Milagros Ramos Rueda

Milagros Ramos Rueda is an experienced Regulatory Affairs professional with a diverse background in the pharmaceutical and clinical research sectors. Currently serving as Regulatory Affairs Manager for the Early Access Program at Bionical Emas, Milagros is responsible for developing regulatory strategies, managing submissions to local authorities, and providing guidance to clients. Previously, Milagros held various regulatory roles at ProductLife Group, including responsibilities for the Spanish market and coordination for Latin America. Additional experience includes positions at Galderma, Boehringer Ingelheim, and Merck, focusing on regulatory compliance, scientific advising, clinical trial coordination, and training. Milagros holds a specialist degree in Quality Assurance and a pharmacy degree, with ongoing professional education in sanitary regulation.