eAdjudication logo

eAdjudication

by Ethical · Since 2014
No reviews yet
ActiveAvailable globallyCloud
Quick facts
VendorEthical
Year launched2014
StatusActive
LocationWartenbergstrasse 40, CH-4052 Basel SWITZERLANDWartenbergstrasse 40, CH-4052 Basel SWITZERLAND
Countries servedGlobal
Languages1
Integrations1+
Free tierN/A
Free trialN/A
Contact salesYES

About eAdjudication

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eAdjudication is a comprehensive software solution designed for efficient data management in clinical trials and research studies. Its primary purpose is to streamline the adjudication process by providing a centralized platform for collecting, reviewing, and analyzing data from multiple sources. Standout features of eAdjudication include customizable workflows, real-time monitoring, and automated notifications. The user interface of eAdjudication is intuitive and user-friendly, making it easy for researchers and clinical trial coordinators to navigate the system. The dashboard layout is well-organized, with clear visual cues that guide users through the various functions and tools available. Unique design elements such as drag-and-drop functionality and customizable templates enhance the user experience, allowing for seamless data entry and workflow customization. One of the core functionalities that sets eAdjudication apart from its competitors is its ability to handle complex adjudication processes with ease. The software supports multiple adjudication models, including independent, consensus, and committee review, allowing for flexible and customizable data review workflows. In addition, eAdjudication offers real-time data validation and discrepancy resolution, ensuring data accuracy and consistency throughout the adjudication process.

Pros & Cons

Pros
  • Highly Customizable Workflows – Designed to adapt to a variety of trial types and adjudication models.
  • Robust Regulatory Compliance – Certified for ISO 27001 and validated under GAMP5, FDA, and GDPR standards.
  • Integrated Imaging & Document Tools – Enables seamless review of documents and images without switching systems.
  • Automation-Enhanced Efficiency – AI tools for redaction and search reduce manual tasks significantly.
  • End-to-End Service – Offers hosting, support, validation, and training—all under one managed solution.
Cons
  • Workflow Complexity – Advanced configuration options may require support or training to fully implement.
  • English-Only Interface – Platform interface and materials are primarily in English; localization options are unclear.
  • Steep Learning Curve – Rich functionality may be overwhelming without structured onboarding.
  • Not Versatile Beyond Clinical Trials – Specifically tailored for adjudication; not general-purpose for other industries.
  • Workflow Complexity – Advanced configuration options may require support or training to fully implement.
  • English-Only Interface – Platform interface and materials are primarily in English; localization options are unclear.
  • Steep Learning Curve – Rich functionality may be overwhelming without structured onboarding.
  • Not Versatile Beyond Clinical Trials – Specifically tailored for adjudication; not general-purpose for other industries.

Features

Key features

Centralized Clinical Event Management
Organizes and assembles data, documents, and images related to clinical endpoint events for adjudication.
Configurable Adjudication Workflows
Supports customized decision pathways, forms, and review structures for any study design.
AI-Powered Redaction
Automatically removes personally identifiable information (PII/PHI) from PDFs and DICOM images.
Integrated DICOM Viewer
Enables seamless review of medical imaging with built-in Orthanc PACS integration.
Zoom Connector for Meetings
Allows virtual adjudication meetings with secure login, recording, and archival of decisions.
Real-Time Dashboards & KPIs
Offers insights into process metrics like turnaround times, disagreement rates, and reviewer activity.
Audit Trail & Regulatory Compliance
Fully traceable actions with secure, validated processes meeting GxP, FDA 21 CFR Part 11, and GDPR.

Additional features

PACS Integration via Orthanc
Integrates with Orthanc server for seamless PACS data ingestion and structured imaging workflows.
Meeting Management and Archiving
Automates scheduling, facilitates virtual meetings, and records decision outcomes with long-term archival.
KPI Monitoring and Adjudication Tracking
Tracks real-time performance metrics like review completion time, committee workload, and backlog.
Regulatory Export Tools
Generates submission-ready, regulator-compliant documentation packages for audits or trial closeout.
GAMP5-Compliant Software Validation
Includes full validation documentation and support for GxP-regulated environments.
Onboarding and Training Resources
Offers online training modules, helpdesk support, and guided onboarding tailored to sponsor or CRO teams.
Secure ISO 27001 Hosting and Backup
Ensures data safety with encrypted cloud storage, access control, and regular disaster recovery backups.

Pricing

Free trial
Free version
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Countries & Languages

Global
Countries served
1
Interface languages
20
Billing currencies

Interface languages

English

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇦🇺AUD🇨🇦CAD🇯🇵JPY🇨🇳CNY🇮🇳INR🇸🇬SGD🇭🇰HKD🇳🇿NZD🇨🇭CHF🇸🇪SEK🇩🇰DKK🇳🇴NOK🇰🇷KRW🇹🇼TWD🇷🇺RUB🇧🇷BRL🇲🇽MXN

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