The following Frequently Asked Questions (FAQs) are provided to address commonly asked questions from researchers about IRB.
Do I Need To Submit to the IRB?
The IRB has jurisdiction over research involving human subjects (participants), more information here.
Visit this page
for assistance in determining whether you need to submit an application to the IRB and if you are doing research involving human subjects.
How do I submit an application to the IRB for review and approval?
IRB applications are submitted online via IRBNet, information can be found here.
Tutorials and screenshots to help you navigate the IRBNet system can be found here.
Information on the type of documents you need to submit for IRB review can be found here.
Where do I find the Application Review Categories?
The review categories can be found on Reference 1, located in IRBNet's Forms and Templates section.
Category A (exempt review) and Category B (expedited review) apply to certain minimal risk studies defined by the federal regulations.
Category C applies to greater than minimal risk research as defined by the federal regulations. Category C studies require that the Full IRB committee meet, discuss and review the application. These are also referred to as Full Board Reviews.
Who should be listed as the Principal Investigator?
The Principal Investigator (PI) must be a full time FAU faculty/employee or otherwise eligible. See PI Eligibility Policy
for more details.
If I am performing a study that may be exempt, do I have to submit it to the IRB?
Yes, the PI does not have the authority to deem his/her proposal as exempt even if it meets all the criteria. All official approvals come from the IRB.
What are the deadlines for submitting an IRB application?
The review process for Category A or B submissions is ongoing. These can be submitted at any time. Category C submissions must undergo Full Board review. IRB meetings are scheduled monthly and you must submit Category C applications by the published deadline. The IRB meeting schedule is posted here.
Who is supposed to electronically sign my IRB submission?
For new protocols: the PI, Department Chair, and in some Colleges, the Dean's representative for research, must sign.If PI is also the Department Chair, then his/her Supervising Authority or the Dean's designee must sign off on the application before it is submitted to the IRB.
For continuing reviews: the PI and Department Chair must sign.
For responses to the IRB and amendments, only the PI must sign.
For adverse event and protocol violation reports, the PI and Department Chair must sign.
The assurance section at the bottom of each form tells you which signatures you need before submitting to the IRB. Please obtain ALL electronic signatures before submitting the IRB application.
How long is the review and approval process?
Please allow 4-6 weeks for the IRB to review and approve your application. You cannot start data collection involving human subjects until after the IRB approves your application.
Now that I have submitted my IRB application, can I start my research?
No. You cannot start data collection involving human subjects until AFTER the IRB approves your submission.
Once the IRB has reviewed my study, how do I respond to their concerns?
IRBNet will generate an e-mail alert if modifications are required. Upon receiving the alert, you should do the following:
Log into IRBNet.
Click My Projects. Click on your project title.
Click Review Details.
Scroll down to Board Documents. You will see a Modifications Required memo.
Review the memo for the specific IRB concerns and instructions on how to submit your response.
Upload Form 5 along with any revised documents that the IRB has requested.
Once the IRB has approved my study what should I do?
IRBNet will generate an e-mail alert where you will receive notification of study approval. You must log into IRBNet to retrieve your approval letter and stamped consent forms. It is important to read that approval letter to understand any requirements or limitations of your approval. Print the IRB stamped consent form and any recruitment material. It is an IRB requirement to use the stamped documents to ensure the material is IRB approved.
Log into IRBNet.
Click My Projects. Click on your project title.
Scroll down to Board Documentsî.
Print Stamped Documents such as Consent Form and Recruitment Material.
Who do I contact with general questions in regards to my human subjects proposal submission?
Contact information for our office can be found in the staff directory.
I am requesting funding. Do I need to have IRB approval before I submit my proposal?
No. You can submit your proposal to the funding agency and list your IRB approval status as pending. With most federal agencies (NIH, NSF, Dept. of Education) you can submit the approval information "just in time" once you receive a fundable score, or when the agency requests the IRB approval information. However, don't wait too long to submit your IRB application because it can delay the funding agency's decision should you be selected to receive a grant. You should also consult the specific granting agency for its guidelines on the use of human subjects.
I haven't received IRB approval but my grant is ready to be funded, what should I do?
FAU and most funding agencies will not release funding until IRB approval has been verified. Contact the Research Integrity office as soon as possible for assistance. We cannot issue an IRB approval immediately, but will work with your granting agency as needed to facilitate the award process.
What is FAU's Federal-Wide Assurance (FWA) Number?
FAU's FWA # is FWA00000157.
