A Researcher Submits A Study To The Irb
Question:
Answer: Determination for Exemption
Question: Where could student researchers and/or student subjects find additional resources regarding the IRB approval process? Select all that apply.
Answer: Faculty Advisor/Research Mentor- IRB Office
Question: In the U.S., the first federal regulations for human subjects research began in 1981 with the codification of the ________.
Answer: Nuremberg Code
Question: Which of the following studies would need IRB approval?
Answer: Studies collecting identifiable information about living individuals.
Question: Which type of IRB review does not require an IRB approval but does require a determination by an individual designated with that task (such as an IRB member or experienced staff person)?
Answer: Exempt
Question:
Answer: Convened Review
Question: Your informed consent form must describe _______.
Answer: all foreseeable risks and discomforts.
Question: In the U.S., the first federal regulations for human subjects research began in 1981 with the codification of the ________.
Answer: common rule
Question: Which of the following studies would need IRB approval?
Answer: Studies collecting identifiable information about living individuals.
Question:
Answer: Not Human Subjects