Institutional review board may temporarily stop the project's progress, at least until adjustments are made.
According to FDA guidelines, an Institutional Review Board is a group that has been specifically given permission to examine and monitor scientific research involving people. According to FDA guidelines, an IRB has the authority to approve, demand adjustments be made (to seek approval), or reject research. This group review strongly protects the rights and welfare of study participants. The purpose of IRB review is to make sure that all required measures are taken to ensure the safety and rights of subjects who are engaging in research, both before and throughout ongoing evaluation.
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