AI-Powered
Document Management System
Get GxP-compliant control over your documents without the complexity. Easily manage the entire lifecycle, from drafting with AI assistance to secure distribution and 21 CFR Part 11 compliant approvals, all in one intuitive, centralised system.
One platform for Global Compliance
The intelligent document management system simplifies how life sciences teams author, approve, and manage their most critical GxP documentation while ensuring regulatory compliance.
Author and Approve SOPs in Record Time
Our intuitive in-built editor with a powerful AI co-author enables your team to create clear, consistent Standard Operating Procedures from templates in minutes, all within a single, controlled document management platform.
Be Permanently Inspection-Ready
Ensure GxP compliance with immutable audit trails, validated FDA 21 CFR Part 11 e-signatures, and automated periodic review cycles. Produce any required document, including version history and approval records, instantly.
Close Training Gaps
Implement new SOPs only after all relevant personnel are trained. This ensures a thorough understanding of process changes prior to their deployment.
A Comprehensive Suite of Features Delivered Through an Intuitive and Accessible Interface
AI- Powered Tools
Industry First Built in AI Document Editor
Our built-in AI-powered document editor generates clear, compliant, and consistent GxP documents from simple prompts, turning weeks of drafting into minutes and ensuring quality and regulatory alignment from the very first word.
Easy Collaboration
Collaborate, Review and Approve in the Same Platform
Our DMS platform brings your entire team together to comment, review, and approve documents with validated e-signatures in one place, creating a cohesive workflow and cutting review cycles in half.
Intelligent Assessments
Create Assessments for Document Training Using AI
Our AI automatically generates relevant assessment questions, allowing you to ensure and document true understanding and create a formidable training record.
Controlled Issuance
Issue Controlled Copies and Ensure GDP and Data Integrity
Our system allows you to issue secure, watermarked, and tracked copies that can be recalled when obsolete. This ensures Good Documentation Practices (GDP) by preventing the use of outdated information, safeguarding both data integrity and operational quality.
When reviewing the platform, it's clear it was engineered with growth in mind. The unified solution is inherently more scalable than trying to bolt on different systems during a high-growth phase.
Jayanth Sridhar
CEO • Biologics, Dr. Reddy's
For brands that outsource manufacturing, this ability to extend GxP control and maintain a single source of truth with their CMOs is a significant leap forward in mitigating risk.
Varun Chandra
Vice President of R&D, Quality, and Regulatory • SeneGence
