Leveraging Technology to Meet FDA 21 CFR Part 11 Brochure

To gain efficiency, many manufacturers have turned to electronic documentation to comply with U.S. Food and Drug Administration regulations. Learn more about how SYSPRO helps companies simplify compliance with 21 CFR Part 11, a set of rules that dictate how FDA-regulated industries manage electronic records and electronic signatures.

“Because electronic documents are subject to greater risks of falsification, misrepresentation, and change than paper records, the FDA determined that electronic documents required special controls. This resulted in the introduction of 21 CFR Part 11.”

– Document Excerpt

A message from our CEO, Phil Duff

Close to our hearts at SYSPRO is the need to protect our loved ones, our families, our colleagues, partners and customers. SYSPRO CEO, Phil Duff, shares his message and thoughts around the COVID-19 Pandemic.