An ongoing clinical protocol at your site includes weekly blood draws to assess an exploratory endpoint. Unfortunately, participants are not happy about visiting the clinic weekly, and they are considering dropping out. Therefore, a protocol amendment is being prepared to remove the weekly blood draw. This change can be implemented: O A. Immediately, as it is not a safety assessment. O B. Once the protocol is finalized and submitted to the FDA. O C. Once the protocol and consent form updates are approved by the IRB. O D. As soon as the study sponsor advises that their decision is final to remove these blood draws. 4. If already serving as a member of the IRB, a clinical investigator can participate in the review of her own clinical protocol.

Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
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Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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3.
An ongoing clinical protocol at your site includes weekly blood draws to assess an exploratory
endpoint. Unfortunately, participants are not happy about visiting the clinic weekly, and they are
considering dropping out. Therefore, a protocol amendment is being prepared to remove the weekly
blood draw. This change can be implemented:
O A. Immediately, as it is not a safety assessment.
O B. Once the protocol is finalized and submitted to the FDA.
O C. Once the protocol and consent form updates are approved by the IRB.
O D. As soon as the study sponsor advises that their decision is final to remove these blood draws.
If already serving as a member of the IRB, a clinical investigator can participate in the review of her
own clinical protocol.
O A. TRUE
O B. FALSE
An 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.
O A. TRUE
O B. FALSE
Transcribed Image Text:3. An ongoing clinical protocol at your site includes weekly blood draws to assess an exploratory endpoint. Unfortunately, participants are not happy about visiting the clinic weekly, and they are considering dropping out. Therefore, a protocol amendment is being prepared to remove the weekly blood draw. This change can be implemented: O A. Immediately, as it is not a safety assessment. O B. Once the protocol is finalized and submitted to the FDA. O C. Once the protocol and consent form updates are approved by the IRB. O D. As soon as the study sponsor advises that their decision is final to remove these blood draws. If already serving as a member of the IRB, a clinical investigator can participate in the review of her own clinical protocol. O A. TRUE O B. FALSE An 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. O A. TRUE O B. FALSE
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