U.S. and EU regulators require human factors and usability testing to bring a medical device to market. Virginia Lang, PhD, president and chief scientist at HirLan Inc., an engineering consultancy ...

The US Food and Drug Administration (FDA) has finalized a revised draft guidance from 2022 on what human factors (HF) information sponsors should include in premarket submissions for medical devices.

Source: Ron Lach / Pexels According to the research, birth rates have steeply declined around the world over the past 15 years—one clear sign that people are spending less time connecting in person.