A signed informed consent form notifies potential research participants of their obligations and ... vulnerable populations or complex interventions. You may use this sample tempate to get started.

Informed consent ... the nature of the research project, why they are candidates for the research, what risks, benefits, and alternatives are associated with the research, and what rights they have as ...

secure the written informed consent of any human subject used in research before involving that subject in the research project. In preparing instructions for subjects being asked to sign this consent ...

The IRB Office published an updated version of the informed consent template. The template and instructions for uploading this form in eRA have been posted to the Forms & Templates page. For your ...

The short form written consent process does not apply when: research is exempt ... the DHHS requirement for documentation of informed consent as codified at §46.117, item (c); or the investigators ...

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 ... whether to participate in research, and the chance to discuss that information. This UB CTSI Educational Modules video: Defines informed consent Outlines where to find the most up ...

Informed consent is one of the primary requirements of research involving human participants ... provided the conditions described on the waiver form are fulfilled.

Furthermore, unless the consent process has been specifically waived by the IRB, no subjects may be included in research unless the investigator has obtained the legally effective informed ... and ...