RESOLUÇÃO-RE nº 1.832, de 12 de julho de 2018
Data de publicação | 16 Julho 2018 |
Data | 12 Julho 2018 |
Páginas | 8-8 |
Órgão | Suplemento ANVISA,Agência Nacional de Vigilância Sanitária,Diretoria de Autorização e Registro Sanitários,Gerência-Geral de Medicamentos e Produtos Biológicos |
RESOLUÇÃO-RE nº 1.832, de 12 de julho de 2018
O Gerente-Geral de Medicamentos e Produtos Biológicos no uso das atribuições que lhe foram conferidas pela Portaria nº 390, de 23 de março de 2018, aliado ao disposto no art. 54, I, § 1º do Regimento Interno aprovado nos termos do Anexo I da Resolução da Diretoria Colegiada - RDC nº 61, de 3 de fevereiro de 2016, resolve:
Art. 1º Conceder a revalidação automática do registro dos medicamentos similares, genéricos, novos, específicos, dinamizados, fitoterápicos, biológicos sob o nº. de processos constantes do anexo desta Resolução, nos termos do § 6º do art. 12 da Lei nº. 6.360, de 1976.
Art. 2º A revalidação abrange os pedidos que ainda não foram objetos de qualquer manifestação por parte da Anvisa.
Parágrafo único. Não constam do anexo desta Resolução os expedientes protocolados fora do prazo estabelecido nos termos da Lei nº. 6360, de 1976.
Art. 3º A revalidação automática não impedirá a continuação da análise da petição de renovação de registro requerida, podendo a Administração, se for o caso, indeferir o pedido de renovação e cancelar o registro que tenha sido automaticamente revalidado, ou ratificá-lo deferindo o pedido de renovação.
Art. 4º Os medicamentos revalidados podem ser consultados, assim como suas...
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