Laurie Jullien

PharmD., Master in International Drug Development and Registration. Laurie Jullien started at Genentech (USA) in Product Drug Development and was then appointed Regulatory Affairs Labelling Manager at Roche (UK). She joined Acticor Biotech in 2016 and started as Regulatory and Quality Manager, working from the non-clinical studies to the Phase 1 trial . In 2018 she was appointed Head of Regulatory Affairs and Quality , ensuring the regulatory strategy and the development of the quality policy of the company. From November 2020, she is taking the role of Head of Regulatory Affairs full time, working on the global regulatory strategy and the management of the regulatory department.