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2021 - Risk Management in Medical Devices Industry
Date2021-03-03 - 2021-03-04
Deadline2021-02-21
VenueVirtual Seminar, USA - United States 
KeywordsISO 14971 workshop; ISO 13485; IEC62366-1/-2
Topics/Call fo Papers
Understand the risk management process, the activities, and deliverables as well as the organizational framework necessary
Be able to Interpret and discuss the requirements of ISO 14971:2019
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 14971:2019 into the development process
Know how to document your Risk Management
Explain how your Risk Management system fits into quality systems and business practices.
Perform risk assessments effectively
Be able to Interpret and discuss the requirements of ISO 14971:2019
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 14971:2019 into the development process
Know how to document your Risk Management
Explain how your Risk Management system fits into quality systems and business practices.
Perform risk assessments effectively
Other CFPs
- Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies
- Regulatory Compliance for Dietary Supplements in the US, EU and Canada
- Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
- Coping with FDA Import Delays, including COVID-19, Expedited Imports and Detentions
- Navigating the Medical Device Post-Market Maze and Challenges during COVID-19 Pandemic - Learn what FDA is really thinking on regulation and guidance documents
Last modified: 2021-02-06 21:25:35