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 | 1 |
ISIN 28 Ottobre 2022 - Le attività svolte dall’Ispettorato e lo stato della sicurezza nucleare in Italia
Sul sito dell’Ispettora...
ECHA August 2017
Versione 1.3
The Technical Agreements for Biocides (TAB) is an information document that intends to provide the agreements of the Working Groups of the ...
ID 1849 | Update 26.06.2024 / Testo consolidato ufficiale Giugno 2024 - Testo Certifico Maggio 2024
Regolamento (UE) ...
Testata editoriale iscritta al n. 22/2024 del registro periodici della cancelleria del Tribunale di Perugia in data 19.11.2024