An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971 - 2011
10 Jan 2011
Webinar
This Integrated Risk Management Approach training in ISO 14971 will discuss how to incorporate risk management as per ISO 14971 in all phases of medical device development and what all documentation to be gathered to support the decisions made as a part of risk management process.
Areas Covered in the Seminar:
How are risk management activities integrated throughout the development process.
The roles that Hazard Analysis, FTA, FMEA, HAZOP and PFMEA play in an Integrated Risk Management Process.
How to control and verify risk mitigations.
How to perform a Risk Benefit Analysis on ALARP and INTOLARABLE Hazards.
The importance of maintaing Risk Management documents in the Post Production era.
What information to include in the Risk Management Plan and Report for better auditability.
Who Will Benefit:
This webinar will provide a methodology that medical device companies can use in establishing a risk management process that is integrated with their product development process. The employees who will benefit include:
Systems engineers responsible for developing requirements
Software developers
Test Engineers
Quality System auditors
Engineering managers and personnel
Regulatory Affairs
Past Events
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971 - 2011 - 10 Jan 2011, Webinar (8987)
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971 2026
Important
Please, check "An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971" official website for possible changes, before making any traveling arrangements
