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Your professional EDC partner

Since we were founded in 2002, it has been our aim to support the clinical development of drugs and medical products through the use of efficient software.
With our CDISC-certified EDC system MARVIN and related tools such as the STUDY COMPOSER and the TABULATOR, we offer sponsors, CROs and academic research institutions of every size a reliable, flexible and powerful software suite. This maximizes the value of their clinical IT investment through the use of the CDISC data standard. Our employees regularly participate in international data management conferences as exhibitors and speakers.


Quality management and quality assurance are accorded high priority at XClinical: we work according to GCP and ISO guidelines. ISO 9001 certification is in the pipeline. Our EDC system MARVIN complies with all relevant FDA regulations, in particular with 21 CFR Part 11.
We are an active member of the CDISC* organization because we are convinced that the widespread use of this standard for data interchange, data submission and archiving will facilitate the use of e-Trial technology and working processes in the long term.

What’s in it for you?

With our integrated toolset, we can help you carry out your clinical trials more efficiently with shorter data management processes and by delivering reliable high-quality data throughout the trial. Get in touch with us to find out how our products and services can simplify your clinical trials and increase the satisfaction of your investigators.

*CDISC = Clinical Data Interchange Consortium

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