Gaby Danan,
MD, PhD
Pharmacovigilance Expert
Dr. Danan is board qualified in Hepatology and Internal Medicine, and has conducted studies on drug hepatotoxicity and drug-drug interactions, and authored papers on pharmacovigilance definitions and methodologies. He joined the pharmaceutical industry in 1984 and, until his 2010 retirement, was the European Union Qualified Person for Pharmacovigilance for Sanofi. He has served as a member of the Council for International Organizations of Medical Sciences and International Council on Harmonisation Expert Working Groups, especially as the European Federation of Pharmaceutical Industries and Associations Clinical Safety topic leader of E2B. In 1993, he co-published the Roussel Uclaf Causality Assessment Method for drug-induced liver injury. He was elected to the DIA Board of Directors in 2001 and 2004, and chaired the 2010 DIA Annual Meeting. Dr. Danan co-chaired, with the European Medicines Agency, the EudraVigilance Expert Working Group from its inception until 2009. He continues to serve as a pharmacovigilance and risk assessment consultant and as member of the DIA Content Committee for Europe, Middle East, and Africa.
Fellows of DIA
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PhD •Chair, Fellows of DIA
President, Japan Self-Medication Industry -
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JD • President, B-Henry & Associates -
MD, PhD • Pharmacovigilance Expert -
MD • Professor of Clinical Pharmacology, St. Vincent's Hospital -
MBA • President, International Regulatory Affairs Group LLC -
MPH, PhD • Global Chief, Sci Affairs; Sr VP, Head, Center for Advanced Evidence Generation
IQVIA -
PhD • Senior Advisor, Strategic Programs,Center for Drug Evaluation and Research, US Food and Drug Administration -
MD • Senior VP, Chief Medical Officer, Director, Corporate Medical Affairs HQ, Eisai Co., Ltd. -
MBA • Chairman, CISCRP; Director of Sponsored Research, Tufts Center For the Study of Drug Development -
PhD • Corporate Vice President
PAREXEL International -
MD • Senior Vice-President, Industrie Sante -
MD • Deputy Director, FDA Liaison to the EMA, Office of International Programs, OC -
MD • Deputy Director, Integrated Delivery, and Lead for Global Regulatory Systems Initiatives
Bill and Melinda Gates Foundation -
MD, JD • Senior Vice President, Head of Global Regulatory Affairs and Clinical Safety, Merck & Co., Inc. -
MS • Representative, NM Consulting -
PhD • Advisor, Digital Channels and eCapabilities, Eli Lilly and Company -
MD • Chief Medical Officer & EVP, Horizon Pharma, Inc. -
DVM, MBA • Director Biopeople, University of Copenhagen -
PhD • Professor and Director, Institute of Drug Regulatory Science, Shenyang Pharmaceutical University, Venture Partner, Lilly Asia Ventures