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