Medigen Suite
Medigen Suite: integrated eClinical platform unifying EDC, CTMS, imaging and patient apps to accelerate global trial execution and approvals
Overview
Medigen Suite: integrated eClinical platform unifying EDC, CTMS, imaging and ePRO/eCOA to accelerate global trial execution and approvals
Medigen Suite is an integrated eClinical platform designed to unify electronic data capture (EDC), clinical trial management systems (CTMS), medical imaging, and eCOA/ePRO. It aims to enhance the efficiency and effectiveness of global clinical trials, facilitating faster regulatory approvals.
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- TaglineMedigen Suite: integrated eClinical platform unifying EDC, CTMS, imaging and patient apps to accelerate global trial execution and approvals
- Founder-editedRecorded Source: www.medigensuite.com
- DescriptionMedigen Suite: integrated eClinical platform unifying EDC, CTMS, imaging and ePRO/eCOA to accelerate global trial execution and approvals
- Founder-editedRecorded Source: www.medigensuite.com
- Starting pricePricing information is available upon request.
- Founder-editedRecorded Source: www.medigensuite.com
- Free planNo
- Founder-editedRecorded Source: www.medigensuite.com
- Free trialYes
- Founder-editedRecorded Source: www.medigensuite.com
- IntegrationsLinear
- Founder-editedRecorded Source: www.medigensuite.com
- SummaryMedigen Suite is an integrated eClinical platform designed to unify electronic data capture (EDC), clinical trial management systems (CTMS), medical imaging, and eCOA/ePRO. It a...
- Founder-editedRecorded Source link unavailable
Key Features
- Unified eClinical Ecosystem: Connect EDC, CTMS, eTMF, medical imaging, patient engagement, training, and AI in one modular platform.
- Dynamic eCRF & EDC: Build protocol-driven, multilingual eCRFs with branching logic, edit checks, audit trails, e-signatures, and flexible data exports.
- Medical Imaging & Core Lab: Manage DICOM uploads, image review, measurements, Core Lab workflows, and AI-assisted PHI anonymization within the EDC.
- Safety Event Adjudication: Centralize CEC/DSMB reviews with standardized workflows, secure documentation, automated narratives, and full decision traceability.
- Centralized CTMS: Plan and track studies, countries, sites, activation, milestones, timelines, enrollment, and operational performance from one environment.
- eMVR & Risk-Based Monitoring: Track visits, queries, SDV, locks, freezes, site performance, risk indicators, and monitoring activities in real time.
- Integrated eTMF: Centralize essential trial documents with structured filing, metadata, version control, audit trails, and integrated review and approval workflows.
- AI-Assisted Trial Workflows: Apply AI to generate eCRFs from study protocols, flag data anomalies, manage queries, review imaging, support safety coding and narratives, and identify risk signals.
- Clinical Trial LMS: Deliver study-specific training with video modules, quizzes, certificates, completion tracking, and inspection-ready training records.
- Data Validation & Reporting: Monitor data quality, protocol compliance, queries, deviations, SDV and lock status, and export analysis-ready clinical trial data.
Who Is It For
Organizations conducting global clinical trials that require a comprehensive and integrated approach to data management and patient engagement.
Site management organizations seeking eSource solutions.
Strengths & Weaknesses
Classification
Alternatives to Medigen Suite
Community
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