Abstract
Advisory committees play an important role in the interactions that occur between the pharmaceutical industry and the Food and Drug Administration (FDA). This article highlights the time points at which advisory committee meetings are typically held—end of Phase I and end of Phase II; prior to New Drug Application (NDA) submission; and following FDA review of an NDA—and the type of discussions held at each meeting. The role of advisory committees, and the presentations made by the sponsor and the FDA at advisory committee meetings, are explained. Each advisory committee member must satisfy him/herself that the proposed new drug is safe and effective before recommending that it be approved by FDA.
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The views expressed in this article are solely those of Richard L. Schilsky, MD and should not be construed as representing official policies of the Oncologic Drugs Advisory Committee, the Food and Drug Administration, or the United States Government.
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Schilsky, R.L. Preparing for FDA Advisory Committee Presentations: Perspective of an Advisory Committee Member. Ther Innov Regul Sci 34, 301–304 (2000). https://doi.org/10.1177/009286150003400138
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DOI: https://doi.org/10.1177/009286150003400138