BSI, a world-class Notified Body providing regulatory and quality management reviews for medical devices, is kicking off its “Passport to Europe” Programme.
FOCUS ZONE REPORT – BSI is launching a new speed-to-market programme, CE-Onsite FastTrack Review, for Class III medical devices needing European CE Marking Design Dossier Reviews.
A Publicly Available Specification (PAS) that defines the terms commonly used in the field of regenerative medicine has been published by BSI British Standards.
