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Posts Tagged ‘FDA’

Spring Brings Hope–Even about Transparency and Accountability in Government

There is some good, albeit modest, news about the Food and Drug Administration and the way the agency addresses conflicts of interest on FDA advisory panels that consider the safety and efficacy of drugs and medical devices. Read More

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Finding Glimmers of Hope on Capitol Hill

The holidays are always a good time to take stock of the year, and to be grateful for the good things that happened. Although the media has labeled this the “do nothing” Congress, the news wasn’t all bad. Read More

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The Consequences of Killer Cantaloupes

If you follow food safety, you may have heard last week that brothers Eric and Ryan Jensen pled not guilty in federal court to charges of introducing adulterated food into interstate commerce. Read More

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We Don’t Have To Give Up Our Place To Special Interests: Democracy Gives Us Options

There is a practice in the Senate, primarily of corporate lobbyists, to hire low-income folks, usually minorities, to hold their place in line before Supreme Court or congressional hearings. There are firms that actually hire the standees, and contract with lobbying firms or corporations. Depending on the interest in the issue, standees can wait for hours before a hearing starts.  Last time I checked with one of them, a standee told me he earned $10 an hour. Read More

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Its Master’s Voice: The FDA’s Dependence on Drug Industry Fees

I’ve spent many years wondering why the Food and Drug Administration (FDA) has been so slow to curb the rampant overuse of antibiotics in agriculture. Read More

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Following Science, Judge Orders Over-the-Counter Access to Emergency Contraception drug Plan B

Chalk up a win for science. Federal Judge Edward Korman today ordered the Food and Drug Administration (FDA) to make “Plan B” emergency contraception available to women of all ages without a prescription, calling efforts to stop the FDA from doing so “arbitrary, capricious, and unreasonable.”

A federal judge has accomplished what two administrations failed to do: make a decision about access to a drug based on medical evidence. It’s just common sense for the government to make drug approval and access decisions solely based on the best available science, not on hunches or political calculations. The decision brings a decade of politics trumping science to an end.  Read More

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Freedom to Tweet: Grading Social Media Policies in the Federal Government

Social media can transform debates, inform discussions and, as we saw with the Arab spring, help spread democracy. And information and science have a key role to play in democracy (hence the new Center for Science and Democracy here at UCS). Scientists working for government agencies such as NASA, NOAA, the EPA, and the FDA have a lot to contribute to discussions about the science-based challenges we face. Unfortunately, agency policies combined with a culture of timidity are often constraining individual government scientists from jumping into social media. Read More

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Weaker Antibiotic Regulation: Another Problem with FDA’s Voluntary Cooperation Program

Last post, I described some of the features of the voluntary process that might convince veterinary drug companies to give up lucrative approvals to sell antibiotics for production purposes, like growth promotion and feed efficiency. Read More

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Putting the Interests of Patients First: Conference Endorses Science-Focused Health Care

It’s not often that some of the best and most creative minds in medicine, medical ethics and healthcare all gather in one place. It’s even more rare when all these individuals are gathered together to focus on one problem—undue corporate influence on the treatment of patients in the U.S. Read More

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Negotiating with Drug Companies: The Horse-Trading Behind the FDA’s Voluntary Program

After decades of dragging its feet on the issue, the FDA has finally acknowledged that the ongoing massive use of antibiotics in food animal production poses a public health risk that demands a response. Read More

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