C207067Level 4

Clinical Trial Related Documentation

**Semantic type:** Intellectual Product

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

GET/api/v1/systems/nci_thesaurus/nodes/C207067

Official DownloadCC BY 4.0Source

Hierarchy Explorer

Hierarchy ExplorerChevron to expand - click title to open

C115462Clinical Trial Subject Recruitment Advertisement Documentation

C115465Clinical Trial Vendor Confidentiality Agreement Documentation

C115466Clinical Trial Import-Export License Application Documentation

C115469Audit Certificate Documentation

C115474Clinical Trial Data Privacy Agreement Documentation

C115475Clinical Trial Financial Agreement Documentation

C115477Clinical Trial Investigator Regulatory Agreement Documentation

C115479Clinical Trial Randomization Programming Documentation

C115483Clinical Trial Final Analysis Programs Documentation

C115484Clinical Trial Interim Analysis Programs Documentation

C115487Clinical Trial Principal Investigator Curriculum Vitae Documentation

C115488Clinical Trial Sub-Investigator Curriculum Vitae Documentation

C115492Clinical Trial Final Analysis Datasets Documentation

C115493Clinical Trial Interim Analysis Datasets Documentation

C115497Clinical Trial Operation Documentation

C115498Clinical Trial Unblinding Documentation

C115521Clinical Trial Corrections to Entered Data Documentation

C115526Clinical Trial Investigator Brochure Documentation

C115528Clinical Trial Specimen Label Documentation

C115530Clinical Trial Import or Export Documentation

C115531Clinical Trial Filenotes Master List Documentation

C115533Clinical Trial Master Randomization List

C115535Clinical Trial Biological Sample Storage Condition Log Documentation

C115544Clinical Trial Investigator Newsletter Documentation

C115551Clinical Trial Notification of Safety or Other Trial Information Documentation

C115554Clinical Trial Final Analysis Output Documentation

C115555Clinical Trial Interim Analysis Output Documentation

C115556Clinical Trial Oversight Committee Information

C115557Clinical Trial Publication Policy Documentation

C115559Clinical Trial Subject Questionnaire Documentation

C115570Clinical Trial Record of Retained Biological Samples Documentation

C115573Clinical Trial Bioanalytical Report Documentation

C115580Clinical Trial Status Report Documentation

C115582Clinical Trial Final Statistical Report Documentation

C115585Clinical Trial Interim Statistical Report Documentation

C115589Subject Diary Documentation

C115593Debarment Statement Documentation

C115599Clinical Trial Investigator Meeting Material Documentation

C115600Clinical Trial Kick-off Meeting Material Documentation

C115606Clinical Trial Team Training Material Documentation

C115621Clinical Trial Randomization Validation Documentation

C115628Clinical Study Protocol Synopsis Documentation

C115631Clinical Trial Safety Status Report Documentation

C115635Clinical Trial Biological Sample Import or Export Documentation

C115644Clinical Trial Adjudication Committee Document

C115646Clinical Trial Core Documentation

C115647Clinical Trial Dose Escalation Document

C115648Clinical Trial Financial Documentation

C115649Clinical Trial Indemnity Documentation

C115650Clinical Trial Independent Data Monitoring Committee Charter

C115651Clinical Trial Insurance Documentation

C115653Clinical Trial Interfacility Standardization Methods Documentation

C115654Clinical Trial Investigator Site Documentation

C115656Clinical Trial Management Communication and Tracking Document

C115657Clinical Trial Management Communication Documentation

C115658Clinical Trial Management Tracking Documentation

C115659Clinical Trial Team Details Documentation

C115662Clinical Trial Regulatory Notification of Termination or Closure Documentation

C115663Clinical Trial Notification to Investigators of Safety Information Documentation

C115664Clinical Study Protocol Deviation Documentation

C115666Clinical Trial Regulatory Tracking Document

C115687Clinical Trial System Account Management Documentation

C115690Clinical Trial Vendor Qualification and Compliance Documentation

C115711Investigator Brochure Acceptance Documentation

C115714Clinical Trial Medical Dictionary Coding Documentation

C115717Clinical Trial Notification of Regulatory Identification Number Documentation

C115718Clinical Study Protocol Amendment Signature Page Documentation

C115719Clinical Study Protocol Signature Page Documentation

C115725Clinical Trial Safety and Clinical Database Reconciliation Documentation

C115734Clinical Trial Public Registration Documentation

C115735Clinical Trial Subject Evaluability Criteria and Subject Classification Documentation

