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REACH, 12 Nov. 2009 1 Supply chain communication Tatjana Humar –Jurič, M.Sc. Semira Hajrlahović Mehić, LL.M.

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Presentation on theme: "REACH, 12 Nov. 2009 1 Supply chain communication Tatjana Humar –Jurič, M.Sc. Semira Hajrlahović Mehić, LL.M."— Presentation transcript:

1 REACH, 12 Nov. 2009 1 Supply chain communication Tatjana Humar –Jurič, M.Sc. Semira Hajrlahović Mehić, LL.M.

2 REACH, 12 Nov. 20092 CONTENT Overview of information Communication DOWN the supply chain Communication UP the supply chain Importers and Non - Community companies Guidance, FAQ

3 REACH, 12 Nov. 20093 Basic framework under REACH

4 REACH, 12 Nov. 20094 OVERVIEW REACH TITLE IV : Information in the supply chain; Articles 31-36 Actors: suppliers Communication Instruments:  SDS  CSR/Exposure scenario

5 REACH, 12 Nov. 20095 Actors Supplier of S/P(mix.) means any:  Manufacturer M  Importer I  downstream user DU or  distributor D placing on the market a substance, on its own or in a preparation, or a preparation Producer P of articles Consumer C

6 REACH, 12 Nov. 20096 Actor's roles Different roles in supply chain REACH: majority of obligations apply to M/I Non-EU manufacturers do not have direct obligations under REACH Importer established within the Community, needs to comply with REACH

7 REACH, 12 Nov. 20097 GOALS of Supply Chain Communication Safety use of substance/preparation/article Risk managment (to lower the risk) To pass on information received from supplier to customers M/I of substances should supply the information on risk managment to other professionals such as DS or D P/I of articles should supply information on the safe use of articles to industrial and professional users, and consumers on request.

8 REACH, 12 Nov. 20098 Risk manegment Risk characterisation under REACH: Estimation of incidence and severity of adverse effects likely to occur in a population/ecosystem due to exposure to a substance Addressing several potential toxic effects and human (sub)populations, and considering each (sub)population’s exposure by relevant exposure routes Focus on most critical effect (with consideration of time scale) Quantitative or qualitative provisons

9 REACH, 12 Nov. 20099 Risk manegment: main goal Environmental risk characterisation Human risk characterisation RCR = intake or concentration/DNEL or DMEL Risk controlled if <1

10 REACH, 12 Nov. 200910 Informing of users CHEMICAL SAFETY REPORT (prof. users) SAFETY DATA SHEET (prof. users, DU, distrib.) LABELL (all users) - - - - - - - - - - - - - - - - - - extent of information, tonage….

11 REACH, 12 Nov. 200911 Chemical Safety Report (CSR) and Safety Data Sheet (SDS) = informing of users = risk manegment

12 REACH, 12 Nov. 200912 Communication DOWN the supply chain (1) SDS OBLIGATORY for transmitting safety info on S/P DOWN the supply chain:  S/P meets the criteria for classification as dangerous- hazardous  Substance is PBT or vPvB  Substances to be included in Annex XIV (substances subject to authorisation)

13 REACH, 12 Nov. 200913 Safety Data Sheet-SDS (1) REACH Regulation (Art.31, Annex II) Provides safety information on all classified chemicals and information from the relevant Chemical Safety Report (CSR) down the supply chain Exceptions:  not hazardous preparations (mixtures)  chemicals e.g.: metals in massive form, alloys, compressed gases … (Annex VI, 67/548/EEC) Enable users to take the necessary measures relating to protection of human health and safety at the workplace, and protection of the environment.

