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Digital pathology solutions provider BioImagene has collaborated with the University of Pennsylvania School of Medicine in Philadelphia and Rutgers University in New Brunswick, N.J., in the development of diagnostic tool, Companion Algorithms.
BioImagene, a digital pathology systems provider, and visual search solutions provider Visuvi have created PathSearch, a visual search product for digital pathology.
BioImagene has received FDA 510(K) clearance for its Pathiam system with iScan for assessment of HER2/neuimmunohistochemistry tests. Pathiam provides users with a menu of validated protocols, digital archiving and retrieval, flexible reporting and integration with LIS systems.
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BioImagene has unveiled Crescendo, its new digital pathology workstation, this week at the 2009 College of American Pathologists conference in Washington, D.C.
Digital pathology solutions provider BioImagene has released a new Ki-67 prostate image analysis algorithm, which is used to detect and provide quantitative measurement of the protein biomarker Ki-67, as part of Virtuoso, a suite of web-based software applications for digital pathology.
Siemens Venture Capital has invested in BioImagene, a provider of scalable digital pathology solutions, following a recent closing of a $26 million series D financing round led by Burrill & Company.
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The use of health IT to reduce rehospitalizations will be welcome but also disruptive, said Stephen Jencks, an independent consultant in healthcare safety during a Feb. 24 webinar on the potential use of health IT to mitigate rehospitalizations, sponsored by the Agency for Healthcare Research and Quality (AHRQ).
During the Health IT Standards Committee meeting on Feb. 24 in Washington, D.C., the Clinical Operations Workgroup sought to gather comments on proposed recommendations on implementation specifications for content exchange, vocabulary and code set standards for the Interim Final Rule of meaningful use.
In 2006, the Center for Devices and Radiological Health (CDRH), a branch of the FDA, began examining the number of medical device reports they received. Over the past two years, the number of submitted reports has increased, sparking a demand for the CDRH to make a move to electronic reporting.
A new hospital breaking ground usually isn’t breaking news. But the vision of patient care at one new facility, tentatively named Palomar Medical Center West (PMC West), is currently illegal under California state law.