EPA Releases Findings on Exposure to Diacetyl

EPA has finally released its study of the chemical exposures that occur for consumers of microwave popcorn. EPA had previously refused to release the study to the public. The study includes information on consumer exposure to diacetyl, the butter flavoring chemical known to cause lung disease. Much of the furor over diacetyl has related to those exposed during the manufacturing process, but consumers are also at risk. The Pump Handle blog has an analysis of the study: "EPA Microwave Popcorn Emissions Study Finally Published"

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EPA Official Sets the Record Straight

EPA Deputy Administrator has put up an interesting post on his blog "Flow of the River." EPA is in the middle of a rulemaking which would tighten the air quality standard for ozone, a.k.a. smog. The Clean Air Act requires EPA to set the standard based on public health considerations. Peacock writes, I have something to say today for the sake of those many states, cities, counties and other local entities that have been commenting on EPA's proposal to tighten the National Ambient Air Quality Standard (NAAQS) for ozone:

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Latest Analyses from OMB Watch

Every two weeks, in OMB Watch's e-newsletter The Watcher, we analyze a few recent issues in regulatory policy. Here are the articles from the November 6 issue: Vice President Reemerging in Regulatory Review Meetings

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National Research Council Recommends Greater Openness

The National Research Council of the National Academies issued a report in October calling for policies to improve government openness with regard to scientific information. The report stressed that certain government policies developed after 9/11 overly restrict access to scientific information and thereby harm scientific progress and national security.

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Consumer Products Expose Children to Toxic Chemicals

If you are worried about products exposing you or your children to toxic chemicals, don't look to the federal government for much help. The government, to a large extent, does not require companies to test chemicals for possible health effects before using them in consumer products, nor does it require that such products be fully labeled with chemical ingredients. In the absence of such government activity, public interest groups and the media have stepped into the role of testing and informing the public.

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Congress Told of FDA's Lax Inspection of Foreign Drug Makers -- Again

The Government Accountability Office (GAO) recently told Congress that the U.S. Food and Drug Administration (FDA) inspects an estimated seven percent of foreign drug manufacturing facilities. GAO can only provide an estimate because FDA doesn't know how many foreign facilities are subject to inspection due to inaccurate and uncoordinated databases that have vastly different estimates of the number of drug makers subject to the foreign drug inspection program. At this inspection rate, it would take FDA more than 13 years to inspect all existing facilities one time, assuming no additional facilities were added to the list.

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Vice President Reemerging in Regulatory Review Meetings

Representatives from the office of Vice President Richard Cheney have been involved in three current administration rulemakings. Their presence is indicative of a recent trend in which Cheney has involved his office in high-profile regulations.

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CPSC Reform Efforts Progress as Agency Woes Continue

Congress is working toward passage of legislation that would expand the resources and regulatory authority of the Consumer Product Safety Commission (CPSC). The bill would also address the continuing problem of lead-contaminated children's products by effectively banning the heavy metal's presence in toys and other goods. Senior administration officials are working to derail the legislation.

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Will the White House Turn Over Documents? Of Course Not.

Sen. Barbara Boxer (D-CA) has requested from the White House documents related to the Office of Management and Budget's editing of testimony on climate change given by the head of the CDC. White House Counsel Fred Fielding responded with a letter on Tuesday. Here's an excerpt:

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Information Gaps Hinder FDA's Ability to Monitor Imported Drugs

Today, the House Energy and Commerce Committee held an oversight hearing on FDA's Foreign Drug Inspection Program. While unsafe imported pharmaceuticals have not garnered the same level of attention as unsafe imported foods and toys, the future does not look bright: FDA's drug inspection program is plagued by a lack of basic information. The Government Accountability Office (GAO) released a new report in conjunction with the hearing. Among other things, GAO found:

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