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FDA News & Notes - Week of July 25, 2011
Date:7/25/2011

visory Committee considers strategies for the implementation of quality by design principles within the Office of Pharmaceutical Science review offices. 8 a.m., 10903 New Hampshire Ave, Building 31, Room 1503, Silver Spring, Md.
Press Office Contact: Sandy Walsh, 301-796-4669, sandy.walsh@fda.hhs.gov

Wednesday, 7/27 – American Telemedicine Association Policy Summit
Bakul Patel, policy adviser, and Mary Brady, senior policy analyst, from the Center for Devices and Radiological Health speak on mobile health policy and telehealth. 8:30 a.m., The Westin Washington, D.C., 1400 M Street, N.W., Washington, D.C.
Press Office Contact: Karen Riley, 301-796-4674, karen.riley@fda.hhs.gov

Thursday, 7/28 – FDA Commissioner Hamburg testifies before the Senate Committee on Health, Education, Labor and Pensions on "FDA User Fees: Advancing Public Health." 9:45 a.m., Dirksen Senate Office Bldg., Constitution Ave. and 1st St., N.E., Room 430, Washington, D.C.
Press Office Contact: Karen Riley, 301-796-4674, karen.riley@fda.hhs.gov

Monday, 8/1 –  The first FDA Humanitarian Use Device Workshop provides an opportunity to spend two days developing applications for devices intended to treat or diagnosis a rare disease or condition. 8 a.m., University of Minnesota-Twin Cities Campus, Moos Tower, 515 Delaware Street, S.E., Minneapolis.
Press Office Contact: Sandy Walsh, 301-796-4669, sandy.walsh@fda.hhs.gov

On the Web:
Tuesday, 7/26 – The FDA begins a pilot program
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SOURCE U.S. Food and Drug Administration
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