Download presentation
Presentation is loading. Please wait.
Published byNeal McCarthy Modified over 9 years ago
1
& H AS HEALTH AND SAFETY AUTHORITY REACH and Downstream Users Marie McCarthy REACH GI Inspector Health and Safety Authority
2
& H AS HEALTH AND SAFETY AUTHORITY Am I a Downstream User ?
3
& H AS HEALTH AND SAFETY AUTHORITY Registration As it applies to Downstream Users (DUs)
4
& H AS HEALTH AND SAFETY AUTHORITY Registration - A Phased Process nNon-phase in Substances Registration required before manufacture/import/use nPhase-in Substances –3 years> 1000 t/yr CMRs Cat 1&2 >1 t/yr R50/53 > 100t/yr –6 years >100 t/yr –11 years > 1 t/yr
5
& H AS HEALTH AND SAFETY AUTHORITY Registration of Substances in Articles Required where Substance is present at > 1 t/yr per producer or importer Substance is intended to be released under normal or forseeable conditions Unless substance has already been registered for that use
6
& H AS HEALTH AND SAFETY AUTHORITY Notification of Substances in Articles Required where Substance meets criteria in Art 54 and is identified according to Art 56(1) Substance present at > 1 t/yr/M or I Substance present at > 0.1% w/v Unless M/I can exclude exposure to humans & environment under normal & forseeable conditions of use.
7
& H AS HEALTH AND SAFETY AUTHORITY Low Volume (1-10 t/a) Substances Annex V testing required for Non phase-in substances in all cases Phase-in substances meeting one or both criteria in Annex I ( c ) -Likely to meet criteria for CMR Cat 1,2 or -Wide dispersive use and likely to be classified as dangerous Phase-in substances not meeting criteria in Annex I ( c ) only need physicochemical studies
8
& H AS HEALTH AND SAFETY AUTHORITY Tools used by Industry CSA used to determine which risk management measures and operational conditions are necessary to ensure risks to human health and environment are adequately controlled CSR used to document the appropriate risk management measures and operating conditions to ensure adequate control Exposure scenario (ES) is a description of the set of conditions for use of a substance so that risks are adequately controlled. This must reflect the outcome of the CSA, be documented in the CSR and annexed to SDS SDS used to communicate risk management measures downstream.
9
& H AS HEALTH AND SAFETY AUTHORITY Chemical Safety Assessment n CSA (Annex I) at > 10t/yr n Registrant must ensure that risks are adequately controlled for manufacture and/or each identified use n Must specify risk management measures for each exposure scenario n DU has a right to identify use to M/I n M/I includes this in his CSR if he can support the use n DU may choose not to identify use but may have to notifyChemicals Agency & perform CSA
10
& H AS HEALTH AND SAFETY AUTHORITY Exposure Scenario - conditions ensuring adequate control Physicochemical characteristics Process description Operating conditions Risk management measures Populations exposed Must cover entire life cycle including use in articles, consumer use, waste disposal etc. Process-specific conditions >>>> broad, generic ESs covering multiple uses/substances
11
& H AS HEALTH AND SAFETY AUTHORITY Derivation of an Exposure Scenario Exposure Assessment Exposure Scenarios Existing Knowledge/data Classification and labelling Risk characterisation Adequate control Hazard Identification Hazard Assessment Exposure Scenarios (final) Documented in CSR and SDS
12
& H AS HEALTH AND SAFETY AUTHORITY Substance X in Paints for Brushing/Application by Roller Standardised exposure scenario for group of substances outlining Protective clothing Maximum periods of exposure Cleaning of brushes/rollers etc Disposal of waste
13
& H AS HEALTH AND SAFETY AUTHORITY Substance X used in Spray- painting of Cars Process- specific exposure scenario outlining Maximum periods of exposure Minimum requirements for the equipment (booth, breathing apparatus) Filtering efficiency Cleaning frequency and procedures Protective clothing Hygiene measures Waste disposal
14
& H AS HEALTH AND SAFETY AUTHORITY Is my use covered by my supplier’s registration ?
15
& H AS HEALTH AND SAFETY AUTHORITY Am I covered by Suppliers CSA ? DU Am I inside ES? SDS + Exposure Scenarios (ES) Apply ES No Notify Agency Do targeted CSA and CSR No Make use known to the supplier Yes
16
& H AS HEALTH AND SAFETY AUTHORITY Do I need to act? DU takes no further action in the following situations: He is using less than 1 t/yr He is operating within the conditions of an exposure scenario communicated via SDS and has implemented recommended RMM on his site SDS not required for substance (e.g. not dangerous) CSR not required for M/I ( e.g. < 10 tonnes/yr) He is using it for PPORD
17
& H AS HEALTH AND SAFETY AUTHORITY I need to act The DU must complete a CSR and report to Agency in the following situations: CSR required and He is operating outside exposure scenario communicated in an SDS or He has chosen to keep his use secret or M/I has not taken account of it Methodology for DU CSA in Annex XI Must implement appropriate Risk Management measures (RMM) on own site and inform DUs of appropriate RRM for their use
18
& H AS HEALTH AND SAFETY AUTHORITY DU Report DU Report is not a registration Limited information on identity of DU and supplier, identity of substance and generic use description In limited circumstances, testing proposal may be required – dossier evaluation Reporting not required for small quantities (< 1 tonne)
19
& H AS HEALTH AND SAFETY AUTHORITY Information Flow Through the Supply Chain
20
& H AS HEALTH AND SAFETY AUTHORITY Information flow through the Supply Chain SDS main tool Extended scope & role All dangerous substances and prepartions placed on the market PBTs/vPvBs identified by Annex XII criteria Must be consistent with CSA Exposure scenarios annexed to SDS Information flow up and down supply chain
21
& H AS HEALTH AND SAFETY AUTHORITY Roles for DUs under REACH Check compliance with suppliers exposure scenario If not covered, and where necessary, report to Agency and carry out a CSA Comply with any authorisation and restriction conditions Communication upstream & downstream
22
& H AS HEALTH AND SAFETY AUTHORITY Supports for DUs & SMEs Guidance for downstream users (RIP 3.5) Guidance on articles (RIP 3.8) Tools for SMEs Trade Associations - development of standardised use descriptions National helpdesk – Health and Safety Authority Agency helpdesk
23
& H AS HEALTH AND SAFETY AUTHORITY Benefits for DUs & SMEs Improved access to information Better quality of information Informed decision-making Improved worker safety Reduced liability and compensation costs Increased innovation
24
& H AS HEALTH AND SAFETY AUTHORITY Risks for SMEs and DUs Increased costs Withdrawl of substances Disclosure of confidential business information
25
& H AS HEALTH AND SAFETY AUTHORITY Timelines Nov 2005EP First Reading Dec 2005Council political agreement Autumn 2006Second Reading 2006/2007Development of IT tools and guidance for industry & MS April 2007Entry into force April 2008Agency operational. Registration and other provisions commence
26
& H AS HEALTH AND SAFETY AUTHORITY What should I do now ? Monitor development of REACH and Guidance documents Assess your use of chemicals Think about implications of REACH for your business Dialogue a.s.a.p!!!
27
& H AS HEALTH AND SAFETY AUTHORITY Useful Websites Commission Websites http://europa.eu.int/comm/enterprise/rea ch http://europa.eu.int/comm/environment/ chemicals/reach ECB Websitehttp://ecb.jrc.it/http://ecb.jrc.it/ Health and Safety Authority Website www.hsa.ie www.hsa.ie Queries on REACH wcu@hsa.iewcu@hsa.ie
Similar presentations
© 2024 SlidePlayer.com Inc.
All rights reserved.