Gilles PARGNEAUX
Constituencies
-
France
Parti socialiste
2009/07/14 - 9999/12/31
Groups
-
S&D
Member
Group of the Progressive Alliance of Socialists and Democrats in the European Parliament
2009/07/14 - 9999/12/31
Committees
| Role | Committee | Start | End |
|---|---|---|---|
| Member of | Committee on the Environment, Public Health and Food Safety | 2012/01/19 | 9999/12/31 |
| Substitute of | Committee on Transport and Tourism | 2012/01/19 | 9999/12/31 |
Show earlier commitees...
Delegations
| Role | Delegation | Start | End |
|---|---|---|---|
| Member of | Delegation for relations with Canada | 2009/09/16 | 9999/12/31 |
| Substitute of | Delegation for relations with the Maghreb countries and the Arab Maghreb Union | 2012/07/04 | 9999/12/31 |
| Substitute of | Delegation to the Parliamentary Assembly of the Union for the Mediterranean | 2012/07/11 | 9999/12/31 |
Show earlier delegations...
| Role | Delegation | Start | End |
|---|---|---|---|
| Substitute of | Delegation for relations with the United States | 2009/09/16 | 2012/07/03 |
Contact
Online
- [javascript protected email address]
Brussels
- Phone
- +322 28 45440
- Fax
- +322 28 49440
- Office
- Bât. Altiero Spinelli 14G217
- Full Address
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- City
- Bruxelles/Brussel
- Zip
- B-1047
- Street
- 60, rue Wiertz / Wiertzstraat 60
Strasbourg
- Phone
- +333 88 1 75440
- Fax
- +333 88 1 79440
- Office
- Bât. Louise Weiss T08006
- Full Address
-
- City
- Strasbourg
- Zip
- CS 91024 - F-67070
- Street
- 1, avenue du Président Robert Schuman
Postal
- Parlement européen
- Rue Wiertz
- Altiero Spinelli 14G217
- B-1047 Bruxelles
Rapporteur
| Shadow | 2013/0014(COD) | European Union Agency for Railways. 4th Railway Package |
| Shadow | 2013/0013(COD) | Common rules for the normalisation of the accounts of railway undertakings: repeal. 4th Railway Package |
| Opinion | 2012/0305(COD) | Fluorinated greenhouse gases |
| Responsible | 2011/0421(COD) | Serious cross-border threats to health |
| Opinion | 2011/0409(COD) | Sound level of motor vehicles |
Born
1957/03/24 Harcigny- Parliamentary assistant (1982-1992). Lawyer (1993-1997). Parliamentary liaison officer in the office of the Minister for Employment and Solidarity (1997-1998). Director of in-house resources at a social housing organisation (1999-2008).
- First secretary of the Nord Department Federation of the Socialist Party (since 2005). National secretary of the Socialist Party (since 2004). Member of the National Bureau of the Socialist Party (since 2005).
- Mayor of Hellemmes (since 2001). Vice-Chair of the Lille Métropole Urban Community (since 2001).
Amendments
| Amendments | Dossier |
| 7 |
2008/0142(COD) Patients' rights in cross-border healthcare
2010/05/10
ENVI
7 amendments...
Amendment 106 #
Council position Recital 18 (18) In order to enable patients to make an informed choice when they seek to receive healthcare in another Member State, the Member State of treatment should ensure that patients from other Member States receive on request the relevant information on safety and quality standards enforced on its territory as well as on which healthcare providers are subject to these standards. Furthermore, healthcare providers should provide patients on request with information on specific aspects of the healthcare services they offer. To the extent that healthcare providers already provide patients resident in the Member State of treatment with relevant information on those specific aspects, this Directive should not oblige healthcare providers to provide more extensive information to patients from other Member States. Nothing should prevent the Member State of treatment from also obliging other actors than the healthcare providers, such as insurance providers or public authorities, to provide the information on specific aspects of the healthcare services offered, if that would be more appropriate with regard to the organisation of its healthcare system. All such information should also be made available in formats accessible to persons with disabilities.
Amendment 131 #
Council position Recital 50 (50) The constant progress of medical science and health technologies presents both opportunities and challenges to the health systems of the Member States. Cooperation in the evaluation of new health technologies can support Member States through economies of scale and avoid duplication of effort, and provide a better basis of evidence for optimal use of new technologies to ensure safe, high- quality and efficient healthcare.
Amendment 167 #
Council position Article 7 – paragraph 1 – subparagraph 1 a (new) After obtaining authorisation on the basis of an objective clinical examination, which procedure should be subject to appeal in the event of authorisation being refused, patients affected by rare diseases shall have the right to access healthcare in another Member State and to receive reimbursement, even if the treatment in question is not among the benefits provided for by the legislation, administrative regulations, guidelines and codes of conduct of the medical professions of the Member State of affiliation. However, the Member State of affiliation may require the treatment to be recognised by the European reference networks or, failing that, by international medical science.
Amendment 177 #
Council position Article 8 – paragraph 2 – introductory part 2. Healthcare that may be subject to prior authorisation shall be set out in a list by the Member State of affiliation, to be transmitted to the Commission. It shall be limited to healthcare which:
Amendment 183 #
Council position Article 8 – paragraph 5 – introductory part 5. The Member State of affiliation may refuse to grant prior authorisation for
Amendment 185 #
Council position Article 8 – paragraph 5 – point b b) if this healthcare can be provided on its territory within a time-limit which is
Amendment 220 #
Council position Article 14 – paragraph 1 1. The Union shall support and facilitate cooperation and the exchange of scientific information among Member States
source: PE-450.566
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| 1 |
2008/0225(COD) Visas: third countries whose nationals are subject to or exempt from a visa requirement. Codification
2010/04/05
ENVI
1 amendments...
Amendment 4 #
Proposal for a regulation – amending act – The European Parliament rejects the Commission proposal.
source: PE-441.030
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| 3 |
2008/0241(COD) Waste electrical and electronic equipment (WEEE). Recast
2011/09/13
ENVI
3 amendments...
Amendment 93 #
Council position Article 2 – paragraph 5 - subparagraph 1 a (new) In the event of any change to the scope of this Directive, from one based on an exhaustive list (closed scope) to one based on the principle of automatic inclusion unless otherwise specified (open scope), special attention shall be paid to the definition of exclusions to ensure that equipment that is currently within the scope of Directive 2002/96/EC
Amendment 97 #
Council position Article 3 – paragraph 1 – point c – subparagraph 1 a (new) Equipment listed in Annex IB of Directive 2002/96/EC is excluded from this definition;
Amendment 101 #
Council position Article 3 – paragraph 1 – point h (h) ‘WEEE from private households’ means WEEE which comes from private households and from commercial, industrial, institutional and other sources which, because of its nature and quantity, is similar to that from private households. Waste from EEE
source: PE-472.180
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| 58 |
2008/0256(COD) Medicinal products for human use: information on products subject to medical prescription
2010/05/25
ENVI
58 amendments...
Amendment 28 #
The European Parliament rejects the Commission proposal.
Amendment 35 #
Proposal for a directive – amending act Recital 3 Amendment 38 #
Proposal for a directive – amending act Recital 3 a (new) (3a) In the area of scientific information, Directive 2001/83/EC lays down transparency obligations for National competent authorities, but experience gained from the application of the current legal framework has also shown certain restrictions on the possibilities for the general public to access information from their National competent authorities due to a too extensive interpretation of commercial confidentiality.
