Why Integrated GxP Compliance is More Progressive than Traditional Managed Services Learn why defining and measuring value helps to provide a trusted solution that responds to changes and scales to meet your needs. 0 Michelle Gardner - September 21, 2023 Blogs Biotech, Medical Device, Pharma Information Technology, Quality Assurance
Discover a next-generation business model that drives tangible business outcomes Outcome-based next-generation business models empower Quality teams to be proactive in minimizing risk and ensuring regulatory compliance. 0 Michelle Gardner - September 6, 2023 Blogs Biotech, Medical Device, Pharma Quality Assurance
Integrated GxP Compliance for the Life Sciences Industry What is integrated GxP compliance? It’s a catalyst for innovation, adaptability, and continuous improvement while maintaining compliance of regulated cloud applications and on-premises IT systems. 0 Lisa Om - August 24, 2023 White Papers Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance, Regulatory
Enhancing Regulatory Compliance for a Pharmaceutical Manufacturing Company Learn how USDM seamlessly validated DocuSign for a Pharmaceutical Manufacturing Company. 0 Nithya Sittaramane - August 24, 2023 Case Studies Pharma Information Technology
Streamlining Oracle Clinical One Software Releases Discover how the team of experts at USDM simplified release management for a clinical research firm. 0 Mohamed Mestari - August 15, 2023 Case Studies CRO Information Technology
Enhancing Regulatory Compliance with Argus Safety Database Learn how USDM ensured audit readiness for a global biotech company. 0 Mohamed Mestari - August 15, 2023 Case Studies Biotech Information Technology, Regulatory
