Siddharth Desai (Technical Leader and President, Health Care Evolution Inc.)
Eri Hirumi (Regulatory Affairs Specialist, Microvention)
Laura Jeannel (Senior Technical Specialist, Meridian BioGroup)
Date: Thursday, November 5
Time: 10:00am - 11:00am
Track:
Conference: Product Development Innovation
Vault Recording: TBD
The current industry landscape for innovative medical devices has become more competitive and challenging in recent years, with the ever-impending regulatory hurdles to jump through. Proper collaboration between companies and regulatory bodies is more crucial for development than ever before. During this interactive session, two experts will go into a short discussion on how to bridge the gap between innovator and regulator, and then open the floor to the audience for an extended Q&A session. In this format, the experts will encourage comments, insights or questions from attendees to engage in a collaborative discussion. Join this gathering to hear from your peers, learn from experts, and accelerate the rate at which your innovations are available to the public.
Topics include:
- How the rate of approval by FDA of medical devices has changed in an era of Covid-19 with the EUA designation
- Steps for developing innovative and efficient regulatory strategies and plans
- A timeline and checklist for developing your strategy
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