Medical device labeling is considered as important as classifying a product or creating an insulation diagram. In IEC 60601-1, labeling is deemed "a critical component of a medical device." 1 The ...

This week, on June 14, 2016, the FDA issued a final ruling revising its medical device and certain biological product labeling regulations to allow, for the first time, manufacturers to use graphical ...

The Food and Drug Administration issued a final rule Wednesday allowing drug companies to use standalone symbols on medical devices and in-vitro diagnostic labels in conjunction with international ...

A medical device is an umbrella term for any instrument, software, or other article used alone or in combination for a medical purpose in humans. An estimated 2 million different kinds of medical ...

In the highly regulated field of medical device labeling translation, ensuring that every translated word meets both linguistic and regulatory requirements is critical. A company specializing in ...