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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How veterinary medicines can be advertised.
There must be sufficiently competent personnel to carry out all the tasks for which the wholesale dealer is responsible.
Benefit-Risk Submission Report (BRSR) and Pharmacovigilance Sales Submission (PSS) templates and guidance for completion of BRSRs, PSSs and signal notifications.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Requirements for documentation, procedures and record keeping.
Explainer for the pharmaceutical industry on the implementation of Pharmacovigilance requirements during the transition time from the date the revised VMR have effect in GB to 17 May 2027.
Legal requirements referred to in Schedule 1 of the Veterinary Medicines Regulations, as amended.
Guidance on Pharmacovigilance reporting.
Requirements for suitable and adequate premises and equipment to ensure proper storage and distribution of veterinary medicinal products.
Information on authorised vaccines and vaccination schedules for dogs.
Requirements for handling complaints, returns, suspected counterfeits and recalls.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Clarification for the interpretation of the new elements within the Veterinary Medicines Regulations (VMRs), as amended, relating to combating antimicrobial resistance (AMR).
Legal requirements for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
Operational requirements.
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.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Apply for authorisation of premises for the retail supply of POM-VPS and NFA-VPS veterinary medicines by suitably qualified persons (SQPs).
Guidelines and guidance for vets, farmers and animal keepers on the responsible use of antimicrobials.
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