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A STD Med Inc. recebe registro da ANVISA para Equipamentos Médicos Classe III no Brasil
Date:11/8/2012

STOUGHTON, Massachusetts, 8 de novembro de 2012 /PRNewswire/ -- A STD Med, Inc. tem o prazer de anunciar que recebeu o Certificado de Boas Práticas de Fabricação de Equipamentos Médicos Classe III da Agência Nacional de Vigilância Sanitária do Brasil – ANVISA. Todos os equipamentos médicos devem ser registrados na ANVISA antes de serem comercializados no Brasil. O Certificado de Boas Práticas foi concedido depois de uma auditoria intensiva feita pela agência brasileira nas instalações de fabricação da STD Med. Atualmente, esta auditoria tem uma lista de espera de 2 a 3 anos e é um dos principais obstáculos para o registro de novos produtos de equipamentos médicos no Brasil.

Steven Tallarida, Presidente da STD Med Inc. declarou, "A STD Med é uma das melhores fabricantes de médio porte de equipamentos médicos do mercado e esperamos levar os produtos médicos da mesma qualidade dos Estados Unidos para o sistema de cuidados com a saúde da América do Sul". Rafael Martinelli de Oliveira, Presidente da BMR Medical, uma companhia brasileira de comercialização e distribuição de equipamentos médicos também acrescentou, "A STD Med tem sido nossa parceira fabricante desde 2006 e sempre nos forneceu um serviço excepcional e produtos de alta qualidade. Eles entendem o mercado brasileiro e sua disposição e habilidade para atender às exigências locais sempre foi uma prioridade máxima. Um dos resultados deste compromisso para com o mercado brasileiro é o Certificado de Boas Práticas de Manufatura da ANVISA, que nos permitirá lançar novos produtos de maneira mais rápida e eficiente".

A SyncMedical LLC, uma subsidiária da STD Med Inc., se encontra em uma posição única para fornecer ainda mais assistência no estabelecimento de novas e emergent
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SOURCE STD Med
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