Thiago Souto is the Regulatory Affairs Manager for Latin America at Merck Life Science, supporting the Process Solutions portfolio used in pharmaceutical and biopharmaceutical manufacturing. He provides regulatory guidance to clients and internal teams, focusing on compliance strategies, regulatory implementation, and advocacy. His work includes engagement with health authorities, regulatory intelligence, organizing scientific events, and delivering technical presentations across the region. With over a decade of experience in regulatory affairs, quality, and technical documentation, Thiago has worked with national and multinational companies such as Cristália, Hypera, and Teva. He holds a Pharmacy degree from Universidade Estadual de Goiás, international academic experience from the University of Salford (UK), and an MBA in Pharmaceutical Industrial Management. Passionate about science, innovation, and public health, he is committed to advancing regulatory excellence in Latin America.

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