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 The leading web portal for pharmacy resources, news, education and careers June 26, 2017
Pharmacy Choice - Pharmacy News - June 26, 2017

Pharmacy News

Today's Pharmaceutical and Pharmacy News
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FDA News
6/26/17 - FDA Clears MAGNETOM Vida 3T MRI System From Siemens Healthineers
By a News Reporter-Staff News Editor at Cardiovascular Week-- The Food and Drug Administration has cleared the MAGNETOM Vida 3 Tesla magnetic resonance imaging scanner from Siemens Healthineers, which features new BioMatrix technology that addresses inherent anatomical and physiological differences among patients, as well as user variability.
6/26/17 - Hologic Receives Expanded FDA 510k Clearance to Market Cynosure's SculpSure® for Non-Invasive Body Contouring Lipolysis of Back, Inner and Outer...
By a News Reporter-Staff News Editor at Pharma Business Week-- Hologic, Inc. announced that the U.S. Food and Drug Administration has granted an expanded clearance for Cynosure's non-invasive body contouring product, SculpSure, to treat the back and inner and outer thighs. Developed by Cynosure, a world leader in medical aesthetics and division of
6/26/17 - Interson's Latest FDA 510k Clearance Just Made The Future Of Ultrasound Healthcare More Accessible
By a News Reporter-Staff News Editor at Pharma Business Week-- Interson announced they have received 510 clearance from the U.S. Food and Drug Administration to market their SiMPLi Series ultrasound array probes for medical applications. Interson has been the market leader in open-architecture USB ultrasound imaging products since 2007.
6/25/17 - New FDA-Cleared Smart Heart Monitor Keeps the Cardiologist a Heartbeat Away
By a News Reporter-Staff News Editor at Heart Disease Weekly-- Eko Devices, the leader in mobile acoustic cardiac monitoring tools, has received FDA clearance to market its latest innovation, DUO- a combined digital stethoscope and electrocardiogram. The portable cardiac device was inspired by cardiologists' demand for more effective monitoring too
6/24/17 - FDA Approves CSL Behring`s Self-Administered C1 Esterase Inhibitor HAE Prophylactic [Syrian Arab News Agency]
The FDA approved CSL Behrings subcutaneously administered C1 esterase inhibitor, Haegarda, for routine use in preventing hereditary angioedema attacks in adolescent and adult patients. The FDA approval of Haegarda is an important milestone for the HAE community because it addresses the primary need of patients: to effectively prevent debilitating H
6/24/17 - Genentechs subcutaneous rituximab approved in US [Sport360]
With cheaper biosimilars of the original Rituxan formulation edging closer to the US market, Genentechs owner Roche is looking for ways to maintain sales. Rituximab biosimilars have already been approved in Europe, where the subcutaneous formulation was approved last year. The FDA noted that the US label will include the following previously approv

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