2Good manufacturing requirements -- Part 2: Validation
Printed: January 1997
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The Vaccine Supply and Quality Unit of the Global Programme for Vaccines andImmunizationthanks the following donors whose financial support has made the production of this document possible: the World Bank, USAID, JICA, the Rockefeller Founda-tion and the Governments of Australia, China, Republic of Korea, Denmark, Ire-land, Japan, Netherlands, Norway, Sweden, and the United Kingdom of Great Britainand Northern Ireland.
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Global Training Network
is designed for staff of National Control Au-thorities and selected vaccine manufacturers meeting specific entrancecriteria. This document is designed for use by participants in the GlobalTraining Network, specifically for those participating in curricula re-lated to Good Manufacturing Practices.Curricula and curricula material for the Global Training Network havebeen overseen by Expert Review Panels convened at the request of WHOand comprised of experts internationally known for their profi-ciency in the particular field. The Vaccine Supply and Quality Unit wouldlike to particularly thank the experts who reviewed this document andserved on the Expert Review Panel: Dr Ian Sykes, Pharmaceutical Con-sultancy Service, Haastrecht, Netherlands, Dr Chung K Lee, Salk In-stitute, Swiftwater, Pennsylvania, USA, and Ms Carolyn Woodruff,Therapeutic Goods Administration, Melbourne, Victoria, Australia. TheGlobal Training Network is financed in part through funds donated bythe World Bank.