38 Amendments of Sari ESSAYAH related to 2012/0366(COD)
Amendment 110 #
Proposal for a directive
Recital 16 a (new)
Recital 16 a (new)
Amendment 118 #
Proposal for a directive
Recital 18
Recital 18
Amendment 131 #
Proposal for a directive
Recital 20 a (new)
Recital 20 a (new)
(20a) An effort should be made to eliminate obstacles effectively and by all available means to enable the use of plain packages to be introduced throughout EU territory as quickly as possible.
Amendment 155 #
Proposal for a directive
Recital 24
Recital 24
(24) Tobacco products for smoking, other than cigarettes and roll-your-own tobacco products, which are mainly consumed by older consumers, should be granted an exemption from certain labelling requirements as long as there is no substantial change of circumstances in terms of sales volumes or consumption patterns in relation to young people. The labelling of these other tobacco products should follow specific rules. The visibility of the health warnings on smokeless tobacco products needs to be ensured. Warnings should therefore be placed on the two main surfaces of smokeless tobacco product packaging.
Amendment 165 #
Proposal for a directive
Recital 27
Recital 27
(27) An interoperable tracking and tracing system and a common security feature should be developed. For an initial period only cigarettes and roll-your-own tobacco should be subjected to the tracking and tracing system and the security features. This would allow producers of other tobacco products to benefit from the experiences gained in the meantime.
Amendment 174 #
Proposal for a directive
Recital 29 b (new)
Recital 29 b (new)
(29b) The sale and placing on the market of other types of tobacco for oral use should be prohibited throughout EU territory. The prohibition should particularly apply to tobacco intended for chewing such as snus and chewing tobacco; it should also apply to snuff intended to be sniffed through the nose.
Amendment 185 #
Proposal for a directive
Recital 31
Recital 31
(31) All tobacco products have the potential to cause mortality, morbidity and disability and their consumption should be contained. It is therefore important to monitor developments as regards novel tobacco products. A notification obligation for novel tobacco products should be put on manufacturers and importers, without prejudice to the power of the Member StatesThe aim of the Directive is to reduce smoking and particularly to discourage young people and others from starting to smoke. Widening of the market by permitting new to ban or to authorise them. The Commission should monitor the developments and submit a report 5 years after the date of transposition of this Directive, in order to assess whecco products should therefore be prohibited as contrary to ther amendments toim of thise Directive are necessary.
Amendment 191 #
Proposal for a directive
Recital 32
Recital 32
(32) In order to ensure a level playing field,t is damaging and unnecessary for novel tobacco products, which are tobacco products in the sense of this Directive, should respeto enter the market. It is therefore not justified to permit novel tobacco products the requirements provided for in this Directiveo enter the market and be approved. Permitting novel tobacco products is in conflict with the fundamental aim of the Directive to reduce the use of tobacco products.
Amendment 195 #
Proposal for a directive
Recital 33
Recital 33
(33) Nicotine-containing products are sold on the Union market. The different regulatory approaches taken by Member States to address health and safety concerns associated with these products have a negative impact on the functioning of the internal market, in particular considering that these products are subject to significant cross-border distance sales including via the internet. E-cigarettes, in which nicotine is absorbed into the body together with air inhaled, should be treated equally with other nicotine sources absorbed into the body through air inhaled.
Amendment 204 #
Proposal for a directive
Recital 34 a (new)
Recital 34 a (new)
(34a) All products containing nicotine should be treated in the same way. They should be governed either by this directive or, in the case of large doses used for medicinal purposes, by the medicines legislation of the Member State. The medicines legislation of the Member State would define the limits of medicinal use of nicotine in accordance with the subsidiarity principle. In defining nicotine content, quantities of nicotine should be calculated as a daily dose and in the light of the largest dose.
Amendment 206 #
Proposal for a directive
Recital 35
Recital 35
(35) Labelling provisions should be introduced for nicotine containing products below the threshold set out in this Directive drawing the attention of consumers to potential health risks. Package labelling should correspond to pictorial warnings and package labelling required of tobacco products in this Directive.
Amendment 227 #
Proposal for a directive
Recital 39 a (new)
Recital 39 a (new)
(39a) The Directive should have the purpose of reducing smoking, and the aim should be ultimately to be able to put an end to smoking entirely, bearing in mind the huge and needless losses to public health and the economy.
Amendment 238 #
Proposal for a directive
Recital 41
Recital 41
(41) Member States should remain free to maintain or introduce national legislations applying to all products alike for aspects falling outside the scope of this Directive, provided they are compatible with the Treaty and do not jeopardise the full application of this Directive. Accordingly, Member States could, for instance, maintain or introduce provisions providing standardisation of packaging of tobacco products provided that those provisions are compatible with the Treaty, with WTO obligations and do not affect the full application of this Directive. Special attention should be devoted to implementation of the compulsory pictorial and textual warnings provided for in this Directive, and of other harmonisation rules, for example concerning cocoa. A prior notification is required for technical regulations pursuant to Directive 98/34/EC of the European Parliament and of the Council of 22 June 1998 laying down a procedure for the provision of information in the field of technical standards and regulations and on rules on Information Society services.
