Global Clinical Research eBook: 21 CFR Part 11 vs. EudraLex Annex 11

Looking to ensure that your electronic records and signatures meet regulatory requirements set forth by the FDA and European Commission? Download this guide to learn about the high-level concepts related to the use of computerized systems and how to ensure the accuracy and integrity of your electronic records.

With insights into both Part 11 and Annex 11, this guide is the perfect resource for anyone looking to use computerized systems for regulated activities in a compliant manner.