Lost Password? No account yet? Register

Advertisement

New Media Advertisement
Siemens receives FDA Approval for the VERSANT 440 Molecular System PDF Print E-mail
User Rating: / 0
PoorBest 
Written by Administrator   
Thursday, 21 February 2008

The U.S. Food and Drug Administration has approved Siemens Healthcare’s VERSANT(TM) 440 Molecular System for marketing for use with the VERSANT HCV RNA 3.0 assay for management of HCV-infected patients undergoing antiviral therapy.

The VERSANT 440 Molecular System represents the next generation in automated viral load testing, providing laboratories with greater throughput and less hands-on time, maximizing productivity to meet the evolving needs of the clinical laboratory. We are pleased to offer clinical laboratories leading-edge solutions in molecular diagnostics that support cost-effective and timely screening and treatment of infectious disease.

Siemens Healthcare Diagnostics Division is the leading clinical diagnostics provider in the world. The VERSANT 440 Molecular System is a branched DNA (bDNA) system designed for flexible walk-away automation. Its single room technology and consolidated footprint allow the system the flexibility to fit anywhere in the clinical laboratory. The VERSANT 440 System streamlines workflow by integrating bar code data entry, automated reagent processing, signal amplification detection, and a Laboratory Information System interface for downloading patient work lists and results.


 

 
< Prev   Next >

11.03.2008 | Retailing

Kmart Pharmacy has launch of the American Fare Dollar Program, which offers pharmacy customers a choice of 10 over-the-counter (OTC) medications from Kmart's proprietary American Fare brand for only…     Readmore

Image

09.09.2007 | Outsourcing

The pharmaceutical manufacturers in the United States have attacked the proposed pharma policy of India saying that it would contravene the stated goal of liberalizing the sector, and sought some…     Readmore

Image

09.09.2007 | Homeopathy

The Homeopatic manufacturing units must fulfill the conditions stated by the government of India under 67-G     Readmore

10.07.2008 | FDA

Invitrogen Corporation, a provider of essential life science technologies for research, production and diagnostics,  has received U.S. Food and Drug Administration (FDA) premarket approval (PMA) for its SPOT-Light(R) HER2…     Readmore

17.07.2008 | Biotechnology

Angel Biotechnology Holdings plc, the biopharmaceutical contract manufacturer, is announced pre-GMP process development programme with Angport Limited. The contract is the first to be signed under the EPhaG relationship…     Readmore

07.10.2008 | Nanotechnology

Cambridge is one of four institutes located outside of Japan which will host a satellite of the 'International Center for Materials Nanoarchitectonics' (MANA). (The University of California, Los Angeles,…     Readmore

20.12.2007 | Packaging

Bilcare Research has launched a product to help check the menace of counterfeit drugs. The product has a label with a unique bar code made out of nanotechnology and…     Readmore