a group that has been formally designated to review and monitor biomedical research involving human subjects. In accordance with FDA, an IRB has the right to review, approve, disapprove or modify any proposal for research involving human subjects.
a group that has been formally designated to review and monitor biomedical research involving human subjects. In accordance with FDA, an IRB has the right to review, approve, disapprove or modify any proposal for research involving human subjects.
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