New EU Medical Device Regulation (MDR) – Major Changes that you should know

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 comprehensive overview of the new requirements and a practical step by step guide to prepare for the transition. Lessons learned from on-going transition programs of major medical device manufacturers will be shared with the audience.

Areas Covered in the Session :

• Overview of the major changes brought forward by the new MDR
• Schedule, timelines and validity of certificates issued
• Step by step guide for successful transition
• Tips dispensed based on our experience in prepping manufacturers for the transition

Who Should Attend:

• Medical Device Manufacturers
• Management Teams
• Quality Departments
• Regulatory Affairs Departments
• Manufacturing Departments
• Engineering Departments
• Marketing and Sales Departments
• Clinical Professionals

Course Director: GADI GINOT

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.