“The EU approach to deadlines regarding alternative methods: the Commission’s support activities for 3Rs”
Georgette Lalis
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“The ECVAM’s Business Plan: Realistic approach to deal with the upcoming dead-line challenge”
Elke Anklam
European Commission
Joint Research Centre
Institute for Health and Consumer Protection
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“The Challenge of the Cosmetics Directive 2009 deadline: what do we have ?”
Odile de Silva
Chair of the Colipa Research Committee
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“Improved REACH implementation using new science based tools?”
Gernot Klotz
CEFIC Executive Director for Research & Innovation
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“REACH challenge: can ECHA deal with it?”
Dr. Erwin Annys
CEFIC
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“Replacing Animal Tests – Do Other Continents do it Better?”
Emily McIvor
EU Director
Humane Society International
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“Outline for the revision of Dir 86/609/EEC”
Susanna Louhimies
European Commission – DG Environment
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“Molecular imaging in vitro and in vivo”
Tony Lahoutte, MD PhD
Vrije Universiteit Brussel
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“MicroRNAs: novel players in skin research”
Andor Pivarcsi
KI, Department of Medicine, Unit of Dermatology and Venerology
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“The human Artificial Lymph Node: A Model for Immunofunctional and Immunotoxicological Testing in vitro”
Dr. Christoph Giese,
ProBioGen AG
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“Realistic Basis for Implementation of Legislation and Alternative Methods?! (And what to do next?)”
Dr. Bernward Garthoff
Bayer AG,
ecopa-Treasurer,
EPAA Co-Chair Industry
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“CarcinoGENOMICS: questionnaire and workshop in checking regulator’s role”
Coenraad Hendriksen, Marjolein van Boxel & Arthur van Iersel
Netherlands Vaccine Institute (NVI) & Netherlands Centre Alternatives to Animal Use (NCA), Utrecht University
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“Necessity of regulators and authorities’ input into FP-projects such as carcinoGENOMICS”
Jos Kleinjans
Dept. of Health Risk Analysis & Toxicology
Maastricht University, the Netherlands
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“What can be done from regulatory side?”
Dr. Sonja Beken
Non-Clinical Assessor, Registration Department
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ecopa: Financial Status
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ecopa: Business Matters
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ecopa: Activities 2008, Future activities 2009
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