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Division 5.1 Basic informationF1

United Kingdom

Original text. Later amendments are not shown.

Basic information is required about the potential of the micro-organism to cause adverse effects such as ability to colonise, to cause damage and to produce toxins and other relevant metabolites.

  1. 5.1.1Medical data
  2. 5.1.2Medical surveillance on manufacturing plant personnel
  3. 5.1.3Sensitisation/allergenicity observations, if appropriate
  4. 5.1.4Direct observation, e.g. clinical cases

Annotations

Textual amendments

F1

Repealed (subject to transitional measures in Arts. 3, 4) by Commission Regulation (EU) No 283/2013 of 1 March 2013 setting out the data requirements for active substances, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market Text with EEA relevance.