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Information to support your recovery after COVID-19.
How to conform with the legal requirements for placing medical devices on the market.
Submission dates and how the submissions using the EC decision reliance procedure work.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to change the ownership from one marketing authorisation (MA) holder to another.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Apply for a higher education course, track your application and accept or reject your offers.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
How to apply for marketing authorisation via this new procedure.
The official UK government website for data and insights on COVID-19.
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