The European Chemicals Agency (ECHA) in Helsinki, Finland has revoked "a number of" REACH registrations because the registrants misrepresented their size. Size is important because the registration fee is dependent on the size of the entity submitting the registration. Small and Medium Sized Enterprises (SMEs) are allowed a significant discount to avoid disproportionate costs of registration compared to market value. According to ECHA, this "ensures equal and fair treatment of registrants." Companies declare their size when registering the fee is assigned automatically when the registrant makes their electronic dossier submission. Once submitted registration dossiers pass a completeness check, which includes payment of the fee, the registrant is given a registration. This generally occurs within three weeks of submission.
In their more comprehensive review since the November 2010 submission deadline, ECHA has determined that some companies inappropriately claimed they were SMEs when they did not, in fact, qualify for that designation or the reduced fee. Those companies that cannot document their SME status or pay the full size entity fee are considered to have failed the completeness check. In those cases ECHA has chosen to revoke the registration, which means the companies can no longer legally manufacture or import the chemical substance in question.
More details on the revocation can be found on the ECHA website.
Science, policy, and politics. Focus on science communication and climate change. The Dake Page offers news, analysis and book reviews.
Wednesday, December 5, 2012
Monday, November 19, 2012
Book Review – Am I Making Myself Clear? A Scientist’s Guide to Talking to the Public by Cornelia Dean
A much needed book for scientific and
non-scientific communities alike. Written by science writer (and former
New York Times editor) Cornelia Dean, the book makes the case that
scientists need to make “their work more accessible to the media, and
thus to the public.” This doesn’t come naturally to most scientists, and
so the book gives some practical tips on how scientists can accomplish
this goal.
Dean starts with “an invitation to
researchers” to put aside their natural reticence and distrust of the
media and help themselves and journalists get the key messages of their
science across to the public. Because there are plenty of people out
there who don’t hesitate to misinform the public about the science in
order to protect their own interests (e.g., the climate change debate).
In ensuing chapters she provides some insights into how scientists can
better “know your audience,” help educate and work with journalists, and
how to get the message across on radio and TV, online, and in the
courtroom. She also offers tips on writing books, writing Op-Eds and
letters to news outlets, and writing about science and technology in
other venues.
Two of the most valuable chapters
actually have to do with how journalists cover science issues. In
“Covering Science,” Dean notes some of the differences in style and
communication between journalism and scientific writing. These
differences set up an inherent conflict. Scientific researchers view
journalists as being superficial, insufficiently concerned with
accuracy, focused on controversy, and even “ignorant.” In turn,
journalists view researchers as boring, “caveating things to death,”
prone to incomprehensible jargon, and incapable of drawing a definitive
conclusion. In “The Problem of Objectivity,” Dean discusses the
limitations of journalistic “balance” in which one opposing voice is
given equal weight to the thousands of proponent voices because both
sides are represented. This journalistic trait is exploited by, for
example, climate change deniers, who know that TV interviews with one
scientist and one naysayer (even if he is a non-scientist) looks to the
public like “two sides” of a debate, even when the science is
overwhelmingly in favor of one view. Given that it is often difficult
for a journalist to know the state-of-the-art of the science, this opens
the door for imbalance in an effort to provide balance.
Perhaps
the most valuable chapter to scientists is “The Scientist as Source.”
Here Dean provides some practical hints as to how scientists can best
interact with journalists. Again she encourages scientists to put aside
their hesitations to speak to the press and to embrace the opportunity
to get out a message that accurately reflects both the research itself
and the ramifications of that research to the public.
“Am
I Making Myself Clear?” is quite readable, as one might expect from a
science journalist. I recommend reading this book along with Chris
Mooney and Sheril Kirshenbaum’s Unscientific America and Randy Olson’s Don’t Be Such a Scientist. All three books are
useful to the scientist to help him or her relate better to the public,
and to the public at large to better understand how science works.
Monday, October 1, 2012
FutureTox: Building the Road for 21st Century Toxicology and Risk Assessment Practices
FutureTox: Building the Road for 21st Century Toxicology and Risk Assessment
Practices—October 18–19, 2012
In just a few weeks, scientists will gather to participate in the "FutureTox: Building the Road for 21st Century Toxicology and Risk Assessment Practices" meeting. FutureTox will address the challenges and opportunities associated with effective and efficient implementation of cutting-edge toxicity testing technologies and tools that will inform hazard prediction and risk assessment. This SOT Contemporary Concepts in Toxicology meeting will be held on October 18–19, 2012, in Arlington, Virginia. In addition to SOT, the Dow Chemical Company, US Food and Drug Administration (US FDA), ILSI Health and Environmental Sciences Institute Risk 21, Human Toxicology Project Consortium, and the National Institute of Environmental Health Sciences (NIEHS) are sponsors. FutureTox will provide information of great relevance to scientists in academia, government, and industry.
