A new survey was launched by CORE-MD partners, aiming to assess educational needs of clinicians, notified bodies and regulators related to regulatory affairs. The survey takes around 10-15 minutes to complete and is open until 10th June.
This survey will help to assess what sort of knowledge clinicians have on regulatory affairs (particularly related to medical devices), what sort of training they have followed, and what gaps in the knowledge exist. It will lead to the establishment of a roadmap which will inform policy makers and stakeholders on the needs for methodological expertise and educational requirements for the assessment of high-risk medical devices, specifically in the context of the EU Medical Device Regulation. This activity will be very helpful, as training in regulatory affairs can help clinicians to better contribute to the safety of the devices that they use to treat their patients.
We would be very grateful if you could fill in the survey and share it with clinicians in your network so we can get as many replies as possible.
Fill out the survey here
