Nanomaterijali u skladu s Uredbom o biocidnim proizvodima
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REACH
- Što je REACH
- Identifikacija tvari
- Registracija
- Evaluacija
- Odobrenje
- Ograničenja
- Komunikacija u lancu opskrbe
- Popis tvari kandidata u proizvodima
- Zakonski propisi
- Pokusi na životinjama u skladu s uredbom REACH
- Izvršenje zakona
- Nanomaterijali
- Procjena regulatornih potreba
- PBT assessment
- Endocrine disruptor assessment
- Cooperation with authorities and stakeholders
- Tvari s potencijalno spornim karakteristikama
Nanomaterijali u skladu s Uredbom o biocidnim proizvodima
Nanomaterijali su kemijske tvari ili materijali koji se proizvode i koriste u jako malim razmjerima. Njihova se građa kreće u rasponu od približno 1 do 100 nm u barem jednoj dimenziji.
Nanomaterijali imaju jedinstvene i istaknutije karakteristike u usporedbi s jednakim materijalom bez nanostupanjskih značajki. Stoga se fizičko-kemijske značajke nanomaterijala mogu razlikovati od značajki masivnijih tvari ili većih čestica.
Nanotehnologija se ubrzano širi. Širok raspon proizvoda koji sadržavaju nanomaterijale već se nalazi na europskom tržištu (primjerice baterije, premazi, antibakterijska odjeća, kozmetika, prehrambeni proizvodi). Nanomaterijali otvaraju tehničke i komercijalne prilike, ali mogu predstavljati rizik za okoliš i izazvati zabrinutost u vezi sa zdravljem i zaštitom ljudi i životinja.
- Uredba REACH i Uredba o razvrstavanju, označavanju i pakiranju tvari i smjesa
- Uredba o biocidnim proizvodima (BPR)
- 50 % ili više čestica veličine su od 1 do 100 nm u barem jednoj dimenziji
- čestice su u nevezanom stanju, u obliku agregata ili aglomerata
Nadzor i izvješćivanje
ECHA
- How to prepare registration dossiers covering nanoforms [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]
OECD
- 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
- Search for nanomaterials on the EU market
- ECHA Nanomaterials expert group
- EU nanomaterials observatory (EUON): Overview of REACH Annex modifications and available methods
- Group assessing already registered nanomaterials (GAARN) - meeting reports
News
- 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