Mr. Puderbach has over 13 years of experience in the pharmaceutical industry with companies such as Hoffmann LaRoche, Warner Lambert, Omnicare Clinical Research and Wyeth. His experience has focused in the areas of manufacturing and clinical quality, compliance and validation. Mr. Puderbach’s validation experience includes extensive work in the process, cleaning, equipment/facilities and computer systems areas. He is currently responsible for computer system compliance (21 CFR Part 11) at all Wyeth manufacturing and distribution facilities that are FDA regulated. Mr. Puderbach holds a B.A. in Biology from Lycoming College and an M.B.A. from Pennsylvania State University.

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