Recognizing the importance of early engagement in regulatory thinking is key to shaping your commercial strategy. This webinar will provide valuable insights into strategically navigating clinical risks and providing compelling evidence for the safety and efficacy of your device or diagnostic innovation.

About the presenter:
Tim Bubb, Technical Director at IMed Consultancy, brings extensive experience in navigating the complexities of innovative and complex devices, spanning software, AI, and novel technologies. Join us for a fundamentally informative discussion on the how, when, and why of regulatory strategies aimed at expediting your pathway to markets both in the US and globally.