Gadi Ginot (M.Sc., MBA), CEO & Founder of Physio-Logic Ltd, Israel’s largest and leading provider of accelerated medical device approval, certification and regulatory compliance solutions (www.physio-logic.co.il). Gadi is internationally renowned for mastering medical device registration, quality and clinical development and his track record extends over 25 years in three continents. Gadi streamlined the regulatory approval of over 100 medical devices leveraging his proficiency in regulatory sciences and his signature out of the box regulatory and clinical strategies. Gadi engineered the “Physio-Logic DNA” based on this formula.
The date of application of the new EU Medical Device Regulation (MDR) is nearing. Preparing for smoothly transitioning to the MDR is vital for assuring business continuity and sales in the EU. This webinar will provide participants with a...
This webinar will discuss the impact of incorporating AI on the premarket regulatory requirements from medical devices and healthcare products. The additional evidence that is needed to get AI based products to the healthcare market will be mapped and...