The following table specifies the REACH data points, i.e. the information requirements as laid down in Annexes VI - X and referred to in Article 10 of the REACH regulation, and the corresponding IUCLID sections for recording the required data. In the Remarks column, hints are given as to what specific data entry fields should be completed in order to specify REACH data requirements. This is necessary when several REACH endpoints are covered by one IUCLID section. For example, REACH data point 8.4 Mutagenicity includes three different types of genotoxicity test systems, which are all recorded in IUCLID section 7.6.1 Genetic toxicity: in vitro. The type of test system is documented in fields Type of genotoxicity (e.g. "chromosome aberration") and Type of study (e.g. "in vitro mammalian cell micronucleus test").