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The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
How marketing authorisation holders should provide educational materials to MHRA for assessment and approval prior to launching their products on the UK market.
How to use A/B testing to evaluate your digital health product.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Check the patents journal to find UK-registered patents granted, published and filed
Guidance for industry on flexible approaches we are taking on good distribution practices.
This is advice for UK sponsors whose students are affected by coronavirus (COVID-19).
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Cancel a marketing authorisation, traditional herbal registration or parallel import product licence or withdraw a pending submission.
Find details of recent trade mark applications or amendments by searching the journal
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Affidavit of marital status for British nationals in Vietnam.
Find out about tax charges on scholarships.
How to check that a laboratory is allowed to buy ozone-depleting substances (ODS).
A collection of case studies showing how businesses have used copyright protection to create value from their ideas.
Advice for manufacturers of Class I medical devices for placing products on the UK market
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