Date: 6/15/2011
Location: Goodwin Procter Boston Conference Center, Boston MA
This internally-produced program will cover the recent market changes and recent 510(k) reform efforts, as well as discuss the FDA's expectations for medical device companies. The conversation will cover several hot topics including: the evolution of the 510(k) program; the FDA's approach to compliance; and tips for medical device companies at all stages. Mark Heller and Ray Zemlin are featured speakers.
This post was authored by Founders Workbench.