The European Chemicals Agency (ECHA) has teamed up with several European chemical trade associations to establish a "cross-sector collaborative network to share knowledge, techniques and approaches to building and applying (REACH) exposure scenarios." The new network "aims at identifying good industry practices on drafting exposure scenarios" and sets up a mechanism for "building a dialogue between supply chain actors" in an effort to "improve the protection of human health and the environment."
The new network is called ENES, the Exchange Network on Exposure Scenarios. The trade associations with whom ECHA worked to set up ENES include the European Chemical Industry Council (CEFIC), Eurometaux (the metals association), CONCAWE (the oil companies’ European association), the European Association of Chemical Distributors (FECC) and the International Association for Soaps, Detergents and Maintenance Products (AISE) on behalf of the Downstream Users of Chemicals Coordination Group (DUCC).
According to the ECHA press release, the first meeting will be held in Brussels, on November 24 and 25, 2011. Besides the trade associations listed above, various "sectors of industry, NGOs, Member State authorities and other stakeholders will be invited to participate."
See the ECHA page here for more information.
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Thursday, October 13, 2011
Monday, October 10, 2011
Canada Moves Into Next Phase of Chemical Management Plan
Canada has issued a news release indicating that it will move into the next phase of its ongoing Chemical Management Plan. This is an extension of the plan first launched in 2006. The CMP was designed to apply the rigorous assessment used for new chemicals to 'legacy chemicals' that were introduced in Canada between January 1, 1984, and December 31, 1986. The new phase is seen "as a continuation of Canada's world-leading initiatives in this area and it will ensure the protection of Canadians' health and safety, and their environment," according to Shannon Coombs, President, Canadian Consumer Specialty Products Association, who promised to "continue to work proactively with the government as the plan is implemented."
According to the announcement, new funding is being provided for this next phase of the Plan, "which will focus on:"
More information on Canada's Chemical Management Plan can be found here.
Canada's Chemical Substance main page is here.
According to the announcement, new funding is being provided for this next phase of the Plan, "which will focus on:"
- Further improving product safety in Canada;
- Completing assessments of 500 substances across nine categories including phthalates, primarily used in plastics; and,
- Investing in additional research for substances like Bisphenol A, flame retardants, substances that affect hormone function and substances that affect the environment.
More information on Canada's Chemical Management Plan can be found here.
Canada's Chemical Substance main page is here.
Thursday, October 6, 2011
ECHA Issues 2012 Work Program - Sees Challenges Ahead
The European Chemicals Agency (ECHA) approved its 2012 work program last week and highlighted both its activities and its challenges ahead of the next REACH deadline. Besides the mid 2013 REACH registration deadline, ECHA will take on an expanding role in the new Biocidal Products Regulation (which will replace the current Directive in 2013). In addition, ECHA will have ramped up activities related to other parts of the expansive REACH regulation, including the Evaluation (the "E") and Authorization (the "A") components, as well as Restrictions (the "missing R"). And of course there is still the continuing evaluation of substance dossiers for high productive volume chemicals submitted in the first registration period that ended on November 30, 2010.
All of this leaves ECHA worried that there may not be enough resources to meet obligations efficiently, both within ECHA and in the Member States. The current economic situation in most of Europe, which has caused such severe spending cuts (austerity), has led ECHA Executive Director Geert Dancet to openly state his concerns that Member States may not have enough resources to fully conduct their role in chemical evaluation.
The developing Biocidal Products Regulation (BPR) also offers challenges to ECHA as the agency is expected to take on responsibility for authorizing biocides. Under the current biocides directive this responsibility lies with each Member State. ECHA would also take on new responsibilities related to the Prior Informed Consent Regulation, which involves identifying hazardous chemicals that could not be exported from Europe unless the country of destination is given sufficient information to assess risk.
During the September 29-30, 2011 meeting of the management board, the mandate of the Executive Director was extended. According to the chairman, Dr. Thomas Jakl:
More information and a link to the work program can be found on the ECHA web site.
