Paperless QMS revolutionizes pharmaceutical quality processes through a secure and validated digital platform. Built in compliance with global GMP, USFDA, and EU-GMP standards, this system automates all core Quality Management System (QMS) components including document control, deviation tracking, CAPA, audits, and training workflows — eliminating paperwork, boosting traceability, and ensuring compliance.
Streamline compliance and drive continual improvement with a validated, fully digital QMS platform for pharma.
Digital SOP Management
Change Control & Deviation Handling
Integrated CAPA System
Quality Risk Management
Audit Scheduling & Tracking
Employee Training Record Management
Regulatory-Compliant Workflow
Real-Time Dashboards & Analytics