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Who should I contact with specific IRB procedural questions?
Direct your questions to IRB Chair: Dr. Rhonda Waskiewicz,
Assistant Dean for Academic Affairs and Assessment, Nesbitt College of Pharmacy and Nursing
How long does the review process take?
There are three types of reviews. These three types are: Exempt, Expedited, or Full-Board --depending on risk to subjects, composition of subject population, and other factors. The review and approval process can take between 2 - 6 weeks. Thorough preparation and planning on your part will ensure an efficient application process.
Can I begin my study without IRB approval?
The short answer is NO! Understand, under no uncertain terms, is an investigator or members of the investigative team allowed to commence with human subject research, including recruitment or initial advertisement or distribution of informed consents, without the express permission and authorization granted by the IRB and another required approval depending on department.
Can I submit a proposal for funding or to an outside sponsor without IRB approval?
Yes, provided the sponsor allows it. The IRB office has an Intent to Apply process for all proposals prior to the submission of the application. Complete this online form and download the documents you will need when you do apply to the IRB. This process does not relieve the investigator from the responsibility to secure IRB approval prior to commencing any human subject research, including recruiting of subjects or initial advertisement.
How can I take Human Subject Protection Training?
National Institutes of Health online research ethics course (NIH) is a free ethics training program for researchers conducting research with human subjects. It requires self-registration and the completion of training modules and a quiz. A printable certificate is issued at the end and remains on file in the training site and is required by the IRB.