EDC :: IWRS :: WebPRO :: DDE :: CTMS :: CDISC Tabulation :: Reporting :: Coding
all types of studies :: all therapeutic areas :: phase I-IV :: medical devices
The eClinical Software Solution Marvin comprises a CDISC-certified Electronic Data Capture (EDC) system that integrates with numerous modules such as Randomization (IWRS), Patient Reported Outcomes (WebPRO), Double Data Entry (DDE), Clinical Trial Management (CTM), CDISC Tabulation, Reporting, Coding and more. Our software portfolio enables you to manage the complete lifecycle of a clinical study in one single integrated solution. Marvin is all-in-one single integrated software package delivered as Software-as-a-Service. Marvin provides intuitive, easy to use tools without the need of programming knowledge. This facilitates the conduct of any clinical trial to become easy, streamlined and very cost-effective.
every browser - every language
high-end support services
focusing on you and your trials
automated end-to-end solutions
|Every browser, every language|
|Set-up without programming|
|MedDRA and WHODrug Coding|
|IWRS and Drug Management|
|Device Data import|
|CTMS / Portal|
|CDM / DDM|
|Standard/Customized/Ad hoc Reports|
|Auto generated annotated CRFs, DVP…|
|SDTM mapping/define.xml export|
Would you like a “14 out of 14”? Contact us today!
studies started in 2017
XClinical introduces: Marvin for Sites, our first eLearning Module. It contains relevant examples and scenarios designed to simulate how patient data is entered into Marvin. It allows your site personnel to better understand the functionalities of Marvin.
We are happy to announce the release of the new Marvin SDTM Reviewer. A powerful, web-based data visualization tool featuring modern charts to analyze CDISC SDTM datasets.
Experience the new Reporter, an intuitive self-service ad-hoc web reporting system enabling authorized users to create and publish their own reports and listings without programming knowledge.
Contact us for more information: firstname.lastname@example.org
Come join us! To grow our business in the USA we are looking for clinical data managers who would like to switch their career to business development, as well as from experienced business development managers with a proven track record in the EDC/IWRS/ePRO industry.
Meet us at the CDISC Interchange in Austin, Texas on November 15-16, 2017 and make sure you come by our booth n° 2. We will do a showcase with a live demonstration of our software tools leveraging CDISC xml standards for fast eCRF set-up, metadata management and mapping to SDTM.
Our software suite has been extended to include a new interactive ad-hoc web reporting module, an SDTM visualization tool, and a new version of our auto-coding software for whoDRUG.
To prearrange a meeting, just contact us: email@example.com
XClinical founder, Dr. Philippe Verplancke will also give a presentation on Thursday, November 16, 2017, 08:30 - 10:00, Session 5, Track A - "Metadata Repositories, Version Control and Standards Governance Leveraging CDISC XML Technology”
Many CROs, pharma companies, and medical device manufacturers have already chosen our software and services!
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