Understanding Risk Management in Medical Devices 2011 is a webinar that covers topics such as:
- Risk Management Process
- FDA and ISO 14971
- Risk Evaluation
- Risk Analysis
- Overall Residual Risk Evaluation
- Risk Control
- Production and Post-Production
Understanding Risk Management in Medical Devices brings together Quality Engineers, Quality Manager, Internal and external auditors, Product Developers, FDA inspectors, Management Reps and Consultants.
