About Marvin EDC
Marvin EDC is a clinical data management software from EvidentIQ designed to support comprehensive study management. It combines easy study set-up and management, StudyMetrIQs for data insights, and impressive universal capabilities so users can efficiently manage clinical trials. With over 1,500 studies managed worldwide, Marvin EDC offers solutions tailored for academics and oncology researchers. The platform provides extensive support services, ensuring that users have the necessary resources for effective data collection and analysis. Key capabilities: clinical data management supporting services solutions for academics solutions for oncology universal capabilities Best for: researchers and clinical trial managers that need reliable data management for their studies.
Marvin EDC is a comprehensive eClinical software platform designed to streamline clinical trials for pharmaceuticals, biotechnology, medical devices, cosmetics, and consumer health sectors. With over 1,500 studies managed across 69 countries, Marvin has established itself as one of the most reliable and flexible solutions in the clinical research landscape. Its strength lies in offering a centralized, secure environment that simplifies study setup and management while addressing the unique demands of global, multi-country trials. Marvin supports multi-language use, offline capabilities, and double-data entry (DDE), ensuring that even studies in resource-limited regions can operate smoothly and efficiently. The platform emphasizes usability through an intuitive interface that requires no programming knowledge, making it accessible to CROs, academic institutions, and clinical trial sponsors alike. Marvin integrates a wide range of eClinical modules, from electronic data capture (EDC) and ePRO to randomization and trial supply management, risk-based monitoring, and safety reporting. Its StudyMetrIQs module adds another layer of value by providing real-time dashboards, customizable reporting widgets, and actionable insights for smarter decision-making.
Pros & Cons
- +Comprehensive suite of eClinical modules in one platform.
- +Real-time dashboards and customizable analytics.
- +Flexible, scalable, and adaptable for global studies.
- +Integrated patient-reported outcome and wearable device support.
- +Strong regulatory compliance with audit trails and e-signatures.
- −Advanced modules may require additional training for new users.
- −Initial setup for multi-country trials can be complex.
- −Costs may be higher compared to simpler EDC systems.
- −Internet-based tools may face challenges in low-connectivity regions.
- −Customization may require technical support.
Features
Key features
- StudyMetrIQs Dashboards – Offers real-time visibility into trial data with customizable dashboards and ad-hoc reporting.
- Flexible Study Setup – Simplifies configuration for any study type, supporting global, multi-country trials.
- ePRO Integration – Captures patient-reported outcomes directly into the central database, including wearable device support.
- Randomization & Trial Supply Management – Provides adaptive randomization methods and efficient supply tracking through IWRS.
- Coder Module – Classifies adverse events and medications using MedDRA and WHODrug dictionaries with automated term matching.
- Regulatory Compliance & Audit Trail – Ensures adherence to international standards with complete audit histories and e-signatures.
- Multi-Language & Offline Support – Enables trial execution in any language and in regions with limited internet access.
Additional features
- Electronic Data Capture (EDC) – Secure, web-based data entry and management system.
- StudyMetrIQs Reporting – Interactive reporting module for insights and KPIs.
- Randomization System (IWRS) – Adaptive and CARA randomization for complex trials.
- Drug Supply Management – Tracks and manages materials across global studies.
- Risk-Based Monitoring – Enables proactive trial oversight and early risk detection.
- Coder Module – Automates classification of safety-related terms using dictionaries.
- ePRO Module – Collects patient feedback and integrates wearable device data.
- Double Data Entry (DDE) – Provides hybrid studies with offline and redundant entry options.
- Safety & AE Reporting – Tracks adverse events with automated SAE notifications.
- Customizable Workflows – Supports flexible, role-based workflows tailored to study needs.
Pricing
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About Marvin EDC
Marvin EDC is a clinical data management software from EvidentIQ designed to support comprehensive study management. It combines easy study set-up and management, StudyMetrIQs for data insights, and impressive universal capabilities so users can efficiently manage clinical trials. With over 1,500 studies managed worldwide, Marvin EDC offers solutions tailored for academics and oncology researchers. The platform provides extensive support services, ensuring that users have the necessary resources for effective data collection and analysis. Key capabilities: clinical data management supporting services solutions for academics solutions for oncology universal capabilities Best for: researchers and clinical trial managers that need reliable data management for their studies.
Marvin EDC Details
Marvin EDC's In-App Market Place
Does Marvin EDC have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
NA
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), AUD (A$), CAD (C$), JPY (¥), CHF (CHF), CNY (¥), INR (₹)
Pros & Cons
- Comprehensive suite of eClinical modules in one platform.
- Real-time dashboards and customizable analytics.
- Flexible, scalable, and adaptable for global studies.
- Integrated patient-reported outcome and wearable device support.
- Strong regulatory compliance with audit trails and e-signatures.
- Advanced modules may require additional training for new users.
- Initial setup for multi-country trials can be complex.
- Costs may be higher compared to simpler EDC systems.
- Internet-based tools may face challenges in low-connectivity regions.
- Customization may require technical support.
Marvin EDC's Support Options
Email Address
info@evidentiq.comContact
+49 89 4522775 000Marvin EDC's Alternatives
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