Now more than ever, physician innovators entering into the medical device ecosystem are experiencing a highly regulated and cost constrained environment. Maneuvering through this world is not for the faint of heart and takes more than sheer will: it takes a multidisciplinary team.

Navigating the journey from concept to commercialization for novel new products and devices

Tiffany Wilson, CEO of GCMI and T3 Labs

Tiffany Wilson, CEO of GCMI and T3 Labs

In this information packed 30-minute program, Tiffany Wilson, CEO of the Global Center for Medical Innovation, and Steven Goudy, MD, Director of Pediatric Otolaryngology for Children’s Healthcare of Atlanta, will share with physician innovators how to successfully navigate the medtech approval pathway from concept to commercialization for novel new products and devices. With decades of first-hand experience in medtech innovation each, they will explore:

  1. How to know you are ready for prototyping
    Steven Goudy, MD, Director of Pediatric Otolaryngology for Children’s Healthcare of Atlanta

    Steven Goudy, MD, Director of Pediatric Otolaryngology for Children’s Healthcare of Atlanta

  2.  How value-based care and the ACA impact medtech innovation
  3. Where to find readily available, highly valuable resources needed to commercialize your innovation without wasting thousands of dollars.

Are you a physician, engineer or startup with an idea for a new piece of medical technology and want to know how to get your device or product to market efficiently? Register now via GoToWebinar.

Date/Time: 10/26/2016 – 11:00 am