Question: Please answer the following question. For research that does not entail a demonstration project conducted by or subject to the approval of state or local government officials, an IRB may waive or alter the regulatory elements of informed consent if it finds and documents a number of items, including: Need Assignment Help? A. The waiver or alteration will not adversely affect the rights and welfare of the subjects B. The research will occur in accepted educational or clinical settings. C. The research could be carried out without the waiver or alteration. D. The research involves more than minimal risk to the subjects.