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
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. 0 Mohamed Mestari - July 17, 2023 Case Studies CMO Information Technology, Regulatory
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. 0 Brian Rankin - July 6, 2023 White Papers Medical Device Information Technology, Regulatory
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
An Update on the FDA’s UDI and GUDID Compliance Requirements ON-DEMAND WEBINAR: An update on the FDA’s requirements and notification activities and aims to answer many of the incoming questions our UDI consultants have received recently. 0 Webinars Medical Device Manufacturing, Regulatory
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
