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FDA Regulation: Cosmetic or Drug Product?

Thursday, August 04, 2016
Time: 2:00 pm EDT - 3:00 pm EDT
Cost: $250.00

Webinar: 1 CCS Credit

Over the years, the regulatory lines between cosmetics and drugs have been blurred as companies have created innovative products with inventive claims and product ingredients. This webinar will discuss the various regulatory classifications and explore circumstances in which a product can be considered a drug, medical device, dietary supplement or consumer product. It will also analyze how a personal care product comes to market and identify FDA requirements while exploring applicable regulatory hurdles.

Key Topics

Our Speaker

Shelly Garg is an attorney with Sandler, Travis & Rosenberg’s Food and Drug Law Practice Group. She represents clients across a broad range of FDA-regulated product categories, including food, beverages and dietary supplements, over-the-counter drugs, medical devices and cosmetics. She advises in strategic business planning, product development, testing and approval, labeling, advertisement and promotion, liability risk, inspections, responding to regulatory enforcement matters and related issues. Her keen insights into FDA and its inner workings have proved to be of significant value to her clients in successfully resolving matters before the agency.

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