Quiz


IRB Home \| Historic Research \| Federal Regulations \| Sladen Library		Welcome Ethical Research Practice Institutional Review Board IRB Review Criteria Informed Consent Genetic Testing Types of Review Continuation & Final Reports --Continuing Review --Final Reports --Quiz Serious Adverse Events Frequently Asked Questions Conclusion
Quiz 1. Continuation Review is required in order to ensure: Risks to subjects are minimized. Subject selection is equitable. Informed consent is adequate. All of the above. You are partially correct, but your answer is not complete. What else does continuation review accomplish? Correct! Continuation Review also ensures that risks are reasonable in relation to benefits and that the privacy on subjects is protected. 2. The application for the continuation of approval of your research, or the final report, must be submitted to the IRB Office: Within two years of the start date of your research. At least one month prior to the expiration date to guard against lapse in IRB approval. At a date to be announced by the IRB during Continuation Review. Incorrect. The IRB requires either a Continuation Report or a Final Report one month prior to the expiration date of your research. Incorrect. The expiration date for a research project is established when the IRB approves the project. Correct! If a Continuation Report is not filed on time, research activities must stop. <<< Back