USDM Life Sciences Summit 2023 ON DEMAND: Progressive technology and compliance thinking to speed GxP cloud adoption and maturity. Watch the replay. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
Computer Software Assurance (CSA) Draft Guidance Webinar ON-DEMAND WEBINAR: Please watch our panel of experts, including Francisco Vicenty, Program Manager, Case for Quality, FDA, discuss any changes and implications impacting medical devices, pharma, and biotech organizations. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Regulatory
Automating Validation Across Your Tech Stack ON-DEMAND WEBINAR: This webinar will addresses forward-thinking validation and continuous compliance considerations for modern cloud technologies. Webinars Biotech, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, 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
Box GxP and Cloud Assurance for FDA Submission Case study on Box GxP and Cloud Assurance for FDA Submission. David Blewitt - April 19, 2022 Case Studies Biotech, Pharma Clinical
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