Amendment 41 #
Proposal for a directive – amending act Recital 4 (4) Experience gained from the application of the current legal framework has also shown that
Amendment 43 #
Proposal for a directive – amending act Recital 6 (6) The different national measures are also likely to have an impact on the proper functioning of the internal market for medicinal products, as the possibility for marketing authorisation holders to
Amendment 44 #
Proposal for a directive – amending act Recital 7 (7) In the light of the above and taking into account technological progress with regard to modern communication tools and the fact that patients throughout the European Union have become increasingly active as regards healthcare, it is necessary to amend the existing legislation in order to reduce differences in access to
Amendment 51 #
Proposal for a directive – amending act Recital 8 (8) National competent authorities and health care professionals should remain
Amendment 59 #
Proposal for a directive – amending act Recital 10 (10) Provisions should be established to ensure that only
Amendment 63 #
Proposal for a directive – amending act Recital 11 (11) In order to further ensure that marketing authorisation holders disseminate only
Amendment 71 #
Proposal for a directive – amending act Recital 12 (12)
Amendment 78 #
Proposal for a directive – amending act Recital 14 (14) Monitoring of information on prescription-only medicinal products should ensure that marketing authorisation holders only
Amendment 86 #
Proposal for a directive – amending act Article 1 – point 1 Directive 2001/83/EC Article 86 – paragraph 2 – indent 1 - the labelling which shall always at least specify the International Non-proprietary Name and the accompanying package leaflets, which are subject to the provisions of Title V;
Amendment 87 #
Proposal for a directive – amending act Article 1 – point 1 Directive 2001/83/EC Article 86 – paragraph 2 – indent 2 a (new) “- correspondence, possibly accompanied by material of a non- promotional nature, needed to answer a specific question including those of media organisations about a particular medicinal product;”
Amendment 92 #
Proposal for a directive – amending act Article 1 – point 1 Directive 2001/83/EC Article 86 – paragraph 2 – indent 2 - factual, informative announcements and reference material relating, for example, to information on the environmental risk of the medicinal product, availability, pack changes, adverse-reaction warnings as part of general drug precautions, trade catalogues and price lists, provided they include no product claims and do not induce to or promote the consumption of the medicinal product;
Amendment 97 #
Proposal for a directive – amending act Article 1 – point 1 Directive 2001/83/EC Article 86 – paragraph 2 – indent 4 -
Amendment 98 #
Proposal for a directive – amending act Article 1 – point 1 Directive 2001/83/EC Article 86 – paragraph 2 – indent 4 a (new) - factual, informative announcements for investors and employees on significant business developments, provided they are not use to promote the product to the general public;
Amendment 99 #
Proposal for a directive – amending act Article 1 – point 1 a (new) Directive 2001/83/EC Article 86 – paragraph 2 a (new) (1a) In Article 86, the following paragraph shall be inserted: “(2a) When exemptions to advertising referred to in paragraph 2 are made available, the marketing authorisation holder and any third party acting on behalf of the marketing authorisation holder shall be identified as such.”
Amendment 101 #
Proposal for a directive – amending act Article 1 – point 1 b (new) Directive 2001/83/EC Article 86 – paragraph 2 b (new) (1b) In Article 86, the following paragraph shall be inserted: “2b. To this end, the statement "Conflict of interest: This information has been compiled and disseminated by [the name of the company] which is the producer of [the name of the medicinal product]" shall be included.”
Amendment 106 #
Proposal for a directive – amending act Article 1 – point 2 2001//83/EC Article 88 – paragraph 4 Amendment 115 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 a – paragraph 1 1. Member States shall allow the marketing authorisation holder to
Amendment 122 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 a – paragraph 2 – point a Amendment 123 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 a – paragraph 2 – point b Amendment 130 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 b – introductory part The following
Amendment 141 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 b – point b Amendment 147 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 b – point b a (new) ba) the package leaflet;
Amendment 148 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 b – point c Amendment 155 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 b – point c a (new) ca) the periodic safety update reports;
Amendment 159 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 b – point d d
Amendment 164 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 b – point d a (new) da) the pre-clinical and clinical data on their product.
Amendment 166 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 c Amendment 174 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 c – point a Amendment 187 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 d – paragraph 1 Amendment 191 #
Proposal for a directive – amending act Article 1 – point 5 – introductory part Directive 2001/83/EC Article 100 d – paragraph 2 – introductory part 2. Any
Amendment 193 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 d – paragraph 2 – point b b) a statement indicating that the
Amendment 194 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 d – paragraph 2 – point c c) a statement starting with the indication
Amendment 204 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 d – paragraph 3 – introductory part 3. The
Amendment 206 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 d – paragraph 3 – point a Amendment 209 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 d – paragraph 3 – point a a (new) aa) any inducement to, or promotion of, the consumption of the medicinal product;
Amendment 211 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 d – paragraph 4 a (new) 4a. Within three years of the entry into force of this Directive, the Commission shall, following a public consultation involving patient and consumer organisations, doctor and pharmacist organisations, Member States and other interested parties, present to the European Parliament and the Council an assessment report regarding the readability and the accuracy of the summaries of product characteristics and the packaging leaflets and their value to the general public and healthcare professionals. Following an analysis of the above data, the Commission shall, if appropriate, put forward guideline proposals to improve the layout and the content of the summaries of product characteristics and of the packaging leaflet to ensure they are a valuable source of information for the general public and healthcare professionals.
Amendment 212 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 e – paragraph 1 1. Member States shall ensure that marketing authorisation holders' Internet websites
Amendment 218 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 e – paragraph 1 a (new) 1a. Member States shall ensure that each webpage of the Internet website of the marketing authorisation holders that refers to a medicinal product subject to medical prescription links to the corresponding webpage of the Community database referred to in Articles 57(1)(l) and 57(2) of Regulation (EC) No 726/2004 (hereinafter ‘the Eudrapharm database’).
Amendment 219 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 e – paragraph 1 b (new) 1b. The Agency shall reproduce on the Eudrapharm database, and the competent authorities of Member States on their websites, the last updated version of: - the approved summary of product characteristics; - the approved package leaflet; - the mock-ups of the secondary and primary packaging as well as of any devices also included; - the Public Assessment Reports (PARs), and when available their summary written in a manner that is understandable to the public. The competent authorities of Member States shall, on each webpage that refers to a medicinal product subject to medical prescription, insert a link to the corresponding webpage of the Eudrapharm database.
Amendment 224 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 e – paragraph 1 b (new) 1b. The summary of the European Public Assessment Reports referred to in Article 13 of Regulation (EC) No 726/2004 shall list the other available therapeutic options and whether the new medicinal product brings about a tangible therapeutic advantage.
Amendment 226 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 e – Paragraph 1 c (new) In Article 100 e, the following paragraph shall be inserted: 1c. The summary of the European Public Assessment Reports referred to in Article 13 of Regulation (EC) No 726/2004 shall be hyperlinked with the corresponding studies in in the clinical trials database provided for in Article 11 of Directive 2001/20/EC (hereinafter ‘the EudraCT database’).
Amendment 228 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 e – paragraph 2 2. Member States shall ensure that requests for information to a marketing authorisation holder on a medicinal product subject to medical prescription by a member of the general public may be drafted in any of the official languages of the Community which are official languages in the Member States where the medicinal product is authorised. The reply shall be drafted in the language of the request. The replies shall be kept available for inspections by national competent authorities.
Amendment 229 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 f – paragraph 1 1. Member States shall
Amendment 232 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 g – paragraph 1 – subparagraph 1 1. Member States shall ensure that there are adequate and effective methods of monitoring to avoid misuse when
Amendment 234 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 g – paragraph 1 – subparagraph 2 – introductory part Such methods shall be based on the control of
Amendment 237 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 g – paragraph 1 – subparagraph 2 – indent 2 Amendment 241 #
Proposal for a directive – amending act Article 1 – point 5 2001/838/EC Article 100 g – paragraph 1 – subparagraph 3 Amendment 245 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 g – paragraph 2 After consulting the Member States, patients and consumers organisations, social health insurance organisations and healthcare professionals, the Commission shall draw up guidelines concerning
Amendment 253 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 h – paragraph 1 – subparagraph 2 a (new) After registration of the Internet website, any amendments to the content relating to medicinal products subject to medical prescription shall be subject to monitoring in accordance with paragraph 3.
