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Consent Form Templates

Listed below are several templates to assist you in composing your informed consent document. Instructions specific to items on the templates appear in red text in brackets. Please remove all instructions and non-applicable sections before submitting the informed consent document to the IRB for review and approval.

The informed consent document must be written in lay language (6th - 8th grade reading level), avoiding scientific / technical terms. All abbreviations and acronyms should be defined. A thesaurus from the CDC is available below, which maps medical terms to plain language options.

If you have any questions regarding the use of templates, please call the eIRB help desk at (813) 974-2880.

Consent Guidance Documents

Biomedical Consent Forms

 Title Version  Last Modified   
Word Addendum for Genetic Research
0.01
9/10/2010 8:44 AM
 
Word Adult Informed Consent
0.03
11/4/2010 1:27 PM
 
Word Adult Informed Consent for Minimal Risk Studies
0.01
9/10/2010 8:43 AM
 
Word Assent Form
0.01
9/10/2010 8:44 AM
 
Word Parental Permission Informed Consent
0.03
9/14/2011 3:36 PM
 
Word Parental Permission Informed Consent for Minimal Risk Studies
0.03
9/14/2011 3:37 PM
 
Word Proxy/LAR Informed Consent
0.02
10/26/2012 9:55 AM
 
Word Short Form Informed Consent
0.01
9/10/2010 8:45 AM
 
Social-Behavioral Consent Forms

 Title Version  Last Modified   
Word Adult Informed Consent
0.02
9/10/2010 8:58 AM
 
Word Adult Informed Consent for Minimal Risk
0.06
9/21/2010 3:29 PM
 
Word Assent Form
0.01
9/10/2010 8:47 AM
 
Word Parental Permission Informed Consent
0.02
9/10/2010 8:59 AM
 
Word Parental Permission Informed Consent for Minimal Risk
0.02
9/10/2010 9:00 AM
 
Word Proxy/LAR Informed Consent
0.02
10/26/2012 9:55 AM
 
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