08-04-2024, 11:32 AM
![[Image: 0190d4ac5e390a5c352d406db62946da.jpg]](https://i123.fastpic.org/big/2024/0804/da/0190d4ac5e390a5c352d406db62946da.jpg)
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
![[Image: rwamgY8Q_o.jpg]](https://images2.imgbox.com/0c/00/rwamgY8Q_o.jpg)
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
[To see links please register or login]
![[Image: signature.png]](https://softwarez.info/images/avsg/signature.png)
