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Regulation (EC) No 1107/2009

Preamble
Recitals 59
Chapter I - GENERAL PROVISIONS (Article 1-3) 3
Chapter II - ACTIVE SUBSTANCES, SAFENERS, SYNERGISTS AND CO-FORMULANTS (Article 4-27) 24
Chapter III - PLANT PROTECTION PRODUCTS (Article 28-57) 30
Chapter IV - ADJUVANTS (Article 58) 1
Chapter V - DATA PROTECTION AND DATA SHARING (Article 59-62) 4
Chapter VI - PUBLIC ACCESS TO INFORMATION (Article 63) 1
Chapter VII - PACKAGING, LABELLING AND ADVERTISING OF PLANT PROTECTION PRODUCTS AND ADJUVANTS (Article 64-66) 3
Chapter VIII - CONTROLS (Article 67-68) 2
Chapter IX - EMERGENCIES (Article 69-71) 3
Chapter X - ADMINISTRATIVE AND FINANCIAL PROVISIONS (Article 72-79) 7
Chapter XI - TRANSITIONAL AND FINAL PROVISIONS (Article 80-84) 5
Annexes 5
Amending acts 3

good laboratory practice

Definitions over time (1)

14/12/2009 – 01/07/2013 Article 3, Regulation (EC) No 1107/2009 Scope: Whole act

For the purposes of this Regulation, the following definitions shall apply:

‘good laboratory practice’ means a practice as defined in point 2.1 of Annex I to Directive 2004/10/EC of the European Parliament and of the Council of 11 February 2004 on the harmonisation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their applications for tests on chemical substances (^{18});

Other definitions of this term in this act (1)

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Article 3(19)

Earlier definition records in this act (1)

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Article 3(19) Historical · definitions end 14/12/2019

Used in (0 places in 0 provisions on 12/11/2026)

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