Nanomaterials under Biocidal Products Regulation
Nanomaterials are chemical substances or materials with particle sizes between 1 to 100 nanometres in at least one dimension.
Due to an increased specific surface area by volume, nanomaterials may have different characteristics compared to the same material without nanoscale features. As a result, the physicochemical properties of nanomaterials may differ from those of bulk substances or particles of a larger size.
Many everyday products containing nanomaterials are already on the European market such as batteries, coatings, anti-bacterial clothing and cosmetics. While nanomaterials may offer technical and commercial opportunities, they may also pose risks to our health and the environment. Just like any other substance on the EU market, it is important to ensure that their uses are properly assessed and that any risks are adequately controlled.
ECHA works in close collaboration with Member State competent authorities, the European Commission, NGOs and industry associations as well as international organisations such as the Organisation for Economic Cooperation and Development (OECD), to help implement EU chemicals legislation for nanomaterials.
- 50 % or more of the particles have a size of 1-100 nanometres in at least one dimension
- Particles are in an unbound state or as an aggregate or agglomerate
Monitoring and reporting
- How to report nanomaterial parameters in IUCLID 6 (Annex 8) [PDF] [EN]
- Guidance for identification and naming of substances under REACH and CLP [PDF] [EN]
- ECHA Guidance on Information Requirements and Chemical Safety Assessment for nanomaterials:
- Appendix to Chapter R.6: Guidance on QSARs and Grouping of Chemicals [PDF] [EN]
- Appendix to Chapter R.7a: Endpoint specific guidance [PDF] [EN]
- Appendix to Chapter R.7b: Endpoint specific guidance [PDF] [EN]
- Appendix to Chapter R.7c: Endpoint specific guidance [PDF] [EN]
- Appendix to Chapter R.8: Characterisation of dose [concentration] - response for human health [PDF] [EN]
- Appendix to Chapter R.10: Characterisation of dose [concentration] - response for environment [PDF] [EN]
- Appendix to Chapter R.14: Occupational exposure assessment [PDF] [EN]
- Template to document practical constraints for fulfilling REACH Annex VII and VIII information requirements [PDF] [EN]
- Registering nanoforms: practical advice – 2020 | Webinar Q&A
- Getting ready for revised REACH information requirements for nanoforms – 2019 | Webinar Q&A
- Updated REACH Guidance for nanomaterials - what you need to know – 2017
- How to ensure the safe use of nanomaterials under REACH - Part III: current best practices for human health and environmental exposure assessment and risk characterisation for nanomaterials – 2014
- How to ensure the safe use of nanomaterials under REACH - Part II: Current best practices for human health and environmental hazard assessment for nanomaterials – 2013
- How to ensure the safe use of nanomaterials under REACH Part I – 2012
- New OECD guidance documents for the risk assessment of nanomaterials, News release 27 July 2020
- Companies need to provide more data on nanoforms, News release 24 February 2020
- Updated guidance for registering substances in nanoform, News release 3 December 2019
- Get ready for new REACH requirements for nanomaterials, News release 8 October 2019
- Companies to provide more information on nanomaterials, Press release 3 December 2018