LLMs and Cybersecurity Standards in Life Sciences LLMs present opportunities to advance drug discovery and development, but protecting the data being processed takes precedence. 0 Brian Rankin - October 16, 2024 Blogs Biotech, Medical Device, Pharma Clinical, Information Technology, Regulatory
Good Automated Manufacturing Practice vs. Computer Software Assurance CSA modernizes and refines GAMP 5 practices to make validation more efficient without compromising system quality or compliance. 0 Jim Macdonell - September 23, 2024 Blogs CMO, Medical Device, Pharma Manufacturing, Quality Assurance
Getting Started with the Common Service Data Model ServiceNow Community MVP John Zhang helps to clarify the complexities of CSDM and answers questions from the Ask the Experts webinar. 0 John Zhang - September 11, 2024 Blogs Biotech, Medical Device, Pharma Information Technology
Penetration Testing in Life Sciences Lab Environments Learn what penetration testing is and why it’s a critical component of a comprehensive cybersecurity strategy. 0 Brian Rankin - August 23, 2024 Blogs Biotech, Medical Device, Pharma Information Technology
Q&A: Ensuring AI Compliance and Maximizing the Value of Your GxP Technologies USDM answers questions about starting and scaling AI initiatives in the life sciences industry and protecting sensitive data. 0 Various Authors - August 22, 2024 Blogs Biotech, Pharma Information Technology
Cybersecurity in Medical Devices: How Did 524B Come About? Section 524B of the Federal Food, Drug, and Cosmetic Act (FD&C Act) recognizes the need for robust cybersecurity measures in medical devices. 0 Brian Rankin - August 7, 2024 Blogs Medical Device Information Technology
