Download presentation
Presentation is loading. Please wait.
Published byGervais Burke Modified over 8 years ago
1
The European Engineering Industries Association How Downstream Users REACH? Impacts and challenges of REACH for EU Cutlery, Flatware, Holloware, and Cookware Industries FEC General Assembly 20 November 2007 Françoise Duplat Orgalime secretariat
2
The European Engineering Industries Association ES UK IE BE LU NL CH FR PT IT DE DK NO PL SL CZ SE FI LV LT BG 35 Member Associations 23 European Countries 130 000 Companies €1779 Bn output 2006 (EU-27 estimates for the whole engineering industry) 10.6 Mio employment AT HR
3
The European Engineering Industries Association Brief outline Introduction REACH priorities for DU Communication in the supply chain Substances in articles Authorisation procedures Conclusion
4
The European Engineering Industries Association Why « REACH »? REACH: « Registration Evaluation Authorisation of Chemicals » Before REACH – various legislation relating to chemicals : Directive 67/548/EEC, Directive 1999/45/EC, Regulation (ECC) n° 793/93, Directive 76/769/EEC etc BUT lack of harmonisation between so-called «new» and « existing» substances Therefore elaboration of « REACH Regulation » Publication of the COM Proposal on REACH: 29 Oct. 2003 Negociation European Parliament and Council: end of 2003-Dec. 2006 European Regulation n° 1907/2006 adopted 18 Dec. 2006 Publication in EU Official Journal : 30 Dec. 2006 Creation of European Chemicals Agency (ECHA)
5
The European Engineering Industries Association REACH Regulation n°1907/2006 Entered into force on 1st June 2007 Directly applicable and full harmonisation except enforcement Strengthened industry responsibility to provide and communicate safety information on substances and to properly manage the risk realted to their use. Scope: All substances, on their own, in preparations, in articles Exemption to scope: radioactive, non-isolated intermediates, waste, transport, transit or reexportation, interest of defence Further exemptions to some parts of REACH, e.g. for R&D, acc. to use, nature of substance etc All EU actors of supply chain concerned: from e.g. EU manufacturer/importer (M/I) of substances to downstream users (DU)/article producer or article importer REACH obligations according to role in supply chain
6
The European Engineering Industries Association Orgalime practical guide for downstream users, article producers and article importers to understanding Regulation N°1907/2006 on REACH (May 2007) Available free of charge at www.publications.orgalime.org Structure: Introduction (definitions, acronyms etc.) Overview important dates and deadlines Orgalime quick screens More detailed guidelines on selected issues One page summary on timelines and obligations Substance manufacturer/ importer e.g. chemical industry Formulator of preparations (“1 st level downstream users”) e.g. paint manufacturer Downstream users of substances/ preparations (“2d level downstream users”) Orgalime Industries FEC industries Article producers/ Article importers Orgalime Industries FEC industries What focus for Orgalime?
7
The European Engineering Industries Association REACH priorities for Orgalime industries In the context of registration of substance: Communication in the supply chain Title V (mainly) Registration of substances intentionally released from articles under certain conditions Article 7 Notification of substances of very high concern present in articles under certain conditions Article 7 Communication requirements on substances of very high concern present in articles under certain conditions Article 33 Use of authorised substances/application for authorisation for substances included in Annex XIV REACH Title VII? Check Orgalime quick screens 1,2,3,4
8
The European Engineering Industries Association Establish inventories with key information according to role What is my role in the supply chain? First and foremost… Downstream user? Importer? (« only representative» nominated in the EU?) Article producer/importer? A company may play several roles! Takes time and ressources - early preparation is key Check REACH scope/exemptions? Check Orgalime Guidelines 1,2,3,4 Downstream user means…. “any natural or legal person established within the Community, other than the manufacturer or the importer, who uses a substance, either on its own or in a preparation, in the course of his industrial or professional activities (…) Article producer means…. “means any natural or legal person who makes or assembles an article within the Community”
9
The European Engineering Industries Association Registration procedure in a nutshell Registration of substances on their own or in preparations, intentionally released from articles ≥ 1 t/y per M/I For “non phase-in substances” ≥ 1 t/y: as of 1/06/2008, before manufacturing/importing/putting on the market For “phase-in” substances ≥ 1 t/y: transitional regime ≥1000 t/y, CMR ≥1 t/y, aqu.tox. ≥100 t/y : 30 /11/2010 100 - 1000 t/y: 31/05/2013 1- 100 t/y : 31/05/2018 To benefit from transitional regime: PRE-REGISTRATION required! “No data - no market” DU to communicate uses to allow manufacturer/importer (i.e. supplier) to complete registration dossier ·
10
The European Engineering Industries Association Communication in the supply chain (1) ESSENTIAL to ensure that substances used will be pre-registered/registered by supplier Pre-registration : between 1/06/2008 and 1/12/2008 (Art. 28) DU not considered as potential registrant List of pre-registered substances on the ECHA website by 1/1/2009 Notification to Agency of interest for a non pre-registered substances DU may be part to Substance Information Exchange Forum (SIEF)? Check Orgalime guideline 5 « No data - No market » Possible consequences on continuity of supply Time is running!
