GCP TRAINING QUIZ WITH 100% CORRECT ANSWERS2024

After the IRB reviews and approves your protocol, informed consent, and associated documents, you should receive: A. A phone call telling you the study can now proceed. B. A personal visit from the IRB chair telling you how excited he/she is about your research. C. Written notification of the IRB decision and the approved versions of the protocol and informed consent forms. D. Nothing. If you do not receive a response in 30 days, you can proceed with your study. correct answersC. Written notification of the IRB decision and the approved versions of the protocol and informed consent forms. 4An IRB may perform an expedited review of a protocol or informed consent form change if the change involves no more than minimal risk to study participants. A. TRUE B. FALSE correct answersA. TRUE 2For an IRB review to be required, clinical research must be: A. Federally funded. B. Involve a product regulated by the FDA. C. Fall under local institutional rules requiring IRB approval. D. Any or all of the above A, B or C. correct answersD. Any or all of the above A, B or C. 3The primary purpose of the Institutional Review Board (IRB) is to: A. Investigate allegations of research misconduct. B. Administer compensation for participation to study volunteers. C. Protect the rights and welfare of research participants. D. All of the above. correct answersD. All of the above.