Activities of Karin KADENBACH related to 2012/0366(COD)
Plenary speeches (1)
Manufacture, presentation and sale of tobacco and related products (debate)
Amendments (8)
Amendment 493 #
Proposal for a directive
Article 6 – paragraph 2 – subparagraph 1
Article 6 – paragraph 2 – subparagraph 1
Amendment 546 #
Proposal for a directive
Article 6 – paragraph 7 – subparagraph 1
Article 6 – paragraph 7 – subparagraph 1
Member States shall, based on scientific evidence, prohibit the placing on the market of tobacco products with additives in quantities that increase in an appreciable mannersignificantly, on the basis of an international standard, at the stage of consumption the toxic or addictive effect of a tobacco product.
Amendment 561 #
Proposal for a directive
Article 6 – paragraph 9
Article 6 – paragraph 9
9. In case scientific evidence and the experience gained in the application of paragraphs 7 and 8 shows that a certain additive or a certain quantity thereof amplify in an appreciable mannersignificantly on the basis of an internationally recognised standard at the stage of consumption the toxic or addictive effect of a tobacco product the Commission shall be empowered to adopt delegated acts in accordance with Article 22 to set maximum levels for those additives.
Amendment 726 #
Proposal for a directive
Article 9 – paragraph 2
Article 9 – paragraph 2
2. The combined health warnings shall be divided into three sets rotating on an annual basis. Member States shall ensure that each combined health warning is displayed as nearly as possible on equal numbers of each brand.
Amendment 743 #
Proposal for a directive
Article 9 – paragraph 3 – point c
Article 9 – paragraph 3 – point c
Amendment 908 #
Proposal for a directive
Article 13 – paragraph 3
Article 13 – paragraph 3
Amendment 926 #
Proposal for a directive
Article 13 – paragraph 4
Article 13 – paragraph 4
Amendment 1005 #
Proposal for a directive
Article 14 – paragraph 9 – point b
Article 14 – paragraph 9 – point b
(b) to define the international technical standards and introduce standardised requests for information to ensure that the systems used for the unique identifiersbatch labelling and the related functions are fully compatible with each other across the Union and.