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What is eReconciliation?

With the implementation of the eAdjudication® software managed service, trial leaders gain the ability to efficiently manage timelines, respond to varying situations and outcomes, and monitor provider performance and protocol compliance throughout the extensive duration of clinical trials. This cutting-edge managed software service is instrumental in avoiding unexpected costs and breaches in timelines during Endpoint Adjudication Studies. The eAdjudication® Managed Software Service is recognized as the premier solution for overseeing Endpoint Adjudication (CEC). By partnering with the eAdjudication® platform and the staff at Ethical, study teams, committee members, and clinical organizations can collaborate seamlessly in real-time within a user-friendly and GxP-compliant environment, thus reducing the inefficiencies, expenses, and errors that often accompany manual processes. Moreover, the comprehensive nature of eAdjudication® services promotes the smooth integration and implementation of EA software within eClinical organizations, thereby boosting overall operational efficiency. This approach not only streamlines processes but also enables research teams to concentrate on producing high-quality results without the burden of logistical obstacles, ultimately enhancing the integrity of the trial outcomes.

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.

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

Ethical

Date Founded

2013

Company Location

Switzerland

Company Website

www.endpointadjudication.com

Company Facts

Organization Name

eDeviation

Company Website

www.protocoldeviation.com/eDeviation-software

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

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

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