All of this leaves ECHA worried that there may not be enough resources to meet obligations efficiently, both within ECHA and in the Member States. The current economic situation in most of Europe, which has caused such severe spending cuts (austerity), has led ECHA Executive Director Geert Dancet to openly state his concerns that Member States may not have enough resources to fully conduct their role in chemical evaluation.
The developing Biocidal Products Regulation (BPR) also offers challenges to ECHA as the agency is expected to take on responsibility for authorizing biocides. Under the current biocides directive this responsibility lies with each Member State. ECHA would also take on new responsibilities related to the Prior Informed Consent Regulation, which involves identifying hazardous chemicals that could not be exported from Europe unless the country of destination is given sufficient information to assess risk.
During the September 29-30, 2011 meeting of the management board, the mandate of the Executive Director was extended. According to the chairman, Dr. Thomas Jakl:
"After the first REACH registration deadline was impressively managed by ECHA in 2010, there is no time to rest on our laurels. Challenging further steps of the REACH and CLP implementation lie ahead and the legislator is in the process of entrusting important new regulatory tasks to the Agency. The continuation decision with regard to a selection process for the Executive Director reflects the high satisfaction of the Board with his achievements since 2007."
More information and a link to the work program can be found on the ECHA web site.
Tuesday, October 4, 2011
Summary of GHS Chemical Classification in Various Regions Now Available
The UN Globally Harmonized System of Classification and Labeling of Chemicals (usually referred to as simply GHS) was a way for governments to voluntarily attempt to bring into harmony what had been a wide range of classification schemes for chemicals. Now the Organization for Economic Cooperation and Development (OECD) has created a summary table that brings together in one place the current status of individual government's and region's adoption of GHS.
The table can be seen here and shows which OECD member countries and other organisations have publicly posted their GHS classifications no the internet. The table is based on a survey performed in 2011. Where available, OECD has provided links to the appropriate documents and web access points (e.g., to the 1300+ page CLP in Europe). Other links take you to web sites, for example, Korea's New Chemical Notification and Assessment.
The Fourth Revised Edition of the UN Globally Harmonized System of Classification and Labelling of Chemicals (the "Purple Book") can be downloaded on the United Nations Economic Commission for Europe (UNECE) site.
The table can be seen here and shows which OECD member countries and other organisations have publicly posted their GHS classifications no the internet. The table is based on a survey performed in 2011. Where available, OECD has provided links to the appropriate documents and web access points (e.g., to the 1300+ page CLP in Europe). Other links take you to web sites, for example, Korea's New Chemical Notification and Assessment.
The Fourth Revised Edition of the UN Globally Harmonized System of Classification and Labelling of Chemicals (the "Purple Book") can be downloaded on the United Nations Economic Commission for Europe (UNECE) site.
Monday, October 3, 2011
Is TSCA Reform Happening this Fall?
The short answer is, probably not. But it does appear that Senator Frank Lautenberg's office will be pushing for a markup this fall of the draft bill introduced this past spring. Lautenberg's "Safe Chemicals Act of 2011" included many industry-friendly changes from the original "Kid Safe Chemical Act" (including no longer mentioning kids in the name). The bill introduced in April would have required companies to submit "basic hazard and exposure data to quickly determine the risk and assess the need for further testing or restrictions."
Over the summer the staffs of Senators Lautenberg and Inhofe held a series of stakeholder meetings in an effort to find common ground and a path forward. These meetings included - separately - representatives from NGOs (e.g., Environmental Defense Fund) and industry (e.g., ACC and SOCMA). Topics for the meetings included defining a "safety standard" and coming up with prioritization schemes that would focus efforts on those chemicals deemed most risky. In August, EPA proposed such a prioritization scheme, which was countered by an alternative scheme by the American Chemistry Council.
