Marie-Amélie MARCQ
Senior Advisor in Regulatory and Pharmaceutical Affairs
Doctor of Pharmacy
Master 1 in Health Law, Economics and Marketing
Master 2 in Regulatory Affairs for Health Industries
With more than 10 years of experience in regulatory affairs, Marie-Amélie has worked in both pharmaceutical companies and consulting firms, giving her a comprehensive and pragmatic understanding of industry challenges.
She began her career at major laboratories such as AstraZeneca and Janssen Cilag, where she was responsible for promotional material validation, MA dossier tracking, medical information requests, and quality topics related to external communications. She later transitioned into consulting at BlueReg Pharma Consult and PharmaLex France. There, she contributed to complex projects such as lifecycle management, communication compliance, promotional quality systems, certification audits, and client support during health authority interactions.
At Atessia, Marie-Amélie leverages her dual background in industry and consulting to deliver tailored support to pharmaceutical companies. Her rigor, versatility, and solution-oriented mindset are key strengths for the team.
