Health Sciences Institutional Review Boards
Resources
Information for Sponsors
- UW-Madison Human Research Protection Program Policies
- Health Sciences IRB Compliance and Composition Statement
- Minimal Risk IRB Compliance and Composition Statement
- IRB Fee Policy
- Federal Wide Assurance
UW-Madison Resources
- Certificates of Confidentiality
- Clinical Investigator Preparatory Program (CIPP)
- General Clinical Research Center (GCRC)
- HIPAA Privacy Rule Research Guidance
- Office of Research Policy
- Office of Clinical Trials (OCT)
- Research and Sponsored Programs (RSP)
- UW Hospital & Clinics (UWHC)
- UWHC Safety Committee Policy & Procedure
- UW-Madison Safety Department
- William S. Middleton Memorial VA Medical Center
Federal/National
- Glossary of Terms:
- Certificates of Confidentiality Kiosk (NIH)
- Council for International Organizations of Medical Sciences (CIOMS)
- Department of Health & Human Services (DHHS)
- Food & Drug
Administration (FDA)
- FDA Code of Federal Regulations
- FDA Device Advice Overview
- FDA Device Advice - Early/Expanded Access, Compassionate/Emergency Use
- FDA Information Sheets: Guidance for IRBs and Clinical Investigators
- FDA Good Clinical Practice Guidance
- Center for Biologics Evaluation and Research
- Center for Devices and Radiological Health
- Center for Drug Evaluation and Research
- National Cancer Institute (NCI)
- National Institutes of Health (NIH)
- Office for
Human Research Protections (OHRP)
- 45 CFR 46 (Common Rule)
- International Human Subject Research Protections