Institutional Review Board -01 Gainesville Health Science Center
  News & AnnouncementsFormsDeadlinesWeb Tracking
University of Florida
 
 
IRB-01 Help!
  IRB-01 Home  
  announcements  
  Required Reading  
  Data Use/Storage  
  Full Board Deadlines  
  Drug Research  
  Education/Training  
  IRB-01 Forms  
  Form Instructions  
  Full Board Info  
  GCRC  
  IRB's HIPAA page  
  Newsletters  
  Links  
  Office Information  
  Other Committees  
  PI Responsibilities  
  IRB-01 P&P Manual  
  Position Papers  
  Psychology Info  
  Researcher Tools  
  Submit Paperwork  
  VA Research  
  IRB Web Functions  
  Web Tracking - NEW!  
  UF's WIRB page  
     
 
Search IRB-01:

 
     
     
     
image

Link to MyUFL

Can't see our news banner
or Help topics?
Get Adobe Flash Player



Form Links
Alphabetical listing Forms for NEW studies
Informed Consent Forms Forms for PREVIOUSLY REVIEWED Studies
Introductory Questionnaire Forms Standardized Text for IRB Forms
HIPAA forms Form FAQs


Form FAQs

How do I track changes in the IRB forms?

Step one: unprotect the form. Click here for directions on how to unprotect Microsoft Word documents.

Step two: turn on track changes. Click here for directions on how to use track changes in Microsoft Word.

What if the questions on a form are not appropriate for my submission?

Sometimes a question on a form may not be appropriate for your particular study, or the available answers don't seem to fit. In either case, please provide a cover letter that (1) indicates which question/answer is not appropriate and (2) provides adequate explanation or information to satisfy the general intent of the question. You may also submit additional pages or information to help clarify a question or to inform the Board about the status of your study. If you have any questions, please contact the IRB-01 office.

What if there isn't a form available for the item/information that you want to submit?

Some types of submissions (for example, reporting a protocol deviation) do not have a required form available. If you need to submit information to the Board and a form is not available, please provide a cover letter detailing the content of your submission. If you have any questions about submitting a coverletter or what form you should use, please contact the IRB-01 office.

When must PIs submit the Informed Consent in our current/newest format?

Effective 02/01/2003, PIs are now required to submit their Informed Consent forms in our current/newest format for (1) new protocols, (2) Continuing review if new subjects might be enrolled in the future (open to enrollment), (3) if the Board requests it, and (4) possibly if re-consent is necessary. For more info Click here!

 

 
     
 
 
Copyright 2007
Updated: 12/10/2007 1:47 PM

E-mail the webmaster
IRB-01 IRB RGP UFL UF Privacy UF Information Security HSC SPICE

UF

            COM Clinical Trials Compliance