The Organizing Committee includes James S. Bus and Craig Rowlands, The Dow Chemical Company; Kim Boekelheide, Brown University; Russell S. Thomas, The Hamner Institutes for Health Sciences; Vicki L. Dellarco, US Environmental Protection Agency (US EPA); Marty Stephens, Human Toxicology Project Consortium; George P. Daston, Procter & Gamble; Suzanne Compton Fitzpatrick, US Food and Drug Administration; Raymond R. Tice, NIEHS; Robert J. Kavlock, US EPA; and Laurie C. Haws, ToxStrategies.
For general information, to review the program, and to register, visit the FutureTox website.
In just a few weeks, scientists will gather to participate in the "FutureTox: Building the Road for 21st Century Toxicology and Risk Assessment Practices" meeting. FutureTox will address the challenges and opportunities associated with effective and efficient implementation of cutting-edge toxicity testing technologies and tools that will inform hazard prediction and risk assessment. This SOT Contemporary Concepts in Toxicology meeting will be held on October 18–19, 2012, in Arlington, Virginia. In addition to SOT, the Dow Chemical Company, US Food and Drug Administration (US FDA), ILSI Health and Environmental Sciences Institute Risk 21, Human Toxicology Project Consortium, and the National Institute of Environmental Health Sciences (NIEHS) are sponsors. FutureTox will provide information of great relevance to scientists in academia, government, and industry.
The Organizing Committee includes James S. Bus and Craig Rowlands, The Dow Chemical Company; Kim Boekelheide, Brown University; Russell S. Thomas, The Hamner Institutes for Health Sciences; Vicki L. Dellarco, US Environmental Protection Agency (US EPA); Marty Stephens, Human Toxicology Project Consortium; George P. Daston, Procter & Gamble; Suzanne Compton Fitzpatrick, US Food and Drug Administration; Raymond R. Tice, NIEHS; Robert J. Kavlock, US EPA; and Laurie C. Haws, ToxStrategies.
For general information, to review the program, and to register, visit the FutureTox website.
Friday, September 21, 2012
EOA Posts List of Safer Chemical Ingredients
From the USEPA:
"The U.S. Environmental Protection Agency today posted a List of Safer Chemical Ingredients that contains chemicals that meet stringent criteria applied by the Design for the Environment (DfE) Safer Product Labeling Program. This program recognizes products that are high-performance and cost-effective while using the safest chemical ingredients. At present, more than 2,800 common household and other products carry the DfE Safer Product Label. This list of safer chemical ingredients will help product manufacturers identify chemicals that the DfE program has evaluated and identified as safer alternatives. This list only includes chemicals in products that were voluntarily submitted for evaluation through the DfE Safer Product Labeling Program. There may be other chemicals not included in this list that are also safer."
The safer ingredients list can be found here.
"The U.S. Environmental Protection Agency today posted a List of Safer Chemical Ingredients that contains chemicals that meet stringent criteria applied by the Design for the Environment (DfE) Safer Product Labeling Program. This program recognizes products that are high-performance and cost-effective while using the safest chemical ingredients. At present, more than 2,800 common household and other products carry the DfE Safer Product Label. This list of safer chemical ingredients will help product manufacturers identify chemicals that the DfE program has evaluated and identified as safer alternatives. This list only includes chemicals in products that were voluntarily submitted for evaluation through the DfE Safer Product Labeling Program. There may be other chemicals not included in this list that are also safer."
The safer ingredients list can be found here.
Tuesday, September 18, 2012
Former EPA Administrator Russell Train Has Died
Former EPA Administrator Russell Train passed away at the age of 92 on September 17, 2012. Train was the second Administrator of the Agency, serving under President's Nixon and Ford from 1973 to 1977. Prior to EPA he had founded several wildlife organizations and served as the first vice-president of the World Wildlife Fund (WWF). He was later made Chair Emeritus of the the WWF, returning there after leaving the EPA.
A statement by Carter Roberts at WWF can be read here.
