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
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. 0 Michelle Gardner - August 6, 2024 Blogs Biotech, Medical Device, Pharma Information Technology
Oracle CloudWorld 2024 – Life Sciences Lunch & Learn If you’re attending Oracle CloudWorld, then you’re invited to an exclusive Life Sciences Lunch & Learn. Register today! 0 Michelle Gardner - July 24, 2024 News & Events Biotech, Medical Device, Pharma Information Technology, Regulatory
USDM Sponsors Veeva R&D and Quality Summit 2024 Connect with USDM at the Veeva R&D and Quality Summit in Boston. We've got innovative ideas to share with you! 0 Michelle Gardner - July 23, 2024 News & Events Information Technology, Quality Assurance
Manual Testing vs. Automated Testing Explore the key differences between manual and automated testing and discover the benefits of automated regression testing. 0 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. 0 Brian Rankin - July 17, 2024 Blogs Biotech, Medical Device, Pharma Information Technology, Regulatory
