![]() ![]() How can research conducted as a classroom exercise be reviewed to protect human participants?.Does research conducted as a classroom exercise count as human subjects research?.Can research proceed at a foreign institution if no foreign IRB has reviewed the research?.How should IRBs deal with research in foreign countries?.How should research involving "snowball samples" be handled from a human subjects perspective?.Advice to Researchers on Dealing with IRBs.Advice to IRBs on Dealing with Researchers.What if the researcher and the IRB disagree about the risk and appropriate action to be taken in the project?. ![]() When a Signed Consent Form can Harm a Participant (Vignette).What flexibility does the IRB have in applying the Common Rule?.What does this mean in terms of social science projects that the federal government has declared "exempt"? My university does not have an "exempt" category for research, only "expedited" and "full review" categories.Does this mean that all questionnaire, test, and interview-based studies are exempt?."Unexpected Risk in Classroom Research" (Vignette)."Research-Like Tools Used as Teaching Tools" (Vignette).The Beach versus the Airport (Vignette).Informed Consent in Social and Behavioral Science.What sorts of harm can arise from social and behavioral science research?.What if the project decides to link data from a new survey to existing individual-level data from public data sources after the survey has been completed?.What if the project intends to link data from a new survey to existing individual-level data from public data sources?.What about merging public data files or enhancing a public data file?.Is secondary analysis of data human subjects research?.Are third parties human subjects in research?.Child language studies in "Freedonia" (Vignette).What exemptions of the Common Rule are most appropriate to social science research?.What does the Belmont Report have to do with IRB reviews?.What does "minimal risk" mean in research?.How can oversight be matched to risk in order to achieve the goals of the Common Rule?.What are the overall goals of the federal policy (the Common Rule)?.Does this mean that all research conducted through this institution must comply with the particulars of these subparts? My institution's assurance is with DHHS through OHRP, which has adopted subparts B, C & D.What parts of the regulations are applicable to my institution?.Where can I get authoritative and expert interpretation of the regulations?.Original Agencies, Departments and Offices approving the Common Rule (1991).What are the Subparts of the regulations?.What is the relationship between the Common Rule and the Federal Regulation for the Protection of Human Subjects?.Interpreting the Common Rule for the Protection of Human Subjects for Behavioral and Social Science ResearchĬlick on the applicable heading to go to a specific subject:Įxempt and Expedited Review and Informed Consent ![]()
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |