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Preamble
Recitals 76
Chapter I - SCOPE AND DEFINITIONS (Article 1-3) 3
Chapter II - APPROVAL OF ACTIVE SUBSTANCES (Article 4-11) 8
Chapter III - RENEWAL AND REVIEW OF APPROVAL OF AN ACTIVE SUBSTANCE (Article 12-16) 5
Chapter IV - GENERAL PRINCIPLES CONCERNING THE AUTHORISATION OF BIOCIDAL PRODUCTS (Article 17-24) 8
Chapter V - SIMPLIFIED AUTHORISATION PROCEDURE (Article 25-28) 4
Chapter VI - NATIONAL AUTHORISATIONS OF BIOCIDAL PRODUCTS (Article 29-31) 3
Chapter VII - MUTUAL RECOGNITION PROCEDURES (Article 32-40) 9
Chapter VIII - UNION AUTHORISATIONS OF BIOCIDAL PRODUCTS (Article 41-46) 6
Chapter IX - CANCELLATION, REVIEW AND AMENDMENT OF AUTHORISATIONS (Article 47-52) 6
Chapter X - PARALLEL TRADE (Article 53) 1
Chapter XI - TECHNICAL EQUIVALENCE (Article 54) 1
Chapter XII - DEROGATIONS (Article 55-57) 3
Chapter XIII - TREATED ARTICLES (Article 58) 1
Chapter XIV - DATA PROTECTION AND DATA-SHARING (Article 59-64) 6
Chapter XV - INFORMATION AND COMMUNICATION (Article 65-73) 9
Chapter XVI - THE AGENCY (Article 74-79) 6
Chapter XVII - FINAL PROVISIONS (Article 80-97) 18
Annexes 7

Recital 22

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Recital 22

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(22)Processing aids are covered by existing Union legislation, in particular Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition ¹⁰ and Regulation (EC) No 1333/2008 of the European Parliament and of the Council of 16 December 2008 on food additives ¹¹ . Therefore, it is appropriate to exclude them from the scope of this Regulation.

11 OJ L 354, 31.12.2008, p. 16 . ↩
10 OJ L 268, 18.10.2003, p. 29 . ↩

Official text · the act as publishedFrom the act as published (consolidated texts do not carry recitals or the preamble). Open full page ↗

Metadata

✓ In force

↻ Amendments (2)

25/04/2014 current
23/09/2013
17/07/2012 first version in the database

Used here (2)

food1
use1