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Physio-Control Receives FDA 510(k) Clearance For LIFEPAK(R) 20e Defibrillator/Monitor

Physio-Control, Inc., a wholly owned subsidiary of Medtronic, Inc., (NYSE: MDT) announced today that it has received clearance by the U.S. Food and Drug Administration (FDA) to market the LIFEPAK 20e defibrillator/monitor within the United States. The 20e is an enhancement of the LIFEPAK 20 defibrillator/monitor, which has become the standard of care in many hospitals worldwide since its introduction...

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A New Model for Pharma Research Activity

By Anonymous Covance in $50 million deal to buy Eli Lilly's Indianapolis- based laboratories PHARMACEUTICAL THE BUSINESS MODEL for pharmaceutical research activity is leaving its familiar environs for a cheaper, faster and more efficient way to replenish new-product pipelines at drug companies.

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ResMed Announces First Major Study to Investigate How Breathing Difficulties During Sleep Affect Heart Failure Patients

BERLIN--(BUSINESS WIRE)--ResMed today announced it has launched the SERVE-HF study at the 18th European Respiratory Society’s (ERS) annual congress in Berlin,

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Jules Crittenden Comments On The AP's Changing News Coverage Of Iraq.

U.S. Navy Petty Officer 2nd Class Angela McLane documents U.S. Army soldiers as they provide overwatch security during the opening of a hospital in Khalis, Iraq, Sept. 28, 2008. McLane is a combat cameraman and the soldiers are assigned to the 4th Squadron, 2nd Stryker Cavalry Regiment. DoD photo by U.S. Army Spc. Ronald Wright AP Goes Neo-Con -- Jules Crittenden OK, al-P and reasonable people might...

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Lilly finalizes deal to sell Greenfield site

Indianapolis » Eli Lilly and Co. has closed a deal to sell its Greenfield Laboratories, along with the labs' 450-acre campus in Hancock County, to Covance of New Jersey for $50 million. Covance said Friday that 264 Lilly employees will stay on with Covance. The deal includes a previously announced agreement by Lilly to give Covance $1.

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Health Winners & Losers: Amgen, Mentor

Amgen rises on an upheld court ruling regarding two anemia drugs. Mentor shares fall on UBS rating.

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Covance Inc. Invites You to Join the Webcast of Its Third Quarter 2008 Financial Results Conference Call

PRINCETON, N.J., Oct. 3 /PRNewswire-FirstCall/ -- In conjunction with its third quarter 2008 earnings release (expected to be issued after market close on October 22), Covance Inc. (NYSE: ) is pleased to invite you to listen to its quarterly investor conference call that will be broadcast live over the Internet on Thursday, October 23, 2008 at 9:00 a.m. ET. What: Covance Third Quarter 2008 Earnings...

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Biomet, Inc. Reschedules Fiscal Year 2009 First Quarter Release and Conference Call

WARSAW, Ind.--(BUSINESS WIRE)--Biomet, Inc. announced today that it has rescheduled its Fiscal 2009 First Quarter release and first quarter conference call to Friday, October 10, 2008. The

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Physio-Control Receives FDA 510(K) Clearance For LIFEPAK(R) 20e Defibrillator/Monitor

Physio-Control, Inc., a wholly owned subsidiary of Medtronic, Inc., (NYSE: MDT) announced today that it has received clearance by the U.S. Food and Drug Administration (FDA) to market the LIFEPAK 20e defibrillator/monitor within the United States.

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Reduction Of Frown Lines - Mentor Corporation Announces Completion Of PurTox(R) 3A Study

Mentor Corporation (NYSE:MNT), a leading supplier of medical products for the global aesthetic market, today announced completion of the first of three Phase 3 clinical trials with its purified botulinum Type A neurotoxin (PurTox®) for the reduction of glabellar rhytides (frown lines). This newly completed study involved 400 subjects at ten investigational sites in the United States.

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Medtronic issues warning about pumps

Medtronic Inc. has warned physicians about issues with some of its implantable drug pump systems that have been linked to one patient death. The Food and Drug Administration posted a notice about problems with the tubing connecting the Fridley company's catheters to its drug pumps. The pumps are implanted in the abdomen to deliver drugs to treat chronic pain. A spokeswoman stressed that Medtronic is...

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Medtronic warns doctors of drug pump problems

The Food and Drug Administration on Thursday posted a notice about problems with the tubing connecting the company's catheters to its drug pumps. The pumps are implanted in the abdomen to deliver drugs to treat chronic pain. Minneapolis-based Medtronic warned physicians of the problem in late June.