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
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. Brian Rankin - August 7, 2024 Blogs Medical Device Information Technology
How to Fulfill Expectations for Data Privacy and Security Explore a variety of tools and services to help your organization achieve data confidentiality, integrity, and availability. Michelle Gardner - August 6, 2024 Blogs Biotech, Medical Device, Pharma Information Technology
Manual Testing vs. Automated Testing Explore the key differences between manual and automated testing and discover the benefits of automated regression testing. Hovsep Kirikian - July 17, 2024 Blogs Biotech, Medical Device, Pharma Information Technology
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
Workforce Optimization: Maximizing Employee Efficiency and Productivity Workforce optimization ensures that the right people are performing the right tasks. Find a delivery model that best fits your organization. Jennifer Hawkins - July 12, 2024 Blogs Biotech, Medical Device, Pharma Clinical, Manufacturing, Research & Development
