About me
Health Regulation Expert with over 12 years of experience in the regulatory evaluation and oversight of non-clinical and clinical development of drugs and biological products. She is currently the Deputy Head of the Clinical Trials Office at Anvisa and a Good Clinical Practice (GCP) inspector. She contributed as Anvisa’s representative to the development of the ICH E17 guideline and currently represents the agency in the ICH working groups for E6 (R3) Annex 2 and ICH E22. She also represents Anvisa in the PAHO Clinical Trials Forum and serves as a full member of Brazil’s National Clinical Research Ethics Commission (INAEP). She holds a degree in Biology and a Master’s in Molecular Biology from the University of Brasília.
