Software as a Medical Device: From Regulatory Strategy to Market Readiness
Join MIDI as they provide a practical framework for developing SaMD products with regulatory requirements built into the development process.
From Data Chaos to Trusted AI in MedTech:
Data Quality, Knowledge Graphs & Semantic Layers That Make It Possible
Join Genpact as they provide a practical framework for connecting, governing, and activating service data – and a clear roadmap for scaling AI from pilot to confident business outcomes.
Quality and Regulatory at the Speed of AI: Moving Faster Without Losing Trust
Join Suntra MedTech as they explore how AI is beginning to reshape the work of Quality and Regulatory—and what must not change.
False Claims Act Risks and Enforcement Priorities for the Med Tech Industry
Join Akin Gump as they provide actionable takeaways to minimize compliance risks and position organizations for effective and credible responses when FCA investigations arise.
Investing in Women’s Health Products and Companies
Examine the evolving investment landscape, share lessons learned, and discuss strategies that help women’s health companies attract investment and drive growth.
From Launch to Exit: Leveraging IP to Build and Protect Enterprise Value
Join Cooley LLP as they explore how to evaluate and strengthen your IP position, prepare for competitive challenges, and avoid common pitfalls that can undermine value during due diligence and…
Entering the Japanese Medical Device Market: Regulatory Pathways, Consultation Opportunities, and Practical Insights
Learn how to enter Japan’s medtech market with insights on regulatory pathways, consultation services, and practical insights for U.S. medtech companies.
The Widening AI Gap: Why AI-First MedTech Companies Are Pulling Ahead
Join Boston Consulting Group as they explore how medtech organizations are using AI to transform product development and accelerate innovation.
The MedTech Conference 101 Webinar
Ready to maximize your ROI at the most impactful medtech event of the year? Join us for The MedTech Conference 101: What’s New, Why Attend & How to Maximize ROI…
Stop Counterfeit & Grey Market Medical Devices at the Border
Gain a focused overview of how to record intellectual property with CBP to stop counterfeit & grey market medical Devices at the border