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
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
Q&A: EU MDR Date of Application Readiness Blog article written from the Q&A during the EU MDR Date of Application Readiness webinar. Jay Crowley - April 19, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Is There a Checklist for GCP Audits? Blog article topic: Is There a Checklist for GCP Audits? Bob Lucchesi - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
