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Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How to apply for marketing authorisation via this new procedure.
Find out which country’s VAT rules to use when supplying services abroad.
Find out how to determine the place of supply of your services and how to deal with supplies of services which you receive from outside the UK.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
Submission dates and how the submissions using the EC decision reliance procedure work.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Marketing authorisations granted in 2024
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
The European Union (EU) and European Economic Area (EEA) - which countries are in the EU and EEA, the single market and free movement of goods, capital, services and people
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Innovation can differ in its degree of radicalness and can take various forms
How to renew marketing authorisations for products granted through different routes and at different times.
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.
How the MHRA processes variations to Marketing Authorisations (MAs)
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