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What is KOŚA DMS?

KOŚA DMS is an all-encompassing cloud-based document management system designed for organizations operating in the pharmaceutical, biotechnology, medical device, and wider life sciences industries. It supports the development, review, approval, distribution, and tracking of controlled documents, while also incorporating workflows for standard operating procedures (SOPs), policies, forms, and vital quality records. The solution offers role-based access control, electronic signatures, audit trails, and periodic review features, enabling teams to maintain a clear and compliant document history for regulated activities. Its integration with Microsoft Word simplifies the drafting process, allowing users to create documents in an environment they are already comfortable with, while links to ERP and LIMS systems provide seamless connections to operational workflows. Tailored for teams in quality assurance, quality control, regulatory affairs, and document control, KOŚA DMS effectively coordinates document lifecycle management across multiple locations and functions, fostering adherence to industry regulations. Moreover, the intuitive interface enhances user experience, enabling teams to manage their document processes with ease and efficiency, thereby minimizing potential disruptions. This comprehensive approach not only streamlines operations but also promotes organizational efficiency and compliance.

What is Ideagen Please Review?

Ideagen Please Review is document review and co-authoring software for regulated teams, with redaction and a full audit trail built in. It replaces email chains and manual comment consolidation with one secure, browser-based place to review, approve and sign off documents. Key benefits: - Faster reviews: parallel or sequential workflows, with feedback consolidated in one workspace. Reduces review time by up to 65%. - Fewer version conflicts: reviewers work against a single master document and accepted changes are applied automatically. - Tighter control: paragraph-level permissions, secure external collaboration and EMA Policy 70-ready redaction. - Audit-ready records: every action, comment and change is captured, with instant audit reports. Runs natively inside Ideagen Quality Management and integrates with Veeva Vault.

Media

Media

Integrations Supported

Microsoft Word

Integrations Supported

API Availability

Has API

API Availability

Pricing Information

Pricing not provided
Free Trial Offered?

Pricing Information

Pricing not provided

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Not specified

Training Options

Documentation Hub
Webinars
On-Site Training

Training Options

Not specified

Company Facts

Organization Name

KOŚA

Date Founded

2025

Company Location

India

Company Website

kosa-ai.com/pharmaceutical-document-management-system/

Company Facts

Organization Name

Ideagen

Date Founded

1993

Company Location

United Kingdom

Company Website

www.ideagen.com/solutions/quality/document-review

Categories and Features

Document Control

Not specified

Document Management

Not specified

Document Workflow

Not specified

Categories and Features

Document Management

Access Controls
Collaboration Tools
Compliance Tracking
Document Archiving
Document Retention
File Recovery
File Type Conversion
Offline Access
Version Control

PDF Redaction

Not specified

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