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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Tatsuo Kurokawa,
PhD •Chair, Fellows of DIA
President, Japan Self-Medication Industry -
Martin Harvey Allchurch • Principal International Affairs Officer, European Medicines Agency, European Union
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Minnie Baylor-Henry,
JD • President, B-Henry & Associates -
Gaby Danan,
MD, PhD • Pharmacovigilance Expert -
Richard Day,
MD • Professor of Clinical Pharmacology, St. Vincent's Hospital -
Marie Dray,
MBA • President, International Regulatory Affairs Group LLC -
Nancy A. Dreyer,
MPH, PhD • Global Chief, Sci Affairs; Sr VP, Head, Center for Advanced Evidence Generation
IQVIA -
Ron Fitzmartin,
PhD • Senior Advisor, Strategic Programs,Center for Drug Evaluation and Research, US Food and Drug Administration -
E. Stewart Geary,
MD • Senior VP, Chief Medical Officer, Director, Corporate Medical Affairs HQ, Eisai Co., Ltd. -
Ken Getz,
MBA • Chairman, CISCRP; Director of Sponsored Research, Tufts Center For the Study of Drug Development -
Alberto Grignolo,
PhD • Corporate Vice President
PAREXEL International -
Yves Juillet,
MD • Senior Vice-President, Industrie Sante -
Sandra L. Kweder,
MD • Deputy Director, FDA Liaison to the EMA, Office of International Programs, OC -
Murray M. Lumpkin,
MD • Deputy Director, Integrated Delivery, and Lead for Global Regulatory Systems Initiatives
Bill and Melinda Gates Foundation -
Sandra A. Milligan,
MD, JD • Senior Vice President, Head of Global Regulatory Affairs and Clinical Safety, Merck & Co., Inc. -
Noriaki Murao,
MS • Representative, NM Consulting -
Jennifer Riggins,
PhD • Advisor, Digital Channels and eCapabilities, Eli Lilly and Company -
Jeffrey Sherman,
MD • Chief Medical Officer & EVP, Horizon Pharma, Inc. -
Per Spindler,
DVM, MBA • Director Biopeople, University of Copenhagen -
Ling Su,
PhD • Professor and Director, Institute of Drug Regulatory Science, Shenyang Pharmaceutical University, Venture Partner, Lilly Asia Ventures