Amendment 264 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 h – paragraph 2 – subparagraph 2 Internet websites registered in accordance with paragraph 1 shall not allow the identification of members of the general public which have access to those websites or the appearance therein of unsolicited material actively distributed to the general public or members thereof. Those websites shall not contain web-TV or video broadcast materials.
Amendment 273 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 h – paragraph 3 3. The marketing authorisation holder shall send the new contents and changes to the competent authorities of the Member State where the Internet website has been registered
Amendment 277 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 h – paragraph 5 5. Member States shall
Amendment 297 #
Proposal for a directive – amending act Article 1 – point 5 (new) Directive 2001/83/EC Article 100 l a (new) Article 100 la) Under the coordination of the Agency, national competent authorities shall organise independent health and treatment literacy campaigns on the following topics: - Rational use of medicines: what is the INN; what does a risk and harm-benefit balance mean; what is an adverse drug reaction; what to do when experiencing an ADR; how to report an ADR; what is compliance; - Good governance: what is a conflict of interest; what is transparency; - Patient and Consumer Rights in Clinical trials: what is a clinical trial; what is informed consent; what are your rights as a participant; what are surrogate endpoints.
Amendment 298 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 l b (new) Article 100 lb Under the coordination of the Agency, national competent authorities shall organise independent preventive health information, notably on health determinants, notably by supporting public campaigns on how to deal with an addiction, risk of alcohol addiction and dependence from addictive substances (tobacco, narcotics, etc.), why to opt for a healthier diet, or to do physical exercise on a regular basis, etc.
Amendment 300 #
Proposal for a directive – amending act Article 1 – point 5 Directive 2001/83/EC Article 100 l c (new) Article 100 lc Member States shall make sure that undergraduate education of healthcare professionals ensures the development of their communications skills and their understanding of the basics of evidence based medicine. Member States shall grant financial support to independent drug information centres, encourage the development of independent continuing education programmes for health professionals and the development of their critical appraisal skills. Within three years of the entry into force of this Directive, the Commission shall, following a public consultation with Member States and continuing education programs for health professionals, establish a comprehensive report on best practices among Member States.
source: PE-441.215
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| 8 |
2009/0173(COD) Reduction of CO2 emissions from light-duty vehicles: emission performance standards for new light commercial vehicles
2010/05/21
ENVI
8 amendments...
Amendment 50 #
Proposal for a regulation Recital 23 a (new) (23a) The beneficial effects of speed limitation devices with regard to protection of the environment and energy consumption, the wear and tear of the motor and tyres and road safety will help attain the objectives of this regulation.
Amendment 58 #
Proposal for a regulation Article 1 – paragraph 1 1. This Regulation establishes CO2 emissions performance requirements for new light commercial vehicles. This Regulation sets the average CO2 emissions for new light commercial vehicles at 1
Amendment 72 #
Proposal for a regulation Article 1 – paragraph 2 2. From 2020, this Regulation sets a target of 1
Amendment 146 #
Proposal for a regulation Article 5 a (new) Article 5a For the calendar year commencing 1 January 2014 and each subsequent calendar year, each manufacturer of light commercial vehicles shall ensure that its light commercial vehicles shall be equipped with speed limitation devices for which the maximum speed is set at 100 km/h.
Amendment 214 #
Proposal for a regulation Article 8 – paragraph 2 – subparagraph 1 – point a – subpoint ii – indent 1 ((Excess emissions – 2) ×
Amendment 218 #
Proposal for a regulation Article 8 – paragraph 2 – subparagraph 1 – point a – subpoint iii – indent 1 ((Excess emissions – 1) ×
Amendment 224 #
Proposal for a regulation Article 8 – paragraph 2 – subparagraph 1 – point a – subpoint iv – indent 1 Excess emissions × 15 € × number of new light commercial vehicles.
Amendment 264 #
Proposal for a regulation Article 12 – paragraph 4 – subparagraph 1 – indent 1 –
source: PE-442.811
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| 15 |
2009/2103(INI) Report on the Commission communication on Action against cancer: European partnership
2010/03/15
ENVI
15 amendments...
Amendment 2 #
Motion for a resolution Recital B B. whereas cancer was the second most common cause of death in 2006, accounting for two out of ten deaths in women and three out of ten deaths in men, equating to approximately 3.2 million EU citizens diagnosed with cancer each year; whereas the deaths are due for the most part to lung cancer, colorectal cancer, and breast cancer,
Amendment 12 #
Motion for a resolution Recital H e (new) He. whereas, according to the World Health Organisation, at least 10% of annual cancer-related deaths are caused directly by exposure to carcinogens at the workplace; whereas such exposure could be averted if the carcinogens were replaced by less harmful substances,
Amendment 21 #
Motion for a resolution Recital N a (new) Na. whereas crystalline silica is classed by the WHO as a Group 1 carcinogen and whereas 3.2 million workers in the EU are exposed to this substance for at least 75 % of their working time; whereas 2.7% of lung/bronchial cancer deaths have to be considered attributable to occupational exposure to crystalline silica,
Amendment 27 #
Motion for a resolution Recital W a (new) Wa. whereas there are at present considerable qualitative differences within the EU as regards cancer screening, early detection, and follow-up; whereas the differences relate in particular to the application of procedures for the purposes of early detection, a method making for a cost measurable, cost-effective reduction in the impact of the disease,
Amendment 28 #
Motion for a resolution Recital Z a (new) Za. whereas EudraCT, the European clinical trials database operated by the European Medicines Agency, is not accessible to patients who have difficulties in finding trials suited to their particular circumstances,
Amendment 37 #
Motion for a resolution Paragraph 3 a (new) 3a. Calls on the Commission to specify the nature of, and the sources of funding for, the European Partnership for Action Against Cancer;
Amendment 49 #
Motion for a resolution Paragraph 12 a (new) 12a. Urges the Member States to establish a legal obligation to declare cancer cases, using standardised European terminology, the object being to provide means of evaluating prevention, screening, and treatment programmes, survival rates, and the comparability of data from one Member State to another and, on the basis of the findings, to produce information aimed at the general public;
Amendment 56 #
Motion for a resolution Paragraph 16 a (new) 16a. Notes that the Czech Government has not yet ratified the WHO Framework Convention on Tobacco Control, which entered into force in February 2005, and therefore urges it to do so;
Amendment 67 #
Motion for a resolution Paragraph 18 a (new) 18a. Calls on the Commission to encourage and support initiatives bringing together a wide range of stakeholders with the aim of preventing cancer by reducing occupational and environmental exposure to carcinogens and other cancer-producing substances and by promoting healthy lifestyles, not least by highlighting the main risk factors such as tobacco, alcohol, obesity, poor diet, lack of exercise, and exposure to the sun, placing the emphasis first and foremost on children and teenagers;
Amendment 69 #
Motion for a resolution Paragraph 19 a (new) 19a. Calls on the Commission and the Partnership to review the Council recommendation on cancer screening in the light of the latest scientific developments in order to provide encouragement for future European accreditation/certification programmes in the area of cancer screening, diagnosis, and treatment, to be drawn up on the basis of the European quality assurance guidelines, bearing in mind that such programmes could also serve as an example for other health-care fields;
Amendment 70 #
Motion for a resolution Paragraph 21 a (new) 21a. Calls on the Commission, the Member States, and the European Chemicals Agency to implement Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals, enforce the applicable restrictions (REACH), and update the list of substances of very high concern, which covers carcinogens;
Amendment 71 #
Motion for a resolution Paragraph 21 b (new) 21b. Calls on the Commission, working within the Partnership, to encourage and support initiatives seeking to prevent imports of goods containing cancer- producing chemicals, and to take Europe- wide measures with a view to intensifying checks to detect such chemicals, pesticides included, as might be present in foodstuffs;
Amendment 73 #
Motion for a resolution Paragraph 23 a (new) 23a. Calls on the Commission and the Member States to ensure that EU-wide human bio-monitoring surveys receive the funding required to enable carcinogens and other cancer-producing substances to be monitored for the purpose of gauging policy effectiveness;
Amendment 74 #
Motion for a resolution Paragraph 24 a (new) 24a. Calls on the Commission to revise 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 (the Clinical Trials Directive) with a view to encouraging a greater cancer research effort, focusing in particular on screening, including early detection, without, however, disregarding the impact of the expenditure entailed on the non- commercial research sector, and to improve the information available to patients and the public at large about clinical trials in progress or which have been successfully completed;
Amendment 76 #
Motion for a resolution Paragraph 26 a (new) 26a. Calls on the Member States and the Commission to employ every means required to produce guidelines for a common definition of disability covering persons suffering from chronic diseases or from cancer and, in the meantime, ensure that those Member States which have not yet done so take the necessary steps without delay to include persons in the above categories in their national definitions of disability;
source: PE-439.847
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| 74 |
2010/0253(COD) Single European railway area. Recast
2011/05/31
TRAN
74 amendments...