An EPA biographer of Russell Train can be read here.
An article about Train's passing is here.
More information on Russell Train's career here.
A statement by Carter Roberts at WWF can be read here.
An EPA biographer of Russell Train can be read here.
An article about Train's passing is here.
More information on Russell Train's career here.
Monday, September 17, 2012
ECHA Strengthens Compliance Check Strategy
From the European Chemicals Agency (ECHA):
"To ensure increased compliance of REACH registration dossiers, ECHA carries out both full compliance checks of the dossiers and now more effectively also targets its evaluation to specific parts of them.
In a full compliance check, ECHA addresses the full dossier content in a single evaluation exercise, especially for randomly selected registration dossiers. This means that ECHA performs a systematic evaluation of all information requirements in the technical dossier (e.g. physico-chemical, environmental and human health endpoints), including the corresponding elements and conclusions provided in the chemical safety report (i.e. PBT/vPvB assessment, classification and labelling, exposure assessment and risk characterisation). Where a dossier is non-compliant with an information requirement, ECHA will request the information in a single decision. The decision is taken in cooperation with the Member States.
In a targeted compliance check, ECHA evaluates only a specific part of the registration dossier based on specified concerns. Selected (groups of) endpoints or criteria, called areas of concern, have been identified that are in particular relevant for the safe use of substances. The ultimate goal is to focus on those endpoints that matter for human health and the environment. Emphasis will be given to Persistent, Bioaccumulative and Toxic (PBT); Carcinogenic, Mutagenic or Toxic to reproduction (CMR); or sensitising (S) properties of a substance. IT-assisted targeting combined with expert judgement will help to achieve the necessary increased compliance of the registration dossiers. The chances of non-compliant dossiers being picked up for compliance check are now higher. Dossiers submitted individually outside an existing joint submission and dossiers with obviously incomplete essential elements will be automatically selected for compliance check."
The full press release can be read here.
"To ensure increased compliance of REACH registration dossiers, ECHA carries out both full compliance checks of the dossiers and now more effectively also targets its evaluation to specific parts of them.
In a full compliance check, ECHA addresses the full dossier content in a single evaluation exercise, especially for randomly selected registration dossiers. This means that ECHA performs a systematic evaluation of all information requirements in the technical dossier (e.g. physico-chemical, environmental and human health endpoints), including the corresponding elements and conclusions provided in the chemical safety report (i.e. PBT/vPvB assessment, classification and labelling, exposure assessment and risk characterisation). Where a dossier is non-compliant with an information requirement, ECHA will request the information in a single decision. The decision is taken in cooperation with the Member States.
In a targeted compliance check, ECHA evaluates only a specific part of the registration dossier based on specified concerns. Selected (groups of) endpoints or criteria, called areas of concern, have been identified that are in particular relevant for the safe use of substances. The ultimate goal is to focus on those endpoints that matter for human health and the environment. Emphasis will be given to Persistent, Bioaccumulative and Toxic (PBT); Carcinogenic, Mutagenic or Toxic to reproduction (CMR); or sensitising (S) properties of a substance. IT-assisted targeting combined with expert judgement will help to achieve the necessary increased compliance of the registration dossiers. The chances of non-compliant dossiers being picked up for compliance check are now higher. Dossiers submitted individually outside an existing joint submission and dossiers with obviously incomplete essential elements will be automatically selected for compliance check."
The full press release can be read here.
Wednesday, August 22, 2012
Industry Groups Say Safe Chemical Act Does Not Include Republican Input
On Monday the Environmental Defense Fund issued a summary of the main provisions of the Safe Chemicals Act and how they "fulfill every detail" of the Industry "10 Principles" for TSCA reform as put forth by the American Chemistry Council. On Tuesday Industry addressed a letter to the Senate disagreeing with that contention, though not specifically rebutting it. The letter was signed by 69 chemical organizations representing "each step in the supply chain."
The basic premise of the letter is that Republican member input was not fully considered in the present Safe Chemicals Act passed out of the Environment and Public Works Committee late last month. The letter notes that "attempts have been made to characterize the current version of S. 847 as a compromise bill that could gain the support of Republicans and industry." The letter goes on to say that "this is not the case for the bill in its current form."
The industry letter confirms that industry "wholeheartedly support the continuation of a bipartisan process to discuss the right concepts needed in legislation to effectively reform the [EPA's] ability to regulate chemicals." Industry does not, however, believe that the current bill accomplishes this goal.
