RAPS Convergence 2024 0 Lisa Om - August 11, 2024 News & Events Medical Device Manufacturing, Regulatory
GxP Primer: Where Do Good Practices Come From and Why Do We Need Them? Global health regulators home in on critical requirements for life sciences organizations. 0 Michelle Gardner - June 3, 2024 Blogs Regulatory
Join Us for Happy Hour During the ASQ World Conference Join USDM Life Sciences for Happy Hour during the ASQ World Conference with our partner ZenQMS 0 Ryan McDonald - May 2, 2024 News & Events Quality Assurance
Unique Architecture Blueprint Supports High Performance Computing The USDM team built and validated the architecture that enabled AWS-based tools for big data processing and analysis. 0 Michelle Gardner - March 18, 2024 Case Studies Biotech Information Technology, Quality Assurance
A Few Surprises in FDA’s Quality Management System Regulation For most manufacturers, the new QMSR will simplify their approach to quality system compliance. Learn about two important issues to be aware of. 0 Jay Crowley - March 1, 2024 Blogs Medical Device Regulatory
Best Practices for Complaint and Adverse Event System Implementation Guidance for data management and system implementation for complaints handling 0 Jim Macdonell - January 3, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Safety
