ISO 14971: Medical Device Risk Management Masterclass
Category: Tutorials
- views: 186
- date: 4 August 2024
- posted by: AD-TEAM

ISO 14971: Medical Device Risk Management Masterclass
Published 7/2024
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz, 2 Ch
Language: English | Duration: 1h 50m | 2.26 GB
Become an expert in ISO 14971 (RM) for medical device. Create p/DFMEA, HAZOP, HACCP document from scratch
What you'll learn
Gain a deep understanding of ISO 14971 standard, including its purpose, scope, key terms, and specific requirements for a compliant RM system
Learn to apply the ISO 14971 risk management process to real medical devices. Master techniques for identifying hazard, analyzing risks, implementing controls.
Develop a comprehensive risk management plan. Learn to create a traceable risk management file to document the entire process
Master the pre-release risk management review. Collect and review information during production and post-prod, adapting and ensuring continuous improvement.
Requirements
No experience or prior curriculum required
More info

https://rapidgator.net/file/15beb8d4030eb3953b6554c9d18e1cab/ISO.14971.Medical.Device.Risk.Management.Masterclass.part1.rar
https://rapidgator.net/file/60bfffbd735b93cd8a7909b72fd71606/ISO.14971.Medical.Device.Risk.Management.Masterclass.part2.rar
https://filestore.me/aq5klijdpujj/ISO.14971.Medical.Device.Risk.Management.Masterclass.part1.rar
https://filestore.me/pgauya0998ft/ISO.14971.Medical.Device.Risk.Management.Masterclass.part2.rar
What you'll learn
Gain a deep understanding of ISO 14971 standard, including its purpose, scope, key terms, and specific requirements for a compliant RM system
Learn to apply the ISO 14971 risk management process to real medical devices. Master techniques for identifying hazard, analyzing risks, implementing controls.
Develop a comprehensive risk management plan. Learn to create a traceable risk management file to document the entire process
Master the pre-release risk management review. Collect and review information during production and post-prod, adapting and ensuring continuous improvement.
Requirements
No experience or prior curriculum required
More info

https://rapidgator.net/file/15beb8d4030eb3953b6554c9d18e1cab/ISO.14971.Medical.Device.Risk.Management.Masterclass.part1.rar
https://rapidgator.net/file/60bfffbd735b93cd8a7909b72fd71606/ISO.14971.Medical.Device.Risk.Management.Masterclass.part2.rar
https://filestore.me/aq5klijdpujj/ISO.14971.Medical.Device.Risk.Management.Masterclass.part1.rar
https://filestore.me/pgauya0998ft/ISO.14971.Medical.Device.Risk.Management.Masterclass.part2.rar
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