Erik Paulsen

Devices & Diagnostics

Fight against medical device tax gains ground

Rep. Erik Paulsen (R-Minn.) appears to be gaining ground in ginning up support for his resurrected “Defend Medical Innovation Act,” which seeks to block the 2.3 percent tax on medical device company revenues prescribed by President Barack Obama’s health care overhaul last year. Paulsen’s “Dear Colleague” letter urging legislators to repeal the tax which, “unfairly […]

Policy

Minnesota Congressman looks to Web for medical device tax repeal

U.S. Rep. Erik Paulsen, one of the top boosters for the medical device industry in Congress, doesn’t see a major repeal of health reform taking place. Still, the Minnesota Republican is hopeful some aspects of the law will change, including an upcoming tax on medical devices that Paulsen believes will stifle innovation. The nearly 50-member […]

Devices & Diagnostics

Medical device tax will face three-pronged repeal attempt

Opponents of the medical device tax have filed three bills in an attempt to defeat the measure, which would tax the makers of new innovative medical devices $20 billion over 10 years. "A $20 billion tax hike on medical device manufacturers to fund Obamacare will cripple an important engine of opportunity, job growth and innovation, while hurting the advancement of technologies essential to improving patient care," Republican Sen. Orrin Hatch state.

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A Deep-dive Into Specialty Pharma

A specialty drug is a class of prescription medications used to treat complex, chronic or rare medical conditions. Although this classification was originally intended to define the treatment of rare, also termed “orphan” diseases, affecting fewer than 200,000 people in the US, more recently, specialty drugs have emerged as the cornerstone of treatment for chronic and complex diseases such as cancer, autoimmune conditions, diabetes, hepatitis C, and HIV/AIDS.

Devices & Diagnostics

Minnesota senators recruit buddies to pressure FDA over 510(k)

Minnesota Sens. Amy Klobuchar and Al Franken along with Rep. Erik Paulsen have championed the medical device industry, giving speech after speech and writing letter after letter to the Food and Drug Administration about upcoming changes to its 510(k) approval program. I doubted the campaign would do much. But Wednesday, a bipartisan group of 15 senators sent a letter to FDA Commissioner Dr. Margaret Hamburg urging her agency, among other things, to adopt a more deliberate, cautious approach to amending 510(k).

News

Klobuchar, Paulsen urge FDA not to quash Minnesota device industry

Minnesota’s medical device community has enlisted some big guns to lobby the Food and Drug Administration against proposed changes that the industry says will hurt innovation and the state’s economy: United States Sen. Amy Klobuchar and Congressman Erik Paulsen. In a letter to FDA Commissioner Dr. Margaret Hamburg, Klobuchar, chair of the Senate Commerce Subcommittee […]