CDISC TMF-RM Site Management Zone Terminology

Preferred Label : CDISC TMF-RM Site Management Zone Terminology;

NCIt synonyms : TMF-RM Site Management Zone;

NCIt related terms : Site Management Zone;

NCIt definition : The CDISC TMF terminology codelist relevant to the Site Management 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 Site Management Zone.;

Details

Origin ID

C208280;

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- CDISC TMF Terminology [NCIt concept]
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]
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- Clinical Study Protocol Amendment Signature Page Documentation [NCIt concept]
- Clinical Study Protocol Deviation Documentation [NCIt concept]
- Clinical Study Protocol Signature Page Documentation [NCIt concept]
- Clinical Trial Agreement Documentation [NCIt concept]
- Clinical Trial Coordinating Investigator Documentation [NCIt concept]
- Clinical Trial Data Privacy Agreement Documentation [NCIt concept]
- Clinical Trial Filenote Documentation [NCIt concept]
- Clinical Trial Financial Agreement Documentation [NCIt concept]
- Clinical Trial Financial Documentation [NCIt concept]
- Clinical Trial Indemnity Documentation [NCIt concept]
- Clinical Trial Investigator Regulatory Agreement Documentation [NCIt concept]
- Clinical Trial Investigators Financial Disclosure Form [NCIt concept]
- Clinical Trial Medical Device Investigators Agreement Documentation [NCIt concept]
- Clinical Trial Meeting Material Documentation [NCIt concept]
- Clinical Trial Notification to Investigators of Safety Information Documentation [NCIt concept]
- Clinical Trial Principal Investigator Curriculum Vitae Documentation [NCIt concept]
- Clinical Trial Relevant Communications Documentation [NCIt concept]
- Clinical Trial Site Additional Monitoring Activity Documentation [NCIt concept]
- Clinical Trial Site Feasibility Documentation [NCIt concept]
- Clinical Trial Site Initiation Monitoring Report Documentation [NCIt concept]
- Clinical Trial Site Investigator Confidentiality Agreement Documentation [NCIt concept]
- Clinical Trial Site Monitoring Visit Follow-up Documentation [NCIt concept]
- Clinical Trial Site Monitoring Visit Report Documentation [NCIt concept]
- Clinical Trial Site Other Personnel Curriculum Vitae Documentation [NCIt concept]
- Clinical Trial Site Personnel Contact Detail Documentation [NCIt concept]
- Clinical Trial Site Staff Qualification Supporting Information Documentation [NCIt concept]
- Clinical Trial Site Task Assignment Documentation [NCIt concept]
- Clinical Trial Site Training Completion Documentation [NCIt concept]
- Clinical Trial Site Training Material Documentation [NCIt concept]
- Clinical Trial Site Visit Log Documentation [NCIt concept]
- Clinical Trial Source Data Documentation [NCIt concept]
- Clinical Trial Source Data Verification Documentation [NCIt concept]
- Clinical Trial Sub-Investigator Curriculum Vitae Documentation [NCIt concept]
- Clinical Trial Subject Eligibility Verification Form and Worksheet Documentation [NCIt concept]
- Clinical Trial Subject Identification Log Documentation [NCIt concept]
- Clinical Trial Subject Log Documentation [NCIt concept]
- Clinical Trial Tracking Information Documentation [NCIt concept]
- Final Clinical Trial Site Close Out Monitoring Report Documentation [NCIt concept]
- Form FDA 1572 [NCIt concept]
- Investigational Product Clinical Trial Site Release Documentation [NCIt concept]
- Investigator Brochure Acceptance Documentation [NCIt concept]
- Pre-Clinical Trial Site Evaluation Report Documentation [NCIt concept]
- Unselected Clinical Trial Site Documentation [NCIt concept]

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