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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How initial teacher training (ITT) providers can offer a physics ITT course designed for engineers.
How to use an ethnographic study to evaluate your digital health product.
Pharmacovigilance system requirements
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to apply for authorisation to import, move or keep specified material and the fees you must pay.
By getting an approved framework, you’ll be able to show when a material has reached end of waste status.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
How to apply for marketing authorisation via this new procedure.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance for copyright owners on how to grant a licence for, sell or market their work.
How commercial plant growers can grow FPCS-certified stock, and find out the benefits of using it in commercial plantations.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
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