EU To U.S. Market: Understanding 3 Core Regulatory Contrasts

By Becky Blankenship, Technical Writer, Cannon Quality Group

The expansion of the United States (U.S.) market offers millions of customers access to transformative medical device technologies. Although both the U.S. and European Union (EU) markets are subject to stringent regulations, significant differences in medical device compliance exist that should be carefully evaluated prior to entering the market. Recognizing three key regulatory differences can considerably impact the success of your market entry. Continue reading to explore these three core contrasts.