# Commission Directive 2011/29/EU of 7 March 2011 amending Council Directive 91/414/EEC to include etridiazole as active substance and amending Commission Decision 2008/934/EC (Text with EEA relevance), Annex

Extent: E+W+S+N.I.

The following entry shall be added at the end of the table in Annex I to Directive 91/414/EEC:
Further details on identity and specification of active substance are provided in the review report.
No
Common Name, Identification Numbers
IUPAC Name
Purity
Entry into force
Expiration of inclusion
Specific provisions
‘332
Etridiazole
CAS No: 2593-15-9
CIPAC No: 518
ethyl-3-trichloromethyl-1,2,4-thiadiazol-5-yl ether
≥ 970 g/kg
1 June 2011
31 May 2021
PART A
Only uses as fungicide in non-soil bound systems in greenhouse may be authorised.
PART B
In assessing applications to authorise plant protection products containing etridiazole for uses other than on ornamental plants, Member States shall pay particular attention to the criteria in Article 4(1)(b), and shall ensure that any necessary information is provided before such an authorisation is granted.
For the implementation of the uniform principles of Annex VI the conclusions of the review report on etridiazole, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 28 January 2011, shall be taken into account.
In this overall assessment Member States shall:
1.. pay particular attention to the risk to operators and workers and ensure that conditions of use include the application of appropriate risk mitigation measures;
2.. ensure that appropriate waste management practices are applied as regards waste water from irrigation of non-soil bound growing systems; Member States permitting the release of waste water into the sewage system or into natural water bodies, shall ensure that an appropriate risk assessment is carried out;
3.. pay particular attention to the risk to aquatic organisms and ensure that conditions of use include the application of appropriate risk mitigation measures.
The Member States concerned shall request the submission of confirmatory information as regards:
1.. the specification of the technical material, as commercially manufactured, by appropriate analytical data;
2.. the relevance of the impurities;
3.. the equivalence between the specifications of the technical material, as commercially manufactured, and those of the test material used in the ecotoxicity dossiers;
4.. the relevance of the plant metabolites 5-hydroxy-ethoxyetridiazole acid and 3-hydroxymethyletridiazole;
5.. indirect exposure of groundwater and soil-dwelling organisms to etridiazole and to its soil metabolites dichloro-etridiazole and etridiazole acid;
6.. long-range and short-range transport through the atmosphere of etridiazole acid.
The Member States concerned shall ensure that the applicant submits to the Commission the information set out in points 1, 2 and 3 by 1 December 2011 and the information set out in points 4, 5 and 6 by 31 May 2013.’

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Source: https://www.legislation.gov.uk/eudr/2011/29/annex (the official version)
Page: https://openlegislation.uk/eu-directive-2011-29/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

