MDSAP Ready in 4 Months Through Assessment and Remediation Case study on MDSAP Ready in 4 Months Through Assessment and Remediation. Jim Macdonell - April 1, 2022 Case Studies Medical Device Clinical, Manufacturing, 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
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
Data Migration Guidance Blog article topic: Data Migration Guidance. Joseph Cassella - February 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
An Introduction to Software Validation Blog article topic: An Introduction to Software Validation. David Blewitt - February 25, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
