About me
Pharmaceutical professional with a degree in Industrial Clinical Pharmacy and a Master’s degree in Pharmaceutical Sciences. Has been working as Health Regulation Expert for Anvisa for over 12 years working as a drug product registration reviewer, quality management professional and GMP inspector of pharmaceutical manufacturing sites. Currently works in the area responsible for the assessment of drug substance dossiers and the issuance of CADIFA. Represented Anvisa as Topic Leader in the EWG/IWG ICH Q2(R2)/Q14 and at present as alternate in ICH M7 nitrosamines subgroup.
