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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.
Adopted EU recommendation GEN-021. UK approved recommendation on the responsibility of UK Approved Bodies for testing conducted by independent laboratories.
Check the veterinary product information database to find out if a medicine is safe to use on your pet or has been removed from sale
The locations for a Marketing Authorisation Holder (MAH) and a Qualified Person responsible for Pharmacovigilance (QPPV)
Check the availability and any issues affecting the approval and set up of your agent services account if you are not based in the UK.
How the MHRA processes variations to Marketing Authorisations (MAs)
Upper Tribunal Administrative Appeals Chamber decision by Judge Citron on 13 August 2023.
First published during the 2022 to 2024 Sunak Conservative government
Responsible authorities within the Licensing Act 2003 include police, fire authorities, health and safety authorities, local planning authorities…
First published during the 2010 to 2015 Conservative and Liberal Democrat coalition government
Guidance on the use of the sensitive words accreditation, accredit, accredited and accrediting, in a company, Limited Liability Partnership or business name.
A short guide giving details of the current proposals for press self-regulation, in the wake of the Leveson Report.
Employment Tribunal decision.
Marketing Authorisations Information Service (MAVIS) Hub edition 118
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