Louise Blythe
Head of Regulatory and Scientific Affairs
Management
Emd Serono
Canada
Biography
As a seasoned regulatory affairs executive with over 18 years of experience in the pharmaceutical industry, Louise Blythe brings a wealth of expertise to her work with EMD Serono.Louise joined EMD Serono in 2016 as Head of Regulatory and Scientific Affairs. In this role, she provides overall leadership and direction to Regulatory Affairs for EMD Serono's full line of investigational and marketed products and devices in Canada. As a member of the local Leadership Team, Louise provides representation for Regulatory Affairs, Drug Safety (Pharmacovigilance) and Quality Operations.Prior to joining EMD Serono, Louise served as Director of Regulatory Affairs, Quality Assurance & Drug Safety at Forest Laboratories Canada, where she was instrumental in establishing Forest Laboratories' Canadian subsidiary and building the Regulatory and Quality Assurance department. She has also held various positions within Regulatory Affairs at AstraZeneca Canada, including Head of Strategic Product Development & Lifecycle Management, and was the Vice President, Global Regulatory Affairs at Cipher Pharmaceuticals.Louise holds a Master of Science degree in Pharmacology from the University of Toronto and a Bachelor of Science degree (with honours) from Queen's University (Kingston, Ontario).
Research Interest
Regulatory and Scientific Affairs.
