WebThe IRB may require that informed consent for secondary analysis be obtained from subjects whose data will be accessed. Alternatively, the IRB can consider a request for a waiver of one or more elements of informed consent under 45 CFR 46.116(d). In order to approve such waiver, the IRB must first be satisfied that the research: Webirb.gatech.edu
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WebJan 20, 2024 · Using the SMART IRB agreement is the preferred method of reliance for all studies where Georgia Tech will rely on an external IRB or serve as the reviewing IRB. … WebThese include the Central IRB, the Joint Georgia State University-Georgia Tech IRB for the Advanced Brain Imaging Center, and the Classified IRB. The IRBs have the responsibility and authority to review, approve, disapprove, or require changes in research activities involving human subjects. All proposed research activities involving human ... WebCOVID-19 Documents for In-Person Research. GT IRB Guidelines: Resuming Non-Essential In-Person Humans Subjects Research (Archived - no longer in effect); GT IRB COVID-19 Pre-Screen Questionnaire/Script (Recommended for use); GT IRB COVID-19 Information Sheet for Human Subject Participants (Recommended for use); Consent and Assent Templates northland village apartments 45240