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Forum on Drug Discovery, Development, and Translation; Board on Health Sciences Policy; Institute of Medicine (IOM); Weisfeld V, Lustig TA, editors. International Regulatory Harmonization Amid Globalization of Drug Development: Workshop Summary. Washington (DC): National Academies Press (US); 2013 Oct 24.

Cover of International Regulatory Harmonization Amid Globalization of Drug Development

International Regulatory Harmonization Amid Globalization of Drug Development: Workshop Summary.

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PLANNING COMMITTEE FOR THE WORKSHOP ON INTERNATIONAL REGULATORY HARMONIZATION AMID GLOBALIZATION OF BIOMEDICAL RESEARCH AND MEDICAL PRODUCT DEVELOPMENT1

  • THOMAS J. BOLLYKY (Co-Chair), Council on Foreign Relations, Washington, DC
  • STEVEN K. GALSON (Co-Chair), Amgen Inc., Thousand Oaks, CA
  • MICHAEL J. BRENAN, Aeras, Rockville, MD
  • RAYMOND CHUA, Singapore Health Sciences Authority
  • HANS-GEORG EICHLER, European Medicines Agency, London, UK
  • JAMES FITZGERALD, Pan American Health Organization, World Health Organization, Washington, DC
  • LYNN D. HUDSON, Critical Path Institute, Tucson, AZ
  • ANDREAS SEITER, World Bank, Washington, DC
  • ALICE E. TILL, PhRMA, Washington, DC
  • MARY LOU VALDEZ, Food and Drug Administration, Silver Spring, MD
  • JANET WOODCOCK, Food and Drug Administration, Rockville, MD

IOM Staff

  • ANNE B. CLAIBORNE, Forum Director
  • TRACY A. LUSTIG, Senior Program Officer
  • REBECCA A. ENGLISH, Associate Program Officer
  • ELIZABETH F. C. TYSON, Research Associate
  • ROBIN GUYSE, Senior Program Assistant
  • ANDREW M. POPE, Director, Board on Health Sciences Policy

Footnotes

1

Institute of Medicine planning committees are solely responsible for organizing the workshop, identifying topics, and choosing speakers. The responsibility for the published workshop summary rests with the workshop rapporteurs and the institution.

Copyright 2013 by the National Academy of Sciences. All rights reserved.
Bookshelf ID: NBK174225

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