Updated Guidance published – Qualitative Risk Characterisation for Human Health
Media enquiries: ECHA Press
The European Chemicals Agency (ECHA) has published an update to the Guidance on Information requirements and chemical safety assessment (IR&CSA) - Part E: Risk Characterisation regarding qualitative risk characterisation for health hazards.
Helsinki, 28 November 2012 – The scope of this consultation on the update of Part E of the Guidance on IR&CSA concerned sections related to qualitative risk characterisation for human health and, in particular, table E.3-1 which makes suggestions for how to do a qualitative risk characterisation when a quantitative risk characterisation is not possible.
The resulting update includes the addition of an entry to also allow decision-making based on CLP hazard statements (instead of only based on the previous Dangerous Substances Directive (DSD) risk phrases). It also introduces new entries for the hazard class Specific Target Organ Toxicity - Single Exposure (STOT-SE). This class was not included in the previous version.
The update results from a regular guidance consultation process. Additionally, sections of Part E outside the scope of the consultation have been updated via a corrigendum covering mainly two topics:
- replacement of references to the DSD by references to the CLP Regulation
- addition of two footnotes to ensure consistency with the new Appendices on "recommendations for nanomaterials" published earlier in 2012.
- Guidance on information requirements and chemical safety assessment
- Support section of the ECHA website
- REACH Regulation
- CLP Regulation
- News Alert- 30 April 2012: Updated Guidance on Information Requirements and Chemical Safety Assessment for nanomaterials
- News Alert- 25 May 2012: Updated Guidance on Information Requirements and Chemical Safety Assessment for nanomaterials