Vice President, Regulatory Affairs & UK Managing Director
- EU Regulatory
- UK/Ireland Regulatory
- Lifecycle Management
Beth has extensive experience in European Regulatory Affairs gained through a number of positions in the pharmaceutical industry over the past 20 years. She has expertise in a wide range of regulatory activities including development and lifecycle management and a full spectrum of regulatory agency interactions both pre- and post-authorisation.
Prior to joining BlueReg Pharma Consulting, Beth was at Allergan Ltd where her most recent role was EU lifecycle management team leader. In this role she led a team of Regulatory professionals and worked in cross functional teams (CMC, regulatory, medical, labelling and marketing) with responsibility for the lifecycle management of all registered products in the EU region.
While at Allergan, Beth also held positions as the Regulatory Head of the UK/Ireland and Nordic affiliates and Regulatory team leader for ophthalmology and neurology therapeutic teams responsible for development and maintenance projects and has a proven track record with successful EU submissions.
Prior to Allergan, Beth worked for Elan Pharma where she was involved in the registration of a new neurology product via the Centralised procedure. Prior to that, she was part of the UK/Ireland team at Pasteur Merieux MSD responsible for the maintenance of registered products, including the registration of the annual flu vaccine.