Hostile corporate insiders and external attackers are on the hunt for information, and they have manufacturers in their crosshairs.
UDI compliance can be costly, but it could also enable better customer relationships and improve patient care.
It's been a full year since Abbott closed its $5.3 billion acquisition of Alere, a deal that almost didn't happen.
A look at how one medical device manufacturer automated quality management along with ideas on how shared intelligence can drive quality from the shop floor to the top floor.
There are a number of money-saving and money-making uses for collaborative robots, shares a speaker at the upcoming MD&M Minneapolis conference.
Thanks to a new validation and part process, molders can now replicate transferable plastic conditions that can save millions of a dollars a year and reduce machine downtime.
A simple design that eases use can overcome challenges faced when changing established medical procedures, said a winner of the 2018 Medical Design Excellence Awards.
Medical device executives are most likely on the edge of their seats with the upcoming elections. Not only is a permanent repeal of the medical device excise tax on their minds, but action on other healthcare issues could impact their business.
Cardiovascular disease (CVD) and stroke produce immense health and economic burdens in the United States and globally. Cardiovascular disease includes coronary artery diseases (CAD) such as angina and myocardial infarction. According to the American Heart Association, the Centers for Disease...
An expert lays out how the medtech industry can adapt to Virtual and Augmented Reality changing the healthcare landscape.
The Pacific Research Institute released a new study that points to five core tax principles and how the 2.3% medical device tax violates each.
So, Boston Scientific might have stumbled a bit this year, but it’s worth noting the setbacks are hardly stopping the company from building itself up, through a series of acquisitions, to be an even stronger medtech powerhouse.
The agency is encouraging innovation in digital health. But is software really so fundamentally different from hardware that it can’t be regulated in the same way?
Industry and FDA are working together to promote actual quality improvement, not just compliance to regulations.
Using a prototype to do some informal bench testing will help you write clear and objective design inputs, according to an expert speaking at MD&M Minneapolis.