Authorization of biocidal products in the European Union is a two-stage process, where the biocidal active substances are approved in a first step at the European level, and the biocidal products are authorized in a second step at a member state level. If an active substance is designated as candidate for substitution during this process, a comparative assessment must be carried out for each biocidal product containing this active substance. Comparative Assessments, and to develop recommendations for improvements.
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