Box GxP and Cloud Assurance for FDA Submission Case study on Box GxP and Cloud Assurance for FDA Submission. David Blewitt - April 19, 2022 Case Studies Biotech, Pharma Clinical
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
Optimized Use of TraceLink Helps Pharma Company Implement Serialization Case study on Optimized Use of TraceLink Helps Pharma Company Implement Serialization. Erin Christy - April 18, 2022 Case Studies Pharma Information Technology, Regulatory
Box GxP for Controlled Clinical Management Case study on Box GxP for Controlled Clinical Management. Kim Hutchings - April 18, 2022 Case Studies Pharma Clinical, Information Technology, Research & Development
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
