It’s important to understand that even though consent may not be documented with a signature, as is the case with ... to your specific research, setting, and participants. There is no need to utilize ...

Informed consent is one of the primary requirements of research involving human participants ... 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.

When submitting a project through the eIRB system, researchers can request either a waiver of the need for signatures/documentation, or a waiver to alter or omit the entire consent process. In either ...

and what rights they have as research subjects. The consent form is one part of the dialogue that investigators have with each subject. It is recommended that forms for adult subjects be written at a ...

If consent form signatures ... then a incident report must be submitted within 48 hours of discovery. It can take up to 3-4 weeks for IRB to provide feedback on your protocol. During high-volume times ...

In these cases, an Assent Form is prepared and the procedure is very similar to that of obtaining consent ... applies to research projects that offer treatment or intervention. When we are finished ...

Give the contact information of the Brandeis University HRPP ([email protected] or 781-736-8133) for questions about the subject's rights as a human subject or concerns about the research. I have read ...