Getting a medical product to market is no simple task. From conception to development, to marketing to appeal to audiences worldwide, every step has its speed bumps, and like a speed bump, and put in place for good measure. Quality control for feasibility and engineering tests both play a part in making sure that the product is functional, viable, and in many cases, FDA approved.On this Sunrise Podcast episode, Adam Jacobs), Chief Technology Officer at Sunrise Labs, discusses how products are submitted and certified by the FDA and what kind of things need to be done during product development, including ISO 13485 certification for medical devices.
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