Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.

“Informed consent is the law and essential to maintaining trust in the patient-provider relationship and respecting patients’ autonomy,” the letter says. Additionally, the Office for Civil ...

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 ...

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 ...

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 ...