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

IRB - HRPP Policies and Procedures

IRB Policies


101 - Human Research Protection Program PDF NEW!
102 - Ethical and Regulatory Mandate to Protect Human Subjects PDF NEW!
103 - The Federalwide Assurance and IRB Registration Process PDF NEW!
104 - Florida State Laws and Regulations PDF NEW!
201 - Institutional Responsibilities for IRB Administration PDF NEW!
202 - Human Research Protection Program Supporting Programs PDF NEW!
203 - Institutional Review Board Membership PDF
204 - Expedited Review of Human Subjects Research PDF
205 - Institutional Review Board Member Conflicts of Interest PDF NEW!
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 NEW!
212 - Reporting Adverse Events and Unanticipated Problems Involving Risk to Human Subjects or Others PDF NEW!
215 - Institutional Conflicts of Interest in USF System Human Subjects Research PDF NEW!
301 - Human Subjects Research PDF NEW!
303 - Exempt Review of Human Subjects Research PDF NEW!
304 - Transnational Human Subjects Research PDF
305 - Human Subjects Research Involving Prisoners PDF NEW!
306 - Human Subjects Research Involving Children PDF
308 - Human Subjects Research Involving Deception PDF NEW!
309 - Human Subjects Research Involving Decisionally Impaired 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 NEW!
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 NEW!
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 NEW!
703 - Continuing and Final Review of Human Subjects Research PDF
705 - Changes to Currently Approved Human Subjects Research 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 NEW!
711 - Requirements for Human Subjects Research Protection Education PDF NEW!
712 - Multi-site Research, Coordinating Centers, and Statistical Centers PDF
713 - Deviations in Human Subjects Research PDF NEW!
714 - Genome Wide Association Studies PDF
715 - Review of Educational Human Subjects Research Outreach Activities PDF
801 - Institutional Roles and Authority PDF
802 - Ad Hoc and Continuing Consultants PDF
803 - Data and Safety Monitoring PDF NEW!
805 - Federal Criteria for Institutional Review Board Approval PDF NEW!
806 - Additional Conditions for Approval PDF
812 - Legally Authorized Representative in Human Subjects Research 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 NEW!
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


  » USF EthicsPoint Hotline

USF is dedicated to providing a safe, secure, and ethical workplace. This hotline provides an easy, anonymous way to discreetly and confidentially report activities that may involve improper conduct or violations of USF policies.

 

 

3702 Spectrum Blvd, Suite 165
Tampa, FL, 33612-9445

Phone: 813.974.5570
Fax: 813.974.4962

Direct comments to
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