Meeting highlights from the Committee for Medicinal Products for Human Use, 18-21 February 2008

摘要

The European Medicines Agency's (EMEA) Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending the granting of a marketing authorisation for the first pre-pandemic influenza vaccine, Prepandrix (split inactivated, adjuvanted, H5N1 influenza vaccine containing antigens from A/VietNam/1194/2004 NIBRG-14), from GlaxoSmithKline Biologicals S.A.