Ace your audits with fully validated software and FDA-compliant features

CERDAAC’s Compliance module was purpose-built to serve the most demanding regulatory requirements in lives-at-stake markets such as life sciences, aerospace and defense. The system is pre-validated and includes features designed to ensure audit readiness.

Compliance Module Benefits


Software validation can be burdensome and time-consuming. SIMCO pre-validates every CERDAAC release to ensure compliance with FDA 21 CFR Part 11, so you don’t need to invest in expensive validation efforts. As new capabilities are added, SIMCO ensures they are validated prior to release.

FDA-Compliant Electronic Signatures

Digital signatures use cryptographic authentication methods in order to verify the identity of the signer and prevent unauthorized users. Fields can be locked down and require approval again if changed. You can set signatures to be role-based, require multiple levels of signatures, and trigger alerts based on a signature to ensure approval.

Learn more about FDA Compliant Digital Signatures

Ace Your Audits

Any modifications made to your records are immediately logged and captured in the extensive audit trails so you can track changes and ensure proper documentation. SIMCO also provides validation/verification audit support in conjunction with the Compliance Module to help you ace your audits.

“I can trust that all of the certificates in CERDAAC can pass an audit. The labeling is correct, the date a part was calibrated and the date due are all correct. We usually shine like stars through an audit as long as it’s a tool that is calibrated by SIMCO.”

Lisa Reid
Senior Quality Engineering Aid & Calibration Administrator
Korry Electronics White Logo

Featured Resources

Interested in learning more about CERDAAC Software? Schedule a demo today to see how CERDAAC can meet your organization’s needs.