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Human factors principles and practices are playing an increasingly important role in medical device design as manufacturers recognise the range of benefits. In this interview Dr. Edmond W Israelski, Director, Human Factors, Abbott Quality and Regulatory, Abbott, joins Andrea Charles from Pharma IQ, to discuss what will top AAMI’s Human Factors subcommittee agenda in 2011 -2012, the impact of the latest standard ANSI/AAMI HE75:2009 and what is next for medical device design. Israelski also shares his top tip for successfully applying human factors in design controls during the design of a medical devices and how to avoid common pitfalls in design.