Dr. MedLaw explains the importance of discussing risks, benefits, and alternatives in a manner the patient fully understands ...

Informed consent is one of the primary requirements of research involving human participants. ... The UAB IRB also offers a sample consent form written for a fictitious protocol. In most places, the ...

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.

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 ...

Department of Health and Human Services (DHHS) regulations for the protection of human participants require that informed consent information be presented in language understandable to the participant ...

The information and sample documents in the compliance form section are provided to help researchers develop consent and assent documents customized to the design of the individual research project.