# Commission Regulation (EU) No 544/2011 of 10 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances (Text with EEA relevance) (repealed), Division (v)

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

There is a need to report all potentially adverse effects found during routine investigations on environmental effects, to undertake and report, where required by the competent authorities, such additional studies which may be necessary to investigate the probable mechanisms involved and to assess the significance of these effects. All available biological data and information which are relevant to the assessment of the ecology profile of the micro-organism must be reported.

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Source: https://www.legislation.gov.uk/eur/2011/544/annex/part/B/division/8/division/1/division/v (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-544/annex/part-B/division-8/division-1/division-v
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.