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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 accelerate your path 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 understanding of modern complex trials. We understand your requirements and help you finding solutions during the entire trial – from eCRF setup to data base lock.

Setup
CDISC SDTM-ready study creation
Process
Amendments without lower quality or 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 - Your Heart of the Study

High-quality data is the backbone of successful clinical trials. Our intelligent data management features facilitate accurate and efficient data collection.
  • CDISC-Native
  • AI-enabled Study Build
  • Guided Data-Entry
  • Managing Large Volumes of Data Efficiently
Design your study with ease

Study Setup

Accelerate study setup with our Marvin Study Designer. Re-use forms and templates for future studies or visits. We are CDISC native and enable teams to create studies and electronic Case Report Forms (eCRFs) quickly as well as to the highest standards. You can choose between or regular study builder or use our AI features to support you with your study desing.
Handling Complex Trial Designs with Ease

Complex Trials

Marvin EDC is built to manage adaptive trials, including platform, basket, and umbrella trials common in oncology. This flexibility allows for modifications based on interim results without compromising data integrity. Utilize complex randomization techniques such as stratified, block-based, and covariate-adjusted response-adaptive randomization to ensure balanced treatment allocation and reduce bias. Implement protocol changes seamlessly, a frequent necessity in long-term oncology studies, without disrupting ongoing data collection.
Complex Trials
Unparalled Data Quality

Data Quality

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.
Data Quality
Randomization and Trial Supply Management

RTSM

Marvin RTSM (Randomization and Trial Supply Management) offers an automated, streamlined solution designed to ensure your investigational products are effectively randomized, distributed, and managed. Marvin supports. Flexible Randomization Methods - Marvin’s randomization feature gives you full flexibility. Choose between site-based or cross-site block randomization, or opt for advanced algorithm-driven methods such as variance minimization, block-wise randomization or CARA - with the option to include various stratification factors for greater balance and precision.

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
  • All amendments possible without downtime
  • Audit trails & Version Control
  • Partial rollout
  • Do it yourself
Audited Batch Case Processing

Local and Central Labs

Handling of Central Lab Data - Seamlessly import and map central lab results directly into your eCRF structure. Saving time, reducing errors, and ensuring data consistency. Lab Data Management - Automatically manage lab normal ranges specific to each site, eliminating the need for manual adjustments at the patient level.
Collect Patient reported outcome

ePRO

Marvin’s intuitive, mobile-friendly design makes it easy for participants to engage, regardless of technical skills, ensuring consistent data entry and high compliance rates.
Ensure Data Accuracy and Completeness

Risk-Based Monitoring

Implement complex validation rules, including cross-form and cross-visit checks, to minimize errors and ensure data consistency. Access up-to-date data and reports to promptly identify and address discrepancies. Enhance data integrity through systematic SDV and focus resources on critical data points with RBM strategies.
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

Embedded query workflow and safety data reconciliation between safety database and EDC. High-data consinstency for fewer steps after Last-Patient-Out.
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

Marvin integrates seamlessly with external systems such as eTMF, CTMS, lab systems, and wearables, ensuring a cohesive flow of data and supporting comprehensive trial documentation.

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 offers an easy-to-navigate interface that reduces training time and improves user adoption among site staff.

Responsive Design

Accessible on any device and browser, allowing site teams to enter and access data wherever they are.

Interactive Images and Scales

Enhance data entry with interactive elements that simplify complex data capture.

Multilingual Support

Facilitate global studies with support for multiple languages, ensuring clear communication with international sites.

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.

Dedicated Support, Training, and Optimization for Academics

With our comprehensive support, training, and dedicated services, CROs can ensure that their teams are fully equipped to leverage our EDC solutions effectively. Our commitment to ongoing support and optimization ensures sustained efficiency, compliance, and success throughout the lifecycle of your clinical trials.

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