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ECHA calls for comments on etridiazole's reproductive toxicity and carcinogenicity
23-05-2013
The proposal for harmonised classification and labelling (CLH) of etridiazole was submitted by the Netherlands in February 2012 and was already subject to a public consultation which ended on 13 April 2012. After the closure of that public consultation, concerns have been raised by the ...
Final weeks before the 2013 registration deadline
ECHA provides final advice for companies registering by the registration deadline of 31 May 2013
16-05-2013
With only a few weeks to go until the second REACH deadline, all registrants should be making the final arrangements for the submission of their dossier. At this stage, lead and member registrants should have already decided how to meet the relevant information requirements and the ...
Public consultations launched on CLH proposals for two borates and a pesticide
03-05-2013
The CLH proposals for the two borates disodium octaborate, anhydrate and disodium octaborate, tetrahydrate, have been submitted by the Netherlands. Neither substance has an existing harmonised classification and for both substances the dossier submitter is proposing classification for ...
The Board of Appeal annuls an ECHA decision
30-04-2013
Following several exchanges of information between the parties and interveners as well as an oral hearing, the Board of Appeal has granted the Appellant’s request to annul an ECHA decision requiring it to carry out a 90-day repeated dose toxicity study in the rabbit by inhalation on the ...
ECHA: Authorisation list updated
25-04-2013
The amendment of Annex XIV of REACH ("Authorisation List") has been published in April in the Official Journal. Eight new substances are now subject to authorisation for being used after the sunset date. This is the third time that substances have been added to the Authorisation List by the ...
New committee starts working for safe biocidal products
02-04-2013
A new scientific committee in ECHA has been established to contribute to the availability of safe biocidal products in the European markets. The Biocidal Products Committee will have an important role in the approval of active substances and the authorisation of biocidal products under the ...
Follow the REACH 2013 registration progress online
25-03-2013
The new information relates to the number of substances registered for the 31 May 2013 deadline. It also breaks down the registrations by their type, their role in the joint submission, company size and whether the registration was submitted by a manufacturer, importer or an only ...
Substance evaluation under REACH: The annual update of the CoRAP published
21-03-2013
The Community rolling action plan (CoRAP) for 2013-2015 covers 115 substances that are suspected of posing risk to human health or the environment. The updated CoRAP list has been prepared in close cooperation with the Member States, taking into account the agreed risk-based criteria for the ...
EU Court confirms ECHA PBT assessment of substances
12-03-2013
ECHA welcomes the EU General Court's conclusions which confirm the Agency's approach in identifying PBTs and vPvBs as substances of very high concern. The ruling confirms that ECHA's approach in identifying UVCB[1] substances as well as other multi-constituent substances as PBTs[2] or ...
First substance evaluation results - further information needed on 32 substances
08-03-2013
The CoRAP lists substances subject to substance evaluation under REACH. In the first year, 2012, the Member States agreed to evaluate 36 substances. The deadline for submitting the results to ECHA was 28 February 2013. In 32 cases the evaluating Member State concluded to request further ...
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