Navigating Regulatory Pathways: Implications for Medical Device Startups 1/23/25

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.