Medical Device Compliance, Regulation and Litigation Conference -- March 4 -- CDRH confirmed

02/6/2013

At this conference, now in its second year, attendees will hear Carolyn "Cassie" Scherer, policy adviser, office of the center director, CDRH, FDA, and Mary Weick-Brady, senior policy adviser, office of the center director, CDRH, FDA, discuss in detail the most significant recent and upcoming medical device compliance, regulatory and enforcement actions. Additionally, legal experts will analyze the most important cases of 2012 and detail what to expect in 2013 in litigation and regulatory developments, including key products liability issues. Register now and save $100.

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