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Division A Safety documentationF1

United Kingdom Repealed

Original text. Later amendments are not shown.

  1. A.0Division A.0
  2. A.1Precise identification of the substance concerned by the application
  3. A.2Relevant pharmacological studies
  4. A.3Toxicological studies
  5. A.4Studies of other effects

Annotations

Textual amendments

F1

Repealed by Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance).