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What is Ketryx?

Ketryx enables life sciences teams to utilize their preferred development tools and automation for generating evidence, ensuring real-time traceability, and reducing process deviations. This automation of documentation allows teams to allocate more time to addressing critical risks that might affect their projects. Ketryx integrates quality management system (QMS) processes into platforms such as Jira and other development tools, effectively preventing process deviations. With its robust automation features, Ketryx supports the swift release of safer software by producing essential documentation, maintaining traceability, and streamlining workflows. Moreover, Ketryx can be integrated into continuous integration and continuous deployment (CI/CD) pipelines, ensuring that teams can verify compliance before any release goes live. By automating the production of crucial documentation and traceability for every release, teams can significantly reduce the time required in each release cycle. Users can also effectively monitor changes across different versions and pinpoint inconsistencies by employing search tools and filters throughout the development lifecycle, which ultimately allows teams to concentrate their attention where it is most impactful. This thorough approach not only boosts operational efficiency but also enhances the overall quality of projects, leading to better outcomes in life sciences development. Additionally, Ketryx's capabilities ensure that teams remain agile and responsive to evolving project needs.

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.

Media

Media

Integrations Supported

Integrations Supported

Microsoft Word

API Availability

API Availability

Has API

Pricing Information

Pricing not provided

Pricing Information

Pricing not provided
Free Trial Offered?

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Online Training

Training Options

Documentation Hub
Webinars
On-Site Training

Company Facts

Organization Name

Ketryx

Company Location

United States

Company Website

www.ketryx.com

Company Facts

Organization Name

KOŚA

Date Founded

2025

Company Location

India

Company Website

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

Categories and Features

Categories and Features

Document Control

Not specified

Document Management

Not specified

Document Workflow

Not specified

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