Philips announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the DigitalDiagnost C90, its newest premium digital radiography (DR) system. Designed to increase patient throughput and decrease the time to diagnosis, the Philips DigitalDiagnost C90...

As part of a federal spending bill passed late Friday, Congress directed the U.S. Food and Drug Administration (FDA) to establish a national minimum standard for including fibroglandular breast density information on mammography reports. While 36 states have already enacted their own breast...

Below are photos from the Healthcare Information Management and Systems Society (HIMSS) 2019 meeting Feb. 11-16 in Orlando, Florida. The conference has about 45,000 attendees and more than 1,300 vendors across a vast show floor.

The value companies place on collaboration was palpable on the floor of the annual meeting of the Healthcare Information and Management Systems Society (HIMSS19...

The U.S. Department of Health and Human Services (HHS) has proposed a new rule to support seamless and secure access, exchange and use of electronic health information (EHI).