Navigating the FDA’s Medical Device Presubmission Process

This webinar provides a comprehensive overview of the FDA’s medical device pre-submission process, a critical step for manufacturers seeking to efficiently bring safe and effective devices to market. The presenters will examine the strategic advantages of utilizing the pre-submission program (Q-Sub), outlining key components and benefits. This webinar is ideal for medical device manufacturers, regulatory professionals, researchers, and anyone involved in developing and commercializing medical devices in the United States.