvement in nursing and medical care of patients must be on the
premises during all the hours of operation of the clinic.
Any on-duty staff member on a ‘rest break’ must at all times be readily available for
active duty during the hours of operation of the clinic.
A written agreement must be entered into with client practices which includes a
written policy on surgical complications of client practice cases and daily reporting of
clinical records back to the client’s practice.
There must be a written policy on answering the telephone, including how to answer
call outs, transport concerns and fee estimates.
There must be an animal ambulance service or agreement with a local animal
transport company for animals to be brought to the clinic.
A dedicated land-based telephone line for the emergency service must be provided.
A practice fulfilling the following requirements
IN ADDITION to all GP Small Animal Standards
may be accredited as a Small Animal Emergency
Service Clinic (ESC) and provide 24-hour
emergency cover to a SA Hospital.
,
GP / ESC
,
The aim for the future is that ESCs will be
required to increase the number of Registered/
Listed veterinary nurses employed by them.
Please refer to the Code of Professional Conduct
and Guidance note 3. While no acceptable
time or distance is specified, as each will be
influenced by local conditions, when making
arrangements for the provision of 24-hour
emergency cover, practices should give
consideration to these factors. Practices should
check carefully that their written contract/
agreement with another practice or Accredited
Emergency Service Centre (ESC) establishes
clearly who is responsible for out-of-hours home
visits, on the rare occasions that such visits may
be necessary
,
,
,
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10.2 Clinical governance
The ESC must have a system in place for monitoring and discussing the clinical
outcomes of cases and acting upon the results. It is expected that outcomes will be
actively followed up with daytime practices/clients.
10.3 Premises and out-patient facilities
Emergency lighting must be provided to allow the ESC to continue to function in the
event of a power-cut or electrical failure. Additional emergency lighting to permit the
completion of essential tasks such as operative surgery, may be provided by back-
up generator, portable rechargeable lighting units, uninterruptible power supplies or
similar devices. Simple torches are not sufficient as emergency back-up in operating
areas.
10.4 In-patient facilities
Suitable facilities for neonatal care must be provided.
An ESC must have the ability to isolate an infectious animal from all other patients.
Isolation facilities must have:
• Separate air space;
• Ventilation that produces a negative air pressure in the facility to reduce the risk of
cross-infection;
• Hand-washing facilities;
• Separate drains to avoid cross-infection.
Isolation facilities can mean either a special area, which has limited access, or a
separate ward. It is recommended that there is a written policy which details the
procedure for isolation and care of cases including barrier nursing requirements.
The written policy must be displayed in an appropriate place and staff must be fully
conversant with its contents.
,
It is recognised that the ESC’s case-load will
differ from that of a SA GP/VH practice.
GP / ESC
Continuous lighting which is suitable to complete
operative surgery must illuminate automatically
in the event of power failure.
,
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There must be an ability to provide close control of fluid replacement by an infusion
pump or syringe driver suitable for infusion of high volumes rapidly or low volumes
slowly.
Facilities must be available for the intensive care of critically ill patients, to include:
• Intravenous fluid therapy;
• Blood transfusion;
• Oxygen therapy;
• Maintenance of body temperature.
Electrosurgery and suction must be available for surgical use and a clock with a
sweeping second hand must be visible from within the operating area.
There must be adequate primary and reserve supplies of oxygen.
10.5 Suitable monitoring of anaesthetised patients
Monitoring must be available, including pulse oximetry and capnography, blood
pressure measurement facility, and oesophageal stethoscope. Records of vital signs
and agents employed must be retained. Evidence of staff training in the use of
monitoring facilities must be provided.
There must be adequate post-anaesthetic monitoring. An anaesthetic monitoring
room or area must be available and records must be maintained until the animal
has recovered. Proper ventilation must be provided to limit staff exposure to exhaled
gases.
10.6 Diagnostic equipment and facilities
The following equipment must be available on site:
• Electrocardiography (ECG) - recordings must be suitably filed and stored;
• Ultrasound system, capable of providing diagnostic quality images of the full range
of species treated;
• Endoscope(s) of an appropriate quality suitable for the workload of the clinic.
GP / ESC
The criteria should not be interpreted to imply
that every piece of monitoring equipment is
required for every operation. What is required
should be based on a risk assessment and will
depend on the number and nature of operations
performed – practices should ensure that
equipment provided is adequate for the work
actually undertaken.
,
Evidence must be provided of training or CPD for
staff in use of all equipment. Reference material
must be available.
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10.7 Laboratory facilities
Laboratory facilities for routine diagnostic tests must be available at all times.
Suitable arrangements must be made for the following detailed investigations:
• Biochemistry;
• Haematology;
• Parasitology;
• Bacteriology.
The following equipment must be provided on the premises:
• Binocular microscope with mechanical stage, electric light source and oil
immersion facility;
• Centrifuge suitable for PCV, blood separation and urine sedimentation;
• Urinary refractometer;
• Biochemistry analyser to include Creatinine, Urea, Glucose, Total Protein and
Calcium;
• Electrolyte analyser.
There must be the ability to look at smears on
site. Evidence must be provided of training or
CPD for staff in use of all equipment and in the
interpretation of results. Reference materials
must be provided.
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APPENDIX 1
Additional resources to be provided by GP-level practices wishing to apply for
accreditation as a Veterinary Nursing TP.
In-patient facilities
There must be a minimum of six kennels or cages for the hospitalisation of patients.
Clinical governance
Relevant caseload for completion of training portfolio by Student VNs.
Minimum caseload requirements include:
• 100 small animal cases/consultations per week;
• 20 general anaesthetic cases per week;
• 10 radiographic exposures per week;
• Level 3 students – 10% of time or one half-day per week to be spent on each of
radiography (including positioning, processing), and biochemistry (including blood
chemistry);
• 10 cases/consultations per week;
• 10 radiographic exposures per week.
(The figures are for guidance only and may vary depending upon the range of cases
and number of students in training.)
Diagnostic equipment and facilities
The practice must have either:
• A range of endoscopes of appropriate quality;
or
• An ultrasound system capable of providing diagnostic quality images,
and must provide SVNs with access to whichever equipment is not on site through
secondment to another practice/hospital.
GP / SA
GP / SA
GP / EQ
GP / SA &
.EQ
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Laboratory facilities
Laboratory facilities for routine diagnostic tests must be available, and the following
equipment provided on the premises:
• Centrifuge and centrifuge tubes;
• Haemotocrit;
• Glass slides;
• Stains for blood films;
• Blood biochemistry analyser.
GP / SA &
.EQ
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