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How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Guidance and application forms for Marketing Authorisations, Animal Test Certificates, Veterinary Homeopathic Remedy, Export and Import certificates, Batch release and Batch control.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
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.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
How to change the ownership from one marketing authorisation (MA) holder to another.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Register as a manufacturer, importer or distributor of active substances.
How to obtain an authorisation to wholesale veterinary medicines.
Use this form when notifying the Intellectual Property Office of your intention to use the Supplementary Protection Certificate (SPC) manufacturing waiver.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
Published standards for regulatory work 2023/24
Guidance to help applicants and licence holders get and maintain a manufacturer licence - MHRA guidance note 5.
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