Home » Office for Research Protections » Institutional Review Board » HRPP Toolkit Resources for Common IRB Submissions
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- Human Research Protection Program (HRPP) Home Page
- About the IRB
- CATS IRB
- Clinical Trials
- COVID-19: Human Subjects
- Expanded Access Submissions
- Find Your IRB Analyst
- HRPP Advisory Committees
- HRPP Quarterly Webinars
- HRPP Toolkit
- Information for Participants
- IRB Basic Steps
- IRB Learning Path
- IRB Resources, Training, and Events
- IRB Policies and Guidelines
- Single IRBs and IRB Authorization Agreements
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- Conflict of Interest
- Controlled Substances
- Drone Operations
- Dual Use Research of Concern (IRE)
- Education
- Export Control
- Human Stem Cells (ESCRO)
- Human Subjects Research (IRB)
- Institutional Biosafety Committee (IBC)
- Radioisotopes (UIC)
- Research Data Management Policy
- Research Integrity
- Research Security
- Responsible and Ethical Conduct of Research (RECR)
- Scientific Diving
- Vertebrate Animal Care and Use (IACUC)
- Quality Assurance
- ORP Team
- ORP Events
- ORP Announcements
HRPP Toolkit Resources for Common IRB Submissions
Below you will find the templates and materials needed for common IRB submissions. All reference materials in the IRB Library can be found on the HRPP Toolkit webpage.
New Studies
Protocol Template
Consent
Study Team Member Qualification Template (if needed)
Reference Materials
New Studies Using Drugs or Devices
Protocol Template
Consent
Study Team Member Qualification Template (if needed)
Reference Materials
Studies Requiring Reliance
Request to Rely on an External IRB (R2R)
Protocol Template
Consent
Reference Materials
Requests for Penn State to Serve as sIRB (R2S)
Protocol Template
Consent
Reference Materials
Not Human Subjects Research
Protocol Template
Reference Materials