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  • On-demand Webinar

10 Most Common Mistakes Made During Risk Analysis for Medical Devices According to ISO 14971 2007/(R)2010

Before marketing of electric or electronic medical devices each manufacturer should conduct a risk analysis. If conducted correctly, the analysis will become useful and will support the manufacturer in the control of product related risks.

Two scientists in a lab working

Learn about 10 most common mistakes made during risk management activities and good practices which helps avoiding such mistakes. This on-line webinar looks at the benefits to manufacturers of proper risk analysis.


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