International Affairs Officer
European Medicines Agency (EMA)
Teams meeting, Netherlands
Carlos currently holds a position as International Affairs Officer at the International Affairs Department of the European Medicines Agency managing technical and policy collaboration initiatives in the America’s Region.
Previously, Carlos has worked as Committee Manager of the Committee of Human Medicinal Products (CHMP) being the main contact points for a wide range of regulatory or scientific topics channeling towards the Committee during the Covid pandemic. Prior to his work at CHMP, Carlos worked in products assessments managing regulatory procedures and focusing on the provision of regulatory and procedural guidance on applications to both Scientific Committees and applicants from the Pharmaceutical Industry. He has also acted as Business Lead for the Product Management Systems (PMS) of SPOR where he led the drafting and publication of the first two versions of the EU Implementation Guide for Medicinal Product Data requirements.
Carlos holds an MSc in Biotechnology and Business Management obtained at the University of Warwick, United Kingdom and a Bachelor in Life Sciences and Biomedical sciences from Universidade de Vigo, Spain.
From Parallel Pathways to Collaborative workstreams: The Evolving EMA–FDA Regulatory Partnership
Thursday, May 7, 2026
08:30 - 09:30 WEST