Adriana Di Marco

Adriana Di Marco has worked in the pharmaceutical industry for over 30 years. Adriana began their career in 1988 as a Lab Technician for Schering-Plough Canada Inc., now Merck. In 1999, they moved to Galderma as a Regulatory Compliance Coordinator. In 2008, they joined Theratechnologies as a CMC Specialist in Pharmaceutical Development. In 2012, they were hired as a QA Supervisor for Winpak. From 2013 to 2016, they worked as a Quality and Compliance Specialist for Valeant Pharmaceuticals. In 2020, they were appointed Director of CMC & Regulatory Affairs at Inversago Pharma. In this role, they provide strategic CMC Regulatory advice to the pharmaceutical industry and authors Quality Sections for Marketing Applications, post-marketing supplements, and drugs in the investigational stages.

Adriana Di Marco completed their BSc in Chemistry from Concordia University between 2005 and 2013. Adriana also obtained a D.E.C in Chemical Technology from Dawson College between 1985 and 1988.