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Guidance for manufacturers, importers and distributors.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out what trade barriers are and how they may affect you when exporting goods or services.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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