Enhancing Regulatory Compliance for a Pharmaceutical Manufacturing Company Learn how USDM seamlessly validated DocuSign for a Pharmaceutical Manufacturing Company. 0 Nithya Sittaramane - August 24, 2023 Case Studies Pharma Information Technology
Reducing Cybersecurity Risks: A Primer for Emerging Life Sciences Firms In the fast-paced landscape of emerging life sciences firms, one critical aspect often overlooked is the need for robust cybersecurity measures. 0 Brian Rankin - July 18, 2023 Blogs Biotech, Medical Device, Pharma Information Technology
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. 0 Roger Davy - July 5, 2023 Blogs Biotech, Medical Device, Pharma Information Technology
Validation Requirements and Responsibilities Who’s responsible for what in the validation process? Get the white paper for more info! 0 Lisa Om - June 15, 2023 White Papers Biotech, Medical Device, Pharma Information Technology, Quality Assurance
Lessons from the USDM Cloud Assurance Box GxP Automated Testing Tool Blog article topic: Lessons from the USDM Cloud Assurance Box GxP Automated Testing Tool. 0 Ryan McDonald - May 22, 2023 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Managing GxP Workflows & Continuous Cloud Compliance with ProcessX and ServiceNow ON DEMAND WEBINAR: Managing GxP Workflows & Continuous Cloud Compliance with ProcessX and ServiceNow 0 Webinars Biotech, Medical Device, Pharma Information Technology
