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Departments, agencies and public bodies
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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Submission dates and how the submissions using the EC decision reliance procedure work.
How the MHRA processes variations to Marketing Authorisations (MAs)
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
The seeds which must be certified before you can market them, how to get them certified and how to get a licence for your seed business.
How to renew marketing authorisations for products granted through different routes and at different times.
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.
Marketing authorisations granted in 2024
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.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Marketing standards for hops producers, manufacturers, retailers and distributors.
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