The basic principle in the Biocidal Products Regulation ((EU) No 528/2012 (BPR)) is that a biocidal product (BP) must be authorised before it can be made available on the market or used in the European Union (EU)/ European Economic Area (EEA).
This takes place in two consecutive steps. As the first step, the active substance is evaluated and, provided the criteria are fulfilled, is then approved in a specified product-type (PT). The second step is the authorisation of each BP consisting of, containing or generating the approved active substance(s).
This document concerns the first step, approval of active substances.
October 2016
Collegati
| Descrizione | Lingua | Dimensioni | Downloads | |
|---|---|---|---|---|
 |
Abbonati Chemicals
|
EN | 5803 kB | 3 |
This publication has been prepared by the European Industrial Gases Association to present data that shows that metallic particles do not migra...
Linea Guida Assogastecnici per la redazione di Etichette e Schede di Dati di Sicurezza per le principali categorie di Miscele
Etichette e Schede di Dati ...
Regolamento delegato (UE) 2020/217 della Commissione del 4 ottobre 2019 che modifica, ai fini dell’adeguamento al progresso tec...
Testata editoriale iscritta al n. 22/2024 del registro periodici della cancelleria del Tribunale di Perugia in data 19.11.2024