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3M Petrifilm Rapid Yeast And Mold Plate Receives AOAC-PTM Approval

2014-01-09 01:45:09| dairynetwork Home Page

3M Food Safety announced today that its new 3M Petrifilm Rapid Yeast and Mold Count Plate has received certification (#121301) from the AOAC Research Institute’s Performance Tested MethodsSM (PTM) Program. The 3M Petrifilm Rapid Yeast and Mold Plate was first introduced in September 2013 as an indicator test that enables the detection of yeasts and molds in as little as 48 hours, faster than conventional agar methods

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CAE receives two contracts from US Navy

2014-01-09 01:00:00| Naval Technology

CAE has received two contracts to provide a range of training systems and services for defence customers.

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US Navy's eCASS test equipment receives Milestone C acquisition approval

2014-01-09 01:00:00| Naval Technology

The US Navy's electronic consolidated automated support system (eCASS) has achieved milestone C acquisition approval, marking a step ahead for limited production and deployment of the next-generation device used to test aircraft avionics.

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Merck Receives FDA Approval for ISENTRESS (raltegravir) for Pediatric Oral Suspension

2014-01-08 14:30:00| Merck.com - Product News

Dateline City: WHITEHOUSE STATION, N.J. WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada, announced today that the U.S. Food and Drug Administration (FDA) recently approved ISENTRESS for oral suspension, a new pediatric formulation of Mercks integrase inhibitor. With this approval, ISENTRESS is now indicated in combination with other antiretroviral (ARV) agents for the treatment of HIV-1 infection in patients four weeks of age and older. Language: English Contact: MerckMedia:Pam Eisele, 267-305-3558orSarra Herzog, 908-423-6154orInvestors:Carol Ferguson, 908-423-4465orJustin Holko, 908-423-5088 Ticker Slug: Ticker: MRK Exchange: NYSE read more

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EarlySense Receives FDA Clearance for New Bedside Monitor

2014-01-08 06:00:00| Industrial Newsroom - All News for Today

Newly Designed Bedside Monitor Launched in the US and will soon be launched in Asia and Europe<br /> <br /> WALTHAM, Mass. - EarlySense, the market leader in Proactive Patient Care Solutions, announced today that the company has received FDA Clearance for EarlySense 2.0 System, a newly designed Bedside Monitor for continuous measurement of respiration rate, heart rate and motion, in an automatic and contact-free manner.<br /> <br /> "The newly designed Bedside Monitor is in line with ...This story is related to the following:Patient Monitoring Equipment

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