Whether the markup happens or not will depend on the legislative calendar, but historically anything that doesn't get done by this fall will likely not get done during the 2012 election year. With the initial changes Lautenberg already made and the Democrats' willingness to compromise the grand reform of TSCA for a more industry-friendly reform, the feedback from the stakeholder meetings suggest that any markup will further limit the extent of "modernization" of the 35-year old chemicals law. Whether you believe that is a good thing or a bad thing may depend on from what perspective you bring to the table.
Over the summer the staffs of Senators Lautenberg and Inhofe held a series of stakeholder meetings in an effort to find common ground and a path forward. These meetings included - separately - representatives from NGOs (e.g., Environmental Defense Fund) and industry (e.g., ACC and SOCMA). Topics for the meetings included defining a "safety standard" and coming up with prioritization schemes that would focus efforts on those chemicals deemed most risky. In August, EPA proposed such a prioritization scheme, which was countered by an alternative scheme by the American Chemistry Council.
Whether the markup happens or not will depend on the legislative calendar, but historically anything that doesn't get done by this fall will likely not get done during the 2012 election year. With the initial changes Lautenberg already made and the Democrats' willingness to compromise the grand reform of TSCA for a more industry-friendly reform, the feedback from the stakeholder meetings suggest that any markup will further limit the extent of "modernization" of the 35-year old chemicals law. Whether you believe that is a good thing or a bad thing may depend on from what perspective you bring to the table.
Friday, September 30, 2011
EPA Will Identify Priority Chemicals by Thanksgiving (or so)
EPA will identify chemicals to be prioritized sometime this fall as it tries to move forward under the old TSCA as Congress makes no progress on developing a new TSCA. To do so EPA will take into consideration feedback they received from a variety of stakeholders in two recent outreach attempts related to their proposed prioritization process.
EPA introduced its proposed prioritization scheme and "discussion guide" back in August. They then had a webinar on September 7th to give an overview of the proposed scheme and to invite feedback. Finally, EPA also invited the public to share their thoughts in an online discussion forum. That discussion forum closed on September 14th.
All comments received from stakeholders are now being assimilated and reviewed by EPA staff, who are working to identify chemicals to be prioritized for review. In general the feedback was very constructive and included both concerns for the data sources being proposed as well as suggestions for other data sources to include in the evaluation. Other stakeholders cautioned that the use of production volume as a surrogate for exposure could lead to chemicals with very low risk being prioritized while chemicals of low production volume by high exposure potential, and thus risk, might be left out. Some stakeholders suggested the addition of additional health effects such as endocrine disruption, neurotoxicity and skin or respiratory sensitization be used early in the prioritization process, while others cautioned that the process could get bogged down in the minutia if too many factors were included in the first step.
More information on the EPA chemical prioritization can be found on the discussion forum web site and EPA's existing chemicals "Identifying priority chemicals for review" page.
EPA introduced its proposed prioritization scheme and "discussion guide" back in August. They then had a webinar on September 7th to give an overview of the proposed scheme and to invite feedback. Finally, EPA also invited the public to share their thoughts in an online discussion forum. That discussion forum closed on September 14th.
All comments received from stakeholders are now being assimilated and reviewed by EPA staff, who are working to identify chemicals to be prioritized for review. In general the feedback was very constructive and included both concerns for the data sources being proposed as well as suggestions for other data sources to include in the evaluation. Other stakeholders cautioned that the use of production volume as a surrogate for exposure could lead to chemicals with very low risk being prioritized while chemicals of low production volume by high exposure potential, and thus risk, might be left out. Some stakeholders suggested the addition of additional health effects such as endocrine disruption, neurotoxicity and skin or respiratory sensitization be used early in the prioritization process, while others cautioned that the process could get bogged down in the minutia if too many factors were included in the first step.
More information on the EPA chemical prioritization can be found on the discussion forum web site and EPA's existing chemicals "Identifying priority chemicals for review" page.
