The European Union is in transition now due to some regulatory changes. EU MDR will be applicable by May 26th, 2021, but in the meantime, other political situations may impact this timeline.
Manufacturers that would like to register their product in Europe need to understand the potential situations that could happen and how this can change your regulatory strategy.
Brexit will apply by January 1st, 2021. Swixit and Turkxit will depend on the EU commission, but this may happen by May 26th, 2021.
This presentation takes a deep dive into the implications of Brexit, Swixit, Turkxit for the European Medical Device Market.
This free in-depth webinar, presented by Monir El Azzouzi , Founder of Easy Medical Device, will cover the current (Winter 2020) Brexit, Swixit, and Turkxit situation for the European Medical Device Market.
★ KEY VIDEO TAKEAWAY★
This presentation originally aired during the 2021 State of Medical Device Virtual Summit.
If you’d like to watch more related videos, browse through the full list of free replays from this track of the virtual summit event: https://youtube.com/playlist?list=PLkchw-at8PkO-O70hkzdbQrzc-LtFPUbM
Plus, download the slides for this presentation for free here: https://www.slideshare.net/greenlightguru/impact-of-brexit-swixit-turkxit-for-the-european-medical-device-market
Are you looking for a QMS solution to help you bring safer medical devices to market faster with less risk? Take a quick tour of Greenlight Guru's Medical Device QMS software: https://www.greenlight.guru/quality-management-software
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