irb.ufl.eduInstitutional Review Board » University of Florida

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Other Offices HIPAA Home HIPAA Identifiers HIPAA Contacts HIPAA Links UF QI Program Services Regulatory Resources Report Noncompliance IRB-02 IRB-02 Home: Campus IRB Contact Us Deadlines for Full Board Review IRB-02 Policies and Procedures Required Training for IRB-02 Report Noncompliance Web-Based Submission Tracking for Paper Studies University of Florida Federalwide Assurance Investigator Information & Guidelines Investigator Guidelines Converting Paper Studies to myIRB Types of Study Review by the IRB FERPA Information for use of Educational Records in Research Lotteries and “Random Awards” as Incentives for Research Participation Guidelines for Revising an Approved Study Definition of Terms Used in IRB02 Documents Student Roles & PI Qualifications for IRB-02 Use of Amazon Mechanical Turk (MTurk) for social/behavioral Research Projects Informed Consent Instructions & Procedures Special Population Requirements Standardized Text for IRB-02 ICF’s Informed Consent Document – Template Consent Document Checklist Common Problems with Informed Consents Consent/Assent Procedures and Instructions IRB-02 Forms Adverse Event Reporting Form Clinical Trials Assessment Form Confidentiality Agreement Continuing Review/Study Closure Form Cumulative Adverse Event Table for Continuing Review Cumulative Deviation Table for Continuing Review Debriefing Form: Sample Deviation/Non-Compliance Reporting Form Legacy Paper Study Submission Form Legacy Paper Study Revision Form myIRB Protocol Submission Form Unaffiliated Investigator Form IRB02 WIRB IRB-04 Home Western IRB (WIRB) WIRB Official Site WIRB: Who to Contact WIRB Forms What studies are eligible for WIRB® submission? Report Noncompliance Cost/Fee Schedule Informed Consent Template Submit a New Study to WIRB Revising Your Study Other Submissions sIRB Contact Us UF sIRB Request University of Florida Federalwide Assurance Required Training for UF IRBs Definition of a Human Subject Research HIPAA Home UF QI Program Report Noncompliance Web-Based Submission Tracking for Paper Studies Web Tracking help Research Data is Institutional Property Investigator Requirements for Retaining Research Data Releasing Data to Other Parties Data/Record Storage and Security Destruction of Data Retention of Signed Informed Consent Forms IRB Policies, Guidelines and Guidances IRB Home The University of Florida Institutional Review Boards (IRBs) are charged with protecting the rights and welfare of participants in clinical trials and other human subjects research studies. UF IRBs review all research involving human subjects to ensure the welfare and rights of research participants are protected as mandated by federal and state laws, local policies, and ethical principles. Faculty, staff, and students at the University of Florida, UF Health, and/or the North Florida/South Georgia Veteran’s Health System (NF/SGVHS) must receive approval for any human subjects research from a UF IRB before conducting the research. This includes research conducted off-site by University faculty and staff when acting as University employees or in connection with their University affiliation.This web site is aimed at any University of Florida faculty members, students, and/or staff members who conduct research with human subjects or assists in such studies. UF IRBs only review research from researchers who have a formal affiliation with UF, UF Health, or the NF/SGVHS. Please submit your research to the relevant IRB Office below: IRB 01 — Gainesville HSC IRB 01 Gainesville HSC Peter Iafrate, Pharm.D, Chair Office Voice: (352) 273-9600 Fax: (352) 273-9614 Email: IRB Email Web: /irb01.html Types of Research Reviewed This IRB accepts and reviews all protocols submitted including the broad category of ‘Medical’ research, regardless of funding. Accepts Research From UF Gainesville Health Science Center faculty, staff, or students regardless of where in the US the research is being conducted. UF Jacksonville Health Science Center faculty, staff or students using Gainesville HSC employees, facilities, resources, or patients. UF Campus faculty, staff, or students (primarily if the research involves HIPAA or the HSC facilities). UF Health staff. North Florida/South Georgia Veteran’s Health System ...