1. European Medicines Agency. Pandemic Influenza A(H1N1)v vaccines authorised via the core dossier procedure. Explanatory note on scientific considerations regarding the licensing of pandemic A(H1N1)v vaccines. EMEA/608259/2009 rev, http://www.ema.europa.eu/pdfs/human/pandemicinfluenza/60825909en.pdf [accessed 18.03.11].
2. European Medicines Agency. Committee for Human Medicinal Products (CHMP) Assessment report for Pandemrix. EMEA/CHMP/619109/2009, http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Assessment_Report_-_Variation/human/000832/WC500095422.pdf [accessed 18.03.11].
3. European Medicines Agency. Committee for Human Medicinal Products (CHMP) Assessment report for Focetria. EMEA/CHMP/503605/2009, http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Public_assessment_report/human/000710/WC500023755.pdf [accessed 18.03.11].
4. European Medicines Agency. Committee for Human Medicinal Products (CHMP) Assessment report for Celvapan. EMEA/CHMP/629184/2009, http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Assessment_Report_-_Variation/human/000982/WC500022669.pdf [accessed 18.03.11].
5. European Medicines Agency. CHMP recommendations for the pharmacovigilance plan as part of the risk management plan to be submitted with the marketing authorisation application for a pandemic influenza vaccine. Revision 1.1 adopted by CHMP on 24 September 2009. EMEA/359381/2009, http://www.ema.europa.eu/pdfs/human/pandemicinfluenza/35938109en.pdf [accessed 18.03.11].