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.
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!
At DeviceTalks Boston, Tyler Shultz will give attendees an inside look at Theranos and how he was able to sound the alarm after he realized the company was falling apart. Shultz will take attendees behind the story that everyone is talking about: the rise and fall of Elizabeth Holmes and her diagnostic company, Theranos.
Join Shultz and 1,000+ medical device professionals at the 8th annual DeviceTalks Boston.