University of Southern California
Protection of Research Subjects

Contents

  • Submissions to the IRB
    • University Park IRB Submissions
    • Health Sciences IRB Submissions
  • Informed Consent/Related Forms
    • University Park IRB Forms and Templates
    • Health Sciences IRB Forms and Templates
  • Guidance for PI/Coordinators
    • IRB Application Guidance
    • Not Human Subjects Research (NHSR)Guidance
    • Exempt Study Guidance
    • Expedited Study Guidance
    • Continuing Review Guidance
    • Full Board Review Guidance
    • Other Guidance
  • Special Types of Research
    • Biomedical/Clinical Research
    • GWAS/Stem Cell Research
    • IRB Reviewer Guidelines
    • International Research
    • Collaborative Review Research
    • Internet Research
    • USC Research Subject Pools
  • Info for Students/Med Students
    • The ABC’s of the IRB Process for Student/Medical Student Investigators
    • IRB Training Videos
    • IRB Student Mentor
    • Model IRB Applications
    • Human Subjects Research Brochures
    • Responsible Conduct of Research (RCR)
    • Expedited vs Exempt Studies… perspective of an IRB reviewer
    • Trojan Health Volunteers
  • Education & Training Resources
    • Education Programs
    • Handouts/Guides/Powerpoints
    • Human Subjects Research Brochures
    • Human Subjects Newsletter
    • IRB Community Member Resources
    • IRB Training Videos
    • iStar Training/Resources
    • OPRS Human Subjects Presentations
  • Research at USC
    • USC Research Committees
    • FWAs (Federalwide Assurances) and IRB Registration Numbers
    • Dept of Research Website
    • Research Compliance at USC (USC Office of Compliance)
    • Health Research Association (HRA)
  • Federal Agencies
    • Food & Drug Administration (FDA)
    • Office for Human Research Protections (OHRP)
    • National Science Foundation (NSF)
    • NIH (National Institutes of Health)
    • US Department of Education
    • US Department of Energy
    • US Department of Health and Human Services (DHHS)
    • Other Federal Agencies and Guidance
  • California Research Laws
    • California Health and Safety Code
    • California Penal Code
    • Other California Codes/Resources
  • Ethical Principles
    • Nuremberg Code
    • Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research
    • Belmont Report Historical Archive
    • Declaration of Helsinki (2000)
    • Council for International Organizations of Medical Sciences (CIOMS) Guidelines

Quick Links

  • iStar (IRB Application System)
  • CITI (Human Subjects Training)
  • GCP (Good Clinical Practice)
  • HIPAA (Privacy Rule)
  • HSPP Policies & Procedures
  • RCR Training
  • FDA | OHRP













Childrens Hospital Los Angeles (CHLA) Forms


Permission, Assent and Informed Consent Forms

  • Permission Form
  • Permission Form - Spanish
  • Assent Form for Children 7 to 13 years
  • Assent Form for Children 7 to 13 years - Spanish
  • Addendum Consent for Subjects Turning 18
  • Addendum Consent for Subjects Turning 18 - Spanish
  • Consent / Permission / Assent Form
  • Consent / Permission / Assent Form - Spanish
  • Consent Form for Adults
  • Consent Form for Adults - Spanish

Experimental Subject Bill of Rights

  • Bill of Rights
  • Bill of Rights - Spanish
  • Bill of Rights - Armenian
  • Bill of Rights - Farsi
  • Bill of Rights - French
  • Bill of Rights - Korean
  • Bill of Rights - Russian
  • Bill of Rights - Tagalog
  • Bill of Rights - Thai
  • Bill of Rights - Traditional Chinese
  • Bill of Rights - Vietnamese

Other Forms

  • Agreement for Use of Coded Data and/or Specimens
  • Connectivity Access Review Card (CARD) Form
  • CARD Instructions
  • Research Monitoring Plan
  • Research Monitoring Plan FAQs
  • Conflict of Interest Questionnaire