Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency - Chicago

Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency - Chicago is hosted by Complianceonline which will be held during September 8th - 9th, 2016 at Chicago, Illinois, United States of America.

Learning Objectives:

Upon completion of the course, the participants will have learned how to implement good risk management principles into medical products manufacturing operations such as medical devices, combination products, and pharmaceuticals:

1. Understand what are the current issues and recommended solutions
2. How to implement the ISO 14971 framework
3. Use a Traceability Report for improved risk management operations
4. How to Use Standards to Facilitate Product-to-Market Achievements
5. How to Use Risk Management to Identify the Critical Success Factors
6. Key implementation issues related to Risk Management
7. Using Risk Management to identify key opportunities for the organization
8. Risk Integration Issues, especially related to the Quality System and Design Controls
9. Use of appropriate risk management tools beyond FMEA