eSignature Transforms Workflows for Leading Biotech Company Learn how a leading biotech company improved efficiencies and saved costs with Cloud Assurance for DocuSign. 0 Nithya Sittaramane - April 13, 2023 Case Studies Biotech Regulatory
ZenQMS Partners with USDM Life Sciences to Simplify GxP Quality Assurance for Life Sciences Customers 0 Ryan McDonald - March 21, 2023 News & Events Biotech, Medical Device, Pharma Information Technology, Quality Assurance, Regulatory
Veeva & USDM at Veeva MedTech 2023 in Chicago Join Veeva and USDM at Veeva MedTech Summit in Chicago at May 30 to June 1st. USDM will be speaking. Join us there! 0 Ryan McDonald - March 10, 2023 News & Events Medical Device Information Technology, Regulatory
NetSuite for GxP, Regulated Use Cases ON DEMAND EVENT: Progressive technology and compliance thinking to fast-track your journey from R&D to commercialization. Watch now. 0 On Demand, Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
Fast DocuSign Validation and SOPs for Clinical-Stage Biopharma Needing GxP System Expertise Learn how USDM’s eSignature system experts helped Xequel Bio streamline its document signing process. 0 Nithya Sittaramane - March 1, 2023 Case Studies Pharma Information Technology, Regulatory
USDM Supports Startups Navigating Technology and Compliance 0 Ryan McDonald - February 28, 2023 News & Events Biotech, Medical Device, Pharma Information Technology, Quality Assurance, Regulatory
