Are you ready to bring your groundbreaking medical device to market but feel overwhelmed by the intricate regulatory landscape?

Join University Lab Partners for a comprehensive webinar designed specifically for startups to navigate the path to success in both U.S. and global markets.

Join them Thursday, January 23 from 9:00AM to 10:00AM online.

What You’ll Learn:

Explore key FDA pathways such as 510(k), De Novo, TAP, and SteP—understand how they work and when to utilize them. Discover strategies for meeting rigorous international standards like EU MDR and Health Canada regulations. Gain valuable tips for designing clinical trials, preparing regulatory submissions, and engaging early with authorities to mitigate risks and expedite approvals. Stay informed on evolving policies and programs shaping the medical device industry.

Why Attend?

This session offers actionable insights from industry experts, providing you with the knowledge and tools to confidently tackle regulatory challenges. Whether you’re just starting your journey or scaling your operations, you’ll learn how to minimize time to market while staying agile and compliant.

Don’t miss this opportunity to streamline your regulatory pathway and accelerate your device's success. Register today and take the first step toward transforming your innovation into a market-ready solution!

Registration is free!

Please register here to attend.

Thanks to University Lab Partners for offering this local startup event, the details, and the graphic!