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Data, Freedom of Information releases and corporate reports
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
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.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Marketing authorisations (MAs) granted since January 2014.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
The effectiveness of marketing channel liberalization in increasing competition among traders and prices obtained by farmers for their produce
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
Marketing authorisations granted in 2024
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.
Current and previous editions of the MAVIS newsletter.
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