Greenlight Guru's State of Medical Device Product Development and Quality Management 2020 Report is here.
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HERE'S WHAT YOU CAN EXPECT...

  • Stay on top of the conundrum of the medical device industry’s regulatory changes, including FDA's Case for Quality, EU MDR, ISO 13485:2016, MDSAP, more. 
  • Network with Orange County's top medical device quality, regulatory and engineering professionals and executives
  • Enjoy specially selected hors d'oeuvres, beer, and wine at Eureka Building

THE SPECIFICS...

Join the Greenlight Guru team, Valtronic, Azzur GroupICS, and Orange County's top medical device quality, regulatory, engineering professionals for learning, networking, drinks, and hors d'oeuvres at Eureka Building.
 

Finish the evening with our panel discussion on the future of quality and regulatory trends, and a Fireside Chat + Q/A with Greenlight Guru Founder Jon Speer.

 
 
5:00 PM: Arrivals + Hors D'oeuvre + Drinks + Networking with Medical Device Professionals
 
6:15 PM: Panel Discussion with seasoned medical device professionals
 
7:00 PM: Fireside chat + Q & A with Greenlight Guru Founder Jon Speer
 
7:30 PM: Closing questions, remarks, and final networking

LEARN FROM THESE EXPERTS.

Jon Speer

CEO & Founder at Greenlight Guru

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Matt Romey

Director - Medical Device Consulting at Azzur Group

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Milton Yarberry

Director Medical Programs at Integrated Computer Solutions

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Michael Drues

President at Vascular Sciences

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Christopher Ware

Director of Quality Assurance at Neural Analytics

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Kathryn Zavala

VP, Operations & Business Development at MedTech Innovator

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DON'T WAIT: GRAB YOUR FREE TICKET BEFORE THEY'RE GONE