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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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Register for our webinar at 11am CEST (Central European Summer Time) learn about 10 most common mistakes made during risk management activities and good practices which helps avoiding such mistakes. The webinar will look at the benefits to manufacturers of proper risk analysis.

To register, complete and submit the online form below and will contact you to finalize your registration. Once finalized, you will receive a confirmation reminder one week before the event.

If you find you cannot attend, you will receive a recording of the webinar.

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