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Simbionix nomeia diretora do recém-criado Departamento de Assuntos Regulatórios
  • Latin America - español


News provided by

Simbionix USA Corporation

Apr 05, 2011, 09:00 ET

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CLEVELAND, 5 de abril de 2011 /PRNewswire/ -- A Simbionix USA Corporation, líder mundial em educação médica e produtos para simulação e treinamento para profissionais médicos e do segmento da saúde, tem o prazer de anunciar a nomeação da dra. Yael Friedman para ser a diretora do recém-criado Departamento de Assuntos Regulatórios. A Simbionix tem consolidado sua posição de liderança no mercado de educação e treinamento para o setor de saúde ao expandir suas atividades dentro do mercado clínico, tendo recebido recentemente a autorização do mercado para o uso do software PROcedure Rehearsal Studio (TM), a última palavra em "simulação para paciente específico ".

Com PhD em Biologia e vinte anos de experiência em pesquisa em universidades de primeira linha nos EUA e em Israel, a dra. Friedman está na Simbionix há dez anos como cientista chefe para Projetos Médicos. O profundo conhecimento da dra. Friedman sobre o potencial e as exigências da simulação médica a tem levado a uma longa trajetória de atividades bem-sucedidas no mercado de simulação. Ao trabalhar bem próximo de líderes de opinião, sociedades médicas e associações profissionais para criar produtos de simulação significativos, efetivos e validados cientificamente, seus esforços resultaram na publicação de 130 documentos de validação dos produtos Simbionix, demonstrando e validando seus valores na educação médica. Nos últimos dois anos, a dra. Friedman também assumiu a liderança nas atividades regulatórias da companhia, trafegando com sucesso dentro do processo de obtenção da autorização junto ao FDA 510 (k) para o novo e estimulante software PROcedure Rehearsal Studio (TM) da Simbionix.

"Yael representa os verdadeiros valores da Simbionix, ao criar produtos inovadores que melhoram o cuidado com o paciente e seus resultados, ao mesmo tempo em que respondem às necessidades de simulação deste mercado crescente", disse Gary Zamler, CEO da Simbionix. "Estamos bastante satisfeitos em sermos capazes de levar nossas inovadoras tecnologias de simulação ao mercado clínico e termos criado o Departamento de Assuntos Regulatórios para melhor atender ao mercado, acelerando os futuros produtos do PROcedure Rehearsal Studio (TM) ainda sob desenvolvimento. Segundo o nosso conhecimento, a Simbionix é a única empresa de simulação a receber a autorização do FDA 510 (k) para uma técnica de simulação. Estamos construindo uma experiência bem-sucedida no mercado de treinamento e educação do segmento de cuidado com a saúde e expandindo para criar produtos baseados em simulação assim como para o mercado clínico. Yael é a pessoa ideal para liderar nossas atividades mundiais de Assuntos Regulatórios e também para nos expandirmos dentro do mercado clínico."

Sobre a Simbionix USA Corporation

A Simbionix é a líder mundial em educação médica e produtos para simulação e treinamento para profissionais médicos e do segmento da saúde. Fundada em 1997, a companhia está comprometida a disponibilizar produtos de alta qualidade, desempenho clínico avançado e otimização de resultados de atuação. A Simbionix coopera com médicos regularmente para produzir os mais confiáveis e efetivos sistemas de treinamento e suporte.

Para mais informações sobre a Simbionix, visite http://www.simbionix.com

Contato: [email protected] +1-216-229-2040 ramal 128

FONTE  Simbionix USA Corporation

FONTE Simbionix USA Corporation

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