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Requirements for audits (surveillance and unannounced) under EU MDR and links to the MDSAP program - by Adam Freeman and Frank Blömer
confinis is moving - literally
From “Essential Requirements” to “General Safety and Performance Requirements” (GSPRs) – EU MDR 2017/745 - by Urs Widmer
Technical Documentation for medical devices under the new European MDR - by Nicole Gabathuler
Conformity assessment procedures and premarket scrutiny under EU MDR 2017/745 - by Dr. Sabine Nieba
Classification under the European Medical Device Regulation - by Joachim Makowski
Work in progress regarding MDR implementation - confinis and its partners
confinis - NEW AFFILIATION: clinical project management services - serving the health technology industry for the entire product lifecycle
Your insight to: confinis and its partners - work in progress regarding MDR implementation - effects of MDR on your QMS
Your insight to: confinis and its partners - work in progress regarding MDR implementation
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Are there "Qick Wins" when it comes to MDR implementation?
confinis invites you!