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This consultation aims to seek views on the possible introduction of regulations mandating the disclosure of industry payments to the healthcare sector.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Advice on writing clear notices and maximising replies to your FSNs.
Helping UK healthcare providers to do more business overseas by promoting the UK healthcare sector to overseas markets and supporting healthcare partnerships between the UK and overseas healthcare providers.
These publications specify Defence regulations and associated guidance for UK Ministry of Defence (MOD) healthcare activity within UK and overseas.
This paper presents evidence from interviews in 2013–15 and 2017 in East Africa
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Annual data on the bioscience and health technology sector.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Report describing the state of the digital health market in the UK.
The government’s plan to support a thriving UK medtech sector and make sure the health and care system can reliably access safe, effective and innovative medical technologies to deliver the best outcomes for patients.
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