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
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
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
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
Good Laboratory Practices (GLP): Ensuring Quality and Reliability in Scientific Research This blog delves into the fundamental aspects of Good Laboratory Practices & how it helps life sciences organizations maintain scientific rigor. 0 Hovsep Kirikian - June 14, 2023 Blogs Biotech Clinical
