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Regulation (EU) No 528/2012 of the European Parliament and of the CouncilDangos y teitl llawn

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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Legislation originating from the EU

When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.

Changes over time for: Article 95G

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Point in time view as at 31/12/2020.

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There are currently no known outstanding effects for the Regulation (EU) No 528/2012 of the European Parliament and of the Council, Article 95G. Help about Changes to Legislation

[F1Article 95GU.K.Transitional measures for Regulation (EU) No 528/2012 authorisations

1.This Article applies to authorisations granted by the United Kingdom competent authority before IP completion day under Articles 19, 26, 30, 31, 33, 34, 36, 39 or 44 of Regulation (EU) No 528/2012.

2.The authorisation is to be treated as if it were authorised by the competent authority under the relevant Article of this Regulation.

3.The authorisation must be cancelled and Article 52 of this Regulation will apply where—

(a)the authorisation holder is not established in the United Kingdom within 12 months after IP completion day, or

(b)the authorisation holder does not supply the competent authority with relevant scientific and authorisation data by whichever is the earlier of the following—

(i)the date of any application for renewal or for amendment of the authorisation under Article 50 of this Regulation, or

(ii)within 60 days of any request made by the competent authority to the authorisation holder.]

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