standards > model/format > DOI:10.25504/FAIRsharing.cjyac2
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ready CDISC Clinical Trial Registry XML

Abbreviation: CDISC CTR-XML

General Information
CTR-XML lets technology vendors 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 trials for clinical trial registry submissions primarily to the World Health Organization (WHO), European Medicines Agency (EMA) EudraCT Registry and United States


Countries that developed this resource United States

Created in 2016

Taxonomic range

How to cite this record CDISC CTR-XML; CDISC Clinical Trial Registry XML; DOI:; Last edited: Jan. 8, 2019, 1:39 p.m.; Last accessed: Nov 28 2021 12:03 a.m.

This record is maintained by awhite

Record added: April 7, 2016, 4:05 p.m.
Record updated: Nov. 21, 2018, 7:39 p.m. by awhite.

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No support information provided.

Additional Information

External Links


    No tools defined


No XSD schemas defined

Access / Retrieve Data

Conditions of Use


No publications available

Related Standards

Reporting Guidelines

No guidelines defined

Terminology Artifacts

No semantic standards defined

Identifier Schemas

No identifier schema standards defined


No metrics standards defined

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

Implementing Policies

This record is not implemented by any policy.


Record Maintainer

  • This record is maintained by awhite