Petra Zoellner directs MedTech Europe’s team focusing on implementing EU regulatory systems for medical devices and in-vitro diagnostic products. She represents MedTech Europe to external fora on strategic regulatory policy questions, including the Medical Devices Coordination Group. She also acts as part of MedTech Europe’s leadership team, ensuring collaboration and coherence on topics that cross over to other areas in the medtech ecosystem. Since Zoellner joined MedTech Europe in February 2012, her work has involved leading and representing the association on regulatory policy in various domains, including implementation of the IVD Regulation, CE-marking topics, device labelling, trade in animal by-products, European database, medical technology standards, and regulation of substances and electronic devices, amongst others. Before MedTech Europe, Zoellner worked for the American Chamber of Commerce to the EU (AmCham EU), where she led the policy team handling legislative and regulatory issues. She also worked within the government affairs team of Genzyme.