9.3 Pregnancy and Postpartum Information
https://w3id.org/m11-rdf/C217272.C218621
- Definition
- Section 9.3 of the ICH M11 Protocol standard, Pregnancy and Postpartum Information.
- Section number
- 9.3
- Broader
- 9 ADVERSE EVENTS, SERIOUS ADVERSE EVENTS, PRODUCT COMPLAINTS, PREGNANCY AND POSTPARTUM INFORMATION, AND SPECIAL SAFETY SITUATIONS
- NCIt concept
- http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C218621 (EVS identifier)
NCIT_C218621 (OBO PURL) - EVS term
- http://rdf.ich.org/ich-terminology#C217272.C218621 (EVS term IRI; does not resolve)
Subsections
- 9.3.1 Participants Who Become Pregnant During the Trial
- 9.3.2 Participants Whose Partners Become Pregnant During the Trial
Elements specified in this section
None.
In the ICH M11 Template
- Heading
- Pregnancy and Postpartum Information
- Page
- p. 53
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.