Bench2Market Talks
"FDA Regulatory Strategy: Regulatory Pathway Options and Timing"
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Join us for an online panel discussion on regulatory strategy to help innovators better understand some of the considerations for determining a product’s regulatory route to market. This introduction is for entrepreneurs new to medical device regulatory affairs and looking for an opportunity to learn more about regulatory requirements for bringing products to market. Our panelists, Grace Powers, Erika Tyburski, Sandra Maher, and Cathy Cambria, will cover topics including defining a medical device, reviewing basics about device classification, identifying different types of premarket submissions, and describing how to get a new product to market.
This event is the sixth session for the 2023-2024 Bench2Market Talks series, which was created to provide commercialization guidance to the university research community. For more details on the series, view the full schedule.
