Informed Consent Ontology
320 terms(s) returned
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- description of procedure for obtaining further information
- description of reputational risk
- description of research procedure
- description of voluntary participation
- description of waiver
- designing an informed consent form
- directive about research of biospecimens
- disclosure directive
- drug testing investigation
- economic vulnerability
- educational vulnerability
- effective date specification in informed consent form
- eligibility of candidate participation
- eligibility questionnaire
- eligibility screening process
- eligibility screening role
- ethics directive
- excess material role
- explaining benefits of participation to participant candidate
- explaining record confidentiality to participant candidate
- explaining risks of participation to participant candidate
- explaining sample process and usage to participant candidate
- explaining study derived data usage to participant candidate
- explaining study protocol to participant candidate
- explaining study purpose to participant candidate
- explaining to participant candidate about the study participating information
- explaining to participant candidate in informed consent process
- filled multiple choice text entity
- filled questionnaire
- filling informed consent form
- filling questionnaire
- for-profit research investigation
- future use directive
- genetic testing directive
- has agent
- health information entity
- human population
- human research investigation
- human subject consenter
- human subject research regulatory document
- human subject signature section in informed consent form
- human subject unable to give informed consent
- human subject-specified contact person role
- incomplete informed consent form
- individually identifiable health information entity
- informed assent form
- informed assent form for child or minor
- informed assent form for cognitively impaired
- informed consent form
- informed consent form containing questionnaire