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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 ClinicalTrials.gov.
How to cite this record
FAIRsharing.org: CDISC CTR-XML; CDISC Clinical Trial Registry XML; DOI: https://doi.org/10.25504/FAIRsharing.cjyac2;
Last edited: Jan. 8, 2019, 1:39 p.m.; Last accessed: Jun 03 2020 5:24 p.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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Edits to 'https://fairsharing.org/FAIRsharing.cjyac2' by 'awhite' at 19:39, 21 Nov 2018 (approved):
'organizations' has been modified:
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CDISC|https://www.cdisc.org/|Maintains
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CDISC|https://www.cdisc.org/|Maintains
Innovative Medicines Initiative (IMI), Europe|http://www.imi.europa.eu|Undefined
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Innovative Medicines Initiative (IMI), Europe|http://www.imi.europa.eu|Undefined
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'shortname' has been modified:
Before: CTR-XML
After: CDISC CTR-XML
'name' has been modified:
Before: Clinical Trial Registry XML
After: CDISC Clinical Trial Registry XML
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United Kingdom
United States
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United States
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United Kingdom
Edits to 'https://fairsharing.org/FAIRsharing.cjyac2' by 'awhite' at 16:48, 08 Nov 2018 (approved):
'description' has been modified:
Before: 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 ClinicalTrials.gov.
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 http://www.who.int/ictrp/network/trds/en/.
After: 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 ClinicalTrials.gov.
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download page
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download page
'contactEmail' has been modified:
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After: awhite@cdisc.org
'contact' has been modified:
Before: paul houston
After: Ann White
'shortname' has been modified:
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After: CTR-XML
'homepage' has been modified:
Before: http://www.cdisc.org/ctr-xml
After: https://www.cdisc.org/standards/data-exchange/ctr-xml
Edits to 'https://fairsharing.org/FAIRsharing.cjyac2' by 'The FAIRsharing Team' at 10:19, 15 Mar 2018 (approved):
'miriam_url' has been modified:
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ClinicalTrials.gov
ClinicalTrials.gov is a registry and results database of publicly and privately supported clinical studies of human participants conducted around the world.
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