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CLP > 5. CLP και BREXIT

CLP



5. CLP και BREXIT
CLP

  1. After the end of the transition period, will my UK(Great Britain)-based company still need to classify and label our products according to the EU’s CLP Regulation?
  2. Will my UK(Great Britain)-based company still be obliged to apply the harmonised classification for substances as listed in Annex VI to the CLP Regulation?
  3. Will my UK(Great Britain)-based company still be obliged to seek agreement on the classification of the substances we manufacture in alignment with manufacturers and importers of the same substance within the EU/EEA?
  4. Will my UK(Great Britain)-based company still be obliged to notify the classification of substances in the C&L Inventory?
  5. How will the information that my UK(Great Britain)-based company notified to ECHA be used after the end of the transition period?
  6. When exporting to the UK(Great Britain), will my EU/EEA-based company still need to include in the labels of our products the pictograms and other label elements that the CLP Regulation prescribes?
  7. When our EU/EEA-based company exports to the UK(Great Britain), will the labels affixed to our products still need to be in the English language as required by the CLP Regulation?
  8. How can my UK(Great Britain)-based company transfer C&L notifications to an EU/EEA-based legal entity?
  9. I am an EU/EEA-based company importing mixtures from the UK (Great Britain) supplier. Do I have obligations under Article 45 and Annex VIII (poison centre notifications)? Can I consider my obligations fulfilled by a notification already submitted by my UK supplier?
  10. Can I transfer my poison centres notifications to an EU/EEA-based legal entity?
  11. What will happen after the UK withdrawal, to the Annex VIII data submitted via the ECHA Submission portal by UK-based companies before 1 January 2021?