CLP
- 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?
- 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?
- 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?
- Will my UK(Great Britain)-based company still be obliged to notify the classification of substances in the C&L Inventory?
- How will the information that my UK(Great Britain)-based company notified to ECHA be used after the end of the transition period?
- 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?
- 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?
- How can my UK(Great Britain)-based company transfer C&L notifications to an EU/EEA-based legal entity?
- 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?
- Can I transfer my poison centres notifications to an EU/EEA-based legal entity?
- 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?