The Risk Management in Medical Devices Industry 2019 is a seminar that covers topics such as:
- Risk Management to ISO 14971:2012
- Introduction into Risk Management and Quality System Integration
- Safety / Assurance case
- Software Risk Management (IEC62304 / FDA software reviewers` guidance):
The Risk Management in Medical Devices Industry 2019 brings together:
- Quality Professionals
- Senior Quality Managers
- Compliance Professionals
- Regulatory Professionals
- Design Engineers
- Project Managers
- Process Owners
- Software Engineers