ACI’s FDA Boot Camp – Medical Devices Edition

May 25, 2016

The American Conference Institute (“ACI”) is holding its fourth annual FDA Boot Camp – Medical Devices Edition on Thursday, July 21 to Friday, July 22, 2016 at the InterContinental Chicago Magnificent Mile, Chicago, IL. This year’s program has been revamped to provide both a “basic training” in FDA regulatory law, as well as “advanced training” sessions tailored to the application of this knowledge to real-life situations. Highlights from this year’s program include a “Ripped from the Headlines” panel, containing updates on key developments in the FDA regulatory bar, and an in-depth Post- Conference Master Class, delving into the hot-button topics of in vitro diagnostics, laboratory developed tests, companion diagnostics, and combination products. Hyman, Phelps & McNamara, P.C.’s Jeffrey N. Gibbs will be speaking on “Low to Moderate-Risk Devices – Clarification of the 510(k) Clearance and Dissecting the De Novo Classification.”

You can register for the program here.  FDA Law Blog is a conference media partner, and blog readers can receive 15% off the tuition fee by using discount code P15-999-FDA16 when registering for the conference.  A new price tier for the conference will go into effect later this week.

Categories: Medical Devices