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Regulation (EU) No 528/2012 of the European Parliament and of the CouncilShow full title

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)

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Changes over time for: Article 13

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Point in time view as at 31/12/2020.

Changes to legislation:

There are currently no known outstanding effects for the Regulation (EU) No 528/2012 of the European Parliament and of the Council, Article 13. Help about Changes to Legislation

Article 13U.K.Submission and acceptance of applications

1.Applicants wishing to seek renewal of the approval of an active substance for one or more product-types shall submit an application to the [F1competent authority] at least 550 days before the expiry of the approval. Where there are different expiry dates for different product-types, the application shall be submitted at least 550 days before the earliest expiry date.

2.When applying for the renewal of the approval of the active substance, the applicant shall submit:

(a)without prejudice to Article 21(1), all relevant data required under Article 20 that it has generated since the initial approval or, as appropriate, previous renewal; and

(b)its assessment of whether the conclusions of the initial or previous assessment of the active substance remain valid and any supporting information.

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