Suzanne provides support to SFL clients for the development, registration and maintenance of medicinal products for European, Swiss and US territories. She defines regulatory strategy, coordinates projects, and implements regulatory support throughout the product lifecycle. Suzanne collaborates with multidisciplinary, international and cross-cultural teams by serving as the project manager and primary contact for clients. She has excellent contacts with Regulatory Authorities with whom she has established long-term relationships on a variety of procedures.
Suzanne has overseen a wealth of regulatory activities throughout the lifecycle of medicinal products and worked on numerous projects including small molecules, plasma-derived and recombinant biologicals. She has extensive knowledge of regulatory procedures and is experienced in writing, reviewing and assembling high quality regulatory documents, from strategic planning and gap analyses to MAA & variation filing, including paediatric investigational plans, orphan drug designations, scientific advice and pre-submission meetings.
Before joining SFL, Suzanne was a Scientific Consultant for 17 years in a consultancy company. She holds a PhD in Pharmaceutical Sciences from the University of Geneva. Suzanne’s thesis was on a slow-release formulation for intraocular administration and was awarded the Dissertation Prize from the Swiss Society of Industrial Pharmacists. Subsequently, she took up a postdoctoral fellowship at the INSERM in Paris.
SFL Regulatory Affairs & Scientific Communication Ltd.