Risk Management FAQ
Why do manufacturers need Risk Management?
How is it defined for medical devices? What ISO is applicable?
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risk management report
Risk Management
Risk management in the medtech industry extends beyond product development and manufacturing to become an integral part of your product’s life cycle. Clin-r+ looks at how ISO 14971:2019 specifies the international requirements for medical device risk management systems, as well as best practices for the device’s entire life cycle.