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(Click the title below to leave the MDLinx Network and go to the Journal's Website)

Cell Therapeutics, Inc. announced that it was notified by the European Medicines Agency that pixantrone is eligible to be submitted for a Marketing Authorization Application through the EMEA's centralized procedure. The centralized review process provides for a single coordinated review for approval of pharmaceutical products that is conducted by the EMEA on behalf of all European Union member states.


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