| Literature DB >> 26262044 |
José Augusto Neto1, Jemerson Figueiredo Damásio1, Paul Monthaler1, Misael Morais1.
Abstract
Worldwide medical device embedded software certification practices are currently focused on manufacturing best practices. In Brazil, the national regulatory agency does not hold a local certification process for software-intensive medical devices and admits international certification (e.g. FDA and CE) from local and international industry to operate in the Brazilian health care market. We present here a product-based certification process as a candidate process to support the Brazilian regulatory agency ANVISA in medical device software regulation. Center of Strategic Technology for Healthcare (NUTES) medical device embedded software certification is based on a solid safety quality model and has been tested with reasonable success against the Class I risk device Generic Infusion Pump (GIP).Mesh:
Year: 2015 PMID: 26262044
Source DB: PubMed Journal: Stud Health Technol Inform ISSN: 0926-9630