MedTech Summit 10th Anniversary: Where the MedTech Community Accelerates Regulatory Excellence
Expert guidance from regulators and industry to streamline compliance, stay deadline-ready, and advance patient safety through rigorous science
European Regulatory Affairs • Clinical Evaluations • SaMD & AI • Post Market Surveillance • Global Markets • Biocompatibility
Navigate the Future of MDR: The 2026 Agenda is Here
Step into the future of MDR, with insights to master the upcoming pivotal revisions and keep deadline-ready. Achieve regulatory excellence and position your organisation as a leader in compliance and innovation.
Forge meaningful connections with a community of top regulators and industry leaders, immerse yourself in dynamic workshops and interactive roundtables, and take the first step in shaping your MDR journey today.
Where MedTech Regulation Is Defined — By the People Behind It
With 80+ speakers already confirmed, the MedTech Summit 2026 is the must-attend event of the summer. Join notified bodies, competent authorities, and industry leaders from renowned organisations such as Johnson & Johnson, Philips, Roche, Baxter, and more. Gain actionable insights to streamline compliance, meet critical deadlines, and elevate patient safety through cutting-edge science
Top Tier 1 MedTech Attending in 2026
Who You'll Connect with at MedTech Summit
+
Competent Authority & Notified Body Speakers
+
Leading MedTech Industry Stakeholders
+
Medical Device, Software, and Combination Product Companies Represented
+
Countries Represented
Your Roadmap to Regulatory Excellence
Connect with regulatory, quality, clinical, and biocompatibility professionals, along with notified bodies, consultants, and future leaders, all shaping the future of MedTech. Explore tailored tracks like EU MDR, SaMD & AI, and Clinical & PMS, and gain expert insights, build connections, and overcome challenges with personalised programming. Ready to advance your career? Discover your path to success at MedTech Summit 2026.
From Regulation to Innovation: What’s on the 2026 Agenda?
Stay ahead with expert insights on EU regulations, SaMD, biocompatibility, and global markets. Gain the knowledge you need to innovate, comply, and lead in MedTech.
European Regulatory Affairs
Navigate the intricacies of the evolving European regulatory landscape and ensure you’re deadline and transition ready.
Software as a Medical Device & AI
Stay ahead of the curve in the rapidly evolving SaMD and AI regulations.
Biocompatibility
Explore the latest updates and practical applications of ISO 10993 and gain a deeper understanding of biocompatibility testing methods.
Global Markets
Immerse yourself in the latest global regulatory updates and gain a comprehensive understanding of global requirements and efforts for global reliance.
Clinical Evaluations & PMS
Streamline your clinical processes & stay aligned with current European and global post-market surveillance requirements
Workshop: SME Survival Guide
Strategies and actionable insights for SMEs operating in the rapidly evolving medical device regulatory sector.
Workshop: Biocompatibility
Master biological evaluation and safety assessment for medical devices through hands-on training. Learn practical techniques to ensure compliance with ISO standards and maintain device safety.
*NEW* Workshop: Patient Access & Reimbursement
Delve into the critical intersection between regulatory compliance and market access success for medical device professionals
Engage Quality Decision-Makers at MedTech Summit!
Showcase your services to industry leaders and innovators. Let’s customise a sponsorship package that drives real results for your business.
Contact Neha Singh at Neha.Singh@informa.com