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Florida Gulf Coast University

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Office of Research and Sponsored Programs

Compliance

 
 

Compliance Committees provide our researchers assistance in complying with the various federal, state and university regulations.  Research involving human subjects (IRB), animal subjects (IACUC), radioactive materials, biohazardous materials, and recombinant DNA (Research Safety Committee) have a multitude of laws and regulations with which they must comply.

The Office of Research and Sponsored Programs also provides assistance with inventions and Intellectual Property issues that arise from externally funded projects. 

The FGCU Misconduct in Research procedures apply to individuals (other than students involved in regular classroom assignments) engaged in any form of research and scholarship, funded or otherwise, in every discipline throughout FGCU.

For assistance with IRB, IACUC, and Research Safety Committee applications, please contact Sandy Terranova at 239-590-7522 or sterranova@fgcu.edu.


FGCU Institutional Review Board for the Protection of Human Subjects in Research and Related Activities (IRB)

The IRB is working to increase the number of resources that will assist FGCU researchers with the IRB process.   Please download and save a new copy of the application and forms each time to ensure you are using the current version.  The new postings and updates are documented in the following table.

 

New Postings        

Updated Documents    

May 2011: 
Amendment to IRB Protocol
On-line Survey Consent Template             
Oral Consent Template

May 2011: 
IRB Aplication
Informed Consent Form Template

June 2011: 
Consent Form Model
On-line Survey Consent Model
Oral Consent Model for In-Person or Telephone Interviews 

October 2011:
Informed Consent Form Model 

   

Navigating the IRB

Is IRB Approval Needed for my Research?   [pdf 77kb] (issued March 2011)
A decision tree with a secondary ‘help’, Determination if Research is Humans Subject Research form, to assist in determining if IRB approval is required before the research can be undertaken.


Determining IRB Review Category - Exempt, Expedited, or Full Board Review  [pdf 74kb] (issued March 2011)
A decision tree to assist in selecting the IRB review category.


IRB Review Process   [pdf 54kb] (issued March 2011)
A flow chart of the IRB application submittal to approval process.

 

 IRB Toolkit

IRB Application Form  [.doc 94kb] (updated May 2011)
The application, redesigned in early 2011, guides the investigator in his/her explanation of the study to collect the information the IRB needs to approve a protocol, thereby reducing the time from application submittal to approval.  The new application form incorporates the checklist from the previous application. 



Amendment to IRB Application [.doc 99kb] (issued May 2011)
Use this form to request an amendment to an exempt, expedited or full board review protocol awaiting approval or approved by the IRB.  Protocol amendments may not be instituted until written approval is received from the IRB. 

 

Consent Helps and Models

Is my consent form written at the 8th grade level?   [pdf 140kb] (issued April 2011)
To determine the readability of your consent document(s), activate the Microsoft WordTM readability function following the instructions in the above link.  The function calculates the U.S. grade school level the document is written for and rates one’s ease in understanding the document.

To improve the readibility of your  form Instead of …Try This Word  [pdf 63 kb] (issued April 2011) 
The document provides alternate word selections to increase the readability of your form.



Informed Consent Form Model [.doc - 48kb] (updated October 2011)
The consent model includes instructions, guidance, both suggested and required text, and refers the researcher to the pertinent sections in the application he/she should consult when writing the form.

 

Child Assent and Parental Consent Form Models  [.doc 76kb] (issued April 2011)
The assent and consent models include instructions, guidance, both suggested and required text, and refers the researcher to the pertinent sections in the application he/she should consult when writing the forms.  Guidance in selecting the correct assent form is found in Assent Instructions [pdf 84kb] (issued April 2011).

  

On-line Survey Consent Model [doc. 69kb] (updated June 2011)
The model includes instructions, guidance, both suggested and required text, and refers the researcher to the pertinent sections in the application he/she should consult when writing the form.

 

Oral Consent Model for In-Person or Telephone Interviews [doc. 42kb] (updated June 2011) 
The modelincludes instructions, guidance, both suggested and required text, and refers the researcher to the pertinent sections in the application he/she should consult when writing the oral consent form for telephone or “on the street” interviews.

 

 

Other IRB Guides 

Guidelines for Letters from Agencies Cooperating with the Research [pdf 75 kb] (issued March 2011)
The guidelines identify the critical components to be included when soliciting a letter of cooperation from a cooperating agency.

  

Please send any questions or comments about the new application and resources to Dr. Thomas Roberts, Associate Vice President, Research and Sponsored Programs at troberts@fgcu.edu  or Sandy Terranova, Compliance Coordinator, at sterranova@fgcu.edu.

  

To submit a protocol to the IRB, please review the following documents:

 

IRB Applcation

 IRB Application Form [.doc - 94kb]    Open the document and save it to your computer. 

 

Protocol Submission Deadlines

Protocols qualifying for an Exempt or Expedited Reviews require a minimum of two weeks after submission for approval.  Please submit all protocols requiring Full Board Review to the IRB in the Office of Research and Sponsored Programs at least one month prior to the meeting date.  Please contact Sandy Terranova for protocol assistance.

 

Human Subjects Research Training

The IRB requires completion of human subject training to accompany the protocol.  We recommend the following tutorial.  Please print the certificate at the end of the tutorial and send it to ORSP.

Additional training is available through CITI (Collaborative Institutional Training Initiative).

 

Related Human Subject Sites

 

IRB Meeting Schedule

Technical Reviews are held weekly.  Full Board Reviews are scheduled on a monthly basis as needed.  Faculty and student researchers are invited to attend the meetings.  Please notify Sandy Terranova of your intention to attend so she can ensure adequate seating.