What should I include in my IRB application if the study is funded?
If your protocol is, or will be funded by an outside organization, please note this on the IRB application. You will also need to submit the section of the grant or contract that describes your proposed scope of work with human subjects. Please ensure that the research described in your funding proposal matches the work described in the IRB application, and that the titles match. The IRB must ensure that the research it approves is consistent with what the sponsor is supporting.
When writing the consent form, can I just copy and paste my grant procedures into the consent form?
No. The consent form is meant to inform participants about what is being asked of them in the simplest terms possible. Please do not copy and paste lengthy methodology from a protocol or grant application into the consent form. Ideally, the reading level of a consent form should be at a 6th - 8th grade reading level. Avoid scientific / technical terms and define or spell out all abbreviations and acronyms. Tip: always ask yourself what would you say if you were explaining your research study to a family member.
How can I determine the reading level of my consent form?
In Microsoft Word, there is a tool under Spelling and Grammar that provides a Flesch-Kincaid reading level score. Aim for a score of 8 or less.
Do I always have to obtain a signed consent form for my research study?
No, not all studies required a signed written consent form. Choose the most appropriate consent process for your study. Click here
for more information. If you think your study does not require a signed consent, you must provide the IRB with a justification as to why this requirement should be waived. Refer to the Waiver of Informed Consent Policy here.
What is a child assent and why is it called assent?
Children cannot legally consent for themselves. Therefore, informing them about the study and asking them to agree to participate is called an assent process. Only parents or guardians can give consent for a child to participate in research, unless the IRB waives this requirement. However, even if a parent consents, if the child refuses to assent, the researcher generally should not enroll the child in his/her study.
Are there any tips for writing child assents?
In general, minors between ages 7 and 17 can give their written assent to participate in research. However, researchers sometimes write an assent document that contains long complex sentences and technical terms. An assent must be tailored to the emotional and educational level of the child. Short, simple sentences and friendly, conversational language is preferred. For very young children a verbal assent script that describes what will be said to the child may be more appropriate. It is also acceptable to not provide assent procedures if the child is extremely young or not capable of understanding (parental consent will still be needed).
I am recruiting subjects who do not speak English. Are there certain consent requirements?
Yes. If you plan to recruit subjects who do not speak English, you need to translate the written consent document to obtain true informed consent. However, since the IRB may request changes, please wait until after the IRB has approved the English version of the consent documents before seeking translation services. If you are using a verbal consent process, you still need to provide a translated version of the script that will be spoken to the participant.
CITI Online Training
Who needs to take the CITI training?
All members of the research team must have CITI training certificates before a study can be approved. In short, anyone who will be involved in consenting, recruiting, or obtaining data from study participants must complete CITI Human Subjects Research training, unless it is already on file in the IRB office. Obtain training by going here.
I have already completed the CITI IRB Training Course. How long is my IRB Training valid?
At FAU, CITI IRB training is valid for 3 years. After 3 years, you must complete a refresher course if you are still engaged in human subjects research at FAU.
How long does the CITI IRB Training take to complete?
How quickly you complete CITI Training varies, but it will likely take you between 2 to 4 hours to complete all of the training modules. You do not have to complete the IRB training modules all at once. You may re-enter the site as often as necessary and complete the modules at your own pace.
What is the minimum grade that is required for passing the CITI IRB Training?
You will need to score at least an 80% in order to pass the training course.
I will be doing research with medical records. Are there any additional training requirements for me to take?
Yes, researchers accessing protected health information (PHI) will also be required to complete the CITI Health Information Privacy and Security (HIPS) Training.
I have already completed the CITI Responsible Conduct of Research (RCR) Training. Do I still need to complete the CITI IRB Training?
Yes. Completion of the RCR Training Course from the CITI website does not satisfy the FAU IRB Training requirement. All investigators conducting research involving human subjects must complete the CITI Human Subjects Research Course. Courses to choose from include: Biomedical Research Investigators, Social and Behavioral Research Investigators, and Data or Specimens Only Research.
Can I receive IRB approval before I complete the Online CITI IRB Training Course?
No, you will not receive IRB approval if you have not completed the required IRB training.
Is CITI Human Subjects Research Training required for persons not affiliated with FAU who are collaborating with FAU researchers?
Maybe. CITI Human Subjects Research Training is required for all non-FAU researchers who are collaborating with FAU researchers in conducting human subjects research, if FAU will provide oversight for their role in the study. If the collaborator will be seeking IRB approval from their own institution for their role in the study, then FAU has no oversight over the collaborator and they can use the training required by their home institution.
