What’s new in Veeva Vault 22R1 Blog article topic: What’s new in Veeva Vault 22R1. Hovsep Kirikian - March 21, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
CSV Program and Application Validation in Less than 6 Weeks Case study on CSV Program and Application Validation in Less than 6 Weeks. Erin Christy - March 18, 2022 Case Studies Biotech Clinical
Accelerate Your Journey to the Cloud: Move your GxP Regulated Workloads to Microsoft Azure On-demand webinar topic: Accelerate Your Journey to the Cloud: Move your GxP Regulated Workloads to Microsoft Azure. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
What are Key Performance Indicators for a Life Sciences Project? Blog article topic: What are Key Performance Indicators for a Life Sciences Project? Diane Gleinser - March 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
Virtual Audits and Inspections Video Video on Virtual Audits and Inspections. David Blewitt - March 13, 2022 Videos Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Regulatory
Standard Operating Procedures (SOPs) – Best Practices for Emerging Life Sciences Companies Blog article topic: Standard Operating Procedures (SOPs) – Best Practices for Emerging Life Sciences Companies. Erin Christy - March 12, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Safety