Amendment 247 #
Proposal for a directive
Article 1 – paragraph 1 – introductory part
Article 1 – paragraph 1 – introductory part
The aim of this Directive is toin the long term to put an end to the use of tobacco products and in the short term to reduce their use by approximateing the laws, regulations and administrative provisions of the Member States concerning:
Amendment 433 #
Proposal for a directive
Article 5 – paragraph 4
Article 5 – paragraph 4
4. Member States shall require manufacturers and importers to submit internal and external studies available to them on market research and preferences of various consumer groups, including young people, relating to ingredients and emissions. Member States shall also require manufacturers and importers to report the sales volume data per product, reported in sticks or kilograms, and per Member State on a yearly basis starting from the full calendar year following that of the entry into force of this Directive. Member States shall provide alternative or additional sales data, as appropriate, to ensure that information on sales volume requested under this paragraph is reliable and complete. Ingredients shall be defined in a uniform manner in all Member States, using a clear list common to the Member States.
Amendment 563 #
Proposal for a directive
Article 6 – paragraph 10
Article 6 – paragraph 10
Amendment 756 #
Proposal for a directive
Article 10
Article 10
Amendment 852 #
Proposal for a directive
Article 12 – paragraph 2
Article 12 – paragraph 2
2. Prohibited elements and features may include but are not limited to texts, symbols, names, trade marks, figurative or other signs, misleading colours, inserts or other additional material such as adhesive labels, stickers, onserts, scratch-offs and sleeves or relate to the shape of the tobacco product itself. Cigarettes with a diameter of less than 7.5 mm shall be deemed to be misleading.not be sold within the EU;
Amendment 1011 #
Proposal for a directive
Article 14 – paragraph 10
Article 14 – paragraph 10
Amendment 1021 #
Proposal for a directive
Article 15 – paragraph 1
Article 15 – paragraph 1
Member States shall prohibit the placing on the market of tobacco for oral usesmokeless tobacco products, such as tobacco for oral use, chewing tobacco and snuff, without prejudice to Article 151 of the Act of Accession of Austria, Finland and Sweden.
Amendment 1040 #
Proposal for a directive
Article 16 – paragraph 1 – introductory part
Article 16 – paragraph 1 – introductory part
1. Member States shall oblige retail outlets intending to engage in cross-border distance sales to consumers located in the Union to register with the competent authorities in the Member State where the retail outlet is established and in the Member State where the actual or potential consumer is located. Retail outprohibit distance salets established outside the Union have to register with the competent authorities in the Member State where the actual or potential consumer is located. All retail outlets intending to engage in cross- border distance sales shall submit at least the following information to the competent authorities:of tobacco products.
Amendment 1054 #
Proposal for a directive
Article 16 – paragraph 1 – point a
Article 16 – paragraph 1 – point a
Amendment 1062 #
Proposal for a directive
Article 16 – paragraph 1 – point b
Article 16 – paragraph 1 – point b
Amendment 1070 #
Proposal for a directive
Article 16 – paragraph 1 – point c
Article 16 – paragraph 1 – point c
Amendment 1078 #
Proposal for a directive
Article 16 – paragraph 2
Article 16 – paragraph 2
Amendment 1088 #
Proposal for a directive
Article 16 – paragraph 3
Article 16 – paragraph 3
Amendment 1105 #
Proposal for a directive
Article 16 – paragraph 5
Article 16 – paragraph 5
Amendment 1112 #
Proposal for a directive
Article 17
Article 17
Amendment 1119 #
Proposal for a directive
Article 17 – paragraph 1 – introductory part
Article 17 – paragraph 1 – introductory part
1. Member States shall require that manufacturers and importers of tobacco products notify the competent authorities of Member States of any novel tobacco product they intend to place on the markets of the Member States concerned. The notification shall be submitted in electronic form six months before the intended placing on the market and shall be accompanied by a detailed description of the product in question as well as information on ingredients and emissions in accordance with Article 5. The manufacturers and importers notifying a novel tobacco product shall also provide the competent authorities in question with:prohibit the placing on the market of any novel tobacco product.
Amendment 1132 #
Proposal for a directive
Article 17 – paragraph 2
Article 17 – paragraph 2
Amendment 1137 #
Proposal for a directive
Article 17 – paragraph 3
Article 17 – paragraph 3
Amendment 1155 #
Proposal for a directive
Article 18 – paragraph 1 – introductory part
Article 18 – paragraph 1 – introductory part
1. The following nNicotine-containing products may only be placed on the market if they were authorised pursuant to Directive 2001/83/EC:
Amendment 1179 #
Proposal for a directive
Article 18 – paragraph 1 – point a
Article 18 – paragraph 1 – point a
Amendment 1192 #
Proposal for a directive
Article 18 – paragraph 1 – point b
Article 18 – paragraph 1 – point b
Amendment 1206 #
Proposal for a directive
Article 18 – paragraph 1 – point c
Article 18 – paragraph 1 – point c
Amendment 1217 #
Proposal for a directive
Article 18 – paragraph 2
Article 18 – paragraph 2
Amendment 1230 #
Proposal for a directive
Article 18 – paragraph 3 – introductory part
Article 18 – paragraph 3 – introductory part
Each unit packet and any outside packaging of nicotine-containing products below the thresholds set out in paragraph 1 shall carry the following health warning:
Amendment 1253 #
Proposal for a directive
Article 19 – paragraph 1 – introductory part
Article 19 – paragraph 1 – introductory part
Each unit packet and any outside packaging of herbal products for smoking or nicotine-free products intended for vaporising or smoking shall carry the following health warning: