Federal Register Notice: CDRH and the Office of Regulatory Affairs in cooperation with AdvaMed's Medical Technology Learning Institute will hold a series of three seminars on FDA medical device regulations 3/15-16 in Irvine, CA, 5/22-23 in Lakewood, CO and 6/6-7 in Pittsburgh, PA. The two-day seminars are designed to address the training needs of start up and small device manufacturers and their suppliers and will include industry and FDA perspectives and a question and answer period. Details about dates are posted on AdvaMed's Web site at: http://frwebgate.access.gpo.gov/cgi-bin/leaving.cgi?from=leavingFR.html&log=linklog&to=http://www.advamed.org/irvine.

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