Beth Anderson

Vice President, Head of Global Regulatory @PharmaLex

Marlow, GB
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Dec 2023 — Present

Vice President, Head of Global Regulatory @PharmaLex

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EDUCATION

1993 — 1996

University of Leicester

BSc, Biological Sciences

SKILLS

Regulatory SubmissionsStandard Operating Procedure (Sop)Regulatory RequirementsPharmacovigilanceGmpPharmaceuticsEctdClinical TrialsMedical DevicesBiotechnologyDrug DevelopmentGood Clinical Practice (Gcp)Electronic Common Technical Document (Ectd)GcpLife SciencesPharmaceutical IndustrySopFdaRegulatory AffairsEuropean UnionCmcStrategyU.s. Food and Drug Administration (Fda)Regulatory Documentation

ABOUT BETH ANDERSON

A versatile and dynamic professional with 25 years’ Regulatory experience gained managing European and Global regulatory projects for leading pharmaceutical manufacturers. Leverages deep knowledge of European requirements for regulatory submissions via National, MRP, DCP, Worksharing and Centralised procedures in order to register and maintain a large and commercially successful portfolio of pharmaceutical products. Operates effectively at all levels, whether defining regulatory strategy, leading and engaging cross-functional teams, or negotiating with Regulatory authorities.

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Beth Anderson — Vice President, Head of Global Regulatory at PharmaLex in Marlow, GB | Unifers