Published in Healthcare Mergers, Acquisitions and Ventures Week, December 23rd, 2006
The Committee for Medicinal Products for Human Use (CHMP), which reviews drug applications for all 25 countries in the European Union as well as Iceland and Norway, recommended approval of Lucentis. The European Commission generally follows the recommendation of the CHMP, and delivers its final decision within 2 to 3 months.
The positive opinion in Europe...
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