Demystify FDA Compliance for Public Cloud Workloads in Life Sciences ON DEMAND WEBINAR: Demystify FDA Compliance for Public Cloud Workloads in Life Sciences. 0 Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
ProcessX Explainer Video Video on ProcessX. 0 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. 0 Jay Crowley - April 19, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
USDM’s Guide to 21 CFR Part 11 Blog article topic: USDM’s Guide to 21 CFR Part 11. 0 David Blewitt - April 14, 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? 0 Bob Lucchesi - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
How Do Life Science Companies Qualify Vendors and Software? Automated equipment & systems used by companies are supplied by vendors & are purchased off-the-shelf (OTS). They should audit the vendors development. 0 David Blewitt - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Safety