Wednesday, September 28, 2011
ECHA Goes to Commission on REACH Testing Proposal
How many Member State Competent Authorities does it take to make a decision on REACH testing proposals? Apparently more than they have. The Member State Committee (MSC) at the European Chemicals Agency (ECHA) "could not find unanimous agreement based on scientific and technical arguments on a draft decision for a testing proposal."
Let's go to the Commission! For the first time ECHA will employ Article 51(7) of the REACH Regulation and refer a case to the European Commission for decision making.
This non-decision by the MSC took place last week. Not that they were stymied on all decisions. They did agree on the draft decisions "for all five compliance checks" they were charged with reviewing. And they did come to unanimous agreement on two of the four draft decisions on "testing proposal examinations." But two testing proposals were particularly tricky. For one, the MSC refined the proposal during the meeting and expect to agree in writing shortly.
The final testing proposal reached stalemate, hence the referral to the Commission. The proposal:
No information on when (or if) the Commission will make its decision.
More on what the Member States Committee does can be found on their web page here.
Let's go to the Commission! For the first time ECHA will employ Article 51(7) of the REACH Regulation and refer a case to the European Commission for decision making.
This non-decision by the MSC took place last week. Not that they were stymied on all decisions. They did agree on the draft decisions "for all five compliance checks" they were charged with reviewing. And they did come to unanimous agreement on two of the four draft decisions on "testing proposal examinations." But two testing proposals were particularly tricky. For one, the MSC refined the proposal during the meeting and expect to agree in writing shortly.
The final testing proposal reached stalemate, hence the referral to the Commission. The proposal:
"concerns a testing proposal examination where the registrant has proposed to perform a two-generation reproductive toxicity test in accordance with the EU test method B.35. This information would be necessary to fill the data gap regarding reproductive toxicity for the substance that is produced in quantities of over 1000 tonnes per annum. Some MSC members preferred to ask the registrant to use the recently adopted OECD test guideline 443, the extended one-generation reproductive toxicity study (EOGRTS). Others wanted to maintain the present requirement of performing a two-generation study."
No information on when (or if) the Commission will make its decision.
More on what the Member States Committee does can be found on their web page here.
Tuesday, September 27, 2011
REACH Chemical Regulation Group Offers Advice and Recommendations
The Director's Contact Group (DCG) has issued a report on the "Achievements, Lessons Learned and Recommendations" garnered from its supporting role for last year's first REACH registration deadline. The DCB was formed to deal with a wide range of issues related to REACH chemical regulation - 28 different issues in all. And now the DCG has been renewed until the end of September 2013 so that it can address any issues that might arise with the next registration deadline, which is May 30, 2013.
The DCG report gives a summary of its achievements, and presents many of the lessons learned from the experience. All of this sets the stage for recommendations that hopefully will ease the burden for companies preparing for the 2013 (and 2018) registration deadlines. An annex of the report gives short summaries of the 28 issues addressed by the group to date.
Issues that are expected to be priority for the next deadline include:
The DCG report can be downloaded as a PDF here.
More information on REACH can be found on the ECHA web site.
The DCG report gives a summary of its achievements, and presents many of the lessons learned from the experience. All of this sets the stage for recommendations that hopefully will ease the burden for companies preparing for the 2013 (and 2018) registration deadlines. An annex of the report gives short summaries of the 28 issues addressed by the group to date.
Issues that are expected to be priority for the next deadline include:
- Organizational issues within SIEFs, the Substance Information Exchange Forums, that had mixed reviews during the first round of registrations,
- Guidance on how to deal with situations in which the companies have merged or spun off units during the registration period (which is especially important for the many small and medium size entities that are expected to be part of the second round),
- Guidance on communication within the supply chain, again a difficult issue for small and medium sized companies with less resources
- Updating of information technology tools like IUCLID, REACH-IT, and guidance documents
The DCG report can be downloaded as a PDF here.
