Abstract
Part 1 of this article describing the EU new regulatory framework for GM food was published in the last issue of this journal. Part 1 dealt with the new authorisation procedure. In that context some attention was given to the developments that led to the new framework and to administrative review. The main topics discussed in this final part are the traceability requirements and labelling requirements. These are followed by supervision and emergency measures. At the end transitional measures are treated
Original language | English |
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Pages (from-to) | 158-162 |
Journal | Journal of International Biotechnology Law |
Volume | 2 |
Issue number | 4 |
Publication status | Published - 2005 |