QEdge is an integrated Quality Management System (QMS) tailored for pharmaceutical manufacturing and life sciences industries. Designed to meet stringent regulatory standards like FDA, EU-GMP, and ICH guidelines, QEdge streamlines quality processes across Change Control, Deviation, CAPA, Document Management, Training, and Vendor Qualification. With features like SOP lifecycle management, SCORM-based eLearning, and audit-ready compliance tracking, QEdge ensures operational excellence, data integrity, and regulatory readiness for GxP environments.
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
PQR/APQR automation
Auto-generate PQR reports with data from multiple sources.
Vendor qualification
Simplify vendor communication and approval processes.
Edge out your quality management hassled with QEdge
Impact
1
+
Implementations
1
k+
Users
1
+
Quality processes
1
k+
Documents managed
1
+
SOP's implemented
1
+
Trainers qualified
1
+
PQR submissions
1
+
Vendors qualified
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
Want to know more about QEdge