Good morning,

Recent changes within the FDA’s 510(k) program have left many companies in a state of confusion and at times downright frustration. Join us on November 9 as the Council hosts Heather Rosecrans, Senior Regulatory Advisor, Greenleaf Health LLC and former Director of the Device Evaluation Group within the FDA’s Center for Devices and Radiological Group, to speak to some of these changes.

The session will also be coupled with a panel of regulatory representatives from area companies who will be on hand to share some tricks of the trade.

Sponsored by:
K&L Gates | Regulatory & Quality Solutions

Making Sense of the FDA’s 510(k) Program
Date: Wednesday, November 9, 2011
Time:
7:00 am Registration, Networking, and Coffee
7:30 am Breakfast & Program
11:15 am Adjournment

Venue:
Westin Convention Center Hotel , 1000 Penn Avenue, Pittsburgh, PA 15222

Cost: $55 Member | $175 Non-Member
(Want the Member rate? E-mail our Membership Team)

Register: Online | events@pghtech.org | 412.918.4229

-RTK

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