I have 30 years experience in drug development building on an expertise in respiratory diseases, inflammation and fibrosis. My work experience in France and the USA is in large and small companies at all stages of drug development. I have experience designing creative product profiles and clinical development plans for approval in Europe and the USA. I am familiar with the early integration of a pharmacoeconomic strategy to fully document clinical effectiveness and with the development of biomarker strategy for a translational medicine approach.

In 2011, I created Baucis Global LLC to offer strategic and clinical development support to build value and increase the probability of success of the clinical development of new products. My main consulting services are:

Clinical development plans: Definition of patient populations, product profiles, clinical risk-management plans, biomarker strategy

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Medical and scientific advisory boards: Formation of boards and evaluation of clinical development approaches

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Evaluation of licensing opportunities: Evaluation of risks and liabilities

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Medical monitoring of clinical studies in the USA and in Europe: Data monitoring boards

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