Regulation and Device Development: Tips for Optimizing Your Experience With the Food and Drug Administration.
PMID: 28673647 · 2017
Abstract
Physician-inventors are in a unique position to identify unserved patient needs, and innovate solutions to clinical problems. These solutions may also have associated commercial opportunities. The logistics of developing these medical products, however, can seem a daunting task. One of the primary barriers in the United States is the regulatory process of the Food and Drug Administration (FDA). In this article, we will explore the risk-based approach used by the FDA which forms a framework to co
Official Source
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