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.

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 ...

The Forms and Templates page includes templates for informed consent documents. However, because each human participants research (HSR) proposal is different and carries unique risks to participants, ...

This Informed Consent for Telehealth Sessions contains important information focusing on doing psychotherapy and advocacy using internet-based video sessions. Please ...

Keep in mind that obtaining informed consent is a continuous process throughout the research, not simply a one-time event when a subject signs a form. To ensure informed consent, researchers should: ...

Note: The IRB must be provided with “sponsor verification” in the form of a letter signed by the sponsor(s ... private information or identifiable biospecimens: In seeking informed consent, the ...

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 ...

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.

Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...