Enhancing Regulatory Compliance with Argus Safety Database Learn how USDM ensured audit readiness for a global biotech company. 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. 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. 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. 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. 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. Mohamed Mestari - June 8, 2023 Case Studies CRO Information Technology, Regulatory
