2nd Annual Biocompatibility Testing In Medical
Devices 2025 Conference
- 06 — 7 March 2025
CLIN-r+ are delighted to announce their participation at the 2nd Annual Biocompatibility Testing In Medical Devices 2025 Conference!
Our Director of Clinical and Regulatory Affairs, Jacqueline van Druten will be discussing
Biocompatibility Evaluations for Gas Pathways: Insights into 2024 ISO 18562-Series Updates
Date 7 March 2025 | Time: 11:20am – 12:00pm | Duration: 30minutes presentation + 10 min Q&A
Explore the latest updates to the ISO 18562 series and gain insights into testing methodologies, regulatory expectations, and practical considerations for ensuring compliance and safety in rspiratory and ventilatory medical devices.
More about 2nd Annual Biocompatibility Testing
in Medical Devices 2025 Conference:Register for your place here!
Welcome to the 2nd Annual Biocompatibility Testing in Medical Devices 2025 Conference in the captivating city of Porto, Portugal! We are delighted to welcome back esteemed professionals and extend a warm greeting to new participants joining us this year.
Over the two days, engage deeply with pivotal discussions and advancements shaping the landscape of medical device safety and efficacy. The conference will address pressing regulatory challenges, including navigating compliance with ISO 10993 standards and understanding the impact of extractables and leachables in medical devices. Attendees will gain insights into cutting-edge biocompatibility testing methods, comparing in vitro and in vivo approaches, and practical considerations when collaborating with third-party laboratories.
Moreover, sessions will delve into the latest updates under EU MDR, focusing on biological equivalence and effective post-market surveillance strategies. Global harmonization efforts and their implications for biocompatibility standards will also be explored.
Join us in driving innovation and setting new benchmarks to ensure the highest standards of safety and effectiveness for medical devices worldwide. We look forward to productive discussions, valuable networking opportunities, and collectively shaping the future of Biocompatibility Testing in medical devices.
KEY POINTS:
• Notified Bodies: Challenges in Regulatory Compliance for Biocompatibility
• Regulatory Requirements for Biocompatibility: ISO 10993 Series
• Extractables and Leachables (E&L) in Medical Devices
• Chemical Characterization and Risk Assessment
• Biological Equivalence Under EU MDR
• Post-Market Surveillance and Regulatory Compliance
• Advances in Biocompatibility Testing Methods: In Vitro vs. In Vivo
• Practical Considerations for Testing with Third-Party Laboratories
• Global Harmonization of Biocompatibility Standards
MORE INFO ON THE CONFERENCE:
+420792618393 | info@vna-events.com | www.vna-events.com
Biocompatibility Testing In Medical Devices 2025 Conference
