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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Advice to give pregnant women on infections that can be transmitted via contact with animals that are or have recently given birth.
How to use an interrupted time series to evaluate your digital health product.
Information on how the CMA investigated the merger, and how you can find out more.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How sellers deal with VAT for goods from overseas that they sell direct to customers in the UK.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to work out the customs value of imported goods that are free of charge, used, rented or leased if you're an importer or clearing agent.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to use a quasi-experimental study to evaluate your digital health product.
Using an ecological momentary assessment to evaluate your digital health product.
How to use a cost utility analysis to evaluate your digital health product.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
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