4.2.7 Rationale for Other Trial Design Aspects
https://w3id.org/m11-rdf/C217272.C218543
- Definition
- Section 4.2.7 of the ICH M11 Protocol standard, Rationale for Other Trial Design Aspects.
- Section number
- 4.2.7
- Broader
- 4.2 Rationale for Trial Design
- NCIt concept
- http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C218543 (EVS identifier)
NCIT_C218543 (OBO PURL) - EVS term
- http://rdf.ich.org/ich-terminology#C217272.C218543 (EVS term IRI; does not resolve)
Elements specified in this section
| Element | IRI | Conformance | TS block |
|---|---|---|---|
| Rationale for Other Trial Design Aspects | C217345.C218735 | Conditional: when <Overall Rationale for Trial Design> is not used | 251 |
In the ICH M11 Template
- Heading
- Rationale for Other Trial Design Aspects optional
- Page
- p. 32
- Heading is
- Rationale for Other Trial Design Aspects (TS term, section)
| Field | Template | Page | Realises | Linked by |
|---|---|---|---|---|
<Enter Rationale for Other Trial Design Aspects> | optional | p. 32 | Rationale for Other Trial Design Aspects | ts-term / verb-dropped / section |
Draft, not normative. A derived rendering of the ICH M11 Technical Specification, Template, code lists and OID Listing (© ICH, used under the ICH Legal Mentions) and of the ICH M11 Terminology published by NCI EVS (CC BY 4.0). Not an ICH, CDISC or HL7 artifact, and not endorsed or sponsored by ICH.