B.Pharm., M.Sc.,PhD. CChem
Dr James Rowe has over 40 years experience in the pharmaceutical industry and academia in Australia and the United Kingdom. His appointments include positions at Lilly, Bristol Myers Squibb and Abbott laboratories in the design and evaluation of pharmaceutical dosage forms and analytical chemistry development and validation. He has appeared as an Expert Witness in many litigation proceedings involving formulation issues in pharmaceutical patents in Australia, New Zealand, Canada and the United States. He has held an academic position at the School of Pharmacy, University of London and was a part-time lecturer in pharmaceutics at the University of Sydney. In recent years he was a Director of a consulting company in Australia concerned with the development and testing of a range of new products for the pharmaceutical, veterinary and personal care industries.