The goal of the informed consent ... sections of this consent form must be completed for consideration and/or final IRB approval. If you are requesting a waiver of the standard written consent ...

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 Document Template. Child Assent and Parental Consent Form When children/minors under eighteen are involved in research, assent must be obtained from both the parent and the ...

Moreover, the informed consent should not merely be a list of isolated facts. Many consent forms are not as good as they could be in terms of aiding decision-making. The goal is to help people process ...

Informed consent forms and scripts should be written at an eighth-grade reading level to ensure that prospective subjects are truly informed. See the Informed Consent Template for an example of ...

The Forms and Templates page includes templates for informed consent documents. However, because each human participants research (HSR) proposal is different and carries unique risks to participants, ...

Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2. Names and Affiliations ...

The Informed Consent Form should be in the primary language of the research ... vulnerable populations or complex interventions. You may use this sample tempate to get started.

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.