This is the third event in a four-part series of fireside chats that are part of the WE-REACH Biomedical Innovation Bootcamp. These events highlight industry experts, startup founders, and investors who share insights and advice to help new innovators ramp up quickly.
Most new innovators don’t realize how much needs to be done to meet the requirements and gain clearance or approval from the FDA allowing them to market their products. Even after a product is on the market specific quality systems must be maintained. Don’t be caught off-guard, come learn about the design, testing, monitoring, and data reporting necessary to move from a bench prototype to a commercial product, whether it’s a medical device or therapeutic. Panelists will bring stories based on their experience as they highlight key FDA processes and associated product development steps.