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The Guidance document on the Registration has been updated. The updated document describes when and how to register a substance under REACH. It consists of 2 parts: one on the Registration tasks and obligations and the other on the preparation of the Registration dossier.
The most important updates have been made on the following points:
Consequence of changes in legal entities Only Representative More information about the structure of the registration number. … In appendix 3 of the guidance document you can find the list with updates.
The RIP for Intermediates has been updated and describes when and how specific provisions for the registration of intermediates under REACH can be used. Appendix 3 shows the total list of updated parts of the text.
Appendix 1 gives the update of the total document. This updated document describes specific provisions under REACH for substances manufactured, imported and used in scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD).
Source: ECHA-website
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