ISO 14971 Risk Management in Medical Devices Training
PURPOSE: EN ISO 14971 Risk Management in Medical Devices Training helps define, assess, control risks in the life cycle of a product in medical devices and implement a risk management framework within the framework of continuous compliance.
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Clinical Assessment Training
All medical devices new or old that are introduced to the market within the borders of the European Union must have an up-to-date Clinical Assessment Report as part of their Technical File.
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PMS and Vigilance Training
Active and systematic collection, recording and analysis of data related data concerning the quality, performance and risklessness of a medical device throughout its economic life after it has been introduced into the market, determination...
MoreUDEM Certificate
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