Risk Management in Medical Devices Industry is a conference that covers topics such as:
- The requirements of ISO 14971
- The risk management process, the activities, and deliverables as well as the organization framework necessary
- Risk analysis team meetings
- Developing a risk analysis framework document
- How to apply ISO 14971 into development process
- How and where to use the various techniques during the design life cycle
- How Risk Management system fits into quality system and business practices
- How to document your Risk Management
- Performing risk assessments effectively
Risk Management in Medical Devices Industry brings together:
- Risk managers
- Project managers
- Quality Assurance personnel
- Engineering management
- System and design engineers
- Regulatory and Compliance professionals responsible for FDA / notified body interactions
- Usability Engineers
- Software Engineers
- Production Managers
- Verification / validation personnel
