Introductie: RIVM Introductie CLP

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1 Introductie: RIVM Introductie CLP Martijn Beekman RIVM Bureau REACH Introductie RIVM Rijksinstituut voor Volksgezondheid en Milieu in Bilthoven (Ministerie van VWS) (5 22 ) Onafhankelijk Sinds 1909 ~ 1500 medewerkers Hoe gezond is Nederland? Hoe blijven we infectieziekten de baas? Hoe houden we onze leefomgeving gezond en veilig? 2 1

2 Bureau REACH (en CLP) Onderdeel van het centrum Veiligheid, Stoffen en Producten ~ 15 medewerkers In opdracht van de Ministeries I&M, VWS en SZW Uitvoering REACH en CLP (in alle facetten, m.u.v. handhaving) 3 Voorlichting REACH / CLP helpdesk in samenwerking met RWS Website Risico s van Stoffen: Diverse bijeenkomsten/overleggen 4 2

3 REACH - IT Toegang tot informatie REACH registraties Communicatie met ECHA 5 Opstellen en reageren op stoffen -dossiers Restrictie SVHC Classificatie Stofevaluaties 6 3

4 Comités Bureau REACH adviseert en ondersteunt: RAC (Risk Assessment Committee) SEAC (Socio Economic Assessment Committee) MSC (Member State Committee) RiME (Risk Management Evaluation meeting) CARACAL (Competent Autority meeting REACH and CLP) REACH Committee Management board ECHA Diverse subgroepen en expert groepen 7 Diversen Richtsnoeren (guidance) Overige internationale overleggen bijvoorbeeld OECD en VN GHS Nieuwe ontwikkelingen, risico s 8 4

5 Introductie CLP Classification, labelling and packaging Regulation (EC) No. 1272/2008 Consolidated version, including 1 st ATP, 2 nd ATP and 3 rd ATP 4 th ATP: update due to 4 th revision GHS 5 th ATP: update Annex IV and Annex VI 6 th ATP: update Annex III, IV an VI ATP: Soluble packaging 7 th (Annex VI), 8 th (5 th revision GHS) and 9 th (Annex VI) ATP under discussion

6 Key elements of CLP Identify Manufacturers, importers and downstream users identify and store relevant information Classify Manufacturers, importers and downstream users classify substances and mixtures Label and package Suppliers label and package them in accordance with CLP Communicate Harmonise Manufacturers, importers and downstream users notify substance to ECHA s classification and labelling inventory Suppliers communicate information to Poison Centres CLP implements UN Globally Harmonised System The classification of certain substances is harmonised (Annex VI) 11 Main roles of industry Manufacturer: manufactures a substance Importer: imports chemicals from outside the EEA Downstream user: formulators producer of articles professional user industrial user Distributor: stores or distributes chemicals 12 6

7 Hazard classes Physical hazards Health hazards Environmental hazards 13 C&L inventory Notification to ECHA: Discussion possibility between companies Information is important for both other users and authorities 14 7

8 Harmonised classification (Annex VI) Art. 37.2: Industry proposal for harmonised classification (new entry) Art. 37.1: Member state proposal for harmonised classification (revision and new): Priority for carcinogenic, mutagenic, reprotoxic and respiratory sensitising substances Obligation for plant protection products and biocidal products [In NL the CLH proposals are prepared by RIVM] Procedure: Registry of Intention Submission of the dossier RAC opinion (including public consultation) ATP (adaptation to technical progress): commission proposal 15 CLP and other EU chemicals legislation CLP works together with other EU/national legislation such as: REACH (Regulation 1907/2006) Chemical agents at work (Directive 98/24/EC) Carcinogens or mutagens at work (Directive 2004/37/EC) Industrial emissions (Directive 2010/75/EU) Biocidal Products (Regulation 528/2012) Transport of Dangerous Goods 16 8

9 Important developments and deadlines 1 June 2015: Deadline for classification and labelling of mixtures according to CLP Harmonisation of information for poison centres Improvement of C&L inventory ATPs with new harmonised classification (once per year) Revision GHS every two years, followed by implementation in CLP (ATP) 17 9

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