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
Quality System Upgrade to Meet EU MDR and EU IVDR Case study on Quality System Upgrade to Meet EU MDR and EU IVDR. Jay Crowley - March 18, 2022 Case Studies Medical Device Manufacturing, Regulatory
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
