XClinical GmbH
AB Cube Germany GmbH (formerly EvidentIQ Germany GmbH) provides an all-in-one eClinical software platform that supports electronic data capture, patient-reported outcomes, IWRS/randomization, reporting, medical coding and integrations. The platform supports traditional randomized trials and adaptive designs across therapeutic areas and medical devices, offers real-time dashboards and analytics, open APIs for interoperability, and an AI assistant for study management. The company offers custom implementations for CROs and academic institutions and integrates with pharmacovigilance and CTMS systems.
Industries
Nr. of Employees
small (1-50)
Products
All-in-one eClinical platform
A unified clinical platform combining EDC, ePRO, IWRS/randomization, reporting, medical coding, dashboards and integration capabilities for end-to-end study management.
Marvin
A comprehensive eClinical solution supporting adaptive and innovative clinical trial designs, offering advanced randomization, real-time data handling, and regulatory-ready reporting.
Marvin RTSM/ IWRS
A centralized, web-based platform fully integrated with Marvin EDC for advanced patient randomization and comprehensive trial supply management in clinical research.
Marvin ePRO
Patient engagement and electronic patient-reported outcomes (ePRO/eCOA) tool with a patient-centric design, multi-device support, and integration capabilities into various Electronic Data Capture (EDC) systems.
Marvin ODS
A browser-based platform designed for efficient cancer registry reporting, management of certified oncological centers, and comprehensive tumor documentation.
Marvin OTB
A flexible, guideline-compliant oncology tumor board platform designed to optimize and standardize multidisciplinary case reviews and clinical workflows.
All-in-one eClinical platform
A unified clinical platform combining EDC, ePRO, IWRS/randomization, reporting, medical coding, dashboards and integration capabilities for end-to-end study management.
Marvin
A comprehensive eClinical solution supporting adaptive and innovative clinical trial designs, offering advanced randomization, real-time data handling, and regulatory-ready reporting.
Marvin RTSM/ IWRS
A centralized, web-based platform fully integrated with Marvin EDC for advanced patient randomization and comprehensive trial supply management in clinical research.
Marvin ePRO
Patient engagement and electronic patient-reported outcomes (ePRO/eCOA) tool with a patient-centric design, multi-device support, and integration capabilities into various Electronic Data Capture (EDC) systems.
Marvin ODS
A browser-based platform designed for efficient cancer registry reporting, management of certified oncological centers, and comprehensive tumor documentation.
Marvin OTB
A flexible, guideline-compliant oncology tumor board platform designed to optimize and standardize multidisciplinary case reviews and clinical workflows.
Services
Configuration, deployment and ongoing support of the eClinical platform tailored to CROs and academic study centers.
Configuration, deployment and ongoing support of the eClinical platform tailored to CROs and academic study centers.
Expertise Areas
- eClinical platform development and deployment
- Clinical data capture and management
- Clinical trial operations and site connectivity
- Adaptive trial design and randomization
Key Technologies
- Electronic data capture (EDC)
- ePRO
- IWRS / randomization systems
- Open APIs and interoperability
News & Updates
Case study describing a multicountry, long-term heart failure study conducted using the platform, highlighting long-term study support and multi-site coordination.
Article describing the process and considerations for replacing a CTMS and integrating the new CTMS with the clinical data platform.
Awarded a platinum-level pharma supplier certification by a third-party certification body.
Case study describing a multicountry, long-term heart failure study conducted using the platform, highlighting long-term study support and multi-site coordination.
Article describing the process and considerations for replacing a CTMS and integrating the new CTMS with the clinical data platform.
Awarded a platinum-level pharma supplier certification by a third-party certification body.