Pharmacovigilance capacity strengthening for WHO prequalification: The case of the trivalent influenza vaccine manufactured by Instituto Butantan

Author:

Koike Marcelo E.ORCID,Gattás Vera L.,Lucchesi Maria Beatriz B.,Moura de Oliveira Mayra M.,Vanni Tazio,Thomé Beatriz da C.,Menang Olga,Socquet Muriel,Precioso Alexander R.ORCID

Funder

U.S. Department of Health and Human Services

Office of the Assistant Secretary for Preparedness and Response

Biomedical Advanced Research and Development Authority

Publisher

Elsevier BV

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Veterinary,General Immunology and Microbiology,Molecular Medicine

Reference16 articles.

1. Influenza vaccine production for Brazil: a classic example of successful North-South bilateral technology transfer;Miyaki;Vaccine,2011

2. Ministério da saúde (BR), Coordenação Geral do Programa Nacional de Imunizações. Informe Técnico: 20a Campanha Nacional de Vacinação Contra a Influenza [Internet]. Brasília (Brasil): Ministério da Saúde; 2018 Abr [cited 2018 Aug 28]. 43p. Available from: http://portalarquivos2.saude.gov.br/images/pdf/2018/abril/18/Informe-Cp-Influenza---01-03-2018-Word-final-28.03.18%20final.pdf.

3. Pandemic potential of a strain of influenza A (H1N1): early findings;Fraser;Science,2009

4. Global vaccine supply. The increasing role of manufacturers from middle income countries;Francis;Vaccine,2014

5. Agência Nacional de Vigilância Sanitária (BR). Resolução n° 4, de 10 de fevereiro de 2009. Dispõe sobre as normas de farmacovigilância para os detentores de registro de medicamentos de uso humano [Directive Resolution n° 4, of February 10th, 2009. Provides the pharmacovigilance regulation for the marketing authorisation holders of medicinal products for human use]. Diário Oficial da União: Seção 1, Brasília, DF, ano 146, n. 29, p. 42-43, 11 mar. 2009.

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