Streamline Document Signing with Built-In Continuous Compliance Learn how USDM validated DocuSign for a biotech company with a remote workforce, enhancing efficiency and flexibility. 0 Nithya Sittaramane - June 21, 2023 Case Studies Biotech Information Technology, Regulatory
Validation Requirements and Responsibilities Who’s responsible for what in the validation process? Get the white paper for more info! 0 Lisa Om - June 15, 2023 White Papers Biotech, Medical Device, Pharma Information Technology, Quality Assurance
Streamlined Supply Chain Management and Continuous Compliance with Oracle SCM Learn how USDM efficiently validated Oracle SCM for a global clinical trial company. 0 Mohamed Mestari - June 8, 2023 Case Studies CRO Information Technology, Regulatory
Simplified Change Control Management and Continuous Validation for Oracle SCM Learn how USDM helped a global medical technology company develop a customized validation and regression testing plan to manage Oracle SCM patches and updates. 0 Mohamed Mestari - June 8, 2023 Case Studies Medical Device Information Technology, Regulatory
GxP System Validation and Monitoring for Half the Cost Learn how an emerging therapeutics company saves more than $400k annually and maintains SaaS systems for half that cost. 0 Lisa Om - June 6, 2023 Case Studies Biotech Information Technology
Lessons from the USDM Cloud Assurance Box GxP Automated Testing Tool Blog article topic: Lessons from the USDM Cloud Assurance Box GxP Automated Testing Tool. 0 Ryan McDonald - May 22, 2023 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
