|Thursday, June 13, 8:00 am - 8:45 am|
|Panelists: Martin Browning, President and Co-Founder, EduQuest, Inc.|
| Matthew Krueger, Chief, Orthopedics and Physical Medicine Device Branch,
Office of Compliance/Center for Devices and Radiological Health
|Mary Gray, Manager Regulatory Affairs, DePuy Synthes Spine|
|Moderator: John Gagliardi, MidWest Process Innovations, LLC|
FDA has considerable reach throughout each link of the supply chain. This Keynote Panel Discussion on Day Two of OMTEC brings together regulatory experts to talk about current and future FDA decisions that may affect your manufacturing processes. Actionable advice will shed light on how FDA changes will manifest themselves regarding innovation and new product releases. Professionals from all departments of medical device companies will leave armed with compliance insight for success.