Peggy Cance has a wealth of experience in regulatory affairs, drug development, and scientific writing. From their time at Alhena Consult as President & consultant to their positions at BlueReg Pharma Consulting and EUDRAC France, Peggy has showcased their skills across multiple domains, emphasizing a client-centric and goal-oriented approach. With a focus on development and registration strategies for Europe, including Orphan Drugs and Pediatric plans, Peggy has a strong background in clinical trial applications and dossier compilation. Their career at Allergan also highlights their expertise in regulatory affairs and clinical data analysis.
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