lexiara

3.

Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance · European Union

Within the 365-day period referred to in paragraph 1, the receiving competent authority shall: draft a report summarising the conclusions of its assessment and the reasons for authorising the biocidal product or for refusing to grant an authorisation (the ‘assessment report’); send an electronic copy of the draft assessment report to the applicant and provide it with the opportunity to submit comments within 30 days; and take due account of those comments when finalising its assessment.

· All articles ·

Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.