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The EUDR is a part of a bigger set of EU policies aimed at fighting climate change and biodiversity reduction, as codified in the European Green Deal. It supersedes the Timber Regulation 2010 . [ 1 ] [ 2 ] It was formally adopted in May 2023 and applies to products placed on the market from 30 December 2024 by medium or big businesses and from ...
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Commission Directive 2007-11-EC of 21 February 2007 amending certain Annexes to Council Directives 86-362-EEC, 86-363-EEC and 90-642-EEC as regards maximum residue levels for acetamiprid, thiacloprid, imazosulfuron, methoxyfenozide, S-metholachlor, milbemectin and tribenuron (Text with EEA relevance)
Commission Directive (EU) 2016-2037 of 21 November 2016 amending Council Directive 75-324-EEC as regards the maximum allowable pressure of aerosol dispensers and to adapt its labelling provisions to Regulation (EC) No 1272-2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures (Text with EEA relevance)
Directive 2001-20-EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use
Council Directive 89-381-EEC of 14 June 1989 extending the scope of Directives 65-65-EEC and 75-319-EEC on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products and laying down special provisions for medicinal products derived from human blood or human plasma
Directive 2014-27-EU of the European Parliament and of the Council of 26 February 2014 amending Council Directives 92-58-EEC, 92-85-EEC, 94-33-EC, 98-24-EC and Directive 2004-37-EC of the European Parliament and of the Council, in order to align them to Regulation (EC) No 1272-2008 on classification, labelling and packaging of substances and ...