For people with food sensitivities, dining out can be a hassle at best and dangerous at worst. But soon, a new portable ...
13don MSN
Seahawks test tactile device from Seattle startup that helps vision-impaired fans follow game action
A fan uses a OneCourt device while watching the Seattle Seahawks at Lumen Field. (Seahawks Photo) The Seattle Seahawks gave ...
Zacks Investment Research on MSN
OraSure files for FDA review of molecular self-test & Colli-Pee device
OraSure TechnologiesOSUR recently announced that it submitted two applications to the FDA seeking approval for its two new at ...
In September 2015, Dr. Dena Marrinucci set out to perfect a tabletop device that could rapidly test a small amount of blood, returning results for more than 30 routine tests in under 30 minutes. If ...
As the Internet of Things in all its manifestations continues to roll out, developers will need a variety of test strategies to ensure low power consumption, suitable RF performance, and even audio ...
The California Air Resources Board (CARB) has certified only one telematics provider to participate in its Clean Truck Check (CTC) program with just over a quarter of the year left before heavy- and ...
Medical device manufacturers use cytotoxicity testing to help prove that devices that come into contact with the human body are biocompatible. Testing results are critical for gaining market access, ...
Developing test systems for R&D through production requires a combination of preparedness and ongoing evaluation. In order to carry out these tasks, the required systems must be capable of performing ...
When it comes to semiconductor device testing, the primary goal is to ensure that each device meets functional and performance specifications. Testing also plays a crucial role in confirming that ...
Please provide your email address to receive an email when new articles are posted on . The FDA granted breakthrough device designation to Quest Diagnostics’ Haystack MRD test for identifying patients ...
Results are detected within just a few minutes, the agency said. The Food and Drug Administration has granted emergency use authorization for a COVID-19 test that uses breath samples -- the first of ...
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