Add an eventCASE STUDY: Implementation of Risk Management for the Whole Life Cycle of Medical Devices
A session at 2nd Annual Software Design for Medical Devices Europe
- Defining roles, responsibilities and activities in the whole Product Risk Management Process
- Carefully documenting Risk Management Activities
- Collecting and validating hazards: techniques and best practices
- Effective handling of production and post-production information
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2nd Annual Software Design for Medical Devices Europe
31st January to 2nd February 2012