How to Align your CSV Program with the FDA’s CSA Approach Blog article topic: How to Align your CSV Program with the FDA’s CSA Approach. Jim Macdonell - April 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
Compliant Data Migration Solutions Blog article topic: Compliant Data Migration Solutions. Joseph Cassella - April 26, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
510(k) Approval Weeks Ahead of Deadline Case study on 510(k) Approval Weeks Ahead of Deadline. Sandy Hedberg - April 24, 2022 Case Studies Medical Device Regulatory
Most Misunderstood and Misapplied UDI Requirements Blog article topic: Most Misunderstood and Misapplied UDI Requirements. Jay Crowley - April 21, 2022 Blogs Medical Device Manufacturing, Regulatory
Demystify FDA Compliance for Public Cloud Workloads in Life Sciences Explore best practices for FDA-compliant cloud adoption in life sciences. Learn about workload analysis, compliance management, and secure cloud strategies. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
ProcessX Explainer Video Video on ProcessX. Vishal Sharma - April 19, 2022 Videos Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
