Article 3
As regards applications to prohibit the marketing of reproductive material in the categories "qualified" or "tested" from approved basic material in the form of seed orchard, parents of family, clone or clonal mixture, the Member State seeking to prohibit the material must provide an assessment of unsuitability made by reference to the individual units of approval. In addition to the information specified in Article 10 of Directive 1999/105/EC, the following information must be provided on request: (a) the selection criteria used for the components of the basic material; (b) the composition of the basic material; (c) the region(s) of provenance in which the original components were selected.