More information on REACH can be found on the ECHA web site.
Monday, September 26, 2011
NSF Announces Steps to Improve Participation of Women in STEM Science Careers
The National Science Foundation (NSF) is announcing steps that will "make it easier for women to pursue careers in engineering and the sciences," according to an Op-Ed by Valerie Jarrett and Tina Tchen in yesterday's Washington Post. They note that "women working in science, technology, engineering and math [STEM] careers earn 33 percent more than those in other occupations, and these 'STEM' skills will become even more important in high-growth, high-tech fields such as health-care technology and advanced manufacturing."
Jarrett and Tchen note that circumstances often work against women:
Ways that NSF is looking to make it easier for women in STEM careers include:
More information is on the National Science Foundation web site.
Jarrett and Tchen note that circumstances often work against women:
As with women throughout the workforce, however, women in STEM jobs are often expected to establish themselves professionally at the same time they are starting families. This forces women to choose between their careers and their responsibilities at home. Understandably, many of our most promising young scientists and engineers drop out of the pipeline.
Ways that NSF is looking to make it easier for women in STEM careers include:
- Working with women researchers who need to delay the start of a funded project for a family-related reason,
- Options to add the lost time if female researchers interrupt research to have a baby,
- Support for research into the effectiveness of flexible workplace policies.
More information is on the National Science Foundation web site.
Friday, September 23, 2011
ECHA Starts REACH 2013 Campaign to Urge Chemical Companies to Act Now!
The European Chemicals Agency (ECHA) has launched a campaign to encourage chemical companies to "Act Now!" to meet their planned registration obligations for the second round of REACH. The next registration deadline - for substances manufactured or imported at tonnages at or above 100 tonnes per year - is May 31 2013.
ECHA's goal is to get companies thinking now about how they will fulfill the data requirements and interact with other members of SIEFs, including any data gathering and compensation to existing data holders. Preparing for and submitting registrations earlier rather than all at the last minute is good for both ECHA and the registering companies.
To do this, ECHA has started a program called REACH 2013 - Act Now!
The web page provides "key information to support you in your preparations for the 2013 registration." It includes "links to all the steps of the registration process: from the formation of the Substance Information Exchange Fora (SIEFs) to data sharing, dossier preparation and online submission."
According to the site, potential registrants need to be getting organized to do:
ECHA's goal is to get companies thinking now about how they will fulfill the data requirements and interact with other members of SIEFs, including any data gathering and compensation to existing data holders. Preparing for and submitting registrations earlier rather than all at the last minute is good for both ECHA and the registering companies.
To do this, ECHA has started a program called REACH 2013 - Act Now!
The web page provides "key information to support you in your preparations for the 2013 registration." It includes "links to all the steps of the registration process: from the formation of the Substance Information Exchange Fora (SIEFs) to data sharing, dossier preparation and online submission."
According to the site, potential registrants need to be getting organized to do:
- Substance identification, hazard information, data-sharing
- Substance identification and sameness of substance: Confirm with the other pre-registrants that you have the same substance;
- Hazard information: Collect all data available on the intrinsic properties of the substance to be registered;
- Data sharing: As part of a joint registration, gather and share existing information, consider alternatives to testing and answer any information request from within your SIEF;
- Chemical safety assessment: Carry out a chemical safety assessment in order to produce a chemical safety report based on the hazard information collected and knowledge on the uses.
Wednesday, September 21, 2011
ACC's Chemical Prioritization Tool - EDFs Analysis is One Thumb Up, One Thumb Down
Last week I reported on an analysis of the EPA's proposed chemical prioritization tool done by Richard Denison of the Environmental Defense Fund (EDF). Today I report on Denison's follow up analysis on the counter-proposal prioritization scheme released by the American Chemistry Council the day prior to EPA's webinar. I'll start with Denison's conclusion:
As suggested, Denison notes that the ACC proposal offers some "refreshing elements and acknowledgements." He describes it as "substantive and specific" and is "welcome in several ways." He goes on to summarize some of the areas he feels are constructive (see his full blog entry). Notwithstanding these kudos, however, Denison does suggest that ACC's proposal seems better suited for a full TSCA Reform element and that implementation of the ACC plan is not likely to be possible under the current (and likely future) resource and funding constraints limiting EPA's activities.
