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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
The Medicines and Healthcare Regulatory Agency (MHRA) has released a statement on CE marking recognition for medical devices and in vitro diagnostics.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Advice on writing clear notices and maximising replies to your FSNs.
The different types of tests and testing kits for COVID-19, and the specifications for manufacturers.
AMRHAI (antimicrobial resistance and healthcare associated infections) is the national reference unit for investigating AMR in healthcare-associated bacteria.
How to conform with the legal requirements for placing medical devices on the market.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
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