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News stories, speeches, letters and notices
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.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
How an innovative funding mechanism is saving lives by speeding up the availability of vaccines and making them affordable.
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 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.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
How the MHRA processes variations to Marketing Authorisations (MAs)
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
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.
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.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
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