Forms and Documents
Investigator Guidance
- HRP-910 INVESTIGATOR MANUAL
- HRP-800 INVESTIGATOR GUIDANCE - Investigator Obligations
- HRP-802 INVESTIGATOR GUIDANCE - Informed Consent
- HRP-803 INVESTIGATOR GUIDANCE - Documentation of Informed Consent
- HRP-810 INVESTIGATOR GUIDANCE - Additional DOD Obligations
- HRP-811 INVESTIGATOR GUIDANCE - Additional DOE Obligations
- HRP-812 INVESTIGATOR GUIDANCE - Additional DOJ Obligations
- HRP-813 INVESTIGATOR GUIDANCE - Additional ED Obligations
- HRP-814 INVESTIGATOR GUIDANCE - Additional EPA Obligations
- HRP-815 INVESTIGATOR GUIDANCE - Additional FDA Obligations
- HRP-816 INVESTIGATOR GUIDANCE - Additional ICH-GCP Obligations
- HRP-817 INVESTIGATOR GUIDANCE - Additional ISO 14155 Obligations
- HRP-818 INVESTIGATOR GUIDANCE - Additional HHS Obligations
- HRP-820 INVESTIGATOR GUIDANCE - Quality Improvement Activities in Health Care
- HRP-821 INVESTIGATOR GUIDANCE - Is it Human Subject Research?
- HRP-822 INVESTIGATOR GUIDANCE: IND Applicability Checklist
General Guidance, Tools & Definitions
- Definitions
- External IRB Reliance
- HRP-900 – BROCHURE: Should I take Part in Research
- Public Data Sets
- Data Use Agreement Toolkit
- Deception in Research
- FERPA and Research with Student Records
- Investigator Requirements for Retaining Research Data
- Is it Human Subject Research
- Research as class requirements
- Types of Consent