Abstract
This paper provides an overview of the Canadian Medical Device Regulations and focuses on those requirements that may impact on human factors and ergonomic issues. Additionally, the paper provides examples of specific incidents with medical devices that occurred in Canada where ergonomic and human factor issues were directly responsible for the problem.
Full Text
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call