Ethical Biosafety Oversight of Gene Transfer Research

The number of drug products under development that incorporate recombinant or synthetic DNA or RNA, viral vectors, and/or genetically-modified organisms (“GMOs”) continues to grow rapidly, and several such products have received marketing approval from the FDA. This paper focuses on important points to consider when planning to initiate clinical trials with these products at sites inside or outside the USA, if the research is subject to rules and regulations of the FDA and/or the
National Institutes of Health (NIH) of the United States. In particular, we focus on the roles of Institutional Biosafety Committees (IBCs) and Institutional Review Boards (IRBs) in approving and facilitating study startup.

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Single-Patient Expanded Access: WIRB experience in 2018
Single-Patient Expanded Access: WIRB experience in 2018

In 2018 WIRB approved 100% of the single-patient EA requests that were submitted for review.

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