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 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., ...

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 ...

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 ...

Data communities may create risks even for those who decline to join, upending the basic bargain of health research and informed consent. The problem is not the form, but the frame. The consent ...

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 ...