Efficient Migration and Validation of SAP Workflows to the Cloud Discover how USDM supported a global clinical trial company in transitioning its SAP workflows to the cloud. Mohamed Mestari - July 17, 2023 Case Studies CMO Information Technology, Regulatory
2023 Life Sciences Dreamin’ Conference Marium Amin - July 17, 2023 News & Events Information Technology
Understanding FD&C 524B – Cybersecurity Requirements for Medical Devices WHITE PAPER: Learn why cybersecurity matters for medical devices and 9 Steps to meet FD&C 524B requirements. Brian Rankin - July 6, 2023 White Papers Medical Device Information Technology, Regulatory
Addressing cybersecurity concerns in the life sciences industry When it comes to preventing cybersecurity incidents, establishing and implementing cybersecurity controls is essential for every life sciences organization. Roger Davy - July 5, 2023 Blogs Biotech, Medical Device, Pharma Information Technology
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. 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! Lisa Om - June 15, 2023 White Papers Biotech, Medical Device, Pharma Information Technology, Quality Assurance
