It passed the first reading in the European Parliament on 17 November , and the Council of Ministers reached a political agreement for a common position on 13 December Advice and Service CIRS can carry out an assessment for you or your suppliers, in accordance with your specific industry and the relevant restriction list to determine which items do not need to be tested, thus improving the efficiency of your testing strategy and saving money on unnecessary testing. Restrict all uses ie, totally prohibited , such as asbestos, dichloro[ dichlorophenyl methyl]methylbenzene, UGILEC Monomethyldibromodiphenyl-methane and so on. Chemical regulators have overreached. The list of harmful substances is continuously growing and requires organizations to constantly monitor any announcements and additions to the REACH scope.
CIRS can carry out an assessment for you or your suppliers, in accordance with your specific industry and the relevant restriction list to determine which items do not need to be tested, thus improving the efficiency of your testing strategy and saving money on unnecessary testing.
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The level of restriction can be divided into two main categories: Restrict the use or existence in certain products such as: Restrict all uses ie, totally prohibited , such as asbestos, dichloro[ dichlorophenyl methyl]methylbenzene, UGILEC Monomethyldibromodiphenyl-methane and so on. Obligations of Suppliers REACH restrictions list covers a great deal of substances, affecting essentially all industries.
Advice and Service CIRS can carry out an assessment for you or your suppliers, in accordance with your specific industry and the relevant restriction list to determine which items do not need to be tested, thus improving the efficiency of your testing strategy and saving money on unnecessary testing.
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About , chemical substances marketed in the European Union were pre-registered by the 1 December deadline. Although pre-registering was not mandatory, it allows potential registrants much more time before they have to fully register.
Supply of substances to the European market which have not been pre-registered or registered is illegal known in REACH as "no data, no market". REACH also addresses the continued use of chemical substances of very high concern SVHC because of their potential negative impacts on human health or the environment. Some uses of SVHCs may be subject to prior authorisation from the European Chemicals Agency, and applicants for authorisation will have to include plans to replace the use of the SVHC with a safer alternative or, if no safer alternative exists, the applicant must work to find one - known as substitution.
To somewhat simplify the registration of the , substances and to limit vertebrate animal testing as far as possible, substance information exchange forums SIEFs are formed amongst legal entities such as manufacturers, importers, and data holders who are dealing with the same substance. However, this creates a series of new problems as a SIEF is the cooperation between sometimes a thousand legal entities that did not know each other at all before but suddenly must:.
Such submission is a mandatory part of the registration process. Under certain circumstances the performance of a chemical safety assessment CSA is mandatory and a chemical safety report CSR assuring the safe use of the substance has to be submitted with the dossier. The aim of REACH is to improve the protection of human health and the environment by identification of the intrinsic properties of chemical substances.
At the same time, innovative capability and competitiveness of the EU chemicals industry should be enhanced. The EC adopted its proposal for a new scheme to manage the manufacture, importation and supply of chemicals in Europe on in October It came into force on 1 June One of the major elements of the REACH regulation is the requirement to communicate information on chemicals up and down the supply chain.
This ensures that manufacturers, importers, and also their customers are aware of information relating to health and safety of the products supplied. For many retailers the obligation to provide information about substances in their products within 45 days of receipt of a request from a consumer is particularly challenging.
Having detailed information on the substances present in their products will allow retailers to work with the manufacturing base to substitute or remove potentially harmful substances from products.
The list of harmful substances is continuously growing and requires organizations to constantly monitor any announcements and additions to the REACH scope. This can be done on the European Chemicals Agency 's website. A requirement is to collect, collate and submit data to the European Chemicals Agency ECHA on the hazardous properties of all substances except Polymers and non-isolated intermediates manufactured or imported into the EU in quantities above 1 tonne per year.
Certain substances of high concern, such as carcinogenic, mutagenic and reproductive toxic substances CMRs will have to be authorised. Chemicals will be registered in three phases according to the tonnage of the substance evaluation:. More than tonnes a year, or substances of highest concern, must be registered in the first 3 years;. In addition, industry should prepare risk assessments and provide controls measures for using the substance safely to downstream users.
Evaluation provides a means for the authorities to require registrants, and in very limited cases downstream users, to provide further information.
Dossier evaluation is conducted by authorities to examine proposals for testing to ensure that unnecessary animal tests and costs are avoided, and to check the compliance of registration dossier with the registration requirements. The relevant authorities perform substance evaluation when there is a reason to suspect that a substance presents a risk to human health or the environment e.
Therefore, all registration dossiers submitted for a substance are examined together and any other available information is taken into account. The REACH proposal sets up a system under which the use of substances with properties of very high concern and their placing on the market can be made subject to an authorisation requirement.
This authorisation requirement ensures that risks from the use of such substances are either adequately controlled or justified by socio-economic grounds, having taken into account the available information on alternative substances or processes.
The Regulation enables restrictions of use to be introduced across the European Community where this is shown to be necessary. Member States or the Commission may prepare such proposals. Downstream users such as plastic pipe producers should provide detail of their uses to their suppliers. In cases where downstream users decide not to disclose this information, they need to have their own CSR. It passed the first reading in the European Parliament on 17 November , and the Council of Ministers reached a political agreement for a common position on 13 December It came into force on 20 January , and will be fully implemented by
52 rows · The table below is the Annex XVII to REACH and includes all the restrictions adopted in the framework of REACH and the previous legislation, Directive 76//EEC. Each entry shows a substance or a group of substances or a substance in a mixture, and the consequent restriction conditions. REACH Annex XVII: REACH Restricted Substance List Little Pro on Views: Update The Annex XVII of REACH regulation contains the list of restrictions of certain hazardous substances, mixtures and articles for their marketing and use on the European market. Restrictions are normally used to limit or ban the manufacture, placing on the market (including imports) or use of a substance, but can impose any relevant condition, such as .