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Mr. Peltier is currently a consultant to Ortec, after working full-time for 5 years. From 1991 to 1999, was
VP of Worldwide Regulatory Affairs, at ConvaTec, a Bristol-Meyers Squibb division, where he was
responsible for regulatory support in more than 100 markets, strategic regulatory guidance to senior
management, and leadership of a global staff of regulatory professionals. Mr. Peltier has management
experience in clinical research and product development with PharmaKenetics Laboratories, Inc., Johnson
& Johnson, America Home Products and Pfizer. Mr. Peltier has a BS in Biology from Fairleigh Dickinson
University (1972), and is certified by the Regulatory Affairs Professional Society (since 1992). He has
more than 25 years of clinical and regulatory experience in the pharmaceutical and medical device industry. | 