Data Submission Manual 5: How to complete a - ECHA - Europa

Data Submission Manual
4.2.2. Section 2.1 - GHS
As indicated in the previous chapter, from 1 December 2010 it is compulsory to include
the information on classification and labelling according to the CLP Regulation in all
registration dossiers (except for members of a joint submission). Therefore, if no
repeatable block has been created in section 2.1, this will be a reason for considering the
dossier as incomplete.
When a repeatable block is created in section 2.1 "GHS", all the requested fields of this
repeatable block will be checked for completeness.
With the entry into force of the CLP Regulation, title XI of the REACH Regulation
has been repealed. Therefore, you need to use section 2.1 of IUCLID 5 to specify
the C&L information requested under Article 40(1- c, d, e and f) of the CLP
Regulation.
More detailed information concerning C&L can be found in the Data Submission
Manual 12 "How to Prepare and Submit a Classification and Labelling Notification
Using IUCLID" available on the ECHA website at:
http://echa.europa.eu/web/guest/support/dossier-submission-tools.
In addition, it is highly recommended to consult Annex I of the CLP Regulation for
the classification criteria and the following guidance document for more detailed
instructions on the application of the C&L criteria:
http://echa.europa.eu/web/guest/guidance-documents/guidance-on-clp.
4.2.2.1. Classification
• For each hazard class or differentiation either the two fields, "Hazard category"
and "Hazard statement" must be indicated; otherwise, the field "Reason for no
classification" must be filled in (Figure 27). Note, that the "Reason for no
classification" is pre-set to "Data lacking" by default.
Figure 27: Entry fields for classification
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