Tracking of New/ Revised Regulation

[SaGaf]

Hi Medical Device Community,
Would you please advise on the best way to track issuance of new/ or revision of regulation/ guidelines for the EU (MDR, MDCGs, ISO)?
We currently don't have any process in place to track changes to regulative requirements, and not sure where to start from to fix this gap.


Thanks in advance!!

 

[Billy Milly]

two suggestions

Medical Devices - Sector

Medical Devices - Sector

health.ec.europa.eu

ISO - Store (mark the relevant standards in your account and get notified on changes)