ShortName = Trial Blinding Role Response Terminology LongName = Trial Blinding Role Response Terminology Version = 1.0 CanonicalUri = 2.16.840.1.113883.3.989.2.3.1.16 CanonicalVersionUri = 2.16.840.1.113883.3.989.2.3.1.16.1 Agency
ShortName = M11 LongName = Clinical Trial protocols Identifier = C217281
| code Id="code" (required) Type="string" |
english-label Id="en" (optional) Type="string" Lang="en" |
M11 Definition Id="en_def" (optional) Type="string" Lang="en" |
current flag Id="cf" (optional) Type="string" Lang="en" |
|---|---|---|---|
| C17445 | Care Provider | The primary person in charge of the care of a patient, usually a family member or a designated health care professional. | y |
| C25936 | Investigator | A person responsible for the conduct of the clinical trial at a trial site. If a trial is conducted by a team of individuals at the trial site, the investigator is the responsible leader of the team and may be called the principal investigator. | y |
| C48660 | Not Applicable | Determination of a value is not relevant in the current context. | y |
| C207599 | Outcomes Assessor | The individual who evaluates the outcome(s) of interest. | y |
| C142710 | Participant | A member of the clinical study population from whom data are being collected. (CDISC Glossary) | y |
| C70793 | Sponsor | An individual, company, institution, or organization that takes responsibility for the initiation, management, and/or financing of a clinical study. (CDISC Glossary) | y |
This file contains a code list co-maintained by ICH M2 ESTRI and CDISC in collaboration with the NCI Enterprise Vocabulary Services (EVS). It is encoded using OASIS genericode. More information on ICH technical standards is available via the M2 ESTRI webpages at www.ich.org.
Change History: v1.0 (November 11 2025)
Report created by ICH_M2_CDISC_Codelist.xsl : [Revision: 1.1 ] : ICH : Harmonisation for Better Health