Integrate Real-World Data
Marvin ePRO:
Patient Engagement and Retention
Our engagement tool with a patient-centric design to ensure patients remain active participants in the study, leading to better compliance and data quality.
User-friendly interface
All Devices
Integration in various EDCs
Marvin your Study
At the heart of every Trial with Marvin is our deep understanding of modern complex trials. We understand your requirements and help you finding solutions during the entire trial – from ePRO setup to data base lock.
Gather Patient Insights, Smart Workflows, Natively Integrated
Features and Advanced Capabilities
Setup
Enhanced Patient Engagement and Usability
Our advanced engagement tools and patient-centric design ensure patients remain active participants in the study, leading to better compliance and data quality.
Patient-Centric Design
Our user-friendly interface supports all devices and channels without the need for downloads or logins. Patients can access the study via a unique link—no passwords or usernames required—simplifying the process and reducing barriers to participation.
Adaptive and Visual Interface
Utilizing icon-based visualization and adaptive design, the interface adjusts according to the patient’s age group. This approach makes it suitable for all demographics, including older adults and children, enhancing usability and encouraging consistent data entry.
Streamlined Workflows
Our fully customizable system accommodates complex study designs and protocols. Configure different workflows, dynamic visit creation, form activation, and conditional logic to suit your study’s unique requirements without the need for technical expertise.
Advanced Engagement Tools
Features like automatic reminders via SMS or email ensure patients complete their assessments on time. Patients can also schedule virtual meetings with site staff directly within the application, enhancing communication and building stronger patient-site relationships.
Compliance & Security by Design - Built on a robust, pre-validated framework aligned with GCP and 21 CFR Part 11 Standards.
Full Compliance with GCP and 21 CFR Part 11 Standards
Our solutions provide complete compliance with Good Clinical Practice (GCP) and 21 CFR Part 11, featuring secure eSignatures and audit trails that simplify regulatory audits and enhance research credibility.
GDPR-Compliant Data Handling and EU Data Storage
We host data securely within the EU, ensuring compliance with GDPR standards for academic institutions in Europe and securing sensitive patient data with SSL encryption.
Secure Audit Trails and Role-Based Access
Maintain detailed audit trails for transparency and role-based access control to safeguard against unauthorized access, ensuring that only approved personnel handle sensitive information.
Trusted by Industry Leaders
“By collaborating with the Marvin team over several years acromion’s data management team has acquired the skills and knowledge of implementing complex and challenging clinical protocols on Marvin, while adding its expertise in clinical data validation, safety reporting and CDISC competence to the final product. All the time we perceived a cooperative, fast and qualified partnership with the Marvin team.”
Oana Braun, Founder acromion
“We think that Marvin is very flexible. It allows us to manage very complex amendments and study design. It’s also very easy to integrate with external parties (using real web services and the REST technology).”
Benoît de Malglaive, Team Leader EDC Specialists, IDDI
“We are currently conducting six oncology studies using Marvin, including a Phase III study. We were quickly convinced by Marvin, as the system is extremely user-friendly. We particularly appreciate the modular structure, which can be flexibly tailored to the requirements of our studies. We don’t have to use all the modules, but it’s reassuring to know that everything is integrated. If something changes during the course of the study, the system can easily be adapted. Marvin has optimized our processes and is extremely user-friendly – it’s easy to navigate and provides everything you need.”
Michael Fuchs, Leiter Studienzentrale der Deutschen Hodgkin Studiengruppe (GHSG)
“I had worked at two companies involving EDC systems. We are lucky and honored that we are in the position using Marvin with our studies. Marvin is a marvelous system.”
Naoko Nakagawa, Data Manager, I’Cros Japan