Amendment 128 #
Draft legislative resolution Citation 2 a (new) – having regard to Article 14 of the Treaty on the Functioning of the European Union and Protocol No 26 thereto on Services of General Interest,
Amendment 128 #
Draft legislative resolution Citation 2 a (new) – having regard to Article 14 of the Treaty on the Functioning of the European Union and Protocol No 26 thereto on Services of General Interest,
Amendment 156 #
Proposal for a directive Recital 6 a (new) (6a) Any restructuring of the provision of transport services and the management of infrastructure should not have a negative impact on the employment and social conditions of workers in the rail sector. The social clauses should be respected in order to avoid the practice of social dumping and distortion of competition by new entrants not complying with the minimum social standards of the rail sector.
Amendment 156 #
Proposal for a directive Recital 6 a (new) (6a) Any restructuring of the provision of transport services and the management of infrastructure should not have a negative impact on the employment and social conditions of workers in the rail sector. The social clauses should be respected in order to avoid the practice of social dumping and distortion of competition by new entrants not complying with the minimum social standards of the rail sector.
Amendment 169 #
Proposal for a directive Recital 10 a (new) (10a) The European Union should explore alternative sources of funding for European rail projects through innovative financial instruments such as EU project bonds.
Amendment 169 #
Proposal for a directive Recital 10 a (new) (10a) The European Union should explore alternative sources of funding for European rail projects through innovative financial instruments such as EU project bonds.
Amendment 172 #
Proposal for a directive Recital 11 Amendment 172 #
Proposal for a directive Recital 11 Amendment 175 #
Proposal for a directive Recital 11 (11)
Amendment 175 #
Proposal for a directive Recital 11 (11)
Amendment 181 #
Proposal for a directive Recital 13 (13) In the case of journeys with intermediate stops, new market entrants should be authorised to pick up and set down passengers along the route
Amendment 181 #
Proposal for a directive Recital 13 (13) In the case of journeys with intermediate stops, new market entrants should be authorised to pick up and set down passengers along the route
Amendment 185 #
Proposal for a directive Recital 14 (14) The introduction of new, open-access, international passenger services with intermediate stops should
Amendment 185 #
Proposal for a directive Recital 14 (14) The introduction of new, open-access, international passenger services with intermediate stops should
Amendment 195 #
Proposal for a directive Recital 19 a (new) (19a) The national regulatory authority must be independent and able to ensure that citizens have access to the SGI and essential services defined by the competent authority. It must be able to act on its own initiative, meet the objectives set by the Member States and conduct investigations in the event of a dispute.
Amendment 195 #
Proposal for a directive Recital 19 a (new) (19a) The national regulatory authority must be independent and able to ensure that citizens have access to the SGI and essential services defined by the competent authority. It must be able to act on its own initiative, meet the objectives set by the Member States and conduct investigations in the event of a dispute.
Amendment 199 #
Proposal for a directive Recital 21 (21) The national regulatory
Amendment 199 #
Proposal for a directive Recital 21 (21) The national regulatory
Amendment 205 #
Proposal for a directive Recital 22 Amendment 205 #
Proposal for a directive Recital 22 Amendment 281 #
Proposal for a directive Article 3 – paragraph 1 – point 12 12) ‘applicant’ means a railway undertaking and other persons or legal entities, such as competent authorities under Regulation (EC) No 1370/2007 and shippers, freight forwarders and combined transport operators, with a public-service or commercial interest in procuring infrastructure capacity where provided for in national rules;
Amendment 281 #
Proposal for a directive Article 3 – paragraph 1 – point 12 12) ‘applicant’ means a railway undertaking and other persons or legal entities, such as competent authorities under Regulation (EC) No 1370/2007 and shippers, freight forwarders and combined transport operators, with a public-service or commercial interest in procuring infrastructure capacity where provided for in national rules;
Amendment 285 #
Proposal for a directive Article 3 – paragraph 1 – point 12 a (new) (12a) The regulatory authority shall be a stand-alone, independent authority established in each Member State under the conditions laid down in Article 55 hereof.
Amendment 285 #
Proposal for a directive Article 3 – paragraph 1 – point 12 a (new) (12a) The regulatory authority shall be a stand-alone, independent authority established in each Member State under the conditions laid down in Article 55 hereof.
Amendment 298 #
Proposal for a directive Article 5 – paragraph 4 Amendment 298 #
Proposal for a directive Article 5 – paragraph 4 Amendment 336 #
Proposal for a directive Article 7 – paragraph 3 a (new) 3a. If structural changes are required to bring the national organisations in line with this directive, all transfers of staff shall respect the relevant national legislation and regulatory provisions on health, safety, social conditions and the rights of workers and shall not lead to any deterioration of the social and working conditions of workers.
Amendment 336 #
Proposal for a directive Article 7 – paragraph 3 a (new) 3a. If structural changes are required to bring the national organisations in line with this directive, all transfers of staff shall respect the relevant national legislation and regulatory provisions on health, safety, social conditions and the rights of workers and shall not lead to any deterioration of the social and working conditions of workers.
Amendment 348 #
Proposal for a directive Article 8 – paragraph 3 3. Within the framework of general policy determined by the State and taking into account the rail infrastructure development strategy referred to in paragraph 1 , the infrastructure manager shall adopt a business plan including investment and financial programmes. The plan shall be designed to ensure optimal and efficient use, provision and development of the infrastructure while ensuring financial balance and providing means for these objectives to be achieved. The infrastructure manager shall ensure that applicants a
Amendment 348 #
Proposal for a directive Article 8 – paragraph 3 3. Within the framework of general policy determined by the State and taking into account the rail infrastructure development strategy referred to in paragraph 1 , the infrastructure manager shall adopt a business plan including investment and financial programmes. The plan shall be designed to ensure optimal and efficient use, provision and development of the infrastructure while ensuring financial balance and providing means for these objectives to be achieved. The infrastructure manager shall ensure that applicants a
Amendment 367 #
Proposal for a directive Article 10 – paragraph 2 – subparagraph 4 Amendment 367 #
Proposal for a directive Article 10 – paragraph 2 – subparagraph 4 Amendment 371 #
Proposal for a directive Article 11 – paragraph 1 1. Member States may limit the right of access provided for in Article 10 on services between a place of departure and a destination which are covered by one or more public service contracts conforming to the Union legislation in force. Such limitation shall not have the effect of restricting the right to pick up passengers at any station located on the route of an international service and to set them down at another, including stations located in the same Member State, except where the exercise of this right would compromise the
Amendment 371 #
Proposal for a directive Article 11 – paragraph 1 1. Member States may limit the right of access provided for in Article 10 on services between a place of departure and a destination which are covered by one or more public service contracts conforming to the Union legislation in force. Such limitation shall not have the effect of restricting the right to pick up passengers at any station located on the route of an international service and to set them down at another, including stations located in the same Member State, except where the exercise of this right would compromise the
Amendment 376 #
Proposal for a directive Article 11 – paragraph 2 – subparagraph 1 – introductory part Whether the
Amendment 376 #
Proposal for a directive Article 11 – paragraph 2 – subparagraph 1 – introductory part Whether the
Amendment 379 #
Proposal for a directive Article 11 – paragraph 2 – subparagraph 1 – point d a (new) da) associations representing users and staff.
