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How to conform with the legal requirements for placing medical devices on the market.
Information about the EU Regulations and their implementation in Northern Ireland
Dstl is seeking highly innovative approaches to understand the contribution that engineering biology can make to Defence Capability.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
A report into the skills needs of the pharmaceutical, medical biotechnology, and medical technologies sectors.
Advice on writing clear notices and maximising replies to your FSNs.
This fund will support innovative engineering biology sandboxes which aim to accelerate pro-innovation regulatory reform and encourage business innovation and investment.
The use of ionising radiation in medicine, including recommended dose measurements and guidance on safe radiology practice.
Outlines the aim, scope and definitions of the medical technology innovation classification framework.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Annual data on the bioscience and health technology sector.
Information for patients, public and health care professionals.
Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
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