Morgane De Verdiere


Morgane joined the European Medicines Agency early 2006 as a Scientific Administrator supporting EMA’s human medicines committee (CHMP). In that role she participated in the first efforts of the Agency to increase transparency initiating the publication of the Committee’s meeting agendas and minutes. In 2013 she pursued her career working to meet the public demand for accessing supporting documents underpinning EMA scientific committees’ assessments. Since 2019 she has headed a team of medical writers who produce information on safe and effective use of medicines for patients, healthcare professionals and the general public at large. Prior to joining EMA, she worked as a regulatory affairs professional in the pharmaceutical industry.