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See Latest ArticlesGenzyme Receives Positive Opinion for European Approval of Mozobil
Genzyme, 06/01/09
Genzyme Corp. announced that the European Medicines Agency's Committee for Human Medicinal Products has adopted a positive opinion on the marketing authorization application for Mozobil. The committee's opinion will be forwarded to the European Commission, which will make a final decision on the authorization. The Commission has 66 calendar days to act on the CHMP's opinion.
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