Human Research Protection Program
Jamie Ryan
IRB Administrator
Phone: 316-293-2610
Fax: 316-293-2628
Email: jryan3@kumc.edu
Human Research Protection Program-Wichita
KUSM-W > Research > Human Research Protection Program-Wichita > Links
Links
KUSM-W Resources
- Informed Consent Checklist
- Guidelines for Retrospective Chart Reviews
- Quick Reference Guide on HIPAA Research Requirements
- The Use of Limited Data Sets for Research
- PHI Checklist
- HIPAA Requirements for Research
- Definitions (45CFR46.110)
- Expedited Categories (45CFR46.110)
- Exempt Categories (45CFR46.101)
- Records Retention Policy
- Policy on Research with Coded or De-Identified Data
Federal Regulations and Guidelines
- The Department of Health and Human Services (DHHS) Office for Human Research Protections (OHRP) Code of Federal Regulations on Protection of Human Subjects (The Common Rule) 45 CFR 46
- The Food & Drug Administration (FDA) Code of Federal Regulations on Protection of Human Subjects 21 CFR 50
- The FDA Code of Federal Regulations on Institutional Review Boards 21 CFR 56
- The FDA Code of Federal Regulations on Investigational New Drugs 21 CFR 312
- The FDA Code of Federal Regulations on Investigational Device Exemptions 21 CFR 812
- The FDA Code of Federal Regulations on Financial Disclosure by Clinical Investigators 21 CFR 54
- FDA Instruction Sheets
- OHRP International Compilation of Human Subject Research Protections
- Federal Criteria for Research
Useful Links
- Federal Office for Human Research Protections (OHRP)
- The Belmont Report
- Guidance on Obtaining Certificates of Confidentiality
- Guidance on Obtaining an Investigational New Drug Applications (IND)
- Guidance on HIPAA and Research
- Association of the Accrediation of Human Research Protection Programs (AAHRPP)
Last modified:
Sep 14, 2018