Melissa Larsen

Melissa Larsen is a seasoned professional in regulatory affairs with extensive experience in the pharmaceutical industry. Currently serving as a Senior Regulatory Affairs Specialist at MSD Belgium since June 2023, Melissa manages regulatory activities related to product lifecycle management and maintains crucial relationships with external agencies. Previous roles include QP/RP Expert at Q-support, where responsibilities included inspection readiness and quality management improvements, and Regulatory Affairs Manager at Flen Health, overseeing an international team and product submissions. Melissa has also contributed to various projects as a consultant and has held positions in major companies such as Pfizer and Zoetis. Melissa holds multiple degrees in pharmacy and drug development from Katholieke Universiteit Leuven.