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Simplify your Clinical Trial

Marvin EDC: Experience Germany’s most trusted EDC

AB Cube´s Marvin EDC is a next-generation, cloud-based platform that handles even the most complex trials with ease. It is also highly preferred by sites for its intuitive design and efficiency. Our solution seamlessly combines advanced technology with exceptional usability, enabling you to streamline your clinical trials, enhance data quality, and reduce time to market.

Protocol Amendments with no Down-Time
High Data Quality
Adaptive Trial Design
CDISC-Native
Explore Marvin
Explore Modules

Marvin your Study

At the heart of every trial with Marvin is our deep comprehension of modern complex trials. We understand your requirements and help you find solutions throughout the trial – from eCRF setup to data base lock.

Setup
AI-enabled plus CDISC SDTM-ready study creation
Process
Amendments without loss of quality or the need for rebuilds
Data Collection
Easy data collection from sites and integrated systems, such as our safety database
Submit
Submission-ready data, no reconciliation needed, and SDTM ready

Explore how Marvin supports you along the Clinicial Trial Process

AB Cube — Complexity of Trials
Study Setup
Study Execution
Study Close & Submission

From Setup to Submission

Study Setup with Marvin EDC

Marvin EDC/ eCRF
Study Setup
Complex Trials
Data Quality
RTSM

Marvin EDC - The Heart of Your Study

High-quality data is the foundation of successful clinical trials. Marvin EDC streamlines study build, data collection, and data management to ensure accuracy, efficiency, and scalability from first patient in to database lock.
  • CDISC-Native architecture
  • AI-assisted study build
  • Intuitive guided data entry
  • Manages large volumes of data efficiently
Design Your Study with Ease

Study Setup

Accelerate study setup with Marvin Study Designer. Re-use forms and templates across studies and visits while maintaining full CDISC compliance. Build studies and electronic Case Report Forms (eCRFs) efficiently, with the flexibility to choose between a guided study builder or AI-assisted design support. Designed to help teams launch studies faster while meeting the highest quality standards.
Handling Complex Trial Designs

Complex Trials

Marvin EDC is built to manage adaptive trial designs, including platform, basket, and umbrella studies commonly used in oncology research. The flexibility allows for protocol modifications based on interim analyses while maintaining data integrity and study continuity. Utilize complex randomization methods (including stratified, block, and covariate-adjusted response-adaptive randomization) to promote balanced treatment allocation and reduce bias. Seamlessly implement protocol amendments, a frequent necessity, without disrupting ongoing data collection.
Complex Trials
Unparalled Data Quality

Data Quality

Marvin EDC is built on CDISC standards and utilizes a standardized Operational Data Model (ODM) to ensure consistency across complex clinical data structures. Manage site-specific lab reference ranges automatically, eliminating the need for manual patient-level adjustments. Seamlessly import and map central laboratory data directly into the eCRF structure to reduce manual effort, improve consistency, and accelerate data review. Automated alerts and workflows for out-of-range lab values enable timely action and support patient safety throughout the study.
Data Quality
Randomization and Trial Supply Management

RTSM

Marvin RTSM (Randomization and Trial Supply Management) offers an automated, streamlined solution for managing investigational product randomization, distribution, and supply logistics throughout the study lifecycle. Marvin’s flexible randomization allows you to configure site-based or cross-site block randomization, as well as advanced methodologies such as variance minimization, block-wise randomization, or Covariate-Adaptive Response-Adaptive (CARA). Plus, options to incorporate multiple stratification factors to support balanced treatment allocation, improved precision, and operational flexibility across complex trial designs.
RTSM

Study Execution

Mid-Study Amendments
Local and Central Labs
ePRO
Risk-Based Monitoring
Save Critical Time in Study Amendments

Mid-study Amendments

Mid-study amendments via documented workflow with minimal disruption to sites & live data
  • Targeted, additive changes
  • Amendments without system downtime
  • Full audit trails and version control
  • Controlled partial rollout capabilities
  • Self-service configuration and deployment
Mid-study Amendments
Audited Batch Case Processing

Local and Central Labs

Handling of Central Lab Data - Seamlessly import and map central laboratory data directly into your eCRF structure to reduce manual effort, improve consistency, and accelerate data review.

