VWP Conclusions from the Workshop on Co-administration of Vaccines held on 31 Jan-1 Feb 2006
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European Medicines Agency pandemic-influenza crisis management plan for the evaluation and maintenance of pandemic-influenza vaccines and antivirals
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European Union influenza pandemic process map
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Draft guideline on dossier structure and content of marketing authorisation applications for influenza vaccines with avian strains with a pandemic potential for use outside of the core dossier context
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Core summary of product characteristics for pandemic-influenza vaccines - Superseded
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Guideline on procedural aspects regarding a CHMP scientific opinion in the context of cooperation with the World Health Organization for the evaluation of medicinal products intended exclusively for markets outside the C...
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Note for guidance on the clinical evaluation of vaccines
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Guideline on adjuvants in vaccines for human use (see also explanatory note)
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Concept paper on the development of a Committee for Human Medicinal Products (CHMP) revised guideline on clinical evaluation of new vaccines
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Guideline on submission of marketing authorisation applications for pandemic influenza vaccines through the centralised procedure - Superseded
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Draft guideline on dossier structure and content for pandemic influenza vaccine marketing authorisation application (revision) - Superseded
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Draft guideline on adjuvants in vaccines
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Note for guidance on the development of vaccinia virus based vaccines against smallpox
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