Denison finds that there are "a number of quite problematic aspects of ACC's proposal," including:
"While ACC’s tool has some serious flaws and is not something that EPA has the authority or resources to utilize under current TSCA, ACC has put forth a serious proposal for prioritization that should help to raise the level of debate over this critical issue in TSCA reform."
As suggested, Denison notes that the ACC proposal offers some "refreshing elements and acknowledgements." He describes it as "substantive and specific" and is "welcome in several ways." He goes on to summarize some of the areas he feels are constructive (see his full blog entry). Notwithstanding these kudos, however, Denison does suggest that ACC's proposal seems better suited for a full TSCA Reform element and that implementation of the ACC plan is not likely to be possible under the current (and likely future) resource and funding constraints limiting EPA's activities.
Denison finds that there are "a number of quite problematic aspects of ACC's proposal," including:
- Overly rigid rules applied in lockstep: Denison finds ACC's proposed "equal basis" rule to be "sleight of hand" that will "rule out any types of information that may indicate a hazard or exposure of high concern unless it has been measured across basically all chemicals subject to prioritization." The "high hazard and high exposure" rule would allow prioritization of only those chemicals "for which high hazard and high exposure can be demonstrated;" a proposal that Denison finds to be "simply shortsighted." He also critiques ACC's "persistent and bioaccumulative" rule, which he finds includes "extremely narrow definitions of P and B" that would avoid prioritizing chemicals that would in fact be either P or B (or both).
- Consistent use of the least conservative classification values: Denison points out that the ACC proposal relies on the classification criteria developed under GHS, which he generally supports. However, he does quibble with what he feels are two limitations - GHS doesn't include every endpoint of concern and ACC chooses the least conservative values instead of adhering to GHS' cutoff values faithfully. A choice where Denison feels "ACC fails badly."
- Over-relying on limited exposure information and discounting evidence of hazard: Denison notes that ACC's tool lumps together its health and environmental hazard rankings into a single score while combining scores for its three exposure elements, which "means that a chemical that harms both people and other organisms only gets counted once, while a chemical that is low-volume and used only as an intermediate and is not P or B gets credit for being of low concern for all three attributes." The way the tool handles hazard vs exposure rankings also is likely to skew the results such as to avoid prioritization for chemicals that could indeed be problematic.
Tuesday, September 20, 2011
ECHA Risk Assessment Committee Adopts Seven Scientific Opinions
The following information comes from the ECHA web site:
The Committee for Risk Assessment (RAC) has adopted opinions on seven proposals for harmonised classification and labelling across Europe during its 17th meeting, held from 13-16 September 2011 in Helsinki.
Polyhexamethylene biguanide hydrochloride (PHMB)
RAC agreed with the proposal from France to classify PHMB as acutely toxic by the oral and inhalation route, damaging to the eye, as a skin sensitiser, as toxic to the respiratory tract after repeated exposure, suspected carcinogen and hazardous to the aquatic environment. The classification of this substance is not currently harmonised at EU level. PHMB is used as biocidal product (disinfectant).
Di-n-hexyl phthalate (DnHP)
RAC agreed with the proposal from France to classify DnHP for reproductive toxicity due to the potential for effects on unborn babies as well as on male fertility. The classification of this substance is not currently harmonised at EU level. DnHP is used in the manufacture of plastics.
