standards > model/format > DOI:10.25504/FAIRsharing.cjyac2

ready Clinical Trial Registry XML


General Information
Version 1.0 of the CDISC CTR-XML standard is a provisionally approved standard based on the CDISC Operational Data Model (ODM) for clinical trial registry submissions primarily to the: World Health Organization (WHO), European Medicines Agency (EMA) EudraCT Registry and United States CTR-XML provides a means for generating harmonized messages to each of the registries listed above. The intent of the CTR-XML standard is to provide technology vendors with the ability to implement tools that support a "write once, use many times" solution based on a single XML file that holds the information needed to generate submissions for multiple clinical trial registries. This standard is based upon the common elements mapped between the registries, which are based upon the 20-item WHO Trial Registration Data Set

How to cite this record CTR-XML ; Clinical Trial Registry XML; DOI:; Last edited: March 15, 2018, 11:56 a.m.; Last accessed: Sep 24 2018 4:14 p.m.

This record is maintained by phouston  ORCID

Record added: April 7, 2016, 4:05 p.m.
Record updated: March 15, 2018, 10:19 a.m. by The FAIRsharing Team.

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No XSD schemas defined

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Reporting Guidelines

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Terminology Artifacts

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Implementing Databases (1) is a registry and results database of publicly and privately supported clinical studies of human participants conducted around the world.

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This record is not implemented by any policy.


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