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Procedure for assessing the acceptability, in principle, of vaccines ...

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Acknowledgments<br />

Acknowledgements are due to <strong>the</strong> follow<strong>in</strong>g experts and organizations <strong>for</strong> <strong>the</strong>ir<br />

comments on <strong>the</strong> draft <strong>of</strong> <strong>Procedure</strong> <strong>for</strong> <strong>assess<strong>in</strong>g</strong> <strong>the</strong> <strong>acceptability</strong>, <strong>in</strong> pr<strong>in</strong>ciple, <strong>of</strong><br />

vacc<strong>in</strong>es <strong>for</strong> purchase by United Nations agencies (revision 2010): First draft -<br />

Agence Française de Sécurité Sanitaire de Produits de Santé, France; BioMangu<strong>in</strong>hos,<br />

Oswaldo Cruz Foundation, Brazil; Center <strong>for</strong> Biologics Evaluation and Research, US<br />

Food and Drug Adm<strong>in</strong>istration, USA; Mr RD Morales, Centro Control Estatal de la<br />

Calidad de los Medicamentos, Havana, Cuba; European Medic<strong>in</strong>es Agency, London,<br />

England; Dr M Eisenhawer, Swiss Agency <strong>for</strong> Therapeutic Products Inspectorates,<br />

Bern, Switzerland; Dr I Feavers, National Institute <strong>for</strong> Biological Standards and<br />

Control, Potters Bar, England; Dr M Ferguson, Independent, Norfolk, England; Dr J<br />

Fournier-Caruana, World Health Organization, Geneva, Switzerland;<br />

GlaxoSmithKl<strong>in</strong>e Biologicals, Belgium; International Federation <strong>of</strong> Pharmaceutical<br />

Manufacturers and Associations, Switzerland; Dr S Lambert, World Health<br />

Organization, Geneva, Switzerland; Dr V Maqueda, Independent, Buenos Aires,<br />

Argent<strong>in</strong>a; Dr J McEwen, Therapeutic Goods Adm<strong>in</strong>istration, Woden ACT, Australia;<br />

Dr J Milstien, University <strong>of</strong> Maryland, Maryland, USA; Agency <strong>of</strong> Food and Drug<br />

Control, Indonesia; National Regulatory Authority, Iran; Dr C Nelson, Independent,<br />

Pensylvania, USA; Panacea Biotec Limited, India; Serum Institute <strong>of</strong> India, India;<br />

UNICEF Supply Division, Denmark. Second draft - Agence Française de Sécurité<br />

Sanitaire de Produits de Santé, France; BioFarma, Indonesia; Biologicals E. Limited,<br />

India; BioMangu<strong>in</strong>hos, Oswaldo Cruz Foundation, Brazil; Crucell, Switzerland;<br />

Federal State Unitary Enterprise <strong>of</strong> Chumakov Institute <strong>of</strong> Poliomyelitis and Viral<br />

Encephalitides, Russian Federation; GAVI Alliance, Switzerland; GlaxoSmithKl<strong>in</strong>e<br />

Biologicals, Belgium; GreenCross Corporation, Republic <strong>of</strong> Korea; Japan BCG<br />

Laboratory, Japan; Dr H Langar, WHO Regional Office <strong>for</strong> <strong>the</strong> Eastern Mediterranean,<br />

Cairo, Egypt; Novartis, Italy; Panacea Biotec Limited, India; Dr D Pfeifer, WHO<br />

Regional Office <strong>for</strong> Europe, Copenhagen Denmark; San<strong>of</strong>i Pasteur, France; Serum<br />

Institute <strong>of</strong> India, India; UNICEF Supply Division, Denmark.<br />

43

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