November 9, 2011 – EOS Imaging announced that EOS installation has been completed at New York University Langone Medical Center, a world-class patient-centered integrated academic medical center.  The clinical use of EOS is planned for early 2012. The full body, ultra-low dose 3-D orthopedic imaging system is already available in 10 North American medical centers to perform radiological examinations for the management and surgical planning of common orthopedic conditions such as scoliosis and joint disease.

November 9, 2011 – A group of states and vendors focused on eliminating the barriers to sharing electronic health records (EHRs) issued a set of technical specifications to standardize connections between healthcare providers, health information exchanges (HIEs) and other data-sharing partners.

November 9, 2011 – PETNET Solutions Inc., a wholly owned subsidiary of Siemens Medical Solutions USA Inc., has entered into a nationwide commercial agreement with Eli Lilly and Company that grants Siemens PETNET Solutions the right to manufacture and distribute Lilly’s molecular imaging agent, which is currently under review by the U.S. Food and Drug Administration (FDA) for positron emission tomography (PET) imaging.

November 9, 2011 – USARAD.com announced FindRad.com, a national radiology directory with benefits for both patients and imaging centers. This resource enables patients to search for radiology centers throughout the United States, review background information about the facilities and schedule an appointment online instantly. A comprehensive resource containing almost 14,000 diagnostic imaging sites, FindRad.com lists outpatient imaging centers, hospital radiology departments, mobile radiology companies and physician offices with imaging capabilities.

November 9, 2011 -- Radcal announced that it has signed an agreement with a European manufacturer of medical imaging phantoms, Leeds Test Objects, to distribute its product line to United States customers.

Giotto USA yesterday announced clearance by the U.S. Food and Drug Administration (FDA) of a 510(k) application for the Giotto Image 3D and 3DL digital mammography systems. The systems, the 3D with an 18 by 24 cm bucky and the 3DL with a 24 by 30 cm bucky, may now be marketed in the U.S.

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