Medical Device made Easy Podcast
Technology
In January 29th, 2024, the EU Commission issued a Proposal that discuss mainly the shortage of Medical Devices, the EUDAMED availability and the IVDR transition periods. So apparently this is urgent and needed to avoid shortage. Let’s ask Erik Vollebregt what he thinks about it. Will this really help and when will this become a law as it is only a proposal for now.
Who is Erik Vollebregt?Erik specializes in EU and national legal and regulatory issues relating to medical devices, including eHealth, mHealth, software, and protection of personal data. He is an expert in life sciences regulation at the EU and Dutch level, with a focus on contracts, and regulatory litigation against competent authorities and M&A. Erik was initially trained as intellectual property and competition lawyer, starting his career at the Directorate-General for Competition of the European Commission. He subsequently gained experience in contentious matters, commercial contracts, and transactional work at three large international law firms. He actively contributes to law and policy development at the national and EU levels via membership in specialized committees at branch associations and the European Commission. Erik also works as an arbitrator in medical devices-related disputes and is regularly retained as an expert witness in foreign litigation. Erik worked and lived in Brussels and Stockholm for several years, and is fluent in Dutch, English, French, German, and Swedish. Chambers Europe 2017: Erik is known for his specialism in regulatory work, which covers medical technology, devices, and products as well as for biotechnology. Clients confirm his strong capabilities, with one saying “he stands out to me. Whenever I work with lawyers he has been the best, with a solid scientific background. He has the perfect combination of skills and experience.”
Who is Monir El Azzouzi?
Monir El Azzouzi is the founder and CEO of Easy Medical Device a Consulting firm that is supporting Medical Device manufacturers for any Quality and Regulatory affairs activities all over the world. Monir can help you to create your Quality Management System, Technical Documentation or he can also take care of your Clinical Evaluation, Clinical Investigation through his team or partners. Easy Medical Device can also become your Authorized Representative and Independent Importer Service provider for EU, UK and Switzerland.
Monir has around 16 years of experience within the Medical Device industry working for small businesses and also big corporate companies. He has now supported around 100 clients to remain compliant on the market. His passion to the Medical Device filed pushed him to create educative contents like, blog, podcast, YouTube videos, LinkedIn Lives where he invites guests who are sharing educative information to his audience. Visit easymedicaldevice.com to know more.
Link:The post New EU Proposal – EUDAMED, IVDR & Shortage appeared first on Medical Device made Easy Podcast. hamza benafqir
How to collect Clinical Data within the 21st Century [Jon Bergsteinsson]
How to manage the IVDR transition period? [IVDR 2017/745]
Is it a good idea to sue my Notified Body? [Erik Vollebregt]
Medical Device News – September 2021 Latest Updates
How to Certify a Software as Medical Device? (Dr. Abtin Rad – TÜV SÜD)
Better to be a Consultant or a Full-time employee? [Lifescience industry]
What can we learn from the first MDR audits? [Martin Witte -TÜV SÜD]
Medical Device News – August 2021 Regulatory Update [MDR & IVDR]
How to implement Vigilance Reporting for MDR and IVDR?
System and Procedure Pack the RETURN with Erik Vollebregt
How to interpret the first Expert Panel Opinion? [Bassil Akra]
Medical Device News: The July 2021 Update [MDR IVDR FDA SFDA]
How to build your State-of-the-art for your Medical Devices?
How Intellectual Property is linked to the Medical Device Regulation?
How to perform a good Clinical Investigation with Helene Quie
How to perform a Biological Evaluation for your Medical Device?
Medical Device News – June 2021 Update [EU MDR Date of Application]
EU MDR Survey: What is the Industry’s opinion? [Catherine Higginson]
MDR is coming so brace yourself with Erik Vollebregt
FDA: Is the Emergency Use Authorization worth it? (EUA)
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