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EU Evaluation Of FDA District Offices Under MRA To Begin By Feb. 2001

This article was originally published in The Tan Sheet

Executive Summary

FDA expects European regulators to begin assessing agency district offices in the next six to eight months, Office of Regulatory Affairs Regional Director Deborah Ralston told a June 5 Food & Drug Law Institute meeting in Washington, D.C.

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International Harmonization Should Focus On Post-Marketing Activities - HRG

International harmonization efforts should include an emphasis on post-marketing activities, Public Citizen's Health Research Group Deputy Director Peter Lurie, MD, commented at an FDA public meeting on the future of the International Conference on Harmonization May 16.

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