SÃlvia Storpirtis
University of Sao Paulo (USP), Brazil
Biography
Sílvia Storpirtis has completed PhD in Biopharmacy in 1992. She has published more than 90 scientific papers. She is a Consultant of the Brazilian Health Surveillance Agency (ANVISA) for elaboration of technical regulations for generic and similar drugs (1999-2006). She is the Member of the Bioequivalence Working Group of the Pan American Network for Drug Regulatory Harmonization (PANDRH-PAHO-WHO) between 2000 and 2006, and the Coordinator of the Pharmaceutical Equivalence and Bioequivalence Committee of the Brazilian Pharmacopoeia. She is the Member of the USP Brazil Advisory Group of the United States Pharmacopoeia and the Consultant of regulatory agencies in Peru and Colombia for supporting the implementation of BA/BE regulations
Abstract
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