Monthly Briefing – October 2010 issue
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- Geraint Roberts reports from ECHA's recent stakeholders' day about the agency's expectations about the first REACH registration deadline, C&L notification and next year's challenges;
- Our Editor, Mamta Patel, looks at the issues debated at ECHA's workshop in September on the use of non-testing methods for hazard assessment;
- Sean Milmo examines how scientists on both sides of Atlantic are developing the concept of toxicity testing based on the mapping of toxicological pathways;
- Mamta Patel explains how a debate about deca-BDE raises the question of how to classify a substance if the parent molecule is not hazardous but it breaks down to congeners that are;
- In a joint submission, Geraint Roberts and Philippa Jones look at where strategies on endocrine disrupters are heading in the US and EU;
- With the US mid-term elections looming, Elizabeth Grossman assesses the propsects for TSCA reform if the Republicans make the gains pundits predict;
- US lawyer Lynn Bergeson sets out industry's concerns about the US EPA's proposed changes to information reporting rules;
- Emma Chynoweth looks at how US states and companies like Hewlett-Packard are using an NGO-developed tool to move to less hazardous chemicals;
- Dr REACH, Steffen Erler, explains how a registration number is not necessarily needed straight after the 30 November deadline to prove that a substance is being registered in accordance with REACH;
- Mayer Brown's Jean-Philippe Montfort and Giovanni Indirli look at companies' duties for substances that need reclassification;
- In this month's Guest Column, French MP Gérard Bapt argues that governments must do more to reduce the public's exposure to endocrine disrupters.
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