irb.ufl.eduInstitutional Review Board » University of Florida

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Student Researcher Resources Other Resources Helpful Links CTSI and the IRB Other Committees that Review Research What research is available at UF, Shands, or the VA? Other Offices HIPAA Home HIPAA Identifiers HIPAA Contacts HIPAA Links UF QA Program Services Regulatory Resources Report Noncompliance IRB-02 IRB-02 Home: Campus IRB Contact Us IRB-02 Roster Deadlines for Full Board Review IRB-02 Policies and Procedures Required Training for IRB-02 Report Noncompliance University of Florida Federalwide Assurance Investigator Information & Guidelines Investigator Guidelines 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 Protocol Template Guidelines Debriefing Form Unaffiliated Investigator Form IRB02 Clinical Trials Assessment Form Confidentiality Agreement Cumulative Adverse Event Table for Continuing Review Cumulative Deviation Table for Continuing Review Deviation/Non-Compliance Reporting Form WIRB WCG (WIRB) WIRB Official Site WIRB: Who to Contact WIRB Forms What studies are eligible for WIRB® submission? Report Noncompliance Informed Consent Template Submit a New Study to WIRB Revising Your Study sIRB Contact Us UF sIRB Request IRB Staff University of Florida Federalwide Assurance Required Training for UF IRBs Definition of a Human Subject Research HIPAA Home UF QA Program Report Noncompliance 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 Investigator Guidelines IRB Policies and Guidance IRB Home New: If you intend to submit a non-human or exempt study, you might be eligible for an instant auto-determination without submitting a study to the IRB. To get an instant determination, please use the non-human/exempt auto-determination tool . If the study is eligible for non-human exempt auto-determination, you will have an instant approval to begin the project. If the study is not eligible for the auto-determination (which is evident almost immediately after answering a few short yes/no questions), you’ll need to submit it through myIRB. 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 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 or have a certificate of exemption 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....