Please join us for an exciting evening of networking and a panel discussion on “How to Make the FDA Work for You” featuring greenlight.guru founder & VP QA/RA Jon Speer with special guest moderator Brian Johnson, Co-Founder and Publisher of MassDevice.
This event is co-hosted by Southeastern Medical Device Association (SEMDA) and Global Center for Medical Innovation (GCMI), in conjunction with GCMI’s annual open house.
As you know, FDA regulates the medical device industry in the U.S. And often times, medical device companies are seeking insights on how to prepare for FDA inspections and FDA horror stories.
The event presents an interesting twist, changing the perspective to provide tips and pointers on how you can leverage a positive working relationship with FDA.
It will take place from 5:00 – 7:00pm ET on September 30, 2015 at GCMI in Atlanta, GA. The cost is free and registration is required.
Joining Speer on the panel are a couple other industry veterans:
- Julio Rivera, VP Quality and Regulatory Affairs, SiO2 Medical Products
- Joel Freimuth, CEO & President, Blue Pearl Consulting
- Kyle Rose, Senior Consultant, Rook Quality Systems
“I’m often asked by med device companies to help get prepared for FDA inspections. I’m excited about this panel to help educate attendees on some important tips on working with FDA to be proactive,” says Speer.
We look forward to seeing you there!
