USDM Life Sciences at the American Medical Device Summit Join us for a quality and regulatory workshop presented by USDM’s Jay Crowley and Hovsep Kirikian on October 2. Michelle Gardner - August 14, 2024 News & Events Medical Device Manufacturing, Regulatory
The Importance of CIS Critical Security Controls (CIS18) in Life Sciences Security breaches in life sciences underscore the need for robust cybersecurity measures. Learn how to implement CIS Critical Security Controls to strengthen your cybersecurity posture and mitigate risk. Brian Rankin - July 17, 2024 Blogs Biotech, Medical Device, Pharma Information Technology, Regulatory
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. 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. 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 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. Michelle Gardner - June 3, 2024 Blogs Regulatory
