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.

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.

The IRB Consent Form and Consent Parent Permission Templates(available in IRBNet researcher libraries) include the required basic elements of informed consent, with the exceptions authorized through ...

The short form written consent process does not apply when ... of the research that begins with the key information and includes the basic and required additional elements of informed consent (e.g., ...

Post-hoc analyses of a large, randomized clinical trial have revealed the potential advantages associated with electronic ...

You're required to have all participants in your study complete an Informed Consent Form. See an example of an Informed Consent Form (pdf). Below are the Bethel University Institutional Review Board’s ...

He’s also an expert on informed consent ... have “benefits in the form of health care advances” because studies that would not have been possible if patient consent were required ...

Informed consent has been defined as "an individual's autonomous authorization of a medical intervention or of participation in research". [1] In professional and legal regulations it is widely ...

For basic checkups, implied consent can stand ... Can someone other than the patient sign an informed consent form? Occasionally, someone other than the patient can provide informed consent ...

Such procedures include examination, prophylaxis, cancer screening, application of fluoride, sealants, and basic restorations ... actual informed consent. Remember, any consent form needs to ...