Medical Device Risk Management

Keywords 3-day training course medical devices risk management medical device safety risks medical device
Standards groups

This 3-day training course delivered worldwide provides a comprehensive coverage of topics that are needed for successful management of safety risks of medical devices in conformance with the international standard ISO 14971. The scope of risk management includes both product development, and post market risk management. The course commences with the fundamentals of medical devices risk management, then builds upon the fundamentals, and teaches a practical, sensible and efficient way of performing medical devices risk management. The course includes multiple quizzes and hands-on workshops to deepen the learning, and create an engaging learning experience

Metadata
Document identifier
P1848-007122-1
Date published
2019-05-08
Language
English
Document type
brochure
Pages
2
Defines standard
Replaced/Superseded by document(s)
Cancelled by
Amended by
File MIME type Size (KB) Language Download
PPI-Medical-Device-Risk-Management.pdf application/pdf   215.05 KB English DOWNLOAD!
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Author(s)
Bijan Elahi
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