Claudia Liliana Molina Campos is a seasoned professional in regulatory affairs with extensive experience in the pharmaceutical industry. Currently serving as the Regulatory Affairs Manager at Recordati Rare Diseases Colombia since May 2023, Claudia focuses on compliance with regulations related to orphan drugs and biotechnological products. Prior roles include Regulatory Affairs Lead at Zambon, where strategic input and regulatory support were critical for Marketing Authorization Applications and maintaining authorized products, and Senior Regulatory Affairs Analyst at Boehringer Ingelheim, responsible for the registration of veterinary medicines. Claudia has also held positions at MSD, Pfizer, and TOPHARMA, gaining expertise in regulatory processes across various markets. Claudia holds a Master of Business Administration from CESA and a degree in Química Farmacéutica from Universidad Nacional de Colombia.
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