Amendment 379 #
Proposal for a directive Article 11 – paragraph 2 – subparagraph 1 – point d a (new) da) associations representing users and staff.
Amendment 384 #
Proposal for a directive Article 11 – paragraph 4 Amendment 384 #
Proposal for a directive Article 11 – paragraph 4 Amendment 393 #
Proposal for a directive Article 13 – paragraph 2 – subparagraph 1 The services referred to in Annex III, point 2, shall be supplied by all operators of service facilities in a non-discriminatory manner and requests by railway undertakings may only be rejected if viable alternatives under market conditions exist. If the services are not offered by one infrastructure manager, the provider of the ‘main infrastructure’ shall use all reasonable endeavours to facilitate the provision of these services.
Amendment 393 #
Proposal for a directive Article 13 – paragraph 2 – subparagraph 1 The services referred to in Annex III, point 2, shall be supplied by all operators of service facilities in a non-discriminatory manner and requests by railway undertakings may only be rejected if viable alternatives under market conditions exist. If the services are not offered by one infrastructure manager, the provider of the ‘main infrastructure’ shall use all reasonable endeavours to facilitate the provision of these services.
Amendment 456 #
Proposal for a directive Article 14 – paragraph 1 Amendment 456 #
Proposal for a directive Article 14 – paragraph 1 Amendment 462 #
Proposal for a directive Article 15 – paragraph 2 2. In this context, the Commission shall closely involve representatives of the Member States, particularly from the regulatory authorities, and of the sectors concerned in its work, including the social partners and organisations representing rail users, so that they are able better to monitor the development of th
Amendment 462 #
Proposal for a directive Article 15 – paragraph 2 2. In this context, the Commission shall closely involve representatives of the Member States, particularly from the regulatory authorities, and of the sectors concerned in its work, including the social partners and organisations representing rail users, so that they are able better to monitor the development of th
Amendment 477 #
Proposal for a directive Article 17 – paragraph 1 1. A railway undertaking shall be entitled to apply for a licence in the Member State in which it is established
Amendment 477 #
Proposal for a directive Article 17 – paragraph 1 1. A railway undertaking shall be entitled to apply for a licence in the Member State in which it is established
Amendment 513 #
Proposal for a directive Article 31 – paragraph 3 – subparagraph 2 Amendment 513 #
Proposal for a directive Article 31 – paragraph 3 – subparagraph 2 Amendment 543 #
Proposal for a directive Article 32 – paragraph 3 – subparagraph 1 Trains equipped with the European Train Control System (ETCS) running on lines equipped with national command control and signalling systems shall enjoy a temporary reduction of the infrastructure charge in accordance with Annex VIII, point 5. The infrastructure manager shall be able to ensure that such a reduction does not result in a loss of revenue. This reduction shall be offset by higher charges on the same railway line for trains not equipped with ETCS.
Amendment 543 #
Proposal for a directive Article 32 – paragraph 3 – subparagraph 1 Trains equipped with the European Train Control System (ETCS) running on lines equipped with national command control and signalling systems shall enjoy a temporary reduction of the infrastructure charge in accordance with Annex VIII, point 5. The infrastructure manager shall be able to ensure that such a reduction does not result in a loss of revenue. This reduction shall be offset by higher charges on the same railway line for trains not equipped with ETCS.
Amendment 550 #
Proposal for a directive Article 35 – paragraph 2 – subparagraph 2 Amendment 550 #
Proposal for a directive Article 35 – paragraph 2 – subparagraph 2 Amendment 565 #
Proposal for a directive Article 41 – paragraph 1 1. Requests for infrastructure capacity may be made by applicants
Amendment 565 #
Proposal for a directive Article 41 – paragraph 1 1. Requests for infrastructure capacity may be made by applicants
Amendment 566 #
Proposal for a directive Article 41 – paragraph 3 Amendment 566 #
Proposal for a directive Article 41 – paragraph 3 Amendment 569 #
Proposal for a directive Article 43 – paragraph 1 – subparagraph 2 Amendment 569 #
Proposal for a directive Article 43 – paragraph 1 – subparagraph 2 Amendment 587 #
Proposal for a directive Article 55 – paragraph 1 1. Each Member State shall establish a single national regulatory
Amendment 587 #
Proposal for a directive Article 55 – paragraph 1 1. Each Member State shall establish a single national regulatory
Amendment 592 #
Proposal for a directive Article 55 – paragraph 3 3. The president and governing board of the regulatory
Amendment 592 #
Proposal for a directive Article 55 – paragraph 3 3. The president and governing board of the regulatory
Amendment 609 #
Proposal for a directive Article 56 – paragraph 3 a (new) 3a. The regulatory body shall determine, in accordance with Article 10(2), whether the principal purpose of a service is to carry passengers between stations located in different Member States and, in accordance with Article 11(2), whether the economic equilibrium of a public service contract is compromised by services provided for in Article 10 between a place of departure and a destination which are covered by one or more public service contracts.
Amendment 609 #
Proposal for a directive Article 56 – paragraph 3 a (new) 3a. The regulatory body shall determine, in accordance with Article 10(2), whether the principal purpose of a service is to carry passengers between stations located in different Member States and, in accordance with Article 11(2), whether the economic equilibrium of a public service contract is compromised by services provided for in Article 10 between a place of departure and a destination which are covered by one or more public service contracts.
Amendment 623 #
Proposal for a directive Article 56 a (new) Amendment 623 #
Proposal for a directive Article 56 a (new) Amendment 633 #
Proposal for a directive Article 57 – paragraph 7 – subparagraph 1 Amendment 633 #
Proposal for a directive Article 57 – paragraph 7 – subparagraph 1 Amendment 640 #
Proposal for a directive Article 57 a (new) Article 57a The Commission shall, one year after the transposition of this Directive, submit a report on cooperation among national regulatory bodies in accordance with this Article.
Amendment 640 #
Proposal for a directive Article 57 a (new) Article 57a The Commission shall, one year after the transposition of this Directive, submit a report on cooperation among national regulatory bodies in accordance with this Article.
Amendment 645 #
Proposal for a directive Article 63 – paragraph 3 3. Measures under Articles 10(2), 11(4), 14(2), and 17(5) designed to ensure the implementation of the Directive under uniform conditions shall be adopted by the Commission as implementing acts in accordance with the procedure referred to in Article 64(
Amendment 645 #
Proposal for a directive Article 63 – paragraph 3 3. Measures under Articles 10(2), 11(4), 14(2), and 17(5) designed to ensure the implementation of the Directive under uniform conditions shall be adopted by the Commission as implementing acts in accordance with the procedure referred to in Article 64(
source: PE-467.166
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| 3 |
2010/0377(COD) Control of major-accident hazards involving dangerous substances
2011/06/28
ENVI
2 amendments...
