DMS - AST

Document Management Systtem

Maximize efficiency, ensure compliance, and streamline document handling with DMS .

Document Management System

Document Management Systems revolutionize documentation processes in pharmaceuticals, biotech, and other regulated sectors. Our solutions include version control, documentation collaboration, document obsoletion, and archival management, streamlining operations and ensuring regulatory compliance.

Why DMS ?

Maximize Efficiency

Optimize documentation procedures to save valuable time and effort

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Version Control

Automatic tracking ensures access to the latest document versions, preventing regulatory issues.

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Enhanced Collaboration

Facilitates parallel reviews, ensuring seamless collaboration between departments.

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Secure Access Control

Only authorized users can access, modify, share documents, enhancing data protection

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Top Features of DMS

Manage Documentation Lifecycle

Effectively manage complete SOP, STP, Protocols, reports, BMR, BPR, Quality manuals, site master file, validation master file documentation lifecycle from creation to obsoletion

Document Template Management

Develop documents according to standardized templates with customized Document Number Format (DNF), Control selection, Header control and Signatory control

Document Tracking & Retrieval

Swift document retrieval with predefined mechanisms. Eliminates challenges faced in manual document retrieval with efficient automated processes

Enhanced Productivity

Track pending tasks for enhanced productivity and efficiency. Get real-time tracking, email notifications, reminders, and escalations to ensure adherence to deadlines