Key differences in the requirements for SFDA UDI and US & EU UDI Blog article topic: Key differences in the requirements for SFDA UDI and US & EU UDI. Jay Crowley - January 29, 2022 Blogs Medical Device Manufacturing, Regulatory
EU MDR Date of Application Readiness Guide Learn how to navigate EU MDR compliance for medical devices. Understand key deadlines, classification rules, vigilance, and post-market surveillance. Download now! Jay Crowley - January 17, 2022 White Papers Medical Device Clinical, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
USDM Managed Compliance Program Case study on USDM Managed Compliance Program. John Petrakis - January 15, 2022 Case Studies Biotech Manufacturing
Will Your Company Be Ready for the Next Regulatory UDI Database? Blog article topic: Will Your Company Be Ready for the Next Regulatory UDI Database? Jay Crowley - January 14, 2022 Blogs Medical Device Manufacturing, Regulatory
Another Regional UDI Database: Singapore’s UDI Implementation Blog article topic: Another Regional UDI Database: Singapore’s UDI Implementation. Jay Crowley - January 8, 2022 Blogs Medical Device Manufacturing, Regulatory
The Evolving Global UDI Landscape Blog article topic: The Evolving Global UDI Landscape. Jay Crowley - January 4, 2022 Blogs Medical Device Manufacturing, Regulatory