Now that the bill has been passed out of Committee it becomes eligible for a full debate of its merits on the Senate floor by all members of the Senate. Democrats in the Senate have indicated that they are more than willing to bring the bill up for debate, so it would seem that Industry and their Republican representatives in the Senate will have the opportunity to publicly present their views on what they agree with in the bill and what they do not agree with, along with solutions. Given that all stakeholders - Industry, NGOs, public health and environmental advocacy groups, parent groups, EPA and others - have agreed that TSCA needs to be reformed, it seems that the Safe Chemicals Act bill gives all parties the opportunity to move toward that goal.
The EDF comparison between the Safe Chemical Act and ACC "10 principles" can be viewed here.
The ACC "10 principles" document can be viewed here.
Further information on ACC's position on TSCA reform can be viewed on their web site.
The basic premise of the letter is that Republican member input was not fully considered in the present Safe Chemicals Act passed out of the Environment and Public Works Committee late last month. The letter notes that "attempts have been made to characterize the current version of S. 847 as a compromise bill that could gain the support of Republicans and industry." The letter goes on to say that "this is not the case for the bill in its current form."
The industry letter confirms that industry "wholeheartedly support the continuation of a bipartisan process to discuss the right concepts needed in legislation to effectively reform the [EPA's] ability to regulate chemicals." Industry does not, however, believe that the current bill accomplishes this goal.
Now that the bill has been passed out of Committee it becomes eligible for a full debate of its merits on the Senate floor by all members of the Senate. Democrats in the Senate have indicated that they are more than willing to bring the bill up for debate, so it would seem that Industry and their Republican representatives in the Senate will have the opportunity to publicly present their views on what they agree with in the bill and what they do not agree with, along with solutions. Given that all stakeholders - Industry, NGOs, public health and environmental advocacy groups, parent groups, EPA and others - have agreed that TSCA needs to be reformed, it seems that the Safe Chemicals Act bill gives all parties the opportunity to move toward that goal.
The EDF comparison between the Safe Chemical Act and ACC "10 principles" can be viewed here.
The ACC "10 principles" document can be viewed here.
Further information on ACC's position on TSCA reform can be viewed on their web site.
Monday, August 20, 2012
New Safe Chemicals Act "fulfills every detail" of Industry's principles for moderning TSCA
Dr. Richard Denison, Senior Scientist at the Environmental Defense Fund (EDF), has "developed a detailed 8-page table
that shows, side by side, the principles and the new version of the
Safe Chemicals Act, with citations to each specific provision of the Act." The principles in question are the "10 Principles for Modernizing TSCA" issued by the American Chemistry Council (ACC), the major trade association for the chemical industry.
According to Dr. Denison, "the alignment is strong" between the "10 Principles" and the provisions in the Safe Chemicals Act proposed by Senator Frank Lautenberg and passed by vote out of committee for discussion and vote in the full Senate. The ACC statement issued following the committee vote indicated that "after a cursory review, we believe the bill is still fundamentally flawed in many critical areas." However, Dr. Denison notes that:
He thus reaches the conclusion that "ACC’s complaints are more about politics than about substance."
Denison has provided a PDF link to his side-by-side table that details his comparison of the bill's provisions versus the ACC "10 Principles."
The full blog article by Dr. Denison can be read here.
According to Dr. Denison, "the alignment is strong" between the "10 Principles" and the provisions in the Safe Chemicals Act proposed by Senator Frank Lautenberg and passed by vote out of committee for discussion and vote in the full Senate. The ACC statement issued following the committee vote indicated that "after a cursory review, we believe the bill is still fundamentally flawed in many critical areas." However, Dr. Denison notes that:
The changes made to the Safe Chemicals Act specifically reflected the input received from all stakeholders, including the converging views that have emerged from several industry-NGO dialogues held over the past 18 months.
He thus reaches the conclusion that "ACC’s complaints are more about politics than about substance."
Denison has provided a PDF link to his side-by-side table that details his comparison of the bill's provisions versus the ACC "10 Principles."
The full blog article by Dr. Denison can be read here.
Friday, August 17, 2012
EPA Announces Availability of Risk Assessment Plans for 2012 Work Plan Chemicals
This morning the EPA
published Peer Review Plans for the risk assessments on the seven chemicals previously identified as 2012 work plan chemicals. According to EPA, "the plans, which form part of the Agency's Peer Review
Agenda, describe the focus of the risk assessment being conducted on
each chemical, indicate how peer reviewers will be selected and how the peer
review will be conducted, and provide the time line for the reviews."
