CDISC TMF-RM IP and Trial Supplies Zone Terminology

Preferred Label : CDISC TMF-RM IP and Trial Supplies Zone Terminology;

NCIt synonyms : TMF-RM IP and Trial Supplies Zone;

NCIt related terms : IP and Trial Supplies Zone;

NCIt definition : The CDISC TMF terminology codelist relevant to the IP and Trial Supplies Zone of the Trial Master File Reference Model.;

Alternative definition : CDISC: The terminology codelist for the Trial Master File Reference Model that contains the sections and artifacts relevant to the IP and Trial Supplies Zone.;

Details

Origin ID

C208281;

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- CDISC TMF Terminology [NCIt concept]
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]
subset_includes_concept
- Clinical Trial Filenote Documentation [NCIt concept]
- Clinical Trial Investigational Product Accountability Documentation [NCIt concept]
- Clinical Trial Investigational Product Certificate of Analysis Documentation [NCIt concept]
- Clinical Trial Investigational Product Certificate of Destruction Documentation [NCIt concept]
- Clinical Trial Investigational Product Handling Instruction Documentation [NCIt concept]
- Clinical Trial Investigational Product Quality Complaint Documentation [NCIt concept]
- Clinical Trial Investigational Product Recall Documentation [NCIt concept]
- Clinical Trial Investigational Product Regulatory Release Documentation [NCIt concept]
- Clinical Trial Investigational Product Relabeling Documentation [NCIt concept]
- Clinical Trial Investigational Product Retest and Expiry Documentation [NCIt concept]
- Clinical Trial Investigational Product Return Documentation [NCIt concept]
- Clinical Trial Investigational Product Sample Label [NCIt concept]
- Clinical Trial Investigational Product Shipment Documentation [NCIt concept]
- Clinical Trial Investigational Product Storage Condition Documentation [NCIt concept]
- Clinical Trial Investigational Product Storage Condition Excursion Documentation [NCIt concept]
- Clinical Trial Investigational Product Supply Plan Documentation [NCIt concept]
- Clinical Trial Investigational Product Transfer Documentation [NCIt concept]
- Clinical Trial Investigational Product Treatment Allocation Documentation [NCIt concept]
- Clinical Trial Investigational Product Treatment Decoding Documentation [NCIt concept]
- Clinical Trial Investigational Product Unblinding Plan Documentation [NCIt concept]
- Clinical Trial Investigational Product Verification Statements Documentation [NCIt concept]
- Clinical Trial Maintenance Logs Documentation [NCIt concept]
- Clinical Trial Meeting Material Documentation [NCIt concept]
- Clinical Trial Non-Investigational Product Supplies Documentation of Return [NCIt concept]
- Clinical Trial Non-Investigational Product Supplies Plan Documentation [NCIt concept]
- Clinical Trial Non-Investigational Product Supplies Shipment Documentation [NCIt concept]
- Clinical Trial Non-Investigational Product Supplies Storage Documentation [NCIt concept]
- Clinical Trial Qualified Person Investigational Product Certification Documentation [NCIt concept]
- Clinical Trial Relevant Communications Documentation [NCIt concept]
- Clinical Trial Tracking Information Documentation [NCIt concept]
- Interactive Response Technology User Acceptance Testing Certification Documentation [NCIt concept]
- Interactive Response Technology User Account Management Documentation [NCIt concept]
- Interactive Response Technology User Manual Documentation [NCIt concept]
- Interactive Response Technology User Specification Documentation [NCIt concept]
- Interactive Response Technology Validation Certification Documentation [NCIt concept]

Keyword's position in hierarchy(ies) :

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