1 / 17

Impact of REACh on non-EU industries

Korea-EU Joint Workshop Program Seoul, Dec. 3rd 2007. Impact of REACh on non-EU industries. Attorney-at-Law, Information Scientist Chemistry Stefanie Merenyi. Society for institutional analysis University of applied sciences, Darmstadt, Germany. Overview. (New) principles of REACh

faith
Download Presentation

Impact of REACh on non-EU industries

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Korea-EU Joint Workshop Program Seoul, Dec. 3rd 2007 Impact of REACh on non-EU industries Attorney-at-Law, Information Scientist Chemistry Stefanie Merenyi Society for institutional analysisUniversity of applied sciences, Darmstadt, Germany

  2. Overview • (New) principles of REACh • Approaches to realization • Sanctions • Need for communication • Summary: Effects on Non-EU manufactures

  3. (New) principles of REACh • No marketing of substances with unknown risks: “no data no market” Reduction of animal testing (vertebrates) “only as a last resort” • Principle of territoriality: actors must be established within the EU

  4. Approaches to realization • “no data no market” Need for knowledge of substances Need for testing of substances REACh: by means of registration (AnnexVI-XI) WHO has to register ?

  5. Approaches to realization • “no data no market” Registration obligation: Manufacturers / Importers of 1 t/a • substances on their own • substances in preparations • Substances in articles intended to be released WHEN?

  6. Approaches to realization • “no data no market” Registration obligation starts: 01. June 2008 BUT regarding the testing of Existing Substances (EINECS= European INventory of Existing Commercial Chemical Substances) DELAY is possible Transitional periods depending on tonnage and risks of the substance (max. until 01. June 2018) Only with PRE-REGISTRATION !!!

  7. Phase-in-System: transitional periods EIF of single duties, e. g. registration Only when pre-registered between 01.06. – 30.11.2008 Entry into force (EIF) in general

  8. Approaches to realization • “no data no market”: pre-registration • Care for pre-registration of existing substances • WHEN: Only 01. June – 30. November 2008 • WHERE: http://ec.europa.eu/ • FEES ? None for pre-registration but for registration later (tonnage) no registration fee 1-10 t (data complete) • WHITHOUT: no marketing until registration (testing) = no benefit from the transitional periods

  9. Approaches to realization • “no data no market”: articles Notification obligation: Producers / Importers of articles with 0,1 % w/w SVHC (1 t/a) • Substance of very high concern (e. g. carcinogenic, mutagenic, toxic reprod.) candidate list WHEN? Not before June 2011.

  10. Approaches to realization • “no data no market”: articles Regarding SVHCs in articles: Consumers may demand information on the existence / absence of SVHCs > 0,1 % w/w in articles from any supplier (“black list”) !

  11. Approaches to realization • “no data no market”: articles The Agency may require importers of articles to submit a registration if the Agency has grounds for suspecting that: (i) the substance is released from the articles, and (ii) the release of the substance from the articles presents a risk to human health or the environment. WHO is the importer ?

  12. Approaches to realization • Principle of territoriality REACh actors are established inside the EU.  Importers must be • Company / natural person based in EU • E. g. the European customers (needs to sum up all imported amounts of a substance) • Only-Representative (based in EU) • company / natural person with sufficient background (relevant tonnage per Non-EU-manufacturer)

  13. Sanctions Art. 126 REACh: Member States shall lay down the provisions on penalties  Different penalties in different Member States. • For the Non-EU Manufacturer: --- • For REACh actors inside the EU • Depending on their national legislation • Proposal in Germany: • Until 2 years of imprisonment for manufacturing / marketingwithout registration • Until 5 years of imprisonment if a severe damage is caused

  14. Need for Communication European Importer needs all relevant data for registration / notification If • Importer = European Customer Non-EU-Manufacturer has to provide data to every European customer • Importer = Only Representative Non-EU-Manufacturer has to provide data to the only representative

  15. Need for Communication How can the European Importer get all relevant data for registration / notification ? • From the Non-EU-Exporter Non-EU-Manufacturer has to know / test substance himself  Check for synergies, e.g. from Korean ECL, Toxic Chemicals List, Observational Chem. List, … ! • EU-based Importer will test the substance himself Non-EU-Manufacturer will face “effects” on his profit margin

  16. Summary:Effects on Non-EU manufactures How to proceed to export chemicals from Korea to the EU? • Contact your European Customers (Can they become the importer?) OR • Establish an Only Representative START NOW !

  17. Further information:www.merenyi.net

More Related