The External Review Drafts of the plans still need to be published in the Federal Register, and when that happens and the risk assessments become officially available there will be a 60-day public comment period. There will also be conference calls of the peer review panel in which the public can provide additional comments.
The External Review Drafts of the plans still need to be published in the Federal Register, and when that happens and the risk assessments become officially available there will be a 60-day public comment period. There will also be conference calls of the peer review panel in which the public can provide additional comments.
EPA notes that the public can access and submit comments on the individual peer review plans for each
chemical by using the following links:
Wednesday, August 15, 2012
ECHA Publishes Practical Guide for Reporting Toxicity Data for REACH
ECHA has announced that it has made available a new "practical guide" to assist REACH registrants in "How to prepare toxicological summaries in
IUCLID and how to derive DNELs." The guide "supports registrants in correctly
summarising the toxicological information for substances in section 7 of
IUCLID 5.4."
The most critical part of the guide explains how to undertake the take of "Derivation of No Effect Levels" (DNELs), which are used to compare toxicity to exposure in the assessment of risk. DNELs must be derived for all relevant toxicological endpoints (e.g., oral and dermal exposures) and represent the effects side of the equation for human health concerns. For environmental concerns there is a similar derivation of "Predicted No Effect Levels" (PNECs) for aquatic and terrestrial organisms. PNEC derivation is not discussed in the new practical guide.
More information on the Practical Guide can be found on the ECHA web site.
The Practical Guide in PDF format can be downloaded directly here.
The most critical part of the guide explains how to undertake the take of "Derivation of No Effect Levels" (DNELs), which are used to compare toxicity to exposure in the assessment of risk. DNELs must be derived for all relevant toxicological endpoints (e.g., oral and dermal exposures) and represent the effects side of the equation for human health concerns. For environmental concerns there is a similar derivation of "Predicted No Effect Levels" (PNECs) for aquatic and terrestrial organisms. PNEC derivation is not discussed in the new practical guide.
More information on the Practical Guide can be found on the ECHA web site.
The Practical Guide in PDF format can be downloaded directly here.
Sunday, August 12, 2012
Japan Identifies 18 Chemicals for Closer Look after Priority Risk Assessments
After an extensive review of 86 chemicals, including detailed environmental and human health risk assessments, the Japanese government has identified 18 chemicals for closer review. The Tier I assessments resulted in five chemicals classified as substances that would be further monitored for production or import volume, mainly because they were considered likely to have fairly low levels. But 18 chemicals were deemed to be of significant enough potential risk to necessitate the Tier 2 assessments. Tier 2 assessments include requirements for manufacturers and importers to provide both health and safety hazard data and exposure information.
Eleven chemicals were identified based on their presumed risk to human health:
Seven chemicals were identified based on their presumed risk to the environment:
The Japanese government will perform the assessments in accordance with Japan's Chemical Substance Control regulation.
Eleven chemicals were identified based on their presumed risk to human health:
- hydrazine
- 1,3-butadiene
- dichloromethane
- 1,2-dichloropropane
- chloroethylene
- ethylene oxide
- 1,2-epoxypropane
- formaldehyde
- acrylonitrile
- toluidine
Seven chemicals were identified based on their presumed risk to the environment:
- 1,3-dichloropropene
- n-butyl acrylate
- isopropenylbenzene
- dichlorobenzene
- 2,6-di-tert-butyl-4-methylphenol
- [3-(2-ethylhexyloxy)propylamine]triphenylboron
- 4,4'-(propane-2,2-diyl)bis(phenol)
The Japanese government will perform the assessments in accordance with Japan's Chemical Substance Control regulation.
Thursday, August 9, 2012
EU to Update Stockholm Convention POPs Chemical Plan
The European Commission (EC) has announced that it is reevaluating and updating the implementing plan for the Stockholm Convention on Persistent Organic Pollutants. The Stockholm Convention is a "global treaty to protect human health and the environment from
chemicals that remain intact in the environment for long periods, become
widely distributed geographically and accumulate in the fatty tissue of
humans and wildlife." A plan was originally drawn up in 2007 and "a significant number of the actions identified in the 2007 Plan have now been finalized or are about to be finalised." Hence the need for an update.
A consultation has been opened on the European Commission web site and interested parties have between August 2 to October 25, 2012 to provide comment.
