risk-analysis, DIN 14971, risk-management, medical-devices
Risko analysis, DIN 14971, Risk management Medical devices, In-Vitro-Diagnostics, IVD DEUTSCH | IMPRINT 26.07.2016 FDA notification, CE-marking, EN 1441 Qware® Riskmanager
risk-analysis, DIN 14971, risk-management, medical-devices
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ISO 9000 implementing of a Risk analysis risk control
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risk management versus Risk analysis documentation
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DIN EN ISO 14971 In-Vitro-Diagnostics CE-marking
FDA authorization CE-marking
Qware® Riskmanager
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Likelihood and severity evaluation after measures
DIN EN ISO 14971:2000
assignment with DIN EN ISO 13485_2003
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 directive 93/42/EWG risk evaluation and for risk control
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In-Vitro-Diagnostics IVD FDA authorization CE-marking

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Qware® Riskmanager
A new version of the market-leading software solution for generating technical documentation for medical devices and in-vitro-diagnostics has been released.
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