Preparing Your Team for the EUDAMED Database

Preparing Your Team for the EUDAMED Database

John N. Bradsher, PhD, RAC, Medical Device Regulatory Affairs & Quality Assurance Expert at Celegence will present a webinar: How to Start Preparing your RA/QA Team for the EUDAMED Databse on Tuesday, September 22 at 10 a.m. CST. Read on for John’s...

US Regulators Extend UDI Deadlines Following Security Issue

According to an announcement from Emergo, “Citing security vulnerabilities, the US Food and Drug Administration has extended deadlines for compliance with a key component of the agency’s Unique Device Identification (UDI) system.”  For more information on...