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Data, Freedom of Information releases and corporate reports
Science and Technology Secretary Michelle Donelan set out the importance of the UK’s mission to be a science and technology superpower.
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.
How initial teacher training (ITT) providers can offer a physics ITT course designed for engineers.
Advice on writing clear notices and maximising replies to your FSNs.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
This fund will support innovative engineering biology sandboxes which aim to accelerate pro-innovation regulatory reform and encourage business innovation and investment.
A report into the skills needs of the pharmaceutical, medical biotechnology, and medical technologies sectors.
The use of ionising radiation in medicine, including recommended dose measurements and guidance on safe radiology practice.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Outlines the aim, scope and definitions of the medical technology innovation classification framework.
The Engineering Construction Industry Training Board (ECITB) ensures there are enough trained people to meet industry needs. It gives professional advice and offers skills development and qualifications to help individuals in the sector succeed in their chosen careers. ECITB is...
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).
Information for a letter of initial assessment or college letter, so you can train for an engineer officer certificate of competence (CoC)
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