Update from the FDA on CSV Changes On-demand webinar topic: Update from the FDA on CSV Changes. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Biotech Completes 70% of eSignatures Within 24 Hours Case study on Biotech Completes 70% of eSignatures Within 24 Hours. David Blewitt - April 1, 2022 Case Studies Biotech Information Technology, Regulatory
Veeva Implementation and Validation Maintenance Video on Veeva Implementation and Validation Maintenance. Hovsep Kirikian - March 28, 2022 Videos Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
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
