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.

If the informed-consent form were to explain these points ... There is a long way to go in cleaning up clinical trials before the trust of patients is regained.

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.

as well as its informed consent forms, contain the necessary information to enable a patient, or his or her representative, to make fully-informed decisions about their care, including the right ...

as well as informed consent forms, contain elements and information that allow for a patient, or his or her representative, to make fully informed decisions about the patient’s care. In the ...

Though informed consent often evokes images of thick packets of forms, the process is much broader than that and starts long before it’s time to read the fine print, Agu said. “The FDA ...

A systematic analysis of 124 informed-consent documents for U.S. government-sponsored, multinational HIV/AIDS research conducted in 2006 revealed that the forms spanned more than 20 pages ...

Informed consent may be the biggest misnomer in medicine: Studies show that most patients don't read the forms they sign before undergoing surgery or medical treatment. More than half of those who ...

This UB CTSI Educational Modules video: Defines informed consent Outlines where to find the most up-to-date consent form template, the HRP-502 Identifies the parts of the Informed Consent form Shares ...

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 ...