Office of Clinical Research (OCR)

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Key HOPs & Guidance Framing the UTHSCSA
Human Research Protection Program (HRPP)

Authority HOP 1.3.7 Vice President for Research HOP 1.6.6 Institutional Review Board Charter HOP 1.6.14 HRPP Steering Committee Administration HOP 7.2.1 HRPP Policy HOP 7.2.2 Institutional Review Board Policy
Supporting Committees &/or Programs
Safety HOP 1.7.1 Institutional Biosafety Committee HOP 1.7.15 Radiation Safety Committee HOP 1.7.16 Radioactive Drug Research Committee	Office of Sponsored Programs HOP 7.1.1 Policies and Procedures
Misconduct HOP 7.6.1 Policy Statement Relating to Misconduct or Research Misconduct	Senior Legal Office HOP 10.1.2 Code of Ethics and Standards of Conduct HOP 10.1.7 Conflict of Interest Statements for Non-Academic Staff
Conflict of Interest HOP 1.6.11 Conflict of Interest Committee HOP 10.1.6 Conflicts of Interest in Scholarly, Research, and Clinical Activity HOP 10.1.8 Conflict of Commitment HOP 10.1.12 Institutional Conflict of Interest Policy	Office of Clinical Research HOP 7.2.3 Research Scope of Practice for Study Personnel Sponsor Investigator Policy Policy: Storage and Control of Investigational Drugs and Devices for Clinical Research Clinical Trial Management Education and Training
Office of Regulatory Affairs & Compliance HOP 2.5.1 Office of Regulatory Affairs & Compliance
Institutional Review Board Policies & Procedures and Forms http://research.uthscsa.edu/irb/forms.shtml IRB Home Page http://research.uthscsa.edu/irb/index.shtml Investigator’s Handbook http://research.uthscsa.edu/irb/handbook.shtml