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Your own dedicated model

Marvin brings AI to your study.

We bring AI to your study by integrating smart features to your trial – always bearing the saftey and integrity of your data in mind

Flexible
Scalable
Dynamic
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How Marvin uses AI to simplify trials

Marvins AI enabled features are here to support you simplifiying complex trials

Identify Potential
Identifying potential for AI improvments in Marvin
Potential check
Check potential and feasibility analysis
Compliance
Define data and compliance requirements
Development
Creation and development of MVPs and solutions

Create, Improve, Code and Streamline

Marvin AI enabled solutions

eCRF Design
Edit Checks
Synthetic Testing
eCRF Design from Protocol

eCRF Design

Upload your Study Protocol or describe your requirements via chat. Our Designer generates a fully structured eCRF – forms, item groups, and fields – instantly ready for review
Smart Plausibility & Edit Checks

Edit Checks

AI suggests plausibility rules and edit checks based on your data structure. Accept, refine or reject – and convert suggestions directly into configured validation actions with one click
Synthetic Patient Generation

Synthetic Testing

Generate realistic synthetic patients across diverse permutations to build UAT test cases – validating your eCRF structure and edit checks thoroughly before go-live.

PRIVATE AI – NO OPENAI | NO ANTHROPIC | NO GOOGLE GEMINI

We train and host our own small, dedicated model – entirely within our secure data center. Each customer receives their own AI, trained on 400+ clinical study definition curated by the Marvin team. Your data never leaves your environment.

Features to simplify your life – AI enabled

We know trials and we know painpoints. We are leveraging smart AI-enable features to make your life easier and improving data quality.

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AI Assistant

Our AI assistant for clinical studies helps users understand study data, generate reports and summaries, answer study-related questions, and support compliance and safety workflows.

Coding

Medical coding of (S)AE via our AI coding module. Detection and transformation of your case with MedDRA and WHODrug coding

MedInfo Management

AI-powered omnichannel intake for medical inquiries from calls, emails, and web forms. Integrates with call center platforms (ZenDesk), auto-classifies inquiries, and detects adverse events — turning inquiries into safety cases with no manual effort.

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.