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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 95FA

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[F1[F2Article 95FAU.K.Transitional measures for applications for same biocidal product authorisations under the simplified procedure

1.This Article applies where—

(a)an application was made to the United Kingdom competent authority before IP completion day under Article 4a of Commission Implementing Regulation (EU) No 414/2013 specifying a procedure for the authorisation of same biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council; and

(b)a decision was not made before IP completion day.

2.The application is to be treated as having been made under Article 4a of Regulation (EU) 414/2013.

3.The applicant must—

(a)resubmit the application and any supporting data to the competent authority; or

(b)where the applicant relies on a letter of access—

(i)resubmit the application; and

(ii)ensure that the data owner resubmits the data.

4.Where the applicant does not meet the requirements of this Article, the application must be rejected by the competent authority and Article 89(11) applies as if the application had been submitted in accordance with Article 89(9).

5.For the purposes of this Article, data resubmitted by the applicant or the data owner must include relevant data for the reference product.

6.The resubmission of any application and data referred to in paragraph 3 must be completed in accordance with Article 71 before 31 January 2023.]]

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