Crafted exclusively for the life sciences industry, our all-in-one QMS isn’t just a tool; it’s a complete shift towards an automated, traceable, and compliant quality process.
Don’t believe us? Take a look at Scilife’s most prominent features:
- Document Management: Go beyond simple storage with a system that guarantees electronic signatures and efficient workflow automation. Always in compliance with 21 CFR Part 11.
- Tailored Training: Empower your team with role-specific training modules that guarantee your team is prepared and compliant.
- Integrated Audits: Combine your audit activities with CAPAs, Event Tracking and Risk Management for unmatched supervision and improvement capabilities.
- CAPA Monitoring and Management: Ensure corrective actions are effectively monitored and managed to prevent recurrence of any non-conformities.
Say goodbye to mundane, manual QMS tasks. Make quality a dynamic, integral part of your team’s ethic with Scilife, and watch compliance costs fall, while standards soar.
Ready to see it in action? Reserve a demo and step into the future of quality management today.
Contact us HERE!