by John Asadi | Sep 17, 2024 | EMS, FSMS, Membership, OHS, Other, Publications, QMS
MDR CHECKLISTUnderstanding New CE Marking RegulationsHow this book serves as your EU MDR checklistNavigating the complexities of the European Union Medical Device Regulation (EU MDR) can be a daunting task for many medical device manufacturers and stakeholders. The EU...
by John Asadi | Jun 22, 2024 | EMS, FSMS, Membership, OHS, Other, Publications, QMS
Embrace Excellence with ISO 10002 Certification!SPECIFICALLY to CANADIAN businessesAt ISC International Standard Certification, we are dedicated to championing excellence in customer satisfaction. That’s why we proudly advocate for ISO 10002 certification, the...
by John Asadi | Jun 22, 2024 | EMS, FSMS, Membership, OHS, Other, Publications, QMS
Get your CE, ISO 13485, MDSAP with the power of Artificial IntelligenceSPECIFICALLY to CANADIAN businessesAt ISC, we know the challenges that medical device manufacturers face when striving for MDSAP, CE and ISO 13485 compliance.www.ISCASC.comThe requirements of...
by Helen | Jun 15, 2024 | EMS, FSMS, Membership, OHS, Other, Publications, QMS
MDD 2 MDRWhat is MDD? “MDD” stands for “Medical Device Directive,” and “MDR” stands for “Medical Device Regulation.” In European law, a Directive is a set of guidelines setting minimum standards that can be interpreted by each European Member State.In Europe Region,...