Fenamiphos
RAC agreed with the proposal from the Netherlands to classify Fenamiphos as acutely toxic by the inhalation route and as an eye irritant. Fenamiphos already has a harmonised classification as acutely toxic by the oral and dermal route and as hazardous to the aquatic environment. RAC agreed with the proposal to replace the minimum classification for acute toxicity (indicate by an asterix) with the definite classification based on data. Further, RAC proposed an M-factor of 100 for chronic aquatic toxicity. Fenamiphos is used as a plant protection product.
Trichloromethylstannane (MMTC)
RAC agreed with the proposal from France to classify MMTC as toxic to reproduction. RAC did not agree with the proposal from France, to classify MMTC as mutagenic. The classification of this substance is not currently harmonised at EU level. MMTC is used as an industrial intermediate in the production of other organotin chemicals.
2-ethylhexyl 10-ethyl-4-[[2-[(2-ethylhexyl)oxy]-2-oxoethyl]thio]-4-methyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate (MMT (EHMA))
RAC agreed with the proposal from France to classify MMT(EHMA) as toxic to reproduction. RAC did not agree with the proposal from France, to classify MMT(EHMA) as mutagenic. The classification of this substance is not currently harmonised at EU level. MMT(EHMA) is used as a heat stabiliser in PVC.
Benzenamine, 2-chloro-6-nitro-3-phenoxy- (Aclonifen)
RAC agreed with the proposal from Germany to classify Aclonifen as a suspected carcinogen, as a skin sensitiser and as hazardous to the aquatic environment. Aclonifen already has a harmonised classification as hazardous to the aquatic environment. Aclonifen is used as a plant protection product (herbicide).
Perestane
RAC agreed with the proposal from the UK to classify Perestane as acutely toxic by the oral, dermal and inhalation routes, skin corrosive and as toxic to the eye after single exposure and to remove the classification for mutagenicity. Perestane already has a harmonised classification as acutely toxic by the oral, dermal and inhalation routes, skin corrosive and mutagenic. Perestane is used as a biocide (surface disinfectant).
More information can be found on the ECHA web site.
Monday, September 19, 2011
Denmark Proposes Restriction of Four Phthalates under REACH Chemical Regulation
Denmark has proposed to restrict "the placing on the market and use of certain articles containing four classified phthalates (DEHP, BBP, DBP and DIBP)." These common phthalates are found in a variety of professional and consumer products, including PVC and in dispersions, paints and varnishes. The primary rationale for these restrictions is that these "phthalates are all reported to affect reproductivity."
The Danish proposal is part of the REACH chemical regulation process, in which substances of very high concern can be proposed by Member States to be restricted from further use. All interested parties (e.g., manufacturers and formulators, as well as other Competent Authorities) can comment on the proposal. All comments will be "reviewed and taken into account by ECHA’s Committees for Risk Assessment (RAC) and Socio-economic Analysis (SEAC)." By September 2012 these Committees would provide their opinions, which will be the basis for final decisions on whether to restrict the substances from use in commerce
Comments are requested by December 16, 2011, though officially the 6-month public consultation being announced today ends in March 2012.
According to the ECHA news release:
More information can be found on the ECHA site.
The Danish proposal is part of the REACH chemical regulation process, in which substances of very high concern can be proposed by Member States to be restricted from further use. All interested parties (e.g., manufacturers and formulators, as well as other Competent Authorities) can comment on the proposal. All comments will be "reviewed and taken into account by ECHA’s Committees for Risk Assessment (RAC) and Socio-economic Analysis (SEAC)." By September 2012 these Committees would provide their opinions, which will be the basis for final decisions on whether to restrict the substances from use in commerce
Comments are requested by December 16, 2011, though officially the 6-month public consultation being announced today ends in March 2012.
According to the ECHA news release:
The widespread use of phthalates is raising concern, regarding human exposure from consumer articles. The dossier addresses the combined exposure based on common effects seen with exposure to these phthalates.
