We consider it both a privilege and a responsibility to be a major actor in the blood industry because whatever happens in this ever rapidly evolving world, humanity will always need access to blood.
My role is to make sure the solutions we provide are not only safe, but also qualitative in a way that preserves our agility towards blood banks.”

Raouf Benyamina joined Macopharma in 2014 for a 6-month internship in the course of his final Masters degree year in “Development and control of health products - Medical devices” at the Pharmacy faculty of Nantes and has pursued his career within the company ever since. He started as a Regulatory Affairs officer before taking on managerial positions all the while being the regulatory coordinator for our transition to the MDR and non-DEHP. He is now the Head of Regulatory Affairs, Quality and Materiovigilance.