Statements (50)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
research
|
| gptkbp:aimsTo |
advance scientific knowledge
|
| gptkbp:auditedBy |
regulatory agencies
funding agencies institutional compliance offices |
| gptkbp:canBe |
interviews
surveys medical records biological samples experimental methods observational methods |
| gptkbp:compatibleWith |
federal regulations
state laws institutional policies |
| gptkbp:fundedBy |
gptkb:National_Institutes_of_Health
gptkb:government_agency private foundations |
| gptkbp:governedBy |
gptkb:Common_Rule
gptkb:Belmont_Report |
| https://www.w3.org/2000/01/rdf-schema#label |
Human Subjects Research
|
| gptkbp:involves |
human participants
|
| gptkbp:mayBeConductedBy |
hospitals
research institutes universities |
| gptkbp:mayBePublishedIn |
scientific journals
|
| gptkbp:mayInclude |
gptkb:philosophy
gptkb:Declaration_of_Helsinki biomedical research clinical trials international guidelines vulnerable populations behavioral studies Good Clinical Practice guidelines |
| gptkbp:mayPose |
risks to participants
|
| gptkbp:mustEnsure |
justice
respect for persons beneficence |
| gptkbp:mustMaximize |
benefits to participants
|
| gptkbp:mustMinimize |
risks to participants
|
| gptkbp:mustProtect |
confidentiality of data
privacy of participants |
| gptkbp:regulates |
gptkb:Institutional_Review_Board
gptkb:Office_for_Human_Research_Protections |
| gptkbp:requires |
adverse event reporting
informed consent data monitoring ethical review protocol approval |
| gptkbp:bfsParent |
gptkb:HSR
|
| gptkbp:bfsLayer |
7
|