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What is eDeviation?

eDeviation offers a thorough suite of tools designed for the evaluation and management of Protocol Deviations, simplifying the journey from software development and validation to the collection of essential documentation and the exportation of data for the Trial Master File (TMF). This innovation significantly reduces the workload on clinical teams who may encounter risks associated with poorly evaluated or neglected protocol deviations, regardless of their frequency. As part of Ethical's eClinical Software Platforms, eDeviation® improves the precision and productivity of clinical trial oversight. The software can be customized to fit the unique needs of your research team, whether assessments are made by an independent committee or internally. Its built-in forms, workflows, and export capabilities guarantee compliance with GxP standards while promoting effective study management. Moreover, the platform supports real-time online collaboration among study teams, investigators’ sites, and committee members, which accelerates decision-making and ensures that protocol deviation assessments are addressed promptly. This collaborative environment not only streamlines processes but also fosters a culture of transparency and accountability in clinical trials. Ultimately, eDeviation® plays a crucial role in enhancing the integrity and efficiency of clinical research processes, leading to improved research outcomes.

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.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

eDeviation

Company Website

www.protocoldeviation.com/eDeviation-software

Company Facts

Organization Name

Ketryx

Company Location

United States

Company Website

www.ketryx.com

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Categories and Features

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