{"id":72366,"date":"2021-01-08T16:32:04","date_gmt":"2021-01-08T19:32:04","guid":{"rendered":"http:\/\/jornalbeirario.com.br\/portal\/?p=72366"},"modified":"2021-01-08T16:36:21","modified_gmt":"2021-01-08T19:36:21","slug":"anvisa-confirma-pedidos-de-uso-emergencial-de-vacinas-da-fiocruz-e-do-butantan","status":"publish","type":"post","link":"https:\/\/jornalbeirario.com.br\/portal\/?p=72366","title":{"rendered":"Anvisa confirma pedidos de uso emergencial de vacinas da Fiocruz e do Butantan"},"content":{"rendered":"<p style=\"text-align: justify;\">Horas depois da Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (Anvisa) ter anunciado que recebeu do Instituto Butantan o pedido para o uso emergencial da vacina Coronavac, produzida pelo laborat\u00f3rio chin\u00eas Sinovac, a ag\u00eancia tamb\u00e9m confirmou que recebeu da Funda\u00e7\u00e3o Oswaldo Cruz (Fiocruz), do Rio de Janeiro, na tarde desta sexta-feira, dia 8, o pedido para o uso emergencial da vacina produzida pela Universidade de Oxford, no Reino Unido, em parceria com a empresa anglo-sueca AstraZeneca.<\/p>\n<p style=\"text-align: justify;\">O pedido, de acordo com o instituto carioca, se refere ao uso emergencial de 2 milh\u00f5es de doses de vacinas, que devem ser importadas do laborat\u00f3rio Serum, da \u00cdndia, um dos fabricantes do imunizante.<\/p>\n<p style=\"text-align: justify;\">A Anvisa, em seu comunicado, destaca que &#8220;j\u00e1 iniciou a triagem dos documentos presentes no pedido&#8221;. As primeiras 24 horas ser\u00e3o utilizadas para fazer uma triagem do processo e checar se os documentos necess\u00e1rios est\u00e3o dispon\u00edveis. Se houver informa\u00e7\u00e3o importante faltando, a Anvisa pode solicitar as informa\u00e7\u00f5es adicionais ao laborat\u00f3rio. O prazo de 10 dias n\u00e3o considera o tempo do processo em status de exig\u00eancia t\u00e9cnica.<\/p>\n<p style=\"text-align: justify;\">Ainda de acordo com a nota, a Anvisa vai utilizar em sua avalia\u00e7\u00e3o as informa\u00e7\u00f5es apresentadas junto com o pedido e tamb\u00e9m as informa\u00e7\u00f5es j\u00e1 analisadas pela Anvisa por meio da Submiss\u00e3o Cont\u00ednua. A an\u00e1lise do pedido de uso emergencial \u00e9 feita por uma equipe multidisciplinar, envolve especialistas das \u00e1reas de registro, monitoramento e inspe\u00e7\u00e3o. A equipe vem atuando de forma integrada, com as a\u00e7\u00f5es otimizadas e acompanhadas pela Comiss\u00e3o que envolve tr\u00eas diretorias da Ag\u00eancia.<\/p>\n<p style=\"text-align: justify;\">PEDIDO DO BUTANTAN CONFIRMADO<br \/>\n<a href=\"https:\/\/jornalbeirario.com.br\/portal\/?p=72319\">Quase 24 horas ap\u00f3s o Instituto Butantan anunciar o pedido para o uso emergencial da Coronavac<\/a>, a Anvisa j\u00e1 havia anunciado na manh\u00e3 desta sexta-feira que recebeu a solicita\u00e7\u00e3o do instituto paulista. A triagem dos documentos encaminhados tamb\u00e9m j\u00e1 foi iniciada e a documenta\u00e7\u00e3o passar\u00e1 pela mesma an\u00e1lise do material enviado pela Fiocruz. A previs\u00e3o para a conclus\u00e3o tamb\u00e9m \u00e9 de at\u00e9 10 dias.<\/p>\n<p><em>Foto: Andr\u00e9 Az (CCS\/Fiocruz)<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Horas depois da Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (Anvisa) ter anunciado que recebeu do Instituto Butantan o pedido para o uso emergencial da vacina<\/p>\n","protected":false},"author":1,"featured_media":72374,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"pmpro_default_level":"","footnotes":""},"categories":[227,35,18],"tags":[],"class_list":["post-72366","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-manchete","category-nacional","category-saude","pmpro-has-access"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Anvisa confirma pedidos de uso emergencial de vacinas da Fiocruz e do Butantan - 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