π Navigating the Challenges of the New Medical Device Regulations π
We're excited to share the highlights of our recent in-person gathering, where 30+ passionate individuals came together for an engaging session!
π’ Event Title: "EU-MDR Clinical and Post-Market Surveillance Requirements for High-Risk and Up-Classified Devices"
A shoutout to our special guest, SGS, a global leader in testing and certification. Thanks to them, we had a fantastic talk from their Technical Director-Medical Audit, Balazs Bozsik. The discussion dove deep into the world of implantables and class III devices, offering a treasure trove of insights.
πββοΈ Interactive and Insightful: Our audience was on fire during the Q&A. They brought many thought-provoking questions, making it an engaging knowledge-sharing experience.
π Heartfelt Thanks: A big round of applause to SGS, our dedicated volunteers, and all attendees. Your enthusiasm made this event a smashing success. We're grateful for our supportive community.
Stay tuned for more exciting events and discussions in the pipeline. Let's keep learning and growing together!
π Applause to All Attendees and Sponsors π
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Kalyanasundar Balasubramanian
Aspiring Regulatory Compliance Specialist
Belmont CA
United States
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