14 Amendments of Adam BIELAN related to 2012/0366(COD)
Amendment 78 #
Proposal for a directive
Recital 22
Recital 22
(22) The labelling provisions also need to be adapted tso new scientific evidence. For example tthat they do not mislead consumers. The indication of the yields for tar, nicotine and carbon monoxide on cigarette packets have proven tomay be mislreading as it by consumers as it often makes consumers believe that certain cigarettes are less harmful than others. Evidence also suggests that large combined health warnings are more effective than text-only warnings. In this light combined health warnings should become mandatory throughout the Union and cover significant and visible parts of the packet surface. A minimum size should be set for all health warnings to ensure their visibility and effectiveness.
Amendment 228 #
Proposal for a directive
Article 8 – paragraph 4 – point b
Article 8 – paragraph 4 – point b
(b) to define the position, format, layout and design of the health warnings laid down in this Article, including their font type and background colour.
Amendment 269 #
Proposal for a directive
Article 9 – paragraph 3 – point c
Article 9 – paragraph 3 – point c
c) define the position, format, layout, design, rotation and proportations of the health warnings;
Amendment 378 #
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 outlets established outside the Union have to register with the competent authorities in the Member State where the actual or potentialnot allow cross-border distance sales of tobacco products to 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: in the Union.
Amendment 382 #
Proposal for a directive
Article 16 – paragraph 1 – point a
Article 16 – paragraph 1 – point a
Amendment 386 #
Proposal for a directive
Article 16 – paragraph 1 – point b
Article 16 – paragraph 1 – point b
Amendment 390 #
Proposal for a directive
Article 16 – paragraph 1 – point c
Article 16 – paragraph 1 – point c
Amendment 396 #
Proposal for a directive
Article 16 – paragraph 2
Article 16 – paragraph 2
Amendment 401 #
Proposal for a directive
Article 16 – paragraph 3
Article 16 – paragraph 3
Amendment 406 #
Proposal for a directive
Article 16 – paragraph 4
Article 16 – paragraph 4
Amendment 411 #
Proposal for a directive
Article 16 – paragraph 5
Article 16 – paragraph 5
Amendment 450 #
Proposal for a directive
Article 18 – paragraph 5
Article 18 – paragraph 5
5. The Commission shall be empowered to adopt delegated acts in accordance with Article 22 to adapt the requirements in paragraphs 3 and 4 taking into account scientific and market developments and to adopt and adapt the position, format, layout, design and rotation of the health warnings.
Amendment 472 #
Proposal for a directive
Article 25 – paragraph 1
Article 25 – paragraph 1
1. Member States shall bring into force the laws, regulations and administrative provisions necessary to comply with this Directive by [Publications Office, please insert the exact date: entry into force + 1824 months] at the latest. They shall forthwith communicate to the Commission the text of those provisions.
Amendment 473 #
Proposal for a directive
Article 26 – paragraph 1 – introductory part
Article 26 – paragraph 1 – introductory part
Member States may allow the following products, which are not in compliance with this Directive, to be placed on the market until [Publications Office, please insert the exact date: entry into force + 248 months]: