The Human Factors for Medical Device course will inform attendees of how to streamline their medical device approval process
The course will inform attendees of how to streamline their medical device approval process
The course by AAMI will take place on 6 – 8 October 2015 at the Castleknock Hotel, Ireland.
The course will include representation from the FDA’s office of Device Approvals, information on the process of applying Human Factors Design Controls into medical devices and insights into best ways to go about obtaining pre-market clearances in the USA.
This course is led by Dr Robert North, Dr Edmund Israelski and offers Q&As with Shannon Hoste from the FDA.