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
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
Cellular Therapy Regulations Blog article topic: Cellular Therapy Regulations. Diane Gleinser - March 12, 2022 Blogs Biotech Clinical, Regulatory, Research & Development
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
Huge Productivity Gains and Decreased Costs with Salesforce Discover how USDM helped a Fortune 500 medical device manufacturer streamline workflows, save $750K annually, and achieve compliance with Salesforce GxP. Jim Macdonell - March 6, 2022 Case Studies Medical Device Information Technology, Regulatory
Remanufacturing of Medical Devices, New DIs, and Software Updates Blog article topic: Remanufacturing of Medical Devices, New DIs, and Software Updates. Jay Crowley - March 1, 2022 Blogs Medical Device Manufacturing
