HRPP guidance documents
Find resources for researchers and others interacting with Geisinger’s Institutional Review Board.
Browse by topic
Involved in research with human participants? Explore our guidance documents for conducting research and working with Geisinger’s Institutional Review Board (IRB).
- General
- Emergency Use of a Test Article
- Requirements for Study Physician Involvement - Investigational Drug (IND) & Device (IDE) Studies
- Special Considerations for the Oversight of Research Protocols in FDA regulated Drug or Device Studies
- Search for FDA Guidance Documents
- Drugs
- Expanded Access Program (EAP) for Drugs
- Sponsor-Investigator Research Requirements (When a Investigator holds the IND)
- Devices
- Humanitarian Use Device (HUD)
- IDE Early/Expanded Access for Devices
- IRB Review of Medical Device Research
- Significant and Non-Significant Risk Medical Device Studies
- Sponsor-Investigator Research Requirements (When a Geisinger Investigator Holds the IDE)
- Sponsor-Investigator Research Requirements (When a Geisinger Investigator is the Sponsor on a non-significant risk device study)