The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers; Public Seminar

Resumen

The Food and Drug Administration's (FDA's) Center for Devices and Radiological Health and Office of Regulatory Affairs, in cooperation with AdvaMed's Medical Technology Learning Institute, is announcing a series of three seminars on FDA medical device regulations. These 2-day seminars, which are designed to address the training needs of start up and small device manufacturers and their suppliers, will include both industry and FDA perspectives and a question and answer period. Dates: The seminars are planned for the following dates: 1. March 15 and 16, 2007, in Irvine, CA 92614. Details about dates are posted on AdvaMed's Web site at: www.advamed.org/irvine.\1\ ---------------------------------------------------------------------------