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Any evolutions related to new REACh rules ?

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Hello,

According to the European court of justice decision, the threshold should not be considered at the product level but at the article (component) level. As product manufacturers, we must communicate where the concerned substances are located in our products and what are the instructions for safe use.

-> How can we record these new sets of data at the parts level (data received from our suppliers) ?

-> How can we report this set of data at our products level (in BOM reports) ?

Regards,

Pierre.


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