Vice President, Regulatory and UK Managing Director @ (January 2017 - July 2018)
Director, European Regulatory Affairs @ (October 2015 - January 2017)
Director, European Regulatory Affairs @ (February 2013 - June 2015)
Associate Director, European Regulatory Affairs @ (November 2006 - February 2013)
Senior Manager, European Regulatory Affairs @ (April 2002 - November 2006)
Senior Regulatory Manager @ (January 2001 - January 2002)
Regulatory Affairs Manager @ (January 1999 - January 2001)
Regulatory Associate, UK and Ireland @ Pasteur Merieux (January 1997 - January 1999)
Beth Anderson Education
University of Leicester
BSc (Biological Sciences)
1993-1996
Beth Anderson Skills
Regulatory Affairs
European Union
Regulatory Submissions
Regulatory Documentation
CMC
Medical Devices
eCTD
Clinical Trials
Pharmacovigilance
Pharmaceutical Industry
Regulatory Requirements
GMP
FDA
SOP
Pharmaceutics
GCP
Biotechnology
Drug Development
Strategy
Life Sciences
Electronic Common Technical Document (eCTD)
Good Clinical Practice (GCP)
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
Consulting
Good Clinical Practice Gcp
u.s. Food and Drug Administration Fda
Electronic Common Technical Document Ectd
Standard Operating Procedure Sop
Standard Operating Procedure
Electronic Common Technical Document
Good Clinical Practice
u.s. Food and Drug Administration
Beth Anderson Summary
Beth Anderson, based in Marlow, GB, is currently a Vice President, Head of Global Regulatory at Cencora PharmaLex. Beth Anderson brings experience from previous roles at PharmaLex, Atlas Regulatory Ltd and Regulis Consulting Ltd. Beth Anderson holds a 1993 - 1996 BSc in Biological Sciences @ University of Leicester. With a robust skill set that includes Regulatory Affairs, European Union, Regulatory Submissions, Regulatory Documentation, CMC and more. Beth Anderson has 2 emails on RocketReach.
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