Does Ideagen Quality Management adhere to Title 21 CFR Part 11?
Ensuring compliance with the U.S. FDA’s Title 21 CFR Part 11 regulation is essential for maintaining the integrity of your electronic records and signatures.
In this document we detail how Ideagen Quality Management aligns to each clause in the regulation. An essential companion piece for any pharmaceutical, biotechnology, or medical device manufacturer that needs to ensure consistency, confidentiality, and integrity in their electronic records.
Download guide
Download your guide nowI confirm that I have read and understood the Ideagen Privacy Policy. I consent to the personal data that I submit being processed by Ideagen, including consent to receive emails regarding Ideagen’s products and services. I understand that I may unsubscribe at any time.