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Better Data Quality. Better Research.

Marvin eClinical Suite:

Simplify your Clinical Trial

Give your team the tools to manage complex clinical trials and real-world oncology data for better and integrated data.

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Our Platform Adapts to Your Needs

Built for every Organization from Academic Institutions to Biotech

CROs

Academic Institutions

(Non) Governmental Institutions
Biotechs
Pharmaceutical or Medical Device Companies
Your Trusted Partner in Clinical Research and Oncology

What is Marvin?

Our eClinical software, Marvin, is a robust CDISC-certified EDC system that includes numerous modules. Designed from the ground up with its end user’s needs in mind, Marvin simplifies clinical trial data management.

On top with our EHR cancer files & tumour board solutions (Marvin ODS and Marvin OTB) you can capture real-world oncology data from hospitals and connects it to clinical trial workflows.

Marvin EDC: Modules and Solutions for a smarter Trial

EDC/ eCRF
Simplify complex Trials

eClinical EDC built for complex oncology and cardiology trials. Fully configurable, CDISC-native and AI enabled.

ePRO
Collecting Patient Data

Collect Quality-of-Life or other real-world data directly from the patient – using predifened  or own ePRO questionnairs.

RTSM

Advanced Patient Randomization and Enrollment

Marvin RTSM offers advanced randomization and material handling capabilities.

Safety

Handling Safety and Vigilance

Seamless integration of Marvin EDC and SafetyEasy® Vigilance Suite for faster, smarter Pharmacovigilance

Why Marvin & AB Cube?

Purpose-Built for Complex Clinical Trials
Vast Trial & Oncology Experience
Highly Configurable
CDISC-Native
Adaptive & Complex Trial Designs
Cost-Effective vs. Global Players
Full Control to Customize Workflows and Fields

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.

AB Cube handles the Complexity of Clinical Trials

AB Cube — Complexity of Trials
Study Setup

Design Flexibility

Basket, umbrella, adaptive and platform designs within standard configuration

Faster Set-Up with AI

AI assisted from protocol, included edit checks and synthetic patients for testing

RTSM

Concurrent randomization across arms and cohorts, no cross system coordination

Study Execution

Adaptive Protocols

Mid-study amendments via documented workflow with minimal disruption to sites & live data

Local lab

Unified lab ingestion for biomarker response data, audit ready, no manual reconciliation.

ePRO & RBM

Improve data quality and trial efficiency with real-time patient insights and targeted monitoring

Study Close & Submission

Built in Compliance

CDISC SDTM mapping built in study design, not post-collection, saving weeks at submission

Ongoing data reconciliation

Embedded query workflow and safety data reconciliation between safety database and EDC

Real-time data cleaning

Inline edit checks and automated queries ensure accurate data from the moment it's entered

Advantage of AB Cube

Faster study start up

Accelerate from design to first patient in for complex trials allowing for amendments

Lower operational risk

Unified data, quality and automation reduce errors and oversights

Accelerated submission

Built-in compliance and reconciled data deliver faster, first-time right submissions

Guiding You Through Every Step

AB Cube offers fast, flexible and focused services ranging from ‘full service’ to ‘do-it-yourself’. Select the services you require and create the ideal mix of professional study setup, consulting and training services to meet your specific needs. Our Customer Success team is here to support you.

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

Frequently Asked Questions

Answers to Help You
Make Decisions

What is Marvin EDC?

AB Cube Germany provides a solution called Marvin that is your powerful EDC to run clinical trials. We have powerful add-on modules like our ePRO or eConsent.

Is AB Cube Germany or Marvin a CRO?

No, AB Cube Germany is not a CRO. We are a dedicated provider of eClinical solutions such as EDC, ePRO or eConsent. Our customer success team can help you set up your eCRF/ eClinical solutions, but we are not a CRO. Through our extensive partner network we can help you find CROs, Data Management providers or service partners

Does Marvin EDC support all kind of Trials

Yes, Marvin EDC supports all phases, all study designs, even complex designs, e.g. adaptive trial designs or RCT´s​.

Is Marvin EDC hosted in a cloud?

Marvin is hosted on differen data centers from two providers in Germany (Noris Network and Hetzner). Our centers are certified according to ISO 27001, TÜVIT, ISAE3402.

Can i integrate Marvin with other systems?

We support integration instead of separation. Marvin is integrated in your eClinical solution architecture and supports all kinds of workflows. The integration works with APIs or our own Data Hub. WIthin the Data Hub we have already build in integrations like with the all-in-one Vigilance solution SafetyEasy®.

Can I do SDTM tabulation with Marvin

Marvin is CDISC-native from the ground up.

SDTM-based architecture end-to-end. Datasets are submission-ready from the start — no post-hoc mapping, no conversion effort.

Can I customize the system to fit my processes?

Absolutely. Marvin is fully modular and customizable and can be configured to fit your workflows.

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