Lab Data Management - Automatically manage site-specific lab reference ranges, eliminating the need for manual patient-level adjustments.

Local and Central Labs
Collect Patient Reported Outcome

ePRO

Marvin’s intuitive, mobile-friendly ePRO experience makes it easy for participants to engage and consistently complete assessments — regardless of technical proficiency. It supports higher compliance rates, and reliable data collection throughout the study.
Ensure Data Accuracy and Completeness

Risk-Based Monitoring

Implement advanced validation rules, including cross-form and cross-visit checks to reduce errors and maintain data consistency throughout the study. Access real-time data and reports to promptly identify and address discrepancies. Strengthen data integrity through systematic Source Data Verification (SDV) and risk-based monitoring strategies focused on critical data points and processes.
Risk-Based Monitoring

Study Closure & Submission

CDISC Native
Data Reconciliation
Reporting
Integrations
Build in Compliance

CDISC Native

Marvin is built upon the CDISC standards and operates with a standardised Operational Data Model (ODM) database ensuring consistency within your intricate data structure. Automatically manage lab normal ranges specific to each site, eliminating the need for manual adjustments at the patient level. Seamlessly import and map central lab results directly into your eCRF structure. Saving time, reducing errors, and ensuring data consistency. Generate automatic alerts and workflows for lab values outside normal ranges, enabling prompt action to ensure patient safety.
CDISC Native
Ongoing Data Reconciliation

Data Reconciliation

Streamline query management and safety data reconciliation through integrated workflows between the EDC and safety database. Maintain high data consistency throughout the study lifecycle, reduce manual reconciliation effort, and minimize post–Last Patient Out activities.
Data Reconciliation
Real-Time Oversight and Reporting

Reporting

Proactive Monitoring - Track documentation completeness and participant progress with real-time statistics for swift issue resolution. Customizable Dashboards - Generate tailored reports specific to adaptive trial needs, including insights from interim analyses. Actionable Insights - Display relevant information like study health and randomization outcomes to inform decision-making and ensure compliance.
Reporting
Seamless System Integration

Integrations

Connect Marvin EDC with key clinical trial systems (including eTMF, CTMS, lab platforms, and wearables) to ensure reliable data flow, improved interoperability, and efficient cross-system collaboration. Support unified trial operations and comprehensive study oversight through seamless integrations.
Integrations

Ready to simplify complexity?

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Seamless User Experience

High-quality data is the backbone of successful clinical trials. Our intelligent data management features facilitate accurate and efficient data collection.

Intuitive Interface

Marvin EDC provides a clean and easy-to-navigate interface that reduces training effort and supports rapid user adoption across study teams.

Responsive Design

Access the platform securely from any device or browser, enabling efficient data entry and study oversight from virtually anywhere.

Interactive Images and Scales

Enhance data capture with interactive visual elements and scales that simplify complex assessments and improve data accuracy.

Multilingual Support

Support global clinical studies with multilingual capabilities that facilitate clear communication across international sites.

Compliance & Security by Design - Built on a robust, pre-validated framework aligned with global regulatory standards and requirements.

Full Compliance with GCP and 21 CFR Part 11 Standards

Our solutions ensure full compliance with Good Clinical Practice (GCP) and are designed to meet the requirements of major regulatory bodies (FDA, EMA, MHRA, PMDA, etc.).

GDPR-Compliant Data Handling and EU Data Storage

We securely host data within the EU, ensuring GDPR compliance for European academic institutions while protecting sensitive patient data with SSL encryption and enterprise-grade security standards.

Secure Audit Trails and Role-Based Access Control

Maintain detailed audit trails for full transparency and enforce role-based access control to ensure that only authorized personnel can access or modify sensitive clinical data.

Dedicated Support, Training, and Optimization

From study setup to long-term platform optimization, Marvin provides dedicated support and training to help academic institutions, research teams, and CROs maximize the value of their clinical trial technology. Our collaborative approach ensures efficient onboarding, sustained compliance, and continuous operational improvement throughout the study lifecycle.

Empowering Teams with Tailored Support and Resources
Extensive Training Programs for All Solutions (EDC, ePRO, Safety, RTSM)
Bilingual Support and Consultation
Continuous Optimization and Platform Updates