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Data, Freedom of Information releases and corporate reports
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Use this form to confirm convention country priority claim relating to UK application for registered design.
Standardisation explained.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
Guidance for manufacturers, importers and distributors.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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.
International trade mark registrations protected in the EU under the Madrid Protocol will no longer enjoy protection in the UK after 1 January 2021.
To help you protect, manage and enforce your intellectual property (IP) rights in Laos.
Pharmacovigilance system requirements
Advice for manufacturers of Class I medical devices for placing products on the UK market
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
To help you protect, manage and enforce your intellectual property (IP) rights in Indonesia.
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