Office of Research: Human Subjects


		Home > Human Subjects


	Research Home

		Human Subjects

	Human Subjects Application Information Consent Process IRB Committee and Staff Info Training Materials Meeting Dates & Deadlines FAQ's News and Events Samples and Forms Policies and Procedures Decision Trees Becoming a Research Volunteer Florida Law & Human Subjects References HIPAA in Research Research @ FSU Cornerstone Council on Research & Creativity (CRC) Federal Relations For Faculty and Staff FSU Research Foundation Human Subjects Committee IP Development & Commercialization Research Compliance Sponsored Research Services Sponsored Research Accounting Services General Information About the VP Contact Information Staff Directory		Download the entire Institutional Review Board Policies and Procedures IRB AUTHORITY AND COMMITMENT Institutional Oversight of Ethical Principles Regarding Research Involving Humans as Subjects Institutional Review Board Jurisdiction/Applicability Policy and Procedures Development IRB REVIEW PROCEDURES Exempt Research Activities Expedited Review Full Committee Review Procedures for reviewing expedited, exempt, and full committee applications Initial Application Materials to be Reviewed at Full Committee IRB Quorum Requirement for Full Committee Review Final Action by the IRB Committee Amendments to Previously Approved Applications Cooperative Project/Multi-site projects – IRB Review IRB Continuing Review (Renewals) IRB Audits and Monitoring Reporting of Unanticipated Problems Involving Risk or Adverse Events Suspension or Termination of IRB Approval for Cause Use of Consultants by Institutional Review Board Non-member Investigator and Other Non-member Attendance at IRB Meetings Procedure for Human Subject Database Information GENERAL IRB POLICIES Prompt Reporting of Serious or Continuing Noncompliance Investigator Qualifications General Responsibilities of Investigator Investigator Checklist Research Involving Pregnant Women, Human Fetuses and Neonates Special Categories of Research: Children in Research Special Categories of Research: Prisoners as Research Subjects HIV Testing Certificate of Confidentiality Recruitment of Subjects Payment to Subjects Compensation or Medical Treatment If Injury Occurs IRB Office Educational Activities – Investigator Training INFORMED CONSENT PROCESS General Requirements for Informed Consent Basic Elements of Consent Documentation of Informed Consent Waiver of Informed Consent Approval and expiration dates informed consent document and stamping Assent of Subjects IRB MEMBERSHIP Membership of IRB Committee Compensation of the IRB Members Local Research Context RECORDS AND DOCUMENTATION IRB Office Records IRB Committee Meeting Agenda – Contents Documentation of IRB Committee Meeting Minutes