Fabienne Herbrecht, PhD
Director, Clinical Development
Dr Herbrecht has over 25 years of experience in the Human and Veterinary Pharmaceutical Industry, working in three main areas: clinical development, quality assurance and regulatory affairs. Dr Herbrecht started her career in 1993 as a CRA in a CRO (FDM Pharma) where she monitored clinical trials, and then as logistical coordinator for the outsourced CRAs. In 1995 she joined the Clinical Development Department of Theramex as a CRA (clinical project managers support, investigators follow-up, contact person for clinical trial management). From 2001, she worked as a QA Officer at Manufacturing perimeter at Teva Pharmaceuticals (maintenance of quality documentation, support to QC and manufacturing teams, audits, non-conformities follow up). Then, from 2006, she took the position of Regulatory Affairs Manager (MA maintenance and geoextension, regulatory strategy, management of answers to health authorities). From 2015, she joined Virbac and acted as Life Cycle Manager of veterinary biological products (pet vaccines) (CMC writing , technical support for affiliates, compliance activities). Over the past 14 years, she has developed an expertise in EU as well as international pharmaceutical regulations in therapeutic areas such as gynaecology, dermatology and, more recently, pet vaccines, by contributing to the writing and maintenance of analytical and production part of Marketing Authorization dossiers.