XClinical Software & Services

Meet Marvin, Your All-In-One eClinical Software Platform

Data is one of the greatest assets for clinical trial teams, yet managing that data remains a challenge. Disparate systems and mismatching data formats are continuing to hold organizations back. XClinical helps clinical study sponsors and CROs overcome these challenges and harness the power of their data to better manage clinical trials. Marvin, XClinical’s electronic all-in-one solution – provides a range of integrated modules in one platform, enabling the seamless flow of data to improve data quality. These modules include EDC, study build, data collection, IWRS and drug management, WebPRO, SDTM tabulation, MedDRA and WHODrug Coding, reporting and CTMS.

Everything is built to CDISC standards and improves access to data by delivering these modules on any web browser, in any language.

experience Marvin

all therapeutic areas :: phase I-IV :: medical devices

EDC :: IWRS :: WebPRO :: DDE :: CTMS :: CDISC Tabulation :: Reporting :: Coding

Software as a Service

every browser - every language

Friendly & professional

high-end support services

Fast response times

focusing on you and your trials

CDISC based

automated end-to-end solutions

Swift & easy

tech transfer

How does your eClinical software solution score?

Your software marvin-white
Every browser, every language  
Set-up without programming  
MedDRA and WHODrug Coding  
Risk-based monitoring  
IWRS and Drug Management  
Device Data import  
CTMS / Portal  
Standard/Customized/Ad hoc Reports  
Auto generated annotated CRFs, DVP…  
SDTM mapping/define.xml export  
CDISC End-to-End  

Would you like a “14 out of 14”? Contact us today!


total studies


studies started in 2018





Marvin in China


If you are also going to the CDISC China Interchange in Beijing on September 19-20, 2019 make sure you come by our booth. For the second time XClinical is a proud exhibitor at this event. At our booth we will show a live demo of our eClinical Solution Marvin

To prearrange a meeting, just contact us: verena.frank@xclinical.com

All about Marvin


He’s traveled the world. He’s managed clinical trials. AND he’s fluent in CDISC.

Here is the story of Marvin, the happy robot and official mascot of XClinical.

CDISC Clear Data – Clear Impact


XClinical actively participates at the CDISC Japan Interchange in the University of Tokyo.
Our experts are available for discussions about XClinical products and our partnership with our Japanese partner I’cros on July 11-12, 2019

On Friday, Our Global Head of Business Development, Dr. Philippe Verplancke will be giving a presentation on "MDR Requirements for Study Build and Implications for the CDISC Library".

Contact us for a live demonstration info@xclinical.com

XClinical at the DIA 2019 Annual Meeting June 24-26


Join XClinical at booth #1955 for the DIA Annual Meeting, the largest global interdisciplinary event that brings together key thought leaders and innovators from around the world to accelerate efforts to enhance health and well-being.

Come and meet Marvin in San Diego!

CDISC Interchange in Amsterdam


Meet the XClinical team at the CDISC Interchange Europe, in Amsterdam, on May 8-9! On Wednesday, Dr. Philippe Verplancke will be giving a presentation on “MDR Requirements for Study Build and Implications for the CDISC 360 project”.

Visit us at our booth n° 4 for more Marvin News

Contact us for a live demonstration info@xclinical.com

New! The XClinical Blog


We’re excited to announce the launch of the XClinical blog! We'll be publishing original content every month to help life science professionals learn about data management, clinical tech trends, trial design, industry news, and more

Be sure to check it out and subscribe to get new posts direct to your inbox.

A small selection of our happy customers

Many CROs, pharma companies, and medical device manufacturers have already chosen our software and services!


Contact us for a free presentation!



+49 89 452 27 75 000


+1 201 340 27 49


+41 61 666 64 01


+33 972 21 24 63


+81 3 3237 3642