ETHOS - Key Persons
Physician with 20 years of experience in the pharmaceutical industry. Medical support and scientific support for marketing activities, scientific documentation, clinical trials, consultancy and services in Pharmacovigilance / "drug safety", P & ID, planning and design of bioavailability, bioequivalence, pharmacoepidemiology, pharmacogenetics, Clinical Studies phase I - IV clinical and academic studies (bioequivalence and clinical phase I study).
Critical Analysis of the medical literature, particularly for R & DI, expertise in clinical research, drug safety and risk management.
Experience in managing R & D projects, from conception to the registration of the drug. Performed this procedure on several projects of incremental and radical innovation, assessing the risks and impacts of the project.