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Data, Freedom of Information releases and corporate reports
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
How to apply for marketing authorisation via this new procedure.
All data on external disclosures made to the CMA
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Information on procedures, potential consequences of non-notification, new and adopted CMA guidance and who to contact.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
British Medical Association trade union: annual returns, rules, statement to members, decisions and other related documents.
How to renew marketing authorisations for products granted through different routes and at different times.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Canada and UK Trade Continuity Agreement enters into force
Information on how to revalidate a UK CoC (and UK GMDSS at the same time).
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
New standards of training certification and watchkeeping (STCW) requirements.
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