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Good distribution practice for veterinary medicinal products must also be observed by third parties involved in the wholesale distribution of veterinary medicinal products and should be part of their contractual obligations.
Requirements for transport of the veterinary medicinal products .
Requirements for stock inventories which must be performed regularly.
Requirements for a self-inspection programme.
Notification to the VMD if they have a reason to suspect, or know of, a threat to the continued supply of a veterinary medicine.
This enforcement policy sets out the general principles and approach taken by the VMD.
This Section lays down specific requirements for identified veterinary medicinal products related to the nature of the active substances contained therein.
Import certificates are required for non-UK licenced veterinary medicinal products which are to be placed on the UK market.
The following requirements shall apply to biological veterinary medicinal products except immunological products or where otherwise set out in Section IV.
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.
Guidelines and guidance for vets, farmers and animal keepers on the responsible use of antimicrobials.
Method of payment for fees charged for the specific activities carried out by the VMD.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Legal requirements and good practice guidance for SQP retailers鈥� premises inspections.
Requirement to analyse samples from food producing animals for residues of veterinary medicines and prohibited substances.
Fees are charged for new marketing authorisation (MA) applications and variations to MAs.
Explainer for businesses and persons regulated by the Veterinary Medicines Regulations 2013, as amended, on the transitional provisions included in the amending legislation: the Veterinary Medicines (Amendment etc.) Regulati鈥�
The VMR sets out the statutory fees associated with various regulatory services provided by the VMD. The statutory fees and fee structure are implemented from 17 May 2024.
The documentation accompanying an application for a marketing authorisation pursuant to Schedule 1 of the Veterinary Medicines Regulations shall be presented in accordance with the requirements set out in this Annex.
The following detailed requirements shall apply to Requirements for Specific Marketing Authorisation Applications.
Don鈥檛 include personal or financial information like your National Insurance number or credit card details.
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