In the report, Denmark suggests a ban for the placing on the market of articles intended for indoor use and articles that may come into direct contact with the skin or mucous membranes, containing one or more of these four phthalates in a concentration greater than 0.1 % by weight of any plasticised material.
More information can be found on the ECHA site.
Thursday, September 15, 2011
Avoiding Paralysis by Analysis - EDF's Analysis of the EPA TSCA Chemical Prioritization Proposal
Last week the USEPA held a webinar to introduce their proposal for how they will attempt to prioritize TSCA chemicals for closer assessment. One day prior to the webinar the ACC announced its own competing prioritization scheme. Earlier this week, Environmental Defense Fund Senior Scientist Richard Denison offered his views on the EPA scheme, which he called "a sensible approach to identifying chemicals of concern." [Note: Denison will be addressing the ACC proposal in a following post on the EDF web site.]
The "paralysis by analysis" noted to in the title refers to the futility of asking EPA to evaluate the entire TSCA Inventory akin to the Canadian approach. The Canadian approach was actually "mandated by statute" (via the 1999 amendments to the CEPA) and both Environment Canada and Health Canada were given "seven years and a major infusion of new resources" just to complete the first phase of the process. According to Denison, with nearly four times as many chemicals on the Inventory, and "without the authority and the resources, well, that's just a recipe for paralysis by analysis" to ask EPA to do the same.
Which is why the EPA proposal is so reasonable, according to Denison. He indicates that EDF and the Safer Chemicals Healthy Families coalition "generally support EPA's approach and believe it strikes the right balance between clarity and transparency and avoiding paralysis by analysis." Denison does, however, offer a series of 10 additional suggestions for improving the EPA proposal. The full list can be seen on the EDF blog page, but include broadening the sources of data specified in Step 1 (perhaps by including some of the source from Step 2), consideration of the published literature, adding specific criteria for children's health and exposure, expanding the range of "vulnerable subpopulations" beyond just children's health, and providing additional clarity on how EPA plans to move from Step 1 to Step 2.
Overall, Denison finds that the attempts by EPA to reintroduce "action" into their proposed prioritization and action plan process are much needed. He welcomes EPA looking at chemicals in commerce to identify those for which it would be prudent to take a closer look at their potential risk. And with the additional actions suggested, he believes that it is a good step in the right direction.
To read EDF's analysis and the full list of suggestions, see Richard Denison's blog entry for September 13, 2011.
The "paralysis by analysis" noted to in the title refers to the futility of asking EPA to evaluate the entire TSCA Inventory akin to the Canadian approach. The Canadian approach was actually "mandated by statute" (via the 1999 amendments to the CEPA) and both Environment Canada and Health Canada were given "seven years and a major infusion of new resources" just to complete the first phase of the process. According to Denison, with nearly four times as many chemicals on the Inventory, and "without the authority and the resources, well, that's just a recipe for paralysis by analysis" to ask EPA to do the same.
Which is why the EPA proposal is so reasonable, according to Denison. He indicates that EDF and the Safer Chemicals Healthy Families coalition "generally support EPA's approach and believe it strikes the right balance between clarity and transparency and avoiding paralysis by analysis." Denison does, however, offer a series of 10 additional suggestions for improving the EPA proposal. The full list can be seen on the EDF blog page, but include broadening the sources of data specified in Step 1 (perhaps by including some of the source from Step 2), consideration of the published literature, adding specific criteria for children's health and exposure, expanding the range of "vulnerable subpopulations" beyond just children's health, and providing additional clarity on how EPA plans to move from Step 1 to Step 2.
Overall, Denison finds that the attempts by EPA to reintroduce "action" into their proposed prioritization and action plan process are much needed. He welcomes EPA looking at chemicals in commerce to identify those for which it would be prudent to take a closer look at their potential risk. And with the additional actions suggested, he believes that it is a good step in the right direction.
To read EDF's analysis and the full list of suggestions, see Richard Denison's blog entry for September 13, 2011.
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