Amendment 55 #
Proposal for a directive Recital 8 a (new) (8 a) As a result of their insularity and small size – specific structural handicaps mentioned in Article 349 of the Treaty on the Functioning of the European Union – the EU’s outermost regions have a limited capacity for electricity generation and import, which influences their security of supply. Given this situation, there is a need to ensure that the provisions of this Directive do not affect the supply of electricity to the islands and that they can be adapted accordingly.
Amendment 118 #
Proposal for a directive Article 4 – paragraph 3 – subparagraph 3 a (new) 3a. Whenever a Member State considers that mentioning a dangerous substance which appears in part 2 of Annex I might affect the supply of electricity to an outermost region or the region’s economic activity, and that the substance might be included in part 3 of the Annex, in accordance with paragraph 1 of Article 4, the Member State shall notify the Commission of this. The Commission shall inform the forum referred to in Article 17(2) of such notifications.
source: PE-467.297
2011/06/30
ENVI
1 amendments...
Amendment 296 #
Proposal for a directive Notes to Annex I – paragraph 6 a (new) 6a. In the case of heavy fuel oil, the thresholds given in Part 2 for ‘Petroleum products’ apply solely to power stations commissioned on or after 1 January 2023.
source: PE-467.346
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| 10 |
2011/0156(COD) Food intended for infants and young children and food for special medical purposes
2012/01/26
ENVI
10 amendments...
Amendment 70 #
Proposal for a regulation Recital 15 (15) A limited number of categories of food constitutes the sole source of nourishment of certain groups of the population or represent a partial source of nourishment; such categories of food are vital for the management of certain conditions and/or are essential to maintain the intended nutritional adequacy for certain well-established vulnerable groups of the population. Those categories of food include infant formulae and follow-on formulae, processed cereal-based food and baby food, milk-based drinks for young children and food for special medical purposes. Experience has shown that the provisions laid down in Commission Directive 2006/141/EC, Commission Directive 2006/125/EC, as well as Commission Directive 1999/21/EC ensure the free movement of such food in a satisfactory manner, while ensuring a high level of protection of public health. It is therefore appropriate that this Regulation focuses on the general compositional and information requirements for infant formula and follow-on formulae, processed cereal-based food and baby food for infants and young children, milk-based drinks for young children and
Amendment 89 #
Proposal for a regulation Recital 19 (19) This Regulation should provide the criteria for the establishment of the specific compositional and information requirements for infant formula, follow-on formula, processed cereal-based food and baby food, milk-based drinks for young children and food for special medical purposes, taking into account Commission Directive 2006/141/EC, Commission Directive 2006/125/EC and Commission Directive 1999/21/EC. In order to adapt the definitions of infant formula, follow-on formula, processed cereal-based food and baby food, milk-based drinks for young children and food for special medical purposes laid down in this Regulation taking into account technical and scientific progress and relevant developments at international level, to lay down the specific compositional and information requirements and the procedure for placing on the market foodstuffs resulting from scientific and technological innovations with respect to the categories of food covered by this Regulation, including for additional labelling requirements to, or derogations from, the provisions of Directive 2000/13/EC and for the authorisation of nutrition and health claims, the power to adopt acts in accordance with Article 290 of the Treaty on the Functioning of the European Union should be delegated to the Commission. It is of particular importance that the Commission carries out appropriate consultations during its preparatory work, including at expert level. The Commission, when preparing and drawing-up delegated acts, should ensure a simultaneous, timely and appropriate transmission of relevant documents to the European Parliament and Council.
Amendment 150 #
Proposal for a regulation Article 2 – paragraph 2 – point g – point ii Amendment 178 #
Proposal for a regulation Article 3 – paragraph 1 a (new) 1a. In the labelling, presentation and advertising of foodstuffs for normal consumption the following shall be prohibited: (a) the use of the words ‘specialised nutrition products’, either alone or in conjunction with other words, to designate those foodstuffs; (b) all other markings or any presentation likely to give the impression that one of the products referred to in Article 1(1) and 1(2) is involved.
Amendment 210 #
Proposal for a regulation Article 10 – paragraph 2 – introductory part 2. Subject to the general requirements of Articles 7 and 9 and taking into account Directive 2006/141/EC, Directive 2006/125/EC and Directive 1999/21/EC, as well as any technical and scientific progress, the Commission shall be empowered to adopt delegated Regulations
Amendment 219 #
Proposal for a regulation Article 10 – paragraph 2 – point c a (new) (ca) due to the additional specific requirements for mandatory information to be provided on labels of certain foods referred to in Article 1(1) of this Regulation, derogations from the minimum font size and from other legibility requirements set out in Article 13(2) of Regulation (EU) No 1169/2011 of the European Parliament and of the Council of 25 October 2011 relating to the provision of food information to consumers1; ______________ 1 OJ L 304, 22.11.2011, p. 18.
Amendment 221 #
Proposal for a regulation Article 10 – paragraph 2 – point e a (new) (ea) the process for the placing on the market of food referred to in Article 1(1) resulting from scientific and technological innovations which do not comply with the rules on composition established by the delegated Regulations;
Amendment 222 #
Proposal for a regulation Article 10 – paragraph 2 – point f a (new) (fa) the requirements for information to be provided on recommendations for appropriate use of foods referred to in Article 1(1);
Amendment 227 #
Proposal for a regulation Article 10 – paragraph 2 a (new) 2a. without prejudice to the criteria for certain contaminants levels laid down in Commission Regulation (EC) No 1881/2006 of 19 December 2006 setting maximum levels for certain contaminants in foodstuffs1, the microbiological criteria laid down in Commission Regulation (EC) No 2073/2005 of 15 November 2005 on microbiological criteria for foodstuffs2 shall apply to milk-based drinks intended for young children on the market during the transition period laid down in Article 18; ______________ 1 OJ L 364, 20.12.2006, p. 5. 2 OJ L 288, 19.10.2006, p. 43.
Amendment 237 #
Proposal for a regulation Article 10 – paragraph 2 b (new) 2b. By the end of the transition period as defined in Article 18 (1), the Commission shall, after consulting the European Food Safety Authority, present to the European Parliament and to the Council a report on the desirability of special provisions regarding the composition and labelling of milk-based drinks intended for young children in regard to the nutritional needs, the pattern of consumption, the nutritional intake and the levels of exposure to contaminants and pesticides of young children taking into account the different legislation that governs normal food and food intended for infants and young children. In the light of the conclusions of that report, the Commission shall either: (a) decide that there is no need for special provisions regarding the composition and labelling of milk-based drinks intended for young children, or (b) present, in accordance with the procedure laid down in Article 114 of the Treaty on the Functioning of the European Union, appropriate proposals with a view to amending this regulation and amend the delegated acts concerned so as to include the relevant specific provisions, in accordance with Article 15.
source: PE-480.592
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| 9 |
2011/0272(COD) European grouping of territorial cooperation (EGTC): clarification, simplification and improvement of the establishment and implementation of groupings
2012/05/06
REGI
9 amendments...
Amendment 25 #
Proposal for a regulation – amending act Recital 3 (3)
Amendment 30 #
Proposal for a regulation – amending act Recital 5 (5) Experience with EGTCs set up so far shows that the new legal instrument is also being used for cooperation in the implementation of other European policies.
Amendment 39 #
Proposal for a regulation – amending act Recital 19 (19) The purpose of an EGTC should be extended to cover the facilitating and promotion of territorial cooperation in general, including strategic planning and the management of regional and local concerns in line with Cohesion and other Union policies, thus contributing to the Europe 2020 strategy or to the implementation of macro-regional strategies.
