Elise Bastian

Elise Bastian has extensive experience in regulatory affairs spanning over 16 years, currently serving as a Senior Regulatory Affairs & CMC Manager in the Development department at SUBSTIPHARM since April 2009. Elise has held multiple roles at SUBSTIPHARM, including US Regulatory Affairs Manager and EU & International Regulatory Affairs Project Manager. Prior to this, Elise worked as a Regulatory Executive on the International Regulatory Affairs Oncology team at GlaxoSmithKline and completed an industrial student placement in European Regulatory Affairs at Ipsen. Academic qualifications include a Master's degree in Drug Development and International Registration from Université Paris XI and an Engineer's Master's degree in Industrial Biology with a specialty in Product Development from École de Biologie Industrielle.