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Guidance for the veterinary pharmaceutical industry on applying for maximum residue limits (MRLs) in the UK.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
Once a VMP is on the UK market an MAH must record and submit the results of their signal management process, alongside sales and worldwide authorisation status data.
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.
Guidance for vets, farmers and animal keepers on what the mg/PCU means and how it is calculated.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Requirements for Biological Veterinary Medicinal Products other than Immunological Veterinary Medicinal Products.
Guidance to the veterinary pharmaceutical industry on moving goods from NI to GB under unfettered access arrangements and placing qualifying NI goods on the GB market.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Information for beekeepers about inspections the Animal and Plant Health Agency carries out on colonies, veterinary medicine records and honey samples.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Guidance for the veterinary pharmaceutical industry on how to apply for and maintain a shared-label for use on veterinary medicines placed on the market in the UK and Ireland.
Requirement to analyse samples from food producing animals for residues of veterinary medicines and prohibited substances.
Details of certificates issued under the Special Import System for the top ten imported veterinary medicines 1 April - 30 June 2023.
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