Human Subjects Research Forms
- Human Research Protections Program
- What to Consider Before Completing an IRB Application
- Training Requirements
- Forms
- Exempt Categories
- Procedures and Policies
- Regulations and Guidance
- Collaborative Research
- NIH Funded Research
- UCSC European Union General Data Protection Regulation (GDPR) Statement of Privacy
- FAQ
- Informed Consent
- HIPAA Research Authorization Forms
- Alternative HSR Training Forms
- Exception to Policy to Act as a Principal Investigator
- Reporting
Informed Consent
Informed Consent Templates (Word documents)
- Adolescent Assent (Age 13-17 Years)
- Adult Consent
- Audio-recording Consent
- Child Assent (Age 6 and Under)
- Child Assent (Age 7-12 Years)
- Experimental Subject's Bill of Rights - To be distributed to subjects when research involves medical procedures (e.g., blood draws, MRIs, etc.)
- GDPR Consent Addendum
- Parental Permission
- Video-recording Consent
Exempt Agreement to Participate Templates (Word documents)
- Exempt Agreement
- Exempt Agreement - Focus Groups
- Exempt Agreement - Interviews
- Exempt Agreement - Surveys
Informed Consent Tools
Alternative HSR Training Forms (Word documents)
HIPAA Research Authorization Forms (PDFs)
Exception to Policy to Act as a Principal Investigator
Reporting
Unanticipated Problems and Adverse Events