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Magazine
Breeding innovation | Unlikely partners are tackling tough problems by setting aside rivalries
By Mike Alkire | March 16, 2013 | Print Magazine Print Magazine Subscription Details
Desperate after a decade of trial and error to make the connection that could usher in a new generation of anti-HIV drugs, University of Washington researchers threw the scientific version of a Hail Mary pass.
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Magazine
Forging a new path | New law offers incentives to develop antibiotics
By Jaimy Lee | February 02, 2013 | Print Magazine Print Magazine Subscription Details
A patient balks at paying $50 for a dose of antibiotics. However, that same patient has no issue paying $50,000 for an oncology drug that may extend life for a few weeks.
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Magazine
Price pressure | As the number of costly specialty drugs grows, insurers and providers push for more reasonable alternatives
By Melanie Evans | January 26, 2013 | Print Magazine Print Magazine Subscription Details
Last year, the Utah-based SelectHealth insurance company paid $1 million to provide just five patients with the critical enzyme-replacement drug Cerezyme.
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Magazine
Growth spurt | As patents expire, focus is on high-priced drugs
By Jaimy Lee | January 26, 2013 | Print Magazine Print Magazine Subscription Details
At least seven of the 35 new drugs approved by the Food and Drug Administration last year cost $9,000 or more per month as manufacturers turn to developing high-priced specialty drugs to shore up bottom lines eroding from the expiration of patents on best-selling drugs that treat common conditions.
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Magazine
Late News: Passing it down | GPOs: Devicemakers billing cost of tax to providers
By Beth Kutscher | January 26, 2013 | Print Magazine Print Magazine Subscription Details
Group purchasing organizations say the medical device industry is passing along the costs of a controversial excise tax to healthcare providers.
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Magazine
Congress backs user-fee law for device industries
By Modern Healthcare | December 22, 2012 | Print Magazine Print Magazine Subscription Details
In one of the few pieces of significant legislation to win bipartisan support in 2012, Congress reauthorizes the Food and Drug Administration's user-fee acts for the drug and medical device industries and establishes first-time user-fee programs for the biosimilars and generic drug sectors.
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Magazine
Price hikes likely | Regs don't keep devicemakers from passing on costs
By Jaimy Lee | December 08, 2012 | Print Magazine Print Magazine Subscription Details
Hospitals will likely pay higher prices for some medical devices as manufacturers seek to pass through the cost of an impending excise tax to providers.
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Magazine
Beyond mammograms | Supplemental screening methods raise questions
By Jaimy Lee | December 01, 2012 | Print Magazine Print Magazine Subscription Details
Manufacturers and patient advocates say providers should inform women if they have dense breast tissue and in many cases offer supplemental breast cancer screening methods for these patients, but some radiologists are pressing for more data about the practices.
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Magazine
More technology, more risks | Top hazards linked to maturing health IT market
By Jaimy Lee | November 03, 2012 | Print Magazine Print Magazine Subscription Details
The growing adoption of complex health technology in hospitals is expected to reduce errors and improve the quality of care, but increased utilization of health IT-based technologies comes with its own set of risks for healthcare providers.
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Information
Second illness is infecting those struck by meningitis
By New York Times | November 03, 2012
Just when they might have thought they were in the clear, people recovering from meningitis in an outbreak caused by a contaminated steroid drug have been struck by a second illness.
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