In late September MHRA released new guidelines on human factors safety considerations and design principles that can help make medical devices "more pleasing” for users. As the Regulatory Affairs Professionals Society noted, these guidelines offer valuable insight on regulators′ perspectives concerning combination product instructions and how to continually improve the user interface in the long term.
Are you fully familiarized with these new guidelines? How can you use them to update your own human factors design techniques? The 3rd Human Factors Engineering & Usability Studies Summit(February 12-13, San Francisco) offers unequaled depth in education and networking about regulatory compliance for medical devices and combination products!
