Art. 89
Biocidal Products Regulation · 32012R0528 · every event for this act · on EUR-Lex
Transitional measures
3 changes recorded across 3 events, newest first.
in force 2024-06-11 DEFERRED+5 −5§
Amended by Regulation (EU) 2024/1398 32024R1398
applies from: 2030-12-31
dates added to the text: 2030-12-31 · dates removed: 2024-12-31
The target date for completing the Commission's work programme on existing active substances was changed from 31 December 2024 to 31 December 2030.
All other text of the provision, including the surrounding transitional rules in paragraphs 2 through 4, remains the same between the two versions.
Cited: Art. 89, v2 · Art. 89, v1
text before / after
02012R0528-20240526 → 02012R0528-20240611
Article 89
Transitional measures
1. The Commission shall carry on with the work programme for the systematic examination of all existing active substances commenced in accordance with Article 16(2) of Directive 98/8/EC with the aim of achieving it by 31 December 2024. 2030. To that end, the Commission shall be empowered to adopt delegated acts in accordance with Article 83 concerning the carrying out of the work programme and specification of the related rights and obligations of the competent authorities and the participants … 740 unchanged words … market with effect from 180 days after the date of the decision of the authority; and
(b) use of existing stocks of the biocidal product may continue for up to 365 days after the date of the decision of the authority.
in force 2014-04-25 MODIFIED§
Amended by Regulation (EU) No 334/2014 32014R0334
applies from: unchanged
Paragraph 2 extends the derogation period a Member State may apply from two years to up to three years after approval of the last active substance, adds an 18-month period for continued use of biocidal products following a non-approval decision, and restructures the description of qualifying products into sub-points covering existing active substances evaluated or being evaluated under Regulation (EC) No 1451/2007 and combinations of such substances with substances approved under this Regulation.
Paragraph 3 lengthens the period within which Member States must ensure authorisations are granted, modified or cancelled from two years to three years after approval, removes the reference to submitting applications to Member States' competent authorities, and rephrases the disposal-and-use language for existing stocks as simply continued use for up to 365 days.
Paragraph 4 is rewritten to also name the Commission, where relevant, alongside the Member State's competent authority as the decision-maker, to cover rejection of authorisation for a product already on the market and decisions imposing conditions requiring a product change, and to replace the prior disposal-and-use wording with a formulation limited to continued use of existing stocks for up to 365 days after the decision.
Cited: Art. 89, v1 · Art. 89, v2
text before / after, on the event page →
in force 2013-09-01 DEFERRED§
Amended by Regulation (EU) No 736/2013 32013R0736 · Regulation (EU) No 334/2014 32014R0334
applies from: 2024-12-31
dates added to the text: 2024-12-31 · dates removed: 2014-05-14
The only change in this provision is the target date by which the Commission aims to complete the work programme for examining existing active substances, which was shifted from 14 May 2014 to 31 December 2024.
All other text in Article 89, including the remaining paragraphs on transitional arrangements for biocidal products, is unchanged between the two versions.
Cited: Art. 89, v1 · Art. 89, v2
text before / after, on the event page →