Head Regulatory Development
M.Sc. Biol (1999)
Sanne Elitha Svendsen is Head Regulatory Development and member of the Operational Management team. Sanne has many years of experience from Regulatory Affairs within the pharmaceutical industry. Areas of expertise include Regulatory Strategy (development strategy, submission strategy, response strategy), management of regulatory submissions (MAA, NDA, BLA, renewals, extensions, and variations/supplements) and management of regulatory procedures (Mutual Recognition Procedure, Decentralised Procedure, Centralised Procedure and National Procedures).
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