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A Risk-based Enterprise Quality Management System
An industry-ready solution for pharma and life sciences that handles all your quality challenges, ensuring full compliance with configurable workflows and comprehensive audit trails.
Effortlessly migrates your work from manual to digital, seamlessly integrating with your existing systems. It is pre-validated and cloud-ready, ensuring a smooth transition. Implement QEdge within just four weeks and experience streamlined, compliant quality management.
What makes Quality Management Sytem by Sarjen stand out!
Process control
Streamline processes with integrated Change Control, CAPA, and more.
DocControl & Issuance
Efficiently manage, track, and distribute critical documents.
Training management
Automate training and certification for regulatory compliance
Vendor qualification
Simplify vendor communication and approval processes.
PQR / APQR
Auto-generate PQR reports with data from multiple sources.
Impact
1
+
Sites audits passed
1
Trusted by companies
1
k+
Users
1
+
Country presence
Features
Always Audit-ready
Easy Process Versioning
Configurable Processes
FDA and EU-compliant Workflows
Field and functional Audit Trails
User Friendly
Other domains served by Sarjen systems
Clinical Research
Pharmacovigilance
Regulatory & Compliant
Manufacturing
Supply Chain
CRM
Want to know more about QEdge


