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Paperless DMS – Pharma Documentation Management is Now Easy

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.

Core Features

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

Documents You Can Manage

SOPs & Work Instructions
BMRs / BPRs
Validation Protocols
Quality Manuals
Audit & Deviation Reports
Change Control Records
Training Records
QMS Documentation
Explore Paperless-DMS