(1)

Alphachloralose was included in Annex I to Directive 98/8/EC of the European Parliament and of the Council (2) as an active substance for use in biocidal products of product-type 14. Pursuant to Article 86 of Regulation (EU) No 528/2012, it was therefore considered approved under that Regulation subject to the conditions set out in Annex I to Directive 98/8/EC.

(2)

On 24 December 2019, an application was submitted in accordance with Article 13(1) of Regulation (EU) No 528/2012 for the renewal of the approval of alphachloralose for use in biocidal products of product-type 14 (‘the application’).

(3)

On 15 October 2020, the evaluating competent authority of Poland informed the Commission that it had decided, pursuant to Article 14(1) of Regulation (EU) No 528/2012, that a full evaluation of the application was necessary. Pursuant to Article 8(1) of that Regulation, the evaluating competent authority is to perform a full evaluation of the application within 365 days of its validation.

(4)

The evaluating competent authority may, as appropriate, require the applicant to provide sufficient data to carry out the evaluation, in accordance with Article 8(2) of Regulation (EU) No 528/2012. In that event, the 365-day period is suspended for a period that may not exceed 180 days in total unless a longer suspension is justified by the nature of the data requested or by exceptional circumstances.

(5)

Within 270 days of receipt of a recommendation from the evaluating competent authority, the European Chemicals Agency (‘the Agency’) is to prepare and submit to the Commission an opinion on renewal of the approval of the active substance in accordance with Article 14(3) of Regulation (EU) No 528/2012.

(6)

Commission Implementing Decision (EU) 2021/333 (3) postponed the expiry date of the approval of alphachloralose for use in biocidal products of product-type 14 from 30 June 2021 to 31 December 2023, in order to allow sufficient time for the examination of the application.

(7)

On 28 April 2023, the evaluating competent authority informed the Commission that the evaluation is delayed due to the need of the evaluating competent authority to assess additional data on the reference specification, and potential carcinogenicity, reproductive toxicity, endocrine disruptor and persistent-bioaccumulation-toxic properties of the active substance.

(8)

Consequently, for reasons beyond the control of the applicant, the approval is likely to expire before a decision has been taken on its renewal. It is therefore appropriate to further postpone the expiry date of the approval for a period of time sufficient to finalize the examination of the application. Taking into account the time-limits for evaluation by the evaluating competent authority, for preparation and submission by the Agency of its opinion and for the Commission to decide whether to renew the approval of alphachloralose for use in biocidal products for product-type 14, the expiry date should be postponed to 30 June 2026.

(9)

After the further postponement of the expiry date of the approval, alphachloralose remains approved for use in biocidal products of product-type 14 subject to the conditions set out in Annex I to Directive 98/8/EC,