Pharmaceutical Company Transitions to CSA Model with USDM Expertise Learn how USDM helped a pharmaceutical company achieve greater efficiencies in their validation process through a hybrid CSA model for testing. Sandy Hedberg - July 26, 2022 Case Studies Pharma Regulatory
Box Meets Complex Security and Global GxP Validation Requirements Discover how USDM enabled FDA-ready Box GxP validation for a global biosciences company, meeting tight deadlines and complex security requirements. David Blewitt - April 24, 2022 Case Studies Biotech Clinical, Regulatory
Veeva Vault Implementation to Maximize GxP Uses Case study on Veeva Vault Implementation to Maximize GxP Uses. Hovsep Kirikian - April 18, 2022 Case Studies Biotech Clinical
ERP Validation in 80% Less Time! Case study on ERP Validation in 80% Less Time!. Diane Gleinser - April 17, 2022 Case Studies Medical Device Quality Assurance, Regulatory
DocuSign in 7 Days to Enable eSignatures for Remote Work Case study on DocuSign in 7 Days to Enable eSignatures for Remote Work. David Blewitt - April 13, 2022 Case Studies Pharma Information Technology, Quality Assurance
Validation of SharePoint for GxP Content Management Solution Case study on Validation of SharePoint for GxP Content Management Solution. Erin Christy - April 12, 2022 Case Studies Biotech Research & Development