How do I transfer my CITI completion records from another institution?
To transfer your completed modules from another institution to FAU, log on to your previous CITI account and click on the Affiliate with another institution link. Choose Florida Atlantic University from the drop-down menu. When prompted, choose the Basic Human Research Course, either Biomedical Research or Social and Behavioral Research to match the coursework that you completed previously. Review the FAU module and complete any modules FAU requires that your former institution did not.
When will I have to take a CITI refresher course?
All CITI course offerings are on a three-year renewal cycle. This means that a refresher course will be due three years after you first complete a course. CITI will send you emails to remind you when a refresher course is due. It is important to adjust your email privacy settings so that you can receive these important emails.
When do I need a data use agreement?
A Data Use Agreement (DUA) is a contractual document used for the transfer of nonpublic data that is subject to restrictions on its use. For the guidance on Data Use Agreement please go here.
Do I need IRB approval for doing a classroom research project?
There is a distinction between research conducted by students and classroom research. Student research refers to human subjects research conducted by students in pursuit of an Honor's thesis, Master's thesis, dissertation, DIS, or other similar research. Student research projects should be submitted to the IRB and be actively monitored by the faculty advisor, who serves as Responsible Principal Investigator. Classroom research refers to students' involvement in course activities that are primarily intended to teach them how to conduct human subjects research, rather than contribute to generalizable knowledge. Results of these activities are generally not published or disseminated outside of an instructional setting. In most cases, classroom research does not need to be reviewed by the IRB. If at a later point, you decide to continue a class project as a research project, submit an IRB application for review and approval.
Are there any special issues I should consider with online research projects?
Yes. Please see our guidance on internet research here
and utilize our internet consent template (consent 7) located within IRBNet.
With regard to keeping participant's research data safe, I am confused by the terms confidential and anonymous. What is the difference?
Anonymity means that an individual subject cannot be identified. No personal identifiers (e.g., name, signature, SS#, address, etc.) will be collected or associated with the data being used for research. Confidentiality means subjects' identities are known but will be protected to some extent by the investigator. For example: If you audiotape or videotape research subjects, their data is NOT anonymous, but you can take certain measures to ensure the data and recordings are kept confidential.
What information does the IRB need on the recruitment procedures for my study?
In addition to describing your recruitment plan in your protocol, don't forget to attach any advertising materials (flyers, scripts for radio or television ads, e-mail, texts, etc.) that will be used. Also, any incentives (money, extra credit, gift cards, etc.) that will be used to attract and retain participants should be described in your protocol and noted in any consent form(s) or procedures.
May I use a lottery as an incentive to attract participants?
No. Due to Florida's strict laws, FAU researchers are not able to use lotteries for prizes or cash as incentives for research participants. Instead, consider incentives that can be given to every participant, such as a candy bar, a scratch-off lottery ticket, a Starbucks gift card, or some other nominal item.
The IRB application asks if we are working with cooperating institutions. What does that mean and how does that affect my IRB submission?
If you are collecting data from persons at an institution outside of FAU, or an outside institution is helping you with recruitment, you are working with cooperating institutions. The IRB requires a letter of cooperation from an appropriate person at that institution. The letter should be on institution letterhead and signed, however an email is sometimes acceptable if sufficient detail is provided. Please refer to Reference #2 in the IRBNet library of forms and templates for a sample letter of cooperation.
I received my IRB approval, so why does another agency also want to review this study?
Some agencies, such as county school districts, the Florida Department of Health, the Florida Department of Corrections, etc. may have their own separate research review processes. Please contact these agencies regarding their specific procedures. These agencies may require an additional review to ensure the study fits within their mission and is conducted according to their logistical or administrative processes. Links to Broward and Palm Beach County Schools research offices can be found here.
I am planning to collect data at one of the FAU K-12 schools. Do they have a separate review process?
Yes. More information here.
I am working with collaborators at other universities. Does my IRB approval cover my collaborators too?
It depends. If your research involves co-investigators at other sites who are enrolling subjects or collecting data, their institution may require them to undergo separate IRB approval. Please check to see if this is a requirement before submitting your IRB application. This will enable all investigators to cross-reference IRB approval and consent documents prior to beginning data collection. In some cases, FAU's IRB can serve as the IRB of record for non-FAU collaborators, but the collaborator will have to fulfill FAU's training requirement and there has to be an agreement between the two IRBs. Contact the IRB office for further information.