Risk Management FAQ
Why do manufacturers need Risk Management?
How is it defined for medical devices? What ISO is applicable?
We have all the answers…
risk management file
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.
