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pharmaREADY® DMS
A centralized Document Management System providing a collaborative workflow across departments to manage documents throughout their life cycle
What is a Document Management System and why does your business need one?
A Document Management System (DMS) is your key to simplifying and streamlining how your organization handles its critical documents and information. By centralizing storage and management, a DMS enables you to easily and efficiently author, review, approve, track, distribute, store, access, control printing, manage reporting, and organize documents and manage business information. An effective DMS serves as your Single Source of Truth, ensuring consistency, transparency, and improved collaboration. It’s not just about document management, it’s about empowering your business to work smarter, not harder.
Documents are omnipresent and managed cross-functionally throughout organizations across the globe. Their management is often business critical and, for life sciences organizations, can mean the difference between compliance with the regulatory authorities, or non-compliance and putting patient safety at risk. Supporting the entire document life cycle process, Navitas Life Sciences’ pharmaREADY® DMS equips your organization to securely manage a wide range of business documents.
Navitas Life Sciences Regulatory Affairs team is using pharmaREADY® DMS to deliver End-to-End Regulatory requirement from IND through NDA and post approval stages, especially the documents pertaining to Module 1 to 5. Client and Navitas users perform co-authoring and review using DMS. The services include Regulatory strategy, CMC Authoring and Review, Clinical and Non-Clinical Document Authoring and Review, Publishing & Submissions, and Archival.
pharmaREADY® DMS utilizes open architecture to enable easy integration with other Enterprise Resource Planning (ERP) systems
pharmaREADY® DMS Supports the management of:
- GxP and non-GxP documents
- SOPs
- Work Instructions
- Preparation, review, and approval of Dossier documents
- Creating submission-ready documents
Built specifically for Life Science organizations, pharmaREADY® DMS is 21 CFR Part 11 compliant and supports controlled printing
Working with Microsoft 365, pharmaREADY® DMS allows for collaborative authoring and review
Get in touch
Available as an independent product, or as part of an integrated package with our other modules, pharmaREADY® DMS is available for
Pharmaceuticals
Biologics and Biosimilars
Medical Devices
Generic Drugs
Animal Health
With a customizable dashboard and pending user actions available on the landing page, we also pride ourselves on our ability to deliver
- A unified licensing model with flexible options, further supported with optimal pricing to include both licensing and maintenance
- Rapid implementation and rollout, with several ‘ready-to-deploy’ features
- Faster legacy data migration with our ‘Bulk Import’ feature
- Unique features including collaborative authoring and consolidated review
- Integration with other ERP systems including, but not limited to, TrackWise® and SAP®
- Meta data-based and keyword-based searches