14 REACH, 12 Nov. 200914 SDS (2) Information provided by SDS shall: Meet the requirements set out in Directive 98/24/EC on the protection of the health and safety of workers from the risks related to chemical agents at work Enable the employer to determine whether any hazardous chemical agents are present in the workplace, and to assess any risk to the health and safety of workers arising from their use

15 REACH, 12 Nov. 200915 SDS (3) Format is given in Annex II of REACH Official language of MS where S/P is placed on the market Free of charge in paper or electronically Enforcement: MS Competent Authorities

16 REACH, 12 Nov. 200916 SDS (4) On request also for preparation not classified as dangerous but containing certain dangerous or very high concern substances (authorisation candidates, PBT, vPvB) No SDS obligations for:  S/P for general public (as well as a sufficient info is provided )  Articles

17 REACH, 12 Nov. 200917 SDS (5) – the content 1. IDENTIFICATION OF THE S/P AND OF THE COMPANY/UNDERTAKING 2. HAZARDS IDENTIFICATION 3. COMPOSITION/INFORMATION ON INGREDIENTS 4. FIRST AID MEASURES 5. FIRE-FIGHTING MEASURES 6. ACCIDENTAL RELEASE MEASURES 7. HANDLING AND STORAGE 8. EXPOSURE CONTROLS/PERSONAL PROTECTION 9. PHYSICAL AND CHEMICAL PROPERTIES 10. STABILITY AND REACTIVITY 11. TOXICOLOGICAL INFORMATION 12. ECOLOGICAL INFORMATION 13. DISPOSAL CONSIDERATIONS 14. TRANSPORT INFORMATION 15. REGULATORY INFORMATION 16. OTHER INFORMATION ANNEX (information from CSR!)

18 REACH, 12 Nov. 200918 SDS (6)- new under REACH  Exposure Scenarios (including use and exposure) in an annex to the SDS  The information on uses of S in SDS must be consistent with the ES in the annex, indicating which uses are covered by the single ES  Results from hazard assessments the should be incorporated into the SDS.  SDS for Substances of Very High Concern subject to Authorisatin (SVHC Candidate list )  Structure changes (sections 2 and 3)  Additional info (registration No., e-mail address..)

19 REACH, 12 Nov. 200919 What is a Chemical Safety Report (CSR)? - Document, which details the process and the results of Chemical Safety Assesment (CSA) - CSR shall be : completed for all substances subject to registration in accordance with in quantities of 10 tonnes or more per year per registrant conducted in accordance with paragraphs 2 to 7 of Art.14 and with Annex I of REACH for: - either each substance on its own or - in a preparation or - in an article or a group of substances.

20 REACH, 12 Nov. 200920 Format of CSR PART A 1. Summary of risk management measures 2. Declaration that risk management measures are implemented 3. Declaration that risk management measures are communicated PART B 1. Identification of the substance, its physical and chemical properties 2. Manufacture and uses 3. Classification and labelling 4. Environmental fate properties 5. Human health hazard assessment 6. Human health hazard assessment of physicochemical properties 7. Environmental hazard assessment 8. PBT and vPvB assessment 9. Exposure assessment 10. Risk characterisation

21 REACH, 12 Nov. 200921 Goals of Chemical Safety Assessment (CSA) To ensure that risks (to workers, consumers and the environment) are controlled - identify and apply the appropriate measures accordingly Shall address all identified uses of the M/I or DU Develop exposure scenarios if substances are classified as dangerous or considered to be a PBT/vPvB Document the assessment in the chemical safety report (CSR), including listing of the exposure scenarios, covering Risk Management Measures (including C&L and down stream consequences) To communicate information using the SDS

22 REACH, 12 Nov. 200922 What is an exposure scenario (ES)? describes the conditions under which a substance (as such, in a preparation or in an article) or a group of substances can be ‘safely’ used. is a major element in the CSA on which the exposure assessment and the risk characterisation is based is an instrument for communicating operational conditions of use and risk management measures that are suitable to ensure adequate control of risk in the supply chain (the ES is integrated into the Safety Data Sheet (SDS) system in Annex !!). shall be developed for both the manufacturer’s own manufacturing process and for identified uses; including both uses by the manufacturer or importer and uses further down the chemical supply chain

23 REACH, 12 Nov. 200923 New under REACH: Any actor in the supply chain who is required to prepare a CRS shall place the relevant : Exposure scenario (ES) in an annex to the SDS covering identified uses and including specific conditions resulting from the application!!

