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  • Human Research Protection Program (HRPP)
    The Human Research Protection Program (HRPP) reviews and monitors research involving human subjects at UCSF and several affiliate institutions to ensure the welfare, safety, privacy, and ethical treatment of participants in human research studies
  • Welcome to iRIS | Human Research Protection Program (HRPP)
    Finding Your IRB Approval Letter: This video shows you how to access and save your past and current IRB approval letters, and discusses the important regulatory information that is included in the letters
  • IRB Review - Human Research Protection Program (HRPP)
    The IRB reviews research projects that involves human subjects performed by UCSF faculty, staff or students or researchers at UCSF-affiliated institutions, as described on the Research Requiring IRB Review page
  • Human Research Protection Program (IRB) | UCSF Websites
    Website URL https: irb ucsf edu Preview Departments EXECUTIVE VICE CHANCELLOR Status Operational Technical Contact Name Ami Patel Business Owner Name Ami Patel Dead Site N MyAccess Required Duplicate
  • Submissions - Human Research Protection Program (HRPP)
    Once you determine that your human subjects research study requires UCSF IRB review, submit a new study using iRIS, our online submission system As your study progresses, submit the following to the IRB as needed:
  • New Study | Human Research Protection Program (HRPP)
    Effective, June 15, 2015, UCSF PIs are no longer required to obtain scientific scholarly review or feasibility analysis prior to submitting a research project to the IRB, unless it is required by the PI's division, department or organization
  • For IRB Members - Human Research Protection Program (HRPP)
    If you are interested in becoming a Community Member of the IRB, and you reside within the San Francisco Bay Area, please complete the UCSF IRB Community Member form
  • Consent | Human Research Protection Program (HRPP)
    Consent and Assent Form Templates Exempt Consent Templates and Guidance Guidelines Consent Guidelines Consenting Non-English Speakers Enrolling Individuals With Cognitive Impairments and Assessing Decisional Capacity Enrolling Subjects Who Are Legally Blind, Illiterate, or Cannot Talk or Write Obtaining and Documenting Informed Consent with Signatures Obtaining and Documenting Informed Consent
  • Contact Us - Human Research Protection Program (HRPP)
    Before reaching out to the IRB, please refer to the resources and contact information below for topics that fall under other offices These areas are outside of the IRB’s scope, and by using the provided links or reaching out to the relevant contacts, you can often find the answers you need directly
  • Current External IRBs - Human Research Protection Program (HRPP)
    The UCSF Cancer Center investigator downloads the application packet and submits to the Cancer Center PRMC Once the Cancer Center PRMC approves the protocol, the investigator submits an abbreviated application to the UCSF IRB via iRIS





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