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Ethical Research Practice
Institutional Review Board
IRB Review Criteria

Informed Consent
--Capacity to Consent
--Freedom from Coercion
--Comprehension of Risks & Benefits
--Informed Consent Document
--Informed Consent Delivery
--Waiver of Informed Consent
--Quiz

Genetic Testing
Types of Review
Continuation & Final Reports
Serious Adverse Events
Frequently Asked Questions
Conclusion

Quiz

1. The informed consent document must provide a complete and clear description of several elements in layman’s terms. These elements are:

Description of how personal health information will be shared with the media, complete financial disclosure for the research organization, and a description of the research study in scientific language.

Explanation of purposes, expected time of involvement, description on the procedures, and reasonably foreseeable risks.

Minimized statement of risks, complete statement on the legal ramifications for HIPAA for the institution, and the detailed financial records for medical equipment used in the research.







2. Which of the following populations are at risk for coercion to participate in research?

Financially disadvantaged individuals, including students and minors.

Prisoners, who may be under stress to participate in hopes of gaining additional freedoms.

Members of the Armed Forces

All of the above






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