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Information to support your recovery after COVID-19.
Submission dates and how the submissions using the EC decision reliance procedure work.
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.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 3 May 2024.
A bogus immigration lawyer with no licence to practise has been jailed for seven-and-a-half years for exploiting at least 19 victims for huge financial gain.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Blogs where government organisations talk about their work and share information and ideas.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
How to apply for marketing authorisation via this new procedure.
How to conform with the legal requirements for placing medical devices on the market.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Apply for a higher education course, track your application and accept or reject your offers.
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