Is Your QMS 21 CFR Part 11 Compliant?

By Johanna Blair, Staff Writer, MasterControl

Gone are the days of paper-based quality systems as the “norm.” Sure, you can still use paper-based records for official documentation and the U.S. Food and Drug Administration (FDA) won’t mind (too much). Sure, you can even keep a web of siloed spreadsheets and/or standalone document folders and/or archived paper documents in cold storage, etc. with handwritten approval signatures. But, why?

With many options for digital transformation available in the quality software sector, there’s never been more opportunity to digitize your quality management system (QMS). Explore the benefits of a digital QMS and more.