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Research & Innovation » Research Integrity & Compliance » Human Research Protection Program

IRB - HRPP Policies and Procedures

IRB Policies

101 - Human Research Protection Program PDF
102 - Ethical and Regulatory Mandate to Protect Human Subjects PDF
103 - The Federalwide Assurance and IRB Registration Process PDF
104 - Florida State Laws and Regulations PDF
201 - Institutional Responsibilities for IRB Administration PDF
202 - Human Research Protection Program Supporting Programs PDF
203 - Institutional Review Board Membership PDF
204 - Expedited Review of Human Subjects Research PDF
205 - Institutional Review Board Member Conflicts of Interest PDF
206 - Noncompliance in Human Subjects Research PDF
207 - Relied Upon Institutional Review Boards PDF
208 - Reporting Concerns/Complaints PDF
209 - Scientific, Scholarly, and Departmental Review for Human Subjects Research PDF
211 - Individual Financial Conflicts of Interest PDF
212 - Reporting Adverse Events and Unanticipated Problems Involving Risk to Human Subjects or Others PDF
215 - Institutional Conflicts of Interest in USF System Human Subjects Research PDF
301 - Human Subjects Research PDF
303 - Exempt Review of Human Subjects Research PDF
304 - Transnational Human Subjects Research PDF
305 - Human Subjects Research Involving Prisoners PDF
306 - Human Subjects Research Involving Children PDF
307 - Parental Permission and Assent Requirements for Human Subjects Research Involving Children PDF
308 - Human Subjects Research Involving Deception PDF
309 - Human Subjects Research Involving Other Vulnerable Populations PDF
310 - Human Subjects Research Involving Pregnant Women, Fetuses, and Neonates PDF
311 - Case Reports and Limited Case Series PDF
312 - Not Human Subjects Research PDF
402 - Emergency Use of a Test Article on Human Subjects PDF
403 - Use of Devices in Human Subjects Research PDF
404 - Use of Drugs and Biologics in Human Subjects Research PDF
501 - Veterans Affairs Regulated Human Subjects Research PDF
601 - Informed Consent Process and Procedures PDF
701 - Investigator Responsibilities PDF NEW!
702 - Initial Review of Human Subjects Research PDF
703 - Continuing and Final Review of Human Subjects Research PDF NEW!
705 - Changes to Currently Approved Human Subjects Research PDF
707 - Research in Schools PDF
708 - Recruitment and Advertising in Human Subjects Research PDF
709 - Conducting Off-Site Human Subjects Research PDF
710 - Privacy and Confidentiality in Human Subjects Research PDF
711 - Requirements for Human Subjects Research Protection Education PDF
712 - Multi-site Research, Coordinating Centers, and Statistical Centers PDF
713 - Deviations in Human Subjects Research PDF
714 - Genome Wide Association Studies PDF
801 - Institutional Roles and Authority PDF
802 - IRB Use of Consultants PDF
803 - Data and Safety Monitoring PDF
805 - Federal Criteria for Institutional Review Board Approval PDF
806 - Additional Conditions for Approval PDF
814 - Administrative Hold, Suspension, Closure or Termination of IRB Approved Human Subjects Research PDF
902 - Establishing & Amending Human Research Protection Policies and Procedures PDF
906 - Records Retention and Accessibility PDF
912 - Documentation of Convened IRB Meetings PDF
1001 - Participants’ Rights and Responsibilities in Human Subjects Research PDF
1002 - Compensation for Human Subjects Research Injury PDF
1003 - Compensation to Human Research Subjects PDF
1004 - Appealing IRB Determinations PDF

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