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Organon Orgaran Stroke Study Cited For Lack of Proper Monitoring By FDA

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Executive Summary

An Organon-sponsored ischemic stroke study for its low molecular weight heparin product Orgaran has been cited for lack of supervision and monitoring by FDA's Bioresearch Monitoring Program.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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