
In-depth on CFR 11
The U.S. Food and Drug Administration (FDA) plays a vital role in protecting public health by regulating medical devices. Part 11 of Title 21 of the Code of Federal Regulations (CFR) lays out the FDA’s requirements for electronic records and electronic signatures used by medical device manufacturers. Implications of CFR 11 This regulation ensures the[…]
Subscribe to our newsletter.
Your go-to destination for insights, best practices, and innovative solutions in supplier quality assurance.
Recent Posts
The ROI of Lean ISO Management Systems
January 31, 2025
The Power of Second Chance Manufacturing Programs
January 30, 2025
The Secret to Customer Delight: Embedded Quality
January 28, 2025
The Psychological Impact of Stress on Quality Outcomes
January 28, 2025
Let's talk to see how PPAP Manager can help your company to save time and money.