Streamline your pharmaceutical document lifecycle with Paperless DMS — a robust Document Management System (DMS) designed for cGMP, WHO-GMP, USFDA, and MHRA compliance. This pharma-ready digital platform centralizes SOPs, BMRs, validation protocols, change controls, and QMS documentation — complete with version control, audit trails, and user access logs.
Empower your pharma operations with secure, traceable, and compliant document management — anytime, anywhere.
Centralized Document Repository
Custom Workflow Management
Version Control & Change History
User & Role-Based Access
CAPA, Deviation & Audit Trail Linking
eSignatures & Approval Flows (21 CFR Part 11)
Automated Review & Retention Reminders
GMP/GLP Compliant Templates
Secure Cloud/On-Premise Storage
Real-Time Access Across Departments