The IRB meeting schedule for academlic year 2010-2011 follows.Meetings may be changed as necessary.  Please watch this website for meeting changes or contact Sandy Terranova for more information.

Friday, November 18, 2011 1:30 pm HE 109  CANCELLED
Friday, December 16, 2011 1:30 pm HE 109  CANCELLED
   
Friday, January 20, 2012 1:30 pm HE 109  CANCELLED
Friday, February 17, 2012 1:30 pm HE 109
Friday, March 16, 2012 1:30 pm HE 109
Friday, April 13, 2012 1:30 pm HE 109

 

 IRB Committee Members

 

Dr. Clifford Renk, Chair

College of Arts & Sciences

Dr. Denise Heinemann College of Health Professions
Mr. Stan Appelbaum Human Rights Advocacy Comm.
Dr. Arthur Rubens College of Business
Dr. Robert Triscari College of Education
Dr. Linda Martin College of Health Professions
Dr. Edward Ferguson Community Member
Dr. Terry Wimberley College of Arts & Sciences
Dr. Thomas J. Roberts, Non-Voting Research & Sponsored Programs

On-Call

Dr. Bret Shannon Orthopedic Surgery, Nemours Children's Clinic
Dr. Margie Morales Pediatric Neurology, Nemours Children's Clinic

Alternates

Dr. Lakshmi Gogate College of Arts & Sciences 
Dr. Katrina Nedley Community Member 
Dr. Rosalyn Gross College of Health Professions 

 


 

FGCU Institutional Animal Care and Use Committee (IACUC)

IACUC meetings are held at a minunum, once a semester in HE 109; the meeting date/time will be published here as soon as possible.

 

Meetings

Protocol Submission Deadlines

to be scheduled  

 

Applications are accepted at any time for an Expedited Approval. If an Expedited Approval is not needed, the IACUC requires applications to be submitted at least two weeks prior to the scheduled meeting.
   

 

Committee Members

Dr. Darren Rumbold, Chair

College of Arts & Sciences 239-590-7527
drumbold@fgcu.edu 
Dr. Dean Croshaw College of Arts & Sciences 239-590-7428
dcroshaw@fgcu.edu 
Walter Fohs Non-Scientist 239-267-3525
wfohs@comcast.net
Dr. Anna Goebel College of Arts & Sciences 239-590-7431
agoebel@fgcu.edu 
Dr. Charles Mesloh College of Professional Studies 239-590-7821
cmesloh@fgcu.edu 
Dr. Dave Nichols Veterinarian 239-481-4746
dbnvet@gmail.com
Dr. Aswani Volety College of Arts & Sciences 239-590-7216
avolety@fgcu.edu 
Dr. Thomas J. Roberts, Non-voting Research & Sponsored Programs 239-590-7021
troberts@fgcu.edu 

 

To submit an application to the IACUC, please review its policy and use the IACUC application form.

Florida Gulf Coast University's Policy on Animal Care and Use in Education & Research [.doc - 120kb]

Application Form [.doc - 82kb]. This form is designed to be completed electronically and then printed. Please use the TAB key to move from one field to the next. 

Related Animal Subject and Guideline Sites

Associations

Online IACUC Training Opportunities

 IACUC animal distress categories

IACUC test Appl

IACUC Animal Log

 


 

 

 FGCU Research Safety Committee
     The mission of the FGCU Research Safety Committee is to promote and facilitate a safe research environment by requiring that research projects meet all federal, state and local research safety regulations.  To ensure compliance, the FGCU Research Safety Committee will review, approve and monitor applicable research projects and serve as an advocate for investigators to meet required infrastructure and personnel training and expertise guidelines.

      The Research Safety Committee was established by President William Merwin in 2002 for the purpose of reviewing, approving and monitoring research projects.  FGCU received its first Radioactive Materials License in January, 2006, from the State of Florida Department of Health, Bureau of Radiation Control.  License Number 3774-1, Category 3L(III) will expire on January 31, 2011. 

 

 Meetings are held at least quarterly.  The next meeting is scheduled for Tuesday, September 20, 2011 at 2:30 HE 109. 

 

 

Committee Members

 
Name
 
College
 
Position/Expertise
 
Contact Information
Rhonda Holtzclaw Arts & Sciences Radiation Safety Officer 590-7224 rholtzcl@fgcu.edu
Takashi Ueda
Arts & Sciences Plants 590-7236 tueda@fgcu.edu
Lewis Johnson Environmental Health and Safety Environmental Health and Safety 590-1036 ljohnso@fgcu.edu

Scott Michael
(Chair)

Arts & Sciences Animals; rDNA technology 590-7439 smichael@fgcu.edu
Diane Bondehagen School of Engineering, Business Environmental Engineering 590-7590 dbondeha@fgcu.edu
Thomas J. Roberts, Ed.D. Associate Vice President for Research Institutional commitments and policies; applicable law; standards of professional conduct and practice (non-voting member) 590-7021 troberts@fgcu.edu

Biological Inventory List:  http://itech.fgcu.edu/hazmat/biological.asp

Chemical Inventory Form:  http://itech.fgcu.edu/hazmat/chemical.asp

 

 


 

Intellectual Property Policy & Invention Disclosure

Dr. Thomas J. Roberts For assistance with Intellectual Property and Commercialization issues,
please contact Dr. Thomas J. Roberts at 239-590-7021.

 

 

 

Send your Questions or Comments to: troberts@fgcu.edu

 

 

 

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