New EU MDR Regulations and Revamp of the Medical Device Directive
CDRH Warns of Potential Device Shortage with Shutdown of Sterigenics Facility in Illinois
EU MDR Supplier Quality Requirements: Convergence of Best Practice and Regulation
EU MDR Post-Market Surveillance: Active, Integrated, Risk-Based, and Planned
Preparing for MDR: Don’t Forget about Class I Reusable Devices