Data in the Cloud Can Be 21 CFR Part 11 Compliant USDM Life Sciences specializes in helping life sciences companies achieve and maintain continuous compliance with their cloud solutions. David Blewitt - March 28, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
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
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
Q&A with the FDA on CSV Changes On-demand webinar topic: Q&A with the FDA on CSV Changes. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance, Regulatory
Accelerating Cloud Content Management for Emerging Life Sciences On-demand webinar topic: Accelerating Cloud Content Management for Emerging Life Sciences. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology
