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Human Research Protection Program and Institutional Review Board

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Resources for the Consent and Assent Process

Guidance and Sample Language for Consent and Assent Documents

Templates for Consent and Assent forms
  • Consent Form for Minimal Risk Studies (DOC)
  • Consent Form for FDA-regulated Studies (DOC)
  • Consent Form for Studies Involving More Than Minimal Risk (DOC)
  • Verbal Consent Guide or Handout (DOC)
  • Assent Form (DOC)
Resources for Participants (in English and Spanish)

Questions to Ask when Deciding Whether to Volunteer for Research

  • English PDF
  • Spanish PDF

Informational Videos

Women in Clinical Trials Handout (in multiple languages)
  • English PDF
  • Spanish PDF
Consent-related Guidance
  • A thorough overview the principle of informed consent can be found in the Stanford Encyclopedia of Philosophy (Fall 2012 Edition), Edward N. Zalta (ed.)
  • For researchers conducting FDA-regulated research
    • Informed Consent Information Sheet: Guidance for IRBs, Clinical Investigators, and Sponsors (PDF)
    • Guidance on Electronic Informed Consent
  • Guidance and Sample Language for Consent and Assent Documents
‹ Exempt Categories Table up Guidance and Sample Language for Consent and Assent Documents ›

Contact Us

Human Research Protection Program, Institutional Review Board
B308 Kerr Administration
Corvallis, OR 97331-2140
irb@oregonstate.edu
Phone: (541) 737-8008

Human Research Protection Program and Institutional Review Board

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Contact Info

Research Office
A312 Kerr Administration
Corvallis, OR  97331-2140
Phone 541-737-3467
Fax 541-737-9041

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