C207073Level 5

Clinical Trial Site Related Documentation

**Semantic type:** Intellectual Product

**Definition:** Documents or documentation related to a clinical trial site.

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C115476Clinical Trial Site Investigator Confidentiality Agreement Documentation

C115536Clinical Trial Site Visit Log Documentation

C115576Clinical Trial Site Initiation Monitoring Report Documentation

C115577Clinical Trial Site Monitoring Visit Report Documentation

C115581Final Clinical Trial Site Close Out Monitoring Report Documentation

C115586Pre-Clinical Trial Site Evaluation Report Documentation

C115604Clinical Trial Site Training Material Documentation

C115668Clinical Trial Site Feasibility Documentation

C115670Clinical Trial Site Management Tracking Document

C115671Clinical Trial Site Personnel Contact Detail Documentation

C115673Clinical Trial Site Task Assignment Documentation

C115674Clinical Trial Site Training Completion Documentation

C115710Investigational Product Clinical Trial Site Release Documentation

C115713Local Laboratory Certification or Accreditation Document

C115737Clinical Trial Site Additional Monitoring Activity Documentation

C115739Unselected Clinical Trial Site Documentation

C115781Clinical Trial Site Communications and Tracking Management Documentation

C125443Clinical Trial Site Monitoring Visit Follow-up Documentation

C207183Clinical Trial Site Other Personnel Curriculum Vitae Documentation

C207184Clinical Trial Site Staff Qualification Supporting Information Documentation

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