Clinical Data Management
As of today, more than 1,300 studies worldwide have been managed using Marvin EDC from XClinical. Marvin is one of the most comprehensive eClinical solutions on the market.
Why choose Marvin to run your Trial?
Marvin provides solutions for pharmaceuticals, biotech, medical devices, cosmetics, and consumer health trials. It is easy to set up and users praise its usability and multiple integrated features.
FLEXIBLE FOR ANY TYPE OF STUDY
Easy Study Set-Up and Management
Enjoy a well-built and flexible modern application to safely collect your clinical data. A versatile software that enables easy study set-up and management. Both customers and end users value the simplicity combined with complex, customizable workflows. The integrated solution comprised of various eClinical modules, optimally supports clinical trial processes and enables seamless data flow.
Marvin is used in 69 Countries
More than 1200 studies realized
with Marvin EDC
BUILT FOR GLOBAL BUSINESS
Impressive universal Capabilities
Most Clinical Trials are conducted internationally spanning multiple countries or even continents. XClinical designed Marvin with a comprehensive vision of the challenges global studies bring. Beginning with a centralized database that is accessible from any web browser, the addition of not just multi-language, but every language became a standard offering. Sensitive to the fact that not all regions have internet access, Marvin also allows for double-data entry (DDE) and hybrid studies.
Marvin – Beyond Data Capture
- Quick and easy implementation of mid study changes
- Advanced query management
- Flexible for any type of study
- Complete Audit Trail
- (S)AE Notifications
- Electronic Signatures
All in One eClinical Software Platform
Scope of Features
The XClinical Randomization System is an IWRS (Interactive Web Response System) integrated into Marvin and does not require an interface to any other external systems. It offers open or double-blind, multi-strata, multi-group randomization based on a block list or a widely configurable range of algorithms like variance minimization. Recently we added CARA randomization to support multi-armed clinical trials.
- Seamless integration with Marvin EDC
- Advanced materials management
- Offers multiple randomization methods
Classify safety-related data such as adverse events or concomitant medications. Coder supports standard MedDRA and WHODrug dictionaries to automatically and manually encode verbatim terms by use of powerful search mechanisms. The coder module is fully integrated with Marvin via a Web Service API.
- Customizable standard user roles and workflows
- Intuitive user interface
- Upgrade dictionary during study conduct
Composer (eCRF Design)
With XClinical’s Composer, you can produce eCRF designs, document links, SDTM Tabulation and more to live in a single intuitive interface for your team. Never again struggle with any traditional office tool. The tool includes an SDTM reviewer as perfect add-on to visualize your SDTM data.
- Smart metadata library functionality
- Easy setup and management of amendments
- Automatic output of the annotated CRF, data validation plan and more
Marvin provides standard reports, custom reports, dashboards and interactive ad-hoc reports. The intuitive self-service reporting system enables users to create and publish their own reports without programming knowledge.
- Real-time data
- Linking of reports to the eCRF
- Pick any CRF data with a simple mouse click
- Report publishing in any format
Marvin is a universal software platform with multiple features to better manage the whole lifecycle of your clinical trial. “Quick set-up” is named top-3 benefit of Marvin compared with other EDC tools. Find out more.