Pharma – Centris Office

Secure, Compliant & Pharma-Ready.

Revolutionize Pharma Industry with Centris

From R&D to Regulatory Compliance - organize, secure, and accelerate your pharmaceutical workflows with ease.

No credit card required.

Why Pharma Companies Need a Smarter DMS

Pharmaceutical organizations manage thousands of critical documents daily - from clinical trials to regulatory submissions. Without a modern system, errors, delays, and compliance risks can cost both time and reputation

Regulatory Pressure

Centris simplifies compliance with built-in audit trails, version control, and secure access, your team stays inspection-ready at all times and reduces regulatory burdens.

Complex Documentation

From clinical trial data to SOPs and quality reports, Centris centralizes everything in one repository. This eliminates silos and makes critical information instantly accessible across departments.

Data Integrity Risks

Centris maintains real-time collaboration with full traceability of edits and approvals. Role-based permissions safeguard sensitive pharma data, ensuring accuracy and accountability at every step.

Slow Approval Cycles

Automate your review and approval workflows with Centris to cut down bottlenecks. Faster sign-offs mean shorter time-to-market for vital drugs and therapies.

Centris Powers Pharma Success

Compliance Made Simple, Innovation Made Faster.

Unified Repository

Store and access regulatory, clinical, and quality documents in one place.

Faster Audits

Instantly retrieve records for FDA, EMA, or WHO inspections

Seamless Collaboration

Connect R&D, Quality, Regulatory, and Manufacturing teams.

Enhanced Security

Protect sensitive IP, patents, trial results with enterprise-grade encryption.

Discover all features

Trusted by Pharma Innovators

Leading pharma companies are already using Centris to transform their documentation processes. Stay ahead and a get free demo now.

See Pharma Use Case Demo

30-days trial, no credit card required.