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Delegations from countries in the Middle East, Africa, Russia and the former Soviet Republics will spend two weeks, from June 17 to 28, 2013, at USP headquarters learning about USP processes and standards-setting activities for chemical and biological medicines, as well for herbal medicines, dietary supplements, and foods.
“Public standards are critically important to help ensure the quality of all medicines,” said Roger L. Williams, M.D., chief executive officer of USP. “The International Training Program is a unique opportunity not only for countries interested in improving their health systems and regulatory framework, but also for USP to expand its understanding of regulatory and compendial issues from an international perspective.”
The program includes speakers from the U.S. Food and Drug Administration, the National Institutes of Health Office of Dietary Supplements, and USP. Speakers will address enforcement and scientific aspects of implementing public standards, and how the global market is influencing the regulation of medicines and dietary supplements, as well as healthcare quality and safety, quality assurance, and global health programs.
“With manufacture and commercialization increasingly crossing borders in the international landscape, it is important to consider the need to exchange information with other regulatory and scientific organizations around the globe,” said Fahad Ibrahim Al-Jenoobi, Ph.D., executive director for the Product Evaluation and Standards Setting division of the Saudi Food and Drug Authority. “USP is one step ahead in contributing to improving health systems by providing the opportunity to openly discuss the issues involved in supplying good quality medicines.”
USP started the ITP in 2012 to foster information exchange among medicines control authorities around the world. For more information about the program and an agenda of events, visit: http://uspgo.to/USP-ITP.
