skip to Main Content
  • This page as PDF

FDA’s Regulation of Mobile Health Technologies: When Is a Mobile Product a Medical Device?


In light of the increasing development of novel mobile technologies designed to improve healthcare outcomes, and FDA recently issuing a final guidance on mobile medical applications, is there a practical framework in place for regulating new and innovative mobile health technologies? Join us as we explore the opportunities and risks associated with the emerging regulatory environment for mobile health technologies from the perspective of FDA, industry and investors, and consider ways to navigate new regulatory expectations while seizing business opportunities.

During this webinar, you will:

    Learn about FDA’s emerging regulatory framework for mobile technologies and how it is expected to evolve
    Understand how different stakeholders view this regulatory framework and related opportunities
    Learn how the current regulatory environment will affect development and commercialization of mobile health technologies

Back To Top