Institutional Review Board -01 Gainesville Health Science Center
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Welcome to the University of Florida Gainesville Health Science Center Institutional Review Board (IRB-01) web site. This site is intended for use by University of Florida, Shands, and NF/SG VHS faculty, staff and students who conduct or participate as investigators in research with human subjects. Federal regulations require that all research involving human subjects must be approved by an IRB prior to the conduct of the research.
CONTACT US at:

Phone: (352) 273-9600
e-mail: ufirb-l@lists.ufl.edu

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REQUIRED READING University of Florida requires everyone who participates in human subject research to read these documents.

News & Announcements Read the latest information and news about research at UF.

Forms ALWAYS download our newest forms for project submissions.

Form Instructions Some forms have instructions on how to complete them. Prior to submitting any paperwork please review these instructions in order to insure you are completing our forms properly.

Submitting Paperwork Effective July 1st, 2002 the IRB-01 Administrative Office has new rules for processing submissions that are incomplete or inaccurate.

Deadlines Submissions requiring Full Board review must be submitted before certain dates in order to be considered at specific Full Board meetings.

Full Board Meetings Where and when the IRB-01 Full Board meets, how protocols are reviewed, attending the meeting, and what happens after the meeting.

Education & Training IRB-01 offers a variety of training and education resources such as newsletters, one-on-one educational sessions, and group workshop.

Office Info How to call, fax, mail, and e-mail our office.

Links to other web resources Links to research related web sites, including UF's other IRBs.

WIRB Submissions UF requirements when submitting paperwork to WIRB. Download UF coverletters to HURRC, Pharmacy, and WIRB.

IRB Position Papers These papers provide information about current IRB positions on
pertinent topics such as advertising, finders fees, phone consents, etc.

IRB-01 Policies & Procedures

Our official polices and procedures manual describes the function of and requirements for IRB-01 review of human subject research.


HURRC, IBC, and VA Reviews of Research Some research protocols must be approved by HURRC, IBC, and/or VA committees before the research may be started. Learn more about submitting your research to these three committees.
 

 

 

 

 

 

 
     
 
 
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Updated: 05/16/2012 11:12 AM


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