The Application of an Integrated Product Development Process to the Design of Medical Equipment

Author:

Canciglieri Junior Osiris,Okumura Maria Lucia Miyake,Young Robert Ian Marr

Publisher

Springer International Publishing

Reference57 articles.

1. ANVISA—Brazilian Health Surveillance Agency (in portuguese: Agência Nacional de Vigilância Sanitária), 2010. Resolução RDC n° 02, de 25 de Janeiro de 2010. Dispõe sobre o gerenciamento de tecnologias em saúde em estabelecimentos de saúde. Brasília. http://wwwbrasilsus.com.br/legislacoes/anvisa/102722-2.html . Accessed 15 Aug 2013

2. WHO, World Health Organization (2003) Medical device regulations: global overview and guiding principles. WHO, France

3. FDA, Food and Drug Administration (2013) Medical device: classify your medical device. http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Overview/ClassifyYourDevice/ . Accessed 10 Aug 2013

4. WHO, World Health Organization (2010) Medical devices: managing the mismatch: an outcome of the priority medical devices project. WHO Press, Geneva

5. Calil SJ, Teixeira MS (1998) Gerenciamento de manutenção de equipamentos hospitalares (Série Saúde & Cidadania, vol 11). São Paulo: Faculdade de Saúde Pública da Universidade de São Paulo

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