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Abstract

A review is made of legislations and recommendations in the European Community on mutagenicity testing on one side for new chemicals in relation with the 6th amendment of the Council Directive 67/548/EEC (Official Journal L 259 + 15 October 1979), on the other side for pharmaceuticals in relation with the Council Directive 83/570/EEC and the Council recommendation of 26 October 1983 concerning tests relating to the placing on the market of proprietary medical products. (Official Journal L 332 + 28 November 1983). Results of mutagenicity testing is considered also as an element of scientific evaluations prepared by advisory Scientific Committees of the Commission.

Additional information

Authors: VAN DER VENNE M TH, CEC LUXEMBOURG;CEC BRUXELLES (BELGIUM);BERLIN A, CEC LUXEMBOURG;CEC BRUXELLES (BELGIUM);SAUER F CEC LUXEMBOURG, CEC LUXEMBOURG;CEC BRUXELLES (BELGIUM);CEC BRUXELLES (BELGIUM), CEC LUXEMBOURG;CEC BRUXELLES (BELGIUM)
Bibliographic Reference: XVITH ANNUAL MEETING OF THE EUROPEAN ENVIRONMENTAL MUTAGEN SOCIETY, BRUXELLES (BELGIUM), AUG. 25-30, 1986 WRITE TO CEC LUXEMBOURG, DG XIII/A2, POB 1907 MENTIONING PAPER E 32815 ORA
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