Why Integrated GxP Compliance is More Progressive than Traditional Managed Services Learn why defining and measuring value helps to provide a trusted solution that responds to changes and scales to meet your needs. 0 Michelle Gardner - September 21, 2023 Blogs Biotech, Medical Device, Pharma Information Technology, Quality Assurance
Integrated GxP Compliance ON-DEMAND WEBINAR: an insightful webinar as we delve into the world of integrated GxP compliance within the life sciences industry. 0 Webinars Biotech, Medical Device, Pharma Information Technology, Quality Assurance
Discover a next-generation business model that drives tangible business outcomes Outcome-based next-generation business models empower Quality teams to be proactive in minimizing risk and ensuring regulatory compliance. 0 Michelle Gardner - September 6, 2023 Blogs Biotech, Medical Device, Pharma Quality Assurance
Integrated GxP Compliance for the Life Sciences Industry What is integrated GxP compliance? It’s a catalyst for innovation, adaptability, and continuous improvement while maintaining compliance of regulated cloud applications and on-premises IT systems. 0 Lisa Om - August 24, 2023 White Papers Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance, 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
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
