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Ana Trullás Jimeno

Senior Scientific Specialist
European Medicines Agency

Ana Trullás Jimeno is a Senior Scientific Specialist who works as Product Lead in the Oncology Office at the European Medicines Agency. Responsible for scientific and regulatory science input for a portfolio of products from pre-submission of initial marketing authorisation through post-authorisation. Further to this, she worked on the implementation of the In Vitro Diagnostics Regulation and is currently one of the main points of reference for scientific and regulatory guidance on companion diagnostics at the Agency. Previously, 2003-2014 Ana worked as Product Team Leader in the area of Quality of Medicines at EMA. Prior to joining the Agency, Ana worked in the Chemical and Pharmaceutical Technology Division at the Spanish Medicines Agency. Ana has over 20 years of experience within the Pharmaceutical framework.

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