About Steadify
Steadify is a training document management platform built specifically for regulated industries that require FDA 21 CFR Part 11 compliance.
Our Mission
To simplify compliance and training management for life sciences companies.
Compliance First
Built from the ground up to meet FDA 21 CFR Part 11 requirements.
Customer Focus
Designed with feedback from QA managers and compliance officers.
What We Do
Steadify helps organizations manage their training documentation with complete audit trails, electronic signatures, and automated training assignments. Our platform ensures that your team stays compliant while reducing administrative overhead.
Why Choose Steadify
- Purpose-built for FDA 21 CFR Part 11 compliance
- Intuitive interface that requires minimal training
- Automated training assignment based on job roles
- Complete audit trail for every action
- Electronic signatures with full traceability
- SOC 2 Type II compliant infrastructure