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Matt Shudtz | June 22, 2009

Medical Device Safety: FDA Can’t Do It Alone

While his colleagues (and former colleagues) jockey for the healthcare reform limelight, Rep. Frank Pallone is quietly busy making sure that, regardless of who pays for healthcare, the sick and injured will have safe and effective solutions to their problems. Last Thursday, Rep. Pallone held a hearing to assess FDA’s ability to properly oversee the […]

Matthew Freeman | March 9, 2009

McGarity columns on Wyeth vs. Levine Preemption Case

CPR Member Scholar Thomas McGarity had op-eds over the weekend in three Texas newspapers — the Dallas Morning News, Houston Chronicle and Austin American-Statesman.  His topic is Wyeth vs. Levine, last week’s blockbuster case from the Supreme Court, in which the Court rejected the Bush Administration’s multi-year effort to use the federal regulatory process as […]

Rena Steinzor | March 6, 2009

The People’s Agents: Rescuing the Occupational Safety and Health Administration

The Occupational Safety and Health Administration (OSHA) is the most maligned and least respected federal agency with responsibility for protecting people’s lives. Now that Hilda Solis has been confirmed as Secretary of the Department of Labor, we can only hope that a new OSHA administrator with a strong stomach, an iron will, and a “yes […]

Matthew Freeman | January 14, 2009

Not just little adults

If you’re a consumer of health and environmental news, you’ve almost certainly heard it said that “children are not just little adults.” The warning comes up a lot in the context of medical research, because children’s bodies metabolize some things differently than do adults. That’s particularly important because somewhere in the vicinity of 80 percent […]

Matthew Freeman | November 28, 2008

Tom McGarity on preemption in November 28 Austin American Statesman

CPR’s Tom McGarity has an op-ed this morning in the Austin American Statesman on Wyeth vs. Levine, the Supreme Court case testing an assertion by pharmaceutical manufacturer Wyeth that FDA approval of its proposed drug label shields the company from tort litigation over harm that drug subsequently causes.  The Court heard oral arguments on the […]