The IRB determines, for each protocol it reviews, which of the following elements and disclosures must be included in the informed ... in the form of a letter signed by the sponsor(s) with the same ...

Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

Informed consent is an agreement between the investigators and the research participants. A signed informed consent form notifies potential research participants of their obligations and rights, and ...

secure the written informed consent of any human subject used in research before involving that subject in the research project. In preparing instructions for subjects being asked to sign this consent ...

Although the geneticists and the university believed that the signed informed-consent forms allowed the pursuit of essentially any biomedical question, the Havasupai claimed that they had never ...

Investigators may request a waiver or alteration of the informed consent process or waiver of consent documentation, provided the conditions described on the waiver form are fulfilled.