With few exceptions, researchers must obtain and document prospective consent from the research subject before initiating any screening or study procedures. Any exceptions must be reviewed and approved by the IRB beforehand. For additional guidance on the informed consent process, please refer to UCSF policy.

UCSF consent form templates
When developing a consent document, you should start with a UCSF Consent and Assent Template. These templates include required regulatory elements and UCSF-specific wording. 

Need assistance? Consult the IRB Website and submit an Ask Andy Form if you are unable to find your answer.