Carl Pinksy, MD, chief medical officer of the National Cancer Institute's biological response modifier program, to VP-medical affairs. Pinsky assisted in the design of the firm's first clinical trial of its Prosorba column in 1983, when he was with Memorial Sloan-Kettering.
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Unfounded expectation some firms have for FDA to protect their investments in preparing successful NDI notifications is part of industry’s overall interest in increased regulation of the market, says Steven Tave, Office of Dietary Supplement Programs director.