KOŚA DMS Description

KOŚA DMS is a comprehensive cloud document management solution tailored for organizations in the pharmaceutical, biotechnology, medical device, and broader life sciences sectors. It facilitates the creation, evaluation, authorization, distribution, and revision tracking of controlled documents, incorporating workflows for standard operating procedures (SOPs), policies, forms, and other essential quality records. With the ability to manage role-specific access, electronic signatures, audit trails, and periodic reviews, teams can ensure that document histories remain traceable for regulated processes. Integration with Microsoft Word enhances the drafting process, allowing users to work within a familiar authoring environment, while connections to ERP and LIMS systems enable seamless documentation linkage with operational workflows. Designed specifically for quality assurance, quality control, regulatory affairs, and document control teams, this system streamlines the coordination of document lifecycle activities across various sites and functions, ensuring compliance with industry regulations. Furthermore, the platform's user-friendly interface allows teams to efficiently navigate and manage their document processes without unnecessary complications.

Pricing

Free Trial:
Yes

Integrations

API:
Yes, KOŚA DMS has an API

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Company Details

Company:
KOŚA
Year Founded:
2025
Headquarters:
India
Website:
kosa-ai.com/pharmaceutical-document-management-system/

Media

KOSA Regulatory Submissions interface listing documents, versions, controlled or approved statuses, dates, version history, and traceability cards.

KOSA Regulatory Submissions interface listing documents, versions, controlled or approved statuses, dates, version history, and traceability cards.

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Product Details

Platforms
Web-Based
Types of Training
Training Docs
Webinars
In Person
Training Videos
Customer Support
Business Hours
Live Rep (24/7)
Online Support

KOŚA DMS Features and Options

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