Amendment 40 #
Proposal for a regulation – amending act Recital 26 (26) It should be clarified that the convention – and given the importance of this issue, not the statutes – should indicate the rules applicable to the EGTC’s staff as well as the principles governing the arrangements concerning personnel management and recruitment procedures. Several options should be available to the EGTCs. One such option is to acquire the status specific to the staff of European Union agencies. However, the specific arrangements concerning personnel management and recruitment procedures should be addressed in the statutes.
Amendment 42 #
Proposal for a regulation – amending act Article 1 – paragraph 2 – subparagraph 2 Regulation (EC) No 1082/2006 Article 2 – paragraph 1 An EGTC shall be considered to be an entity of the Member State where it has its registered office for the purposes of determining the applicable law. However, the other Member States which are stakeholders in the EGTC must recognise the specific provisions adopted by the above procedure.”
Amendment 44 #
Proposal for a regulation – amending act Article 1 – paragraph 3 – point e a (new) (ea) organisations representing civil society.”
Amendment 49 #
Proposal for a regulation – amending act Article 1 – paragraph 8 – point a Regulation (EC) No 1082/2006 Article 7 – paragraph 3 – subparagraph 2 Specifically, the tasks of an EGTC may concern the implementation of cooperation programmes or parts thereof
Amendment 51 #
Proposal for a regulation – amending act Article 1 – paragraph 8 – point a Regulation (EC) No 1082/2006 Article 7 – paragraph 3 – subparagraph 3 Member States may not limit the actions that EGTCs may carry out with
Amendment 52 #
Proposal for a regulation – amending act Article 1 – paragraph 9 – subparagraph 4 Regulation (EC) No 1082/2006 Article 8 – paragraph 2 To allow equal treatment of all staff working at the same location, the national laws and rules, whether of public or private law, may be subject to additional ad hoc rules fixed by the EGTC. These may be modelled on the European status accorded to staff of Union agencies.”
source: PE-491.049
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| 2 |
2011/0294(COD) Trans-European transport network: guidelines
2012/11/10
TRAN
2 amendments...
Amendment 792 #
Proposal for a regulation Annex I – Volume 08/33 Incorporate the Tours-Dijon section into the core network
source: PE-496.673
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| 25 |
2011/0409(COD) Sound level of motor vehicles
2012/05/21
TRAN
7 amendments...
Amendment 21 #
Proposal for a regulation Recital 8 (8) This Regulation should also further reduce noise limits. It should take account of Regulation (EC) No 661/2009 of the European Parliament and of the Council of 13 July 2009 concerning type-approval requirements for the general safety of motor vehicles, their trailers and systems, components and separate technical units intended therefor, which introduced new stricter noise requirements for motor vehicle tyres. Studies highlighting the annoyance and health effects from road traffic noise, and the associated costs and benefits should also be heeded. This Regulation should also take account of Regulation (EC) No 1222/2009 of the European Parliament and of the Council of 29 November 2009 on the labelling of tyres with respect to fuel efficiency and other essential parameters1. __________________ 1 OJ L 342, 22.12.2009, p. 46.
Amendment 26 #
Proposal for a regulation Recital 10 (10) The environmental benefits expected from hybrid electric and pure electric road transport vehicles have resulted in a substantial reduction of the noise emitted by such vehicles. This has resulted in the removal of an important source of audible signal that is used by blind and low vision pedestrians and cyclists, amongst other road users, to become aware of the approach, presence or departure of these vehicles. For that purpose, industry is developing acoustic systems to compensate for this lack of audible signal in electric and hybrid electric vehicles. The performance of approaching vehicle audible systems fitted to vehicles should be harmonised. The fitting of such systems should however, remain an option at the discretion of vehicle manufacturers. The Commission should also be asked to look into the contribution that active safety systems can make to meeting the objective of improving the safety of vulnerable road users in urban areas.
Amendment 35 #
Proposal for a regulation Article 3 – point 21 a (new) (21a) “point of sale” means a location where vehicles are offered for sale to consumers.
Amendment 36 #
Proposal for a regulation Article 3 – point 21 b (new) (21b) "technical promotional material" means technical manuals, brochures, leaflets and catalogues (whether these appear in printed, electronic or online form), as well as websites, the purpose of which is to promote vehicles to the general public.
Amendment 56 #
Proposal for a regulation Annex II – point 3.1 – line 9 Amendment 64 #
Proposal for a regulation Annex III – introductory part The sound level measured in accordance with the provisions of Annex II shall not exceed 90 dB (A), under any driving conditions, at a maximum speed of 130 km/h, in accordance with Annex VIII, and shall remain within the following limits:
Amendment 69 #
Proposal for a regulation Annex 3 – Limit Values Table Vehicle Description of vehicle category Limit values expressed in dB(A) [decibels(A)] category Limit values for Limit values for Limit values for registration, sale Type-approval of Type-approval of and entry into new vehicle new vehicle service of new types types vehicles Phase 1 valid Phase 2 valid Phase 3 valid from from from [2 years after [5 years after [7 years after publication] publication] publication] Off- Off- Off- General General General road * road * road * M Vehicles used for the carriage of passengers no of seats < 9; < 125 kW/ton and a maximum of M1
source: PE-489.511
2012/06/13
ENVI
12 amendments...
Amendment 29 #
Proposal for a regulation Recital 8 (8) This Regulation should also further reduce noise limits. It should take account of Regulation (EC) No 661/2009 of the European Parliament and of the Council of 13 July 2009 concerning type-approval requirements for the general safety of motor vehicles, their trailers and systems, components and separate technical units intended therefor, which introduced new stricter noise requirements for motor vehicle tyres. Studies highlighting the annoyance and health effects from road traffic noise, and the associated costs and benefits should also be heeded. This Regulation should take account of Regulation (EC) No 1222/2009 of the European Parliament and of the Council of 25 November 2009 on the labelling of tyres with respect to fuel efficiency and other essential parameters1. _______________ OJ L 342, 22.12.2009, p. 46.
Amendment 40 #
Proposal for a regulation Recital 10 (10) The environmental benefits expected from hybrid electric and pure electric road transport vehicles have resulted in a substantial reduction of the noise emitted by such vehicles. This has resulted in the removal of an important source of audible signal that is used by blind and low vision pedestrians and cyclists, amongst other road users, to become aware of the approach, presence or departure of these vehicles. For that purpose, industry is developing acoustic systems to compensate for this lack of audible signal in electric and hybrid electric vehicles. The performance of approaching vehicle audible systems fitted to vehicles should be harmonised. The fitting of such systems should
Amendment 44 #
Proposal for a regulation Recital 10 a (new) (10a) In view of the lack of legislation on the level of noise emitted by two- or three- wheel vehicles, the Commission should submit a fresh legislative proposal on this subject. It is in the interests of the Union to adopt provisions concerning noise nuisance caused by these vehicles, in the same way as concerning the four-wheel vehicles dealt with in this Regulation. A regulation specific to motor vehicles with at least two wheels would make it possible, on the basis of an improved testing procedure, to assess possibilities of establishing stricter limits in order to ensure that vehicles placed on the market are genuinely less noisy.
Amendment 45 #
Proposal for a regulation Recital 12 (12) In order to enable the Commission to replace the technical requirements of this Regulation with a direct reference to UNECE Regulations No 51 and No 59 once the limit values relating to the new test method are laid down in those Regulations, or to adapt those requirements to technical and scientific developments, the power to adopt acts in accordance with Article 290 of the Treaty on the Functioning of the European Union should be delegated to the Commission in respect of the amendment of the provisions in Annexes to this Regulation related to the test methods and sound levels. It is of particular importance that the Commission carry out appropriate consultations during its preparatory work, including consultation of experts. The Commission, when preparing and drawing up delegated acts, should ensure a simultaneous, timely and appropriate transmission of relevant documents to the European Parliament and to the Council.
