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Immunogenicity data from the 1st vaccination in adults will end up being submitted to the European Medicines Company within days. The current dosing timetable, as specified in the EMEA mock-up licensure for CELVAPAN using another virus stress, demands two 7. Baxter expects the info from the trial of healthful adults to point whether an individual dose may be easy for CELVAPAN H1N1. This research will determine whether a lesser dose also, 3.. Baxter receives advertising authorization for CELVAPAN H1N1 pandemic influenza vaccine Baxter International Inc.