C115736Clinical Trial Other Committees Decisions Documentation

C115747Clinical Trial Vendor Selection Documentation

C115749Case Report Form Annotation Guideline Documentation

C115750Case Report Form Guideline Documentation

C115752Clinical Trial Medical Monitoring Plan Documentation

C115753Clinical Trial Monitoring Plan Documentation

C115756Clinical Trial Data Management Plan Documentation

C115761Clinical Trial Statistical Analysis Plan Documentation

C115764Clinical Trials Operational Procedure Manual Documentation

C115765Clincial Trial Master File Plan Documentation

C115769Clinical Trial Recruitment Plan Documentation

C115777Clinical Trial Quality Assurance Plan Documentation

C115778Clinical Trial Randomization Plan Documentation

C115779Clincial Trial Standard Operating Procedure List Documentation

C115780Clinical Trial Management Plan Documentation

C115783Clinical Trial Stakeholder Communication Plan Documentation

C116348Clinical Trial Randomization Procedure Documentation

C125421Clinical Trial Operational Oversight Documentation

C125422Clinical Trial Committee Member Financial Disclosure Form Documentation

C125423Clinical Trial Committee Member Contract Documentation

C125424Clinical Trial Committee Member Confidentiality Disclosure Agreement Documentation

C125425Clinical Trial Team Evidence of Training Documentation

C125426Clinical Trial Coordinating Investigator Documentation

C125427Clinical Trial Subject Eligibility Verification Form and Worksheet Documentation

C125428Clinical Trial Ongoing Vendor Oversight Documentation

C125429Clinical Trial Roles and Responsibilities Matrix Documentation

C125431Medical Device Report of Prior Investigations Documentation

C125432Clinical Trial Medical Device Investigators Agreement Documentation

C125433Clinical Trial Source Data Verification Documentation

C125434Clinical Trial Subject Identification Log Documentation

C125438Clinical Trial Database Change Control Documentation

C125440Clinical Trials Vendor Curriculum Vitae Documentation

C125442Clinical Trial Source Data Documentation

C126093Clinical Trial Submission to Other Committees Documentation

C126094Clinical Trial Vendor Management Plan Documentation

C207071Clinical Trial-Related Form

C207073Clinical Trial Site Related Documentation

C207074Clinical Trial Products and Supplies Management Documentation

C207075Clinical Trial Safety Management Documentation

C207167Clinical Trial Risk Management Plans Documentation

C207168Clinical Trial Transfer of Regulatory Obligations Documentation

C207169Clinical Trial Sponsor Team Member Curriculum Vitae Documentation

C207170Clinical Trial Committee Process Documentation

C207171Clinical Trial Committee Member List Documentation

C207172Clinical Trial Committee Output Documentation

C207173Clinical Trial Committee Member Curriculum Vitae Documentation

C207174Clinical Trial Relevant Communications Documentation

C207175Clinical Trial Tracking Information Documentation

C207176Clinical Trial Meeting Material Documentation

C207177Clinical Trial Filenote Documentation

C207178Clinical Study Protocol Amendment Documentation

C207179Clinical Trial Investigators Financial Disclosure Form Summary Documentation

C207180Marketed Clinical Trial Investigational Product Material Legal Documentation

C207181Clinical Trial Regulatory Progress Report Documentation

C207186Clinical Trial Subject Log Documentation

C207194Testing Facility Certification or Accreditation Documentation

C207195Clinical Trial Laboratory Validation Documentation

C207196Clinical Trial Laboratory Results Documentation

C207197Clinical Trial Testing Facility Manual Documentation

C207198Clinical Trial Supply Import Documentation

C207199Clinical Trial Head of Facility Curriculum Vitae Documentation

C207200Clinical Trial Specimen Shipment Records Documentation

C207201Clincial Trial Contractual Agreement Documentation

C207202Clinical Trial Final Subject Data Documentation

C207203Clinical Trial Database Requirements Documentation

C207204Clinical Trial Database Validation Plan Documentation

C207205Clinical Trial Edit Check Programming Documentation

C207206Clinical Trial Data Validation Testing Documentation

C207207Clinical Trial Approval for Database Activation Documentation

C207208Clinical Trial External Data Transfer Specification Documentation

C207209Clinical Trial Data Entry Guidelines From Paper Forms Documentation

C207210Clinical Trial Data Review Documentation

C207211Clinical Trial Database Lock and Unlock Approval Documentation

C207212Clinical Trial Electronic Data Capture System Technical Design Documentation

C207213Clinical Trial Electronic Data Capture System Validation Documentation

C207214Clinical Trial Sample Size Calculation Documentation

C207215Clinical Trial End of Trial or Interim Unblinding Documentation

C207216Clinical Trial Data Definitions for Tabulation and Analysis Dataset Documentation

C207217Clinical Trial Tabulation and Analysis Quality Control Documentation

C207218Clinical Trial Raw Dataset for Interim Tabulation and Analysis Documentation

C207219Clinical Trial Raw Dataset for Final Tabulation and Analysis Documentation

C208325Template Informed Consent Form Documentation

C215490Study Definition Document

C60777Clinical Trial Agreement Documentation

C79176Clinical Trial Reports and Related Information Documentation

C79189Clinical Trial Regulatory Authority Decision Documentation

Cross-system equivalences0

No cross-system equivalences mapped for this node.

Report a data issue