Annex C. EURL ECVAM GIVIMP meeting 24-25 February 2015 - participating experts

Maria Astridou

EFSA, Parma, Italy

Camilla Bernasconi

EURL ECVAM, Ispra, Italy

Gerard Bowe

EURL ECVAM, Ispra, Italy

Ann-Charlotte Bostroem

EURL ECVAM, Ispra, Italy

Sandra Coecke

EURL ECVAM, Ispra, Italy

Thomas Cole

EURL ECVAM, Ispra, Italy

Rita Cortvrindt

Vito, Mol, Belgium

Laureano Cuevas

Centro Nacional de Microbiologia, Majadahonda, Spain

Agnieszka Dudra

Bureau for Chemical Substances, Lodz, Poland

Eugene Elmore

University of California Irvine, Trabuco Canyon, Unites States

Chantra Eskes

SeCAM, Magliaso, Switzerland

Varvara Gouliarmou

EURL ECVAM, Ispra, Italy

Andrew Gray

United Kingdom GLP Monitoring Authority, The MHRA Medicines and Healthcare, London, United Kingdom

John Harbell

JHarbell Consulting LCC, Dallas, United States

Minne Heringa

RIVM, The National Institute for Public Health and the Environment, Centre for Safety of Substances and Products, Bilthoven, The Netherlands

Delyan Ivanov

University of Nottingham, Cancer Biology Queens Medical Centre, Nottingham, United Kingdom

Rob Jaspers

Health Care Inspectorate, The Netherlands

Ingrid Langezaal

EURL ECVAM, Ispra, Italy

Marcel Leist

University of Konstanz, Konstanz, Germany

Thomas Lucotte

ANSM, Inspectorate Department, Saint-Denis, France

Marisa Meloni

Vitroscreen SRL, Milano, Italy

Maurits-Jan Prinz

European Commission, Directorate General Internal Market, Industry, Entrepreneurship and SMEs, Brussels, Belgium

Vittorio Reina,

EURL ECVAM, Ispra, Italy

Glyn N Stacey

United Kingdom Stem Cell Bank, Advanced Therapies Division, NIBSC, United Kingdom

Emanuela Testai

Istituto Superiore di Sanita, Rome, Italy

Frederique van Acker

TNO Triskelion, Zeist, The Netherlands

Iwona Wilk-Zasadna

Novartis Vaccines, Basel, Switzerland.

Maria-Chiara Zorzoli

EURL ECVAM, Ispra, Italy

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