Denise Endo da Costa Bittencourt

Denise Endo da Costa Bittencourt is a professional with extensive experience in regulatory affairs and quality assurance, currently serving as a validation technologist at Instituto de Biologia Molecular do Paraná - IBMP since March 2022, focusing on in vitro diagnostic manufacturing. Previously held positions include regulatory analyst at CRIALI Assuntos Regulatórios and technical responsible at Serion Brasil, where contributions involved developing registration dossiers and maintaining certifications for diagnostic products. Denise has also worked as a pharmacist at Cyclopet Radiofarmacos and served in technical roles at Medplast Importadora e Exportadora de Produtos Médicos Hospitalares and ABBMED Importadora de produtos médicos Ltda., emphasizing quality management systems and regulatory compliance. Educational qualifications include a Master of Science in Microbiology and Immunology from HC-UFPR and a Bachelor of Pharmacy from PUCPR, complemented by a specialization in quality management for pharmaceuticals, cosmetics, and food.