NAMDET members are asked to look at the latest MHRA consultation and make recommendations, suggestions etc. Closing date is January 5th 2024. Please feel free to share with colleagues working in medical device design and development too.
The MHRA is inviting members of the public – including patients, medical device researchers, developers, manufacturers and suppliers, clinicians and other healthcare professionals – to provide their views on proposed changes to the regulatory framework for medical devices that will help us meet these objectives.
NAMDET has shared the link (so please feel free to contribute and share within your colleagues and organisations). Although focussed on regulatory aspects, nevertheless NAMDET’s Chair Paul Lee was disappointed to search the whole 44 pages to only find 2 references to the phrase ‘training’ and neither of these focus on the importance and essential requirements around medical device training.
Members are asked to help the MHRA and feedback all comments before the deadline date of January 5th 2025