Describe exactly what you wish to waive.
Describe why the research involves no more than minimal risk to the subjects.
Describe why the waiver or alteration will not adversely affect the rights and welfare of the
subjects.
Describe why the research could not practically be carried out without the waiver or
alteration of informed consent.
Will subjects be provided with additional pertinent information after or during the research? If
yes, describe how information will be provided to participants.
For studies including participants under the age of 19
IRB – Waiver of Parental Consent
How do you wish to depart from the usual written informed consent procedure? (For example, you
wish to waive the consent from parents of students less than 19 years of age).
The IRB will assess whether the subjects’ rights, such as the “right to privacy” would be violated if
the consent were waived and the potential benefits to participation.
The IRB will assess whether the subjects’ rights, such as the “right to privacy” would be violated if
the consent were waived and the potential benefits to participation.
In social science research involving deception/concealment, subjects should be UWA OSPR
debriefed at the conclusion of the study. This may not be needed in other studies or, if data
Octowere ber 2020 collected without identifies, it may not be possible, since the identity of
subjects would be known.
In social science research involving deception/concealment, subjects should be UWA OSPR
debriefed at the conclusion of the study. This may not be needed in other studies or, if data
Octowere ber 2020 collected without identifies, it may not be possible, since the identity of
subjects would be known.
