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2020 - Risk Management System in Medical Devices Industry
Date2020-04-02 - 2020-04-03
Deadline2020-03-23
VenueZurich, Switzerland, USA - United States 
KeywordsISO 14971 workshop; ISO 13485; IEC62304
Topics/Call fo Papers
Upon completing this course participants should:
Understand the risk management process, the activities, and deliverables as well as the organization framework necessary
Be able to Interpret and discuss the requirements of ISO 14971
Develop a risk analysis framework document
Be able to conduct risk analysis team meetings
Recognize how and where to use the various techniques during the design life cycle.
Understand how to apply ISO 14971 into development process
Know how to document your Risk Management
Explain how your Risk Management system fits into quality system and business practices.
Perform risk assessments effectively
Understand the risk management process, the activities, and deliverables as well as the organization framework necessary
Be able to Interpret and discuss the requirements of ISO 14971
Develop a risk analysis framework document
Be able to conduct risk analysis team meetings
Recognize how and where to use the various techniques during the design life cycle.
Understand how to apply ISO 14971 into development process
Know how to document your Risk Management
Explain how your Risk Management system fits into quality system and business practices.
Perform risk assessments effectively
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Last modified: 2020-02-11 06:03:07