Build Clinical Studies in Minutes
Clinical trial setup is complex, time-consuming, and highly resource-intensive. Marvin Study Designer helps clinical data management teams accelerate this process with AI-assisted study design.
From a short study description or an uploaded protocol, the application generates a complete, review-ready study definition within minutes, including visits, eCRFs, data fields, controlled terminology, validation rules, and edit checks.
AI Designed for Clinical Research
Marvin Study Designer has been developed specifically for sponsors, CROs, and clinical data management teams. Its AI is informed by more than 840 real-world CDISC ODM study definitions, helping teams create consistent, high-quality, and CDISC-compliant study drafts without starting from scratch.
Secure and Fully Controlled
The application runs entirely within AB Cube Germany’s own infrastructure. Protocols, study definitions, and confidential project information are not shared with external AI services or third-party processors.
Experts Remain in Control
Marvin Study Designer follows a human-in-the-loop approach. AI creates the initial draft, while clinical experts review, refine, and approve every visit, form, field, and validation rule before publication in Marvin EDC.
Faster Validation and UAT
In addition to generating study structures, Marvin Study Designer can create edit checks, synthetic patient data, and test users, helping teams accelerate validation, UAT, and study go-live.
“Marvin Study Designer combines the speed of AI with the oversight required for regulated clinical research. It enables clinical teams to reduce manual effort, accelerate study startup, and confidently use AI without compromising data security or quality.”
Manuel Neukum
CEO, AB Cube Germany
Interested in learning more? Contact us to request a demonstration or to be among the first to experience Marvin Study Designer
Learn more about Marvin Study Designer in our full press release
