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Nathalie FRONTCZAK

Lyon

En résumé

Veterinarian in the pharmaceutical industry for over 20 years, I have successfully managed various activities. I have an extensive experience in regulatory affairs and pharmacovigilance. I organize and prioritize workload effectively and work quickly and effectively even under pressure. Flexible and adaptable to change, I work independently or in a team environment, with strong quantitative and analytical skills.

Mes compétences :
Industrie pharmaceutique
Santé animale
Vétérinaire
Pharmacovigilance
Essais cliniques
Affaires réglementaires

Entreprises

  • Merial - EMEA PV Manager/QPPV

    Lyon 2015 - 2020 Manage the activities of pharmacovigilance for EMEA region and conduct a continuous evaluation of the benefits and the risks of the products during the post-authorization period.
    Manage a team of four people (two veterinarians and two specialists).

  • Virbac - Europe Pharmacovigilance Manager, QPPV Deputy

    Carros 2013 - 2015 Manage the activities of pharmacovigilance reports, participate in signal detection and promote the development of technical expertise for the evaluation of the risk / benefit ratio of the products. Manage the documentation and compliance of the department.
    Manage a team of three people (two veterinarians and one technician).

  • Audevard - Regulatory Affairs Director, Qualified Person

    Clichy 2012 - 2013 Maintain the pharmaceutical establishment and the marketing authorizations of veterinary medicinal products (VMP) and biocidal products in Europe.
    Maintain nutritional products by supporting studies and scientific reports.

  • AB Science - International Clinical and Regulatory Affairs Manager

    2010 - 2012 Manage phase II and III clinical trials in oncology, in compliance with ICH-GCP and according to the legislation in the concerned countries.
    Manage a “scientific advice" dossier for a VMP and act as PV manager.

  • Vetoquinol - Project Manager

    Lure cedex 2007 - 2009 Manage a portfolio of fifteen projects in cardiology, nephrology, pain-inflammation and infectious diseases (VMP and nutraceutical products).

  • Vetoquinol - Group Technical Manager

    Lure cedex 2002 - 2007 Develop scientific information for VMP and nutraceutical products. Manage an international clinical study plan (15 post-marketing clinical trials).

  • Vetoquinol - International Regulatory Manager and Pharmacovigilance Manager

    Lure cedex 1999 - 2002 International Regulatory Affairs Manager and PV manager.

Formations

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