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Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
Benefit-Risk Submission Report (BRSR) and Pharmacovigilance Sales Submission (PSS) templates and guidance for completion of BRSRs, PSSs and signal notifications.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Legal requirements for the sale of veterinary medicines on the internet.
Service for Marketing Authorisation Holders.
Effective from 17 May 2024 Definitive fees charged for applications under Schedule 7 of Veterinary Medicines Regulations 2013 (as amended) as they apply to GB.
Information on how your personal data relating to financial transactions may be used in counter-fraud and error data matching exercises.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Requirement to analyse samples from food producing animals for residues of veterinary medicines and prohibited substances.
Method of payment for fees charged for the specific activities carried out by the VMD.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
How to report an adverse event to animal medicine using the VMD's online reporting service.
Legal requirements referred to in Schedule 1 of the Veterinary Medicines Regulations, as amended.
All national applications will be processed on one of six timetables that vary in length depending on the complexity and nature of the application under assessment.
Apply to register, renew, or vary a Veterinary Homeopathic Remedy.
The Veterinary Medicines Regulations require wholesale dealers in Great Britain to adhere to Good Distribution Practice for all distribution processes.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Do not include personal or financial information like your National Insurance number or credit card details.
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