Courtesy of PR Newswire LAS VEGAS, June 10, 2014 /PRNewswire/ -- DigiPath, Inc. (OTCBB and OTCQB: DIGP), a life sciences company that creates digital pathology solutions and is focusing on the botanical nutraceutical industry, is pleased...

PITTSBURGH – April 14, 2014 – GE Healthcare and UPMC today announced that the Omnyx™ Manual Read of the Digital HER2 Application has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). This clearance will allow...

Courtesy of colLABoration: A Sharing of Insights for Enhancing Laboratories and Laboratory Informatics Advisory Panel Recommends HPV as First-line Screen An advisory panel for the Medical Devices Committee of the FDA voted unanimously to...

The New York Times (9/24, A12, Tavernise, Subscription Publication) reports that the Food and Drug Administration announced on Monday that “a small portion of the rapidly expanding universe of mobile health applications” would be...

In the wake of the FDA panel at Pathology Visions 2011 many questions have come to mind.  As a dues paying, card carrying member of the College of American Pathologists, I have benefited in many ways professionally being associated with...

TUCSON, Ariz., Oct. 24, 2011 /PRNewswire/ -- Ventana Medical Systems, Inc. (Ventana), a member of the Roche Group, received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the VENTANA Companion Algorithm HER2...