The full consultation document is available as a PDF download here.
A consultation has been opened on the European Commission web site and interested parties have between August 2 to October 25, 2012 to provide comment.
The full consultation document is available as a PDF download here.
Tuesday, August 7, 2012
ECHA to make more data on chemicals available
According to an ECHA news release:
"Beginning in November, ECHA will make more information from registration dossiers available on its website. This will implement a decision taken by ECHA in 2011 and is in line with Article 119(2)d of REACH. With these new elements, information made available will include the name of the registrant, the registration number of the substance as well as other items normally contained in a Safety Data Sheet (SDS). Companies wishing to request confidentiality on these items need to update their dossiers and justify their requests for confidential treatment."
More information can be found on the ECHA web site.
"Beginning in November, ECHA will make more information from registration dossiers available on its website. This will implement a decision taken by ECHA in 2011 and is in line with Article 119(2)d of REACH. With these new elements, information made available will include the name of the registrant, the registration number of the substance as well as other items normally contained in a Safety Data Sheet (SDS). Companies wishing to request confidentiality on these items need to update their dossiers and justify their requests for confidential treatment."
More information can be found on the ECHA web site.
Monday, August 6, 2012
Senator Lautenberg Calls for Senate Vote on Safe Chemicals Act
Senator Frank Lautenberg (D-NJ) is calling for a vote in the full Senate on his Safe Chemicals Act. Originally introduced April 14, 2011, the bill was passed out of the Environment and Public Works Committee last week. The bill is "designed to protect
Americans from dangerous toxic chemicals that are found in everyday
consumer products." Lautenberg now wants the bill to get a vote in the Senate.
A 174-page Amendment that documents all of the changes to the original bill (S.847) was released by the Committee. The committee also issued a short summary highlighting the key changes. These changes comprehensively alter the bill from its original "NGO-friendly" form to its now very "Industry-friendly" form. Still, Lautenberg has not been able to get any Republican to join the 25 Democratic co-sponsors of the bill. Lautenberg called on his fellow Senators to put the bill to a vote, "either for or against." He noted that "families deserve to know" what Senators from both sides of the aisle "are thinking as we go through this process."
After languishing for nearly one and half years after its introduction, the bill took on new emphasis following an investigative reporting series by the Chicago Tribune. The Tribune reported that there had been collusion between the chemical industry and the tobacco industry to overstate the effectiveness of flame retardants and understate the health risks. A rather contentious hearing was held the day before the Committee vote, during which Senator Boxer went so far as to suggest one of the witnesses should "take a course in ethics."
It is clear that Lautenberg does not expect the bill to pass a full Senate vote since it would need to reach 60 votes to invoke cloture just to bring it to the floor for a real vote. With only 53 Democrats and Independents possibly voting for the bill and all 47 Republicans likely voting against it no matter what changes are made in debate, the bill is essentially dead on arrival. But he does feel that after 7 years of introducing bills and making substantive changes that make the bill more industry-friendly, the public should know what each Senator believes about protecting human health and the environment.
A 174-page Amendment that documents all of the changes to the original bill (S.847) was released by the Committee. The committee also issued a short summary highlighting the key changes. These changes comprehensively alter the bill from its original "NGO-friendly" form to its now very "Industry-friendly" form. Still, Lautenberg has not been able to get any Republican to join the 25 Democratic co-sponsors of the bill. Lautenberg called on his fellow Senators to put the bill to a vote, "either for or against." He noted that "families deserve to know" what Senators from both sides of the aisle "are thinking as we go through this process."
After languishing for nearly one and half years after its introduction, the bill took on new emphasis following an investigative reporting series by the Chicago Tribune. The Tribune reported that there had been collusion between the chemical industry and the tobacco industry to overstate the effectiveness of flame retardants and understate the health risks. A rather contentious hearing was held the day before the Committee vote, during which Senator Boxer went so far as to suggest one of the witnesses should "take a course in ethics."
It is clear that Lautenberg does not expect the bill to pass a full Senate vote since it would need to reach 60 votes to invoke cloture just to bring it to the floor for a real vote. With only 53 Democrats and Independents possibly voting for the bill and all 47 Republicans likely voting against it no matter what changes are made in debate, the bill is essentially dead on arrival. But he does feel that after 7 years of introducing bills and making substantive changes that make the bill more industry-friendly, the public should know what each Senator believes about protecting human health and the environment.
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