Jenny has comprehensive expertise in Regulatory Affairs with more than 30 years experience. She has in depth experience of preparing and implementing a wide range of regulatory strategies relating to various product types, including drug-device combinations. She has designed and delivered training programmes on a wide range of regulatory matters, including compliance, auditing and CMC data requirements and has undertaken audits of a large number of regulatory departments and CROs on behalf of clients.
Jenny is a member of the Royal Pharmaceutical Society (MRPharmS) and a Fellow of The Organisation for Professionals in Regulatory Affairs (FTOPRA).
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