The medical device industry is evolving and expanding with every passing year, with new devices being developed to save lives and treat an array of ailments and health conditions. At the same time, ...

FDA says it is concerned that the lack of standard content and format may translate into increased medical device errors. “Also, there is no single available labeling source for people to view, search ...

Labeling Labeling techniques have undergone many changes since 1979. As a result, the industry has been required to develop new regulations and attitudes toward medical device labels. Dave Olson Dave ...

US regulators plan to launch a new study of medical device labeling in the hopes of determining if a standardized format could help healthcare providers to better understand the risks and benefits of ...

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 ...

The US Food and Drug Administration (FDA) plans to study whether it could standardize device labeling with the use of new content and format standards now under development. At present, there are no ...

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 ...

The Ministry of Health and Family Welfare has mandated medical device manufacturers that outsource sterilisation to disclose the licence number of the facility carrying out the process on the labels ...

The US Food and Drug Administration (FDA) held a 2-day public hearing this week to solicit input about the marketing and use of medications and medical devices for off-label use. It is fairly common ...

WASHINGTON — The federal government is rolling out a consumer labeling system designed to help Americans pick smart devices that are less vulnerable to hacking. Under the voluntary program, called the ...