Companies involved in developing medical devices understand the importance of risk management, but their approaches can vary significantly in terms of the time it takes to manage risk, the ability to connect risks to specific requirements and tests, and the capacity to pull together relevant documentation for an audit. To meet these challenges, medical device developers need a comprehensive approach to risk management.
In this presentation, industry and solution experts will explore how teams can integrate risk-based thinking into their product development lifecycle.
Attendees will learn more about:
Risk management in the medical device industry
Guidance and best practices to follow
How to manage risk analysis
The importance of risk traceability throughout project activities
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