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Workshop on Post-Approval Device Studies

08/19/2009

Federal Register Notice: FDA will hold a public workshop 9/9-10 entitled, “Methodologies for Post-Approval Studies of Medical Devices.” The target audiences are epidemiologists, statisticians, clinicians and regulatory affairs specialists. The workshop will be held from 9 a.m. to 5 p.m. on both days at the FDA White Oak Campus, 10903 New Hampshire Ave., Silver Spring, MD. Contact Daniel Caños (240) 796-6057 or Ellen Pinnow, (301) 796-6066 To view this notice, click here.

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