11
The European Engineering Industries Association Communication in the supply chain (2) Supplier (M/I) to compile registration dossier Technical dossier: starting at 1 t/y Chemical safety report (CSR): starting at 10 t/y CSR to include exposure scenario (ES) if substance is dangerous, PBT or vPvB ES to cover manufacture of sub. and DU identified uses DU «identified use» covered ? DU has the right to make his use known to supplier (« brief description of use ») DU to provide sufficient information to allow supplier to prepare exposure scenario/use and exposure category (ES/UEC) for his use ES annexed to safety data sheet (SDS)? Check Orgalime guideline 5
12
The European Engineering Industries Association Important to BE PRO-ACTIVE and inquire early enough on supplier’s policy towards substance/preparation used Communication in the supply chain (3) Possible uses advised against, but only for reasons of protection of human health or the environment If no SDS but risks management measures (RMMs): Article 32 DU to identify, apply and where suitable recommend RMMs ( listed in SDS or Article 32) 12 Months to comply with Art. 37 after receiving registration number in SDS Further DU communication duties? Check Orgalime guideline 5
13
The European Engineering Industries Association DU own chemical safety report Specific cases : DU to perform own chemical safety report (CSR) and report to ECHA (Art. 37.4, 38 and Annex XII) for: Use outside conditions described ES/UEC of supplier Use advised against (protection of health and the environment) DU to identify, apply and where suitable recommend RMMs of his own CSR Information to be kept available and up to date Exemptions foreseen!? Check Orgalime guideline 6 Requires specific chemical knowledge Time consuming and expensive Make sure supplier’s ES covers DU uses
14
The European Engineering Industries Association Substances in articles What is an « article »? “an object which during production is given a special shape, surface or design which determines its function to a greater degree than does its chemical composition” (Art. 3.3)? Check Orgalime Guidelines 7,8,9 E.g.: electrical and electronic equipment, a screw, a bolt, a motor, cutlery, cookware, etc.
15
The European Engineering Industries Association Registration of substances intentionally released from articles Article producer,article importer/«only representative» to REGISTER any substance in articles if Intentional release under normal or reasonably foreseeable conditions of use AND Total amount of substance present in articles over 1 tonne per producer/ importer per year (Art. 7.1) Same timeline to register as for any other substances (2010- 2013-2018) - Registration fees NO registration of substance in article if substance has already been registered for that use (Art. 7.6) Check Orgalime guideline 7?
16
The European Engineering Industries Association Notification of substances present in articles? Check Orgalime guideline 8 Article producer,article importer/«only representative» to NOTIFY substances in articles if the substance Has been identified as of very high concern (Art.57) i.e. CMR 1 & 2, PBT/ vPvB and any other substance of equivalent concern AND Is present in articles in quantities over 1 t/y AND Has been included in the candidate list (Art.59) AND Is present in the article above a concentration of 0.1% w/w (Art. 7.2) FROM 1/06/2011, 6 months after inclusion in candidate list Notification of substance in article NOT required If substance has already been registered for that use (Art. 7.6) If exposure to human health and the environment, including disposal, can be excluded (appropriate instructions to recipient) (Art. 7.3)
17
The European Engineering Industries Association Further points to consider…. ECHA to possibly require registration for substances present in articles under certain conditions (Art. 7.5) Concentration calculation « 0.1% w/w » at the level of the article Consequences on smooth running of supply chain and just in time delivery of articles
18
The European Engineering Industries Association Communication requirements on substances in articles Supplier of an article to provide sufficient information available to him, as a minimum name of substance, to recipient of article to allow safe use if the substance Is identified as of very high concern AND Is included in the candidate list for inclusion in Annex XIV AND Is present in the article in concentration above 0.1% w/w Extended to consumers upon request (within 45 days free of charge)? Check Orgalime guideline 9
19
The European Engineering Industries Association Authorisation procedure (1) Concerns substances of very high concern on their own/in preparations/ incorporated in articles during process phase « Progressive» procedure: Sub. incorporated in the candidate list Priority list from ECHA no later than 01/06/09 Further inclusion of sub. in Annex XIV Application for authorisation (by M/I/DU - analysis of alternatives - fees!) COM to decide on granting/reviewing authorisation NO tonnage threshold DU may use a substance listed in Annex XIV if authorisation granted for that use up the supply chain Notification to ECHA within 3 months of first supply! Exemption certain uses and categories of uses Further exemptions foreseen! Two routes foreseen? Check Orgalime guideline 10
20
The European Engineering Industries Association Authorisation procedure (2) An authorisation for the use of a substance listed in Annex XIV will be granted only if : Risks adequately controlled, OR Adequate control cannot be demonstrated but it is shown that socio-economic benefits outweigh the risk to human health or the environment arising from the use of the substance and if there are no suitable alternative substances or technologies.? Check Orgalime guideline 10
21
The European Engineering Industries Association Possible consequences of authorisation procedures Substance withdrawal from the market Disruption in the supply chain Technology changes Costly and time consuming procedures (analysis of alternatives and where such alternative exists – substitution plan) DU to make sure that the substance used is authorised for his use up the supply chain
22
The European Engineering Industries Association Guide available free of charge at www.publications.orgalime.org To know more…. Orgalime REACH guide?
23
The European Engineering Industries Association Conclusion REACH : complex legislation New duties for inter alia downstream users, article producers and article importers Important to prepare NOW Orgalime practical guide to understanding REACH Regulation 1907/2006 http://publications.orgalime.org/
24
The European Engineering Industries Association Thank you for your attention! Orgalime Diamant building 5 th floor 80 Boulevard Reyers 1030 Brussels Secretariat@orgalime.org Tel.:0032.(0)2.706.82.35 Fax.:0032.(0)2.706.82.50 www.orgalime.org
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.