BETA

13 Amendments of Sirpa PIETIKÄINEN related to 2010/0208(COD)

Amendment 27 #
Proposal for a regulation - amending act
Recital 5
(5) Experience has shown that cultivation of GMOs is an issue which is more thoroughly addressed by Member States, either at central or at regional and local level. Contrary to issues related to the placing on the market and the import of GMOs, which should remain regulated at EU level to preserve the internal market, cultivation has been acknowledged as an issue with a strong local/regional dimension/territorial dimension and as an issue of particular importance for the self-determination of Member States. In accordance with Article 2(2) TFEU Member States should therefore be entitled to have a possibility to adopt rulebinding legislative provisions concerning the effective cultivation of GMOs in their territory after the GMO has been legally authorised to be placed on the EU market.
2011/03/17
Committee: ENVI
Amendment 38 #
Proposal for a regulation - amending act
Recital 8
(8) According to the legal framework for the authorisation of GMOs, the level of protection of human/animal health and of the environment chosen in the EU cannot be revised by a Member State and this situation must not be altered. However Member States may adopt measures restricting or prohibiting the cultivation of all or particular GMOs in all or part of their territory on the basis of grounds relating to the public interest other thancomplementary to, or differing from, those already addrssessed by the harmonised set of EUnion rules which already. The grounds given by the Member States may include consideration of environmental impacts complementary to those already covered by the risk assessment provided for procedures to take into account the risks that a GMO for cultivation may pose on health and the environmentin Part C of Directive 2001/18/EC, or other legitimate factors, such as: the absence or lack of adequate data on the potential negative impacts of GMOs on the ecosystems or public health in a Member State; the invasiveness or persistence of GM crops; grounds relating to changes in agricultural practices linked to the cultivation of GMOs resulting in negative environmental or health impacts; grounds justifying the maintenance and development of agricultural practices which offer the best combination of production with ecosystem sustainability, or the existence of alternative practices to GMO cultivation and with better technical, economic or environmental performance. Those measures should furthermore be in conformity with the Treaties, in particular as regards the principle of non discrimination between national and non national products and Articles 34 and 36 of the Treaty on the Functioning of the European Union, as well as with the relevant international obligations of the Union, notably in the context of the World Trade Organisation.
2011/03/17
Committee: ENVI
Amendment 46 #
Proposal for a regulation - amending act
Recital 9
(9) On the basis of the subsidiarity principle, the purpose of this Regulation is not to harmonize the conditions of cultivation in Member States but to grant freedom to Member States to invoke otherestrict or gprounds than scientific assessment of health and environmental risks to ban cultivationhibit the cultivation of GMOs on their territory on grounds relating to environmental or health impacts which might arise from the deliberate release or the placing on the market of GMOs on r otheir terrilegitimate factorys. In addition one of the purposes of 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 which is to allow the Commission to consider the adoption of binding acts at EU level would not be served by the systematic notification of Member States’ measures under that Directive. Moreover, since measures which Member States can adopt under this Regulation cannot have as a subject the placing of the market of GMOs and thus does not modify the conditions of placing on the market of GMOs authorised under the existing legislation, the notification procedure under Directive 98/34/EC does not appear the most appropriate information channel for the Commission. Therefore, by derogation, Directive 98/34/EC should not be applicable. A simpler notification system of the national measures prior to their adoption appears to be a more proportionate tool for the Commission to be aware of these measures. Measures which Member States intend to adopt should thus be communicated together with their reasons to the Commission and to the other Member States one month prior to their adoption for information purposes.
2011/03/17
Committee: ENVI
Amendment 58 #
Proposal for a regulation - amending act
Article 1 – point -1 (new)
Directive 2001/18/EC
Article 26 a – paragraph 1
Directive 2001/18/EC shall be amended as follows: (-1) Article 26a(1) shall be replaced by the following: ‘1. Member States shall take appropriate measures to avoid the unintended presence of GMOs in other products, within their borders and on the territory of other Member States.’
