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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.

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THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.

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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