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Departments, agencies and public bodies
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
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Submission dates and how the submissions using the EC decision reliance procedure work.
How to change the ownership from one marketing authorisation (MA) holder to another.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
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 how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
How to apply for marketing authorisation via this new procedure.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
The Marshall Aid Commemoration Commission (MACC) administers the British Marshall Scholarships, which finance young Americans of high ability to study for a graduate degree in the UK. MACC is an executive non-departmental public body, sponsored by the Foreign, Commonwealth &...
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Guidance for the pharmaceutical industry on applying for a marketing authorisation for parallel import (MAPI).
Invitation to comment launched by the CMA on the partnerships between Microsoft and Mistral AI, and Amazon and Anthropic, and Microsoft’s hiring of former employees and related arrangements with Inflection AI.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
The locations for a Marketing Authorisation Holder (MAH) and a Qualified Person responsible for Pharmacovigilance (QPPV)
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
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