AI, Adversarial Attacks, and Insider Threats in Life Sciences With the integration of AI comes significant security risks. Learn how to overcome attacks and threats, starting with an AI risk assessment. 0 Brian Rankin - July 12, 2024 Blogs Biotech, Medical Device, Pharma Information Technology, Regulatory
Q&A: Mandatory Use of EUDAMED Now Starting Q1 2026 Jay Crowley and Lionel Tussau help make medical device manufacturers aware of key dates, requirements, and regulatory implications. 0 Jay Crowley - July 2, 2024 Blogs Medical Device Manufacturing, Regulatory
Mandatory Use of EUDAMED Now Starting Q1 2026 ON-DEMAND WEBINAR: Technical considerations and guidance for managing UDI data to meet the deadline 0 Webinars Medical Device Regulatory
GxP Primer: Where Do Good Practices Come From and Why Do We Need Them? Global health regulators home in on critical requirements for life sciences organizations. 0 Michelle Gardner - June 3, 2024 Blogs Regulatory
Veeva MedTech 2024 in Austin Join Veeva and USDM at Veeva MedTech Summit in Austin from April 29th to May 1st. Jay Crowley will be speaking on Holistic Data Management. 0 Lisa Om - April 4, 2024 News & Events Medical Device Information Technology, Regulatory
Good Machine Learning Practice (GMLP) for Medical Device Development: Guiding Principals Explore the guiding principles of Good Machine Learning Practice (GMLP) and the importance of ethics, data integrity, and model transparency. 0 Jim Macdonell - March 15, 2024 Blogs Medical Device Information Technology, Regulatory
