Description
Key Features and Benefits
- Document Control & Electronic Signatures – Securely manage, track, and approve documents with FDA 21 CFR Part 11 compliance.
- Audit & Compliance Management – Automates audits, CAPA tracking, and compliance with ISO and FDA standards.
- Risk & CAPA Management – Identifies, tracks, and mitigates risks with corrective and preventive actions.
- Training & Employee Management – Links training records to compliance needs, ensuring proper certification.
- Supplier & Nonconformance Management – Evaluates supplier quality and tracks deviations to maintain compliance.
- Customizable Reports & Dashboards – Provides real-time insights with automated email notifications.
Key Differentiators
- All-in-One QMS – Includes 25+ pre-installed modules, eliminating the need for extra customization costs.
- Flexible Deployment – Available as cloud-based or on-premise with access across devices.
- Affordable & Scalable – Starts at $1,700 per year, making it a cost-effective alternative to premium QMS solutions.
- Fast Implementation – User-friendly interface with unlimited training and support for easy adoption.
