Friday, April 26, 2024
4:00 PM - 5:00 PM CET
Medical Device Regulation Ask Me Anything
🌟 Join us on April 19 for an exclusive LinkedIn Live session with Tibor Zechmeister!
🌍 As the landscape of medical device regulation in Europe continues to evolve, staying informed and compliant is more crucial than ever. This session is your golden ticket 🎫 to discuss the complexities of the European Medical Device Regulation (MDR).
🔍 Whether you're a startup navigating the initial certification process, an established manufacturer looking to adapt to the latest regulatory changes, or a professional curious about the intricacies of the MDR, this session is tailored just for you.
💡 Possible Topics in this session:
✅ Overview of the European MDR: Understand the framework, key changes, and how it impacts the medical device industry.
✅ Compliance Pathways: Practical advice on navigating the certification process, including tips for smoother approval.
✅ Risk Management: Strategies for ensuring your device meets the stringent safety and performance requirements.
✅ Post-Market Surveillance: Insights into the ongoing obligations for device monitoring and reporting adverse events.
This is an interactive Q&A: Have your questions answered live. Dive deep into your specific concerns and gain clarity on complex regulations.
🛠️ Who Should Attend:
✅ Medical device manufacturers and startups
✅ Regulatory affairs professionals and consultants
✅ Quality assurance personnel
✅ R&D engineers in the medical device field
✅ Policy makers and healthcare professionals interested in medical device regulations
👩💼 About the Host:
Meet Tibor Zechmeister, a vanguard in the medical device regulatory landscape, with an illustrious career spanning multiple facets of the industry. Tibor's journey began with a deep-rooted passion for merging high-tech solutions with healthcare, aiming to improve lives through innovation.
As a founder of medical device companies, Tibor has firsthand experience in steering companies through the intricate process of regulatory build-up, certification, and quality management systems. His expertise is built on a robust foundation as a regulatory affairs manager, where he has actively contributed to the successful certification and compliance of medical devices.
Adding to his profile, Tibor has served as an auditor for a European Notified Body, providing him with unique insights into the regulatory requirements and challenges faced by companies in the medical device sector.
📅 Mark Your Calendar!
Date: April 26
Time: 1600 CET
Location: LinkedIn Live
✍️ How to Participate:
Follow my LinkedIn page for updates and live session access. Prepare your questions in advance or simply tune in to enrich your knowledge.
🚀 Don't miss out on this opportunity to elevate your understanding of the European Medical Device Regulation and ensure your devices are not just compliant, but also competitive on a global stage. See you there!
Thanks to Tibor Zechmeister for the listing and graphics for this virtual startup event.