Consumer Products & Mobile Apps: Reducing the Risk of FDA Regulatory Oversight of Ad Claims

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This webinar will discuss how consumer products and mobile apps can easily (and, often times, inadvertently) become FDA-regulated medical devices solely based on their advertising claims, and will offer some “tips and tricks” on how to word-smith claim language to help reduce the risk of FDA oversight. FDA regulatory experts, including attorneys from Loeb & Loeb LLP, will analyze example devices (including video games, sports equipment, clothing, mobile apps and cameras, among others) to evaluate risk of FDA regulation and how companies can adjust their advertising and marketing with a few key strategies to help reduce the risk of FDA scrutiny.