2011/03/17
Committee: ENVI
Amendment 80 #
Proposal for a regulation - amending act
Article 1 – point 1
(a) those measures are based on grounds other than those related to the assessment of the adverse effect on health and environment which might arise from the deliberate release or the placing on the market of GMOsrelating to environmental impacts which might arise from the deliberate release or the placing on the market of GMOs, and which are complementary to the environmental impacts examined during the assessment of the negative impacts on the environment conducted under Part C of this Directive, or include other legitimate factors, such as: (i) the absence or lack of adequate data on the potential negative impacts of GMOs on the ecosystems or public health in a Member State; (ii) the invasiveness and persistence of GM crops; (iii) grounds relating to changes in agricultural practices linked to the cultivation of GMOs resulting in negative environmental or health impacts; (iv) grounds justifying the maintenance and development of agricultural practices which offer the best combination of production with ecosystem sustainability, or the existence of alternative practices to GMO cultivation and with better technical, economic or environmental performance;
2011/03/17
Committee: ENVI
Amendment 86 #
Council position
Recital 8
(8) During the authorisation procedure of a given GMO, the possibility should be provided for a Member State to request the Commission to present to the notifier/applicant its demand to adjust the geographical scope of its notification/application submitted in accordance with Part C of Directive 2001/18/EC or in accordance with Articles 5 and 17 of Regulation (EC) No 1829/2003 to the effect that all or part of the territory of that Member State be excluded from cultivation. The Commission should facilitate the procedure by presenting the request of the Member State to the notifier/applicant without delay.deleted
2014/10/20
Committee: ENVI
Amendment 93 #
Council position
Recital 9
(9) The geographical scope of the notification/application should be adjusted accordingly if the notifier/applicant explicitly or tacitly agrees with the Member State's request within an established time-limit from the communication by the Commission of that request. If the notifier/applicant opposes the request, the notifier/applicant should notify the Commission and the Member States. However, a refusal by the notifier/applicant to adjust the geographical scope of the notification/application is without prejudice to the Commission's powers in accordance with Article 19 of Directive 2001/18/EC or Articles 7 and 19 of Regulation (EC) No 1829/2003, as the case may be, to make such an adjustment, where appropriate, in the light of the environmental risk assessment carried out by the European Food Safety Authority ('the Authority').deleted
2014/10/20
Committee: ENVI
Amendment 104 #
Council position
Recital 10
(10) In addition, and only where the notifier/applicant has refused to adjust the geographical scope of the notification/application of a GMO as requested by athere should be the possibility for that Member State, there should be the possibility for that Member State too act as risk manager and adopt reasoned measures restricting or prohibiting the cultivation of thata GMO, or groups of GMOs defined by crop or trait or of all GMOs once authorised in all or part of its territory, on the basis of grounds relating to the public interest, distinct from those assessed according to the harmonized set of Union rules, that is Directive 2001/18/EC and Regulation (EC) No 1829/2003, which are in conformity with Union law. Those grounds may be related to environmental or agricultural policy objectives, or other compelling grounds such as town and country planning, land use,legitimate factors such as socio-economic impacts, where those factors have not been addressed as part of the harmonised procedure provided for in Part C of Directive 2001/18/EC, or to persisting scientific uncertainty. Those measures should be duly justified on socio-economic impacts, co-existence and public policyentific grounds or on grounds relating to other legitimate factors which might arise from the deliberate release or the placing on the market of GMOs. Those grounds may be invoked individually or in combination, depending on the particular circumstances of the Member State, region or area in which those measures will apply.
2014/10/20
Committee: ENVI
Amendment 169 #
Council position
Article 1 – paragraph 1
Directive 2001/18/EC
Article 26 b – paragraph 1
1. During the authorisation procedure of a given GMO or during the renewal of consent/authorisation, a Member State may request, via the Commission, the notifier/applicant to adjust the geographical scope of its notification/application submitted in accordance with Part C of this Directive or Regulation (EC) No 1829/2003, to the effect that all or part of the territory of that Member State is to be excluded from cultivation. This request shall be communicated to the Commission at the latest 30 days from the date of the circulation of the assessment report under Article 14(2) of this Directive, or from receiving the opinion of the Authority under Article 6(6) and Article 18(6) of Regulation (EC) No 1829/2003. The Commission shall communicate the request of the Member State to the notifier/applicant and to the other Member States without delay.deleted
2014/10/20
Committee: ENVI
Amendment 178 #
Council position
Article 1 – paragraph 1
Directive 2001/18/EC
Article 26 b – paragraph 2
2. Where the notifier/applicant opposes a request of a Member State in accordance with paragraph 1, the notifier/applicant shall notify the Commission and the Member States within 30 days from the communication by the Commission of that request. In the event of explicit or tacit agreement of the notifier/applicant, the adjustment of the geographical scope of the notification/application shall be implemented in the written consent or authorisation. The written consent issued under this Directive and, where applicable, the decision issued in accordance with Article 19 as well as the decision of authorisation adopted under Articles 7 and 19 of Regulation (EC) No 1829/2003, shall be issued on the basis of the adjusted geographical scope of the notification/application as explicitly or tacitly agreed by the notifier/applicant.deleted
2014/10/20
Committee: ENVI
Amendment 195 #
Council position
Article 1 – paragraph 1
Directive 2001/18/EC
Article 26 – paragraph 3 – subparagraph 1 – introductory part
3. Where the notifier/applicant opposes the adjustment of the geographical scope of its notification/application corresponding to a request made by a Member State in accordance with paragraph 1 of this Article, that Member State mayA Member State may, following the risk assessment carried out pursuant to this Directive or to Regulation (EC) No 1829/2003 and acting as risk manager, adopt measures restricting or prohibiting the cultivation of thata GMO or of groups of GMOs defined by crop or trait or of all GMOs in all or part of its territory once authorised in accordance with Part C of this Directive or with Regulation (EC) No 1829/2003, provided that such measures are in conformity with Union law, reasoned, proportional and non- discriminatory and, in addition, are based on compelling grounds such as those related to:
2014/10/20
Committee: ENVI
Amendment 228 #
Council position
Article 1 – paragraph 1
(ga) or other legitimate factors where those factors have not been addressed as part of the harmonised procedure provided for in Part C of this Directive , or to persisting scientific uncertainty.
2014/10/20
Committee: ENVI
Amendment 244 #
Council position
Article 1 – paragraph 1
Directive 2001/18/EC
Article 26 b – paragraph 3 – subparagraph 2 a (new)
Those measures shall be duly justified on scientific grounds or on grounds relating to other legitimate factors which might arise from the deliberate release or the placing on the market of GMOs.
2014/10/20
Committee: ENVI