24 REACH, 12 Nov. 200924 SDS (8)- update New information on hazards becomes available Info which may affect the risk management measures Authorisation has been granted or refused Restriction has been imposed Access to SDS and other info is given to workers

25 REACH, 12 Nov. 200925 Communication DOWN the supply chain (3) Supplier of ARTICLES: shall inform consumers about substances of very high concern contained in conc. >0,1% ; Also consumer can request such information Distributor: shall pass on info received from supplier to costumer to ensure safety use of S/P

26 REACH, 12 Nov. 200926 Communication DOWN the supply chain (4) If SDS is not required supplier has to communicate:  key risk info about S, in particular if the S is subject to authorisation or restriction  Other relevant/available info to enable appropriate risk management

27 REACH, 12 Nov. 200927 Communication UP the supply chain (1) Applies if you are using S/P in the context of industrial or professional activities and you do not supply further down the chain Communicate to your supplier next up the chain

28 REACH, 12 Nov. 200928 Communication UP the supply chain (2) Communication of :  NEW INFO on hazardous properties that become available, regardless of the uses concerned  Any other information that might call into question the appropriateness of the risk management measures identified in SDS

29 REACH, 12 Nov. 200929 Communication UP the supply chain (3) Distributors: obligation to pass on info received to the next actor in the supply chain Downstream users:  Have right to make their use known to the supplier  Provide sufficient info to prepare an exposure scenario (important for registrants preparing CSR including ES)

30 REACH, 12 Nov. 200930 DU Follow the RM advice and the operational conditions of use described SDS received from the supplier, including the exposure scenarios If relevant, forward the advice to actors further down the supply chain Obligation to use S according to the conditions laid down in the authorisation granted Notify to ECHA the use of S subject to authorisation

31 REACH, 12 Nov. 200931 DU should inform (in writing) suppliers about use of a substance → supplier considers use in relation to his registration. use be an identified use and have an ES your conditions of use, unless the registrant cannot support the use. Before informing supplier: check the use mappings prepared by industry association, and/or any communication from supplier about the uses he intends to cover. ECHA has published a Fact Sheet that provides background information and further details about the DS’ right to inform their suppliers of the use they make of thesubstance (see gudiance!). If the substance needs to be registered before 1 December 2010: DU must inform the supplier till 30 Nov. 2009!!

32 REACH, 12 Nov. 200932 DU DU obligations when his use is not covered by the SDS-options:  Adapt the conditions of use to those described in the SDS  Implement or recommend ES which includes as a minimum the conditions described in the ES communicated to him  Make the use known to the supplier with the aim of making it an identified use based on the manufacturer’s CSA  Perform your own CSA for that particular use and record it in a Chemical Safety Report - CSR (if the total amount used is 10 t/year or more). Notify your use to ECHA  Switch to another supplier of the substance if that supplier covers your specific use in his SDS

33 REACH, 12 Nov. 200933 Importers and Non - Community companies Non Community manufacturers do not have direct obligations under REACH Non Community manufacturers:  Work with EU importer  Established or use EU-legal entity  Use Only representative

34 REACH, 12 Nov. 200934 Importers Identify which S/P require SDS:  new format, include ES  submit to costumer Identify S subject to restriction/authorisation and pass info down the chain For articles:  Check if article contains SVHC  Provide info on safe use (min. name of S)

35 REACH, 12 Nov. 200935 3.1: Preparing the registration dossier 3.1: Preparing the registration dossier 3.3: Information requirements 3.3: Information requirements 3.2: Preparing the CSR 3.2: Preparing the CSR 3.10: Guidance on substance ID 3.10: Guidance on substance ID 3.5: Guidance for downstream users 3.5: Guidance for downstream users 3.8: Requirements for articles 3.8: Requirements for articles 3.6: Guidance on C&L under GHS 3.6: Guidance on C&L under GHS 3.7: Guidance on applications for authorisation 3.7: Guidance on applications for authorisation 3.9: Guidance on SEA 3.9: Guidance on SEA 3.4: Guidance on data-sharing 3.4: Guidance on data-sharing RIP-3 REACH Guidance for Industry http://ec.europa.eu/echa/

36 REACH, 12 Nov. 2009 36 Thank you! Tatjana.Humar-Juric@gov.si Semira.Mehic@gov.si


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