Amendment 49 #
Proposal for a regulation Article 3 – paragraph 1 – point 21 a (new) (21a) “point of sale” means a location where vehicles are offered for sale to consumers.
Amendment 50 #
Proposal for a regulation Article 3 – paragraph 1 – point 21 b (new) (21b) "technical promotional material" means technical manuals, brochures, leaflets and catalogues (whether these appear in printed, electronic or online form), as well as websites, the purpose of which is to promote vehicles to the general public.
Amendment 83 #
Proposal for a regulation Article 9 – paragraph 1 Where manufacturers
Amendment 84 #
Proposal for a regulation Article 10 – paragraph 1 1. The Commission shall be empowered to adopt delegated acts, in accordance with Article 11, to amend Annexes I to XI.
Amendment 87 #
Proposal for a regulation Article 11 – paragraph 2 2. The power to adopt delegated acts referred to in Article 10(1) shall be conferred on the Commission for a
Amendment 88 #
Proposal for a regulation Article 11 – paragraph 5 5. A delegated act adopted pursuant to Article 10(1) shall enter into force only if no objection has been expressed either by the European Parliament or the Council within a period of two months of notification of that act to the European Parliament and the Council or if, before the expiry of that period, the European Parliament and the Council have both informed the Commission that they will not object. That period shall be extended by
Amendment 89 #
Proposal for a regulation Article 12 Amendment 90 #
Proposal for a regulation Article 13 source: PE-491.112
2012/12/06
ENVI
6 amendments...
Amendment 100 #
Proposal for a regulation Annex II – point 3.1. – paragraph 7 Amendment 117 #
Proposal for a regulation Annex III – paragraph 1 – introductory part The sound level measured in accordance with the provisions of Annex II shall not exceed the following limits and shall not exceed 90 dB(A) under any driving conditions, with a maximum speed of 130 km/h, in accordance with Annex VIII:
Amendment 118 #
Proposal for a regulation Annex III – column 2 – line 6 no of seats
Amendment 121 #
Proposal for a regulation Annex III – limit values – column 2 – line 7 no of seats
source: PE-491.113
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| 6 |
2012/0055(COD) Ship recycling
2012/12/20
ENVI
6 amendments...
Amendment 148 #
Proposal for a regulation Article 2 – paragraph 1 – point 1 a (new) (1a) 'EU ship' means a ship flying the flag of a Member State or operating under its authority (vessels/craft as defined in Article 2(1)(1));
Amendment 171 #
Proposal for a regulation Article 5 – paragraph 4 – point c a (new) and c b (new) (ca) in the case of EU ships, be verified by the administration or a recognised organisation acting on its behalf; (cb) in the case of ships registered under the flag of a third country, be validated by the classification society.
Amendment 174 #
Proposal for a regulation Article 5 – paragraph 6 – point b (b) a list of the waste (both hazardous and non-hazardous) present on board the ship, including waste generated during the operation of the ship (Part II);
Amendment 214 #
Proposal for a regulation Article 11 – paragraph 1 – subparagraph 1 a (new) Where an EU ship does not have a valid inventory certificate or where there is good reason to believe that – the condition of the ship or its equipment does not correspond substantially with the particulars of the certificate and/or Part I of the inventory of hazardous materials or – no procedure for keeping Part I of the inventory of hazardous materials up to date is implemented on board the ship, a detailed inspection may be carried out, with due account being taken of the IMO guidelines and of Directive 2009/16/EC. Where a non-EU ship does not have a Document of Compliance on board, it may be the subject of a detention order issued in connection with an inspection carried out under Directive 2009/16/EC on port State control.
Amendment 233 #
Proposal for a regulation Article 14 – paragraph 1 1.
Amendment 249 #
Proposal for a regulation Article 23 – paragraph 5 5.
source: PE-502.035
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| 11 |
2012/0082(COD) Single Market: simplifying the transfer of motor vehicles registered in another Member State
2012/10/23
TRAN
11 amendments...
Amendment 17 #
Proposal for a regulation Article 1 – paragraph 1 – introductory part 1. This Regulation shall apply to
Amendment 18 #
Proposal for a regulation Article 1 – paragraph 1 – point a Amendment 19 #
Proposal for a regulation Article 1 – paragraph 1 – point b Amendment 23 #
Proposal for a regulation Article 4 – paragraph 1 – subparagraph 1 Where the holder of the registration certificate moves his normal residence to another Member State, he shall request registration, within a period of six months following his arrival, of a vehicle registered and located in another Member State w
Amendment 24 #
Proposal for a regulation Article 4 – paragraph 1 – subparagraph 2 a (new) After the six-month period, the owner of a vehicle registered and located in another Member State may still request registration of his vehicle in the Member State of residence without any administrative or other obstacles being created by the national registration authority.
Amendment 30 #
Proposal for a regulation Article 5 – paragraph 1 – point d a (new) (da) where the vehicle does not match any known type approved and does not meet objective, non-discriminatory criteria which are known in advance in the Member State of destination.
Amendment 34 #
Proposal for a regulation Article 5 – paragraph 2 2. Any decision taken by a vehicle registration authority refusing to register a vehicle registered in another Member State shall be duly substantiated, giving details of appeal procedures and time limits. The person concerned may within a period of one month from
Amendment 38 #
Proposal for a regulation Article 8 – paragraph 1 – point b (b) it builds or distributes vehicles or provides repair, maintenance or testing services for vehicles;
Amendment 40 #
Proposal for a regulation Article 8 – paragraph 1 – point c (c) it has
Amendment 43 #
Proposal for a regulation Article 8 – paragraph 5 – subparagraph 1 The
Amendment 44 #
Proposal for a regulation Article 8 – paragraph 5 – subparagraph 2 source: PE-497.805
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| 6 |
2012/0190(COD) Reducing CO2 emissions from new passenger cars: modalities for reaching the 2020 target
2013/02/28
ENVI
4 amendments...
Amendment 81 #
Proposal for a regulation Article 1 – point 10 – point c Regulation (EC) No 443/2009 Article 13 – paragraph 5 By 31 December 2014, the Commission shall review the specific emissions targets, modalities and other aspects of this Regulation
Amendment 142 #
Proposal for a regulation Article 1 – point 10 – point c Regulation 2009/443/EC Article 13 – paragraph 5 5. . By 31 December 2014, the Commission shall review the specific emissions targets, modalities and other aspects of this Regulation
Amendment 169 #
Proposal for a regulation Article 1 – point 13 Regulation 2009/443/EC Annex I – point 1 – point c – value of letter "a" in the formula a = 0,0
source: PE-506.077
2013/03/22
ENVI
2 amendments...
Amendment 142 #
Proposal for a regulation Article 1 – point 10 – point c Regulation 2009/443/EC Article 13 – paragraph 5 5. . By 31 December 2014, the Commission shall review the specific emissions targets, modalities and other aspects of this Regulation
Amendment 169 #
Proposal for a regulation Article 1 – point 13 Regulation 2009/443/EC Annex I – point 1 – point c – value of letter "a" in the formula a = 0,0
source: PE-506.077
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| 22 |
2012/0266(COD) Medical devices
2013/05/14
ENVI
22 amendments...
Amendment 178 #
Proposal for a regulation Recital 34 (34) The traceability of medical devices by means of a Unique Device Identification (UDI) system based on international guidance should significantly enhance the effectiveness of the post-market safety of medical devices due to improved incident reporting, targeted field safety corrective actions and better monitoring by competent authorities. It should also help to reduce medical errors and to fight against counterfeit devices. Use of the UDI system should also improve purchase-policy and stock-management by hospitals and pharmacists, and be compatible with the other authentication systems already in place in these environments.
Amendment 222 #
Proposal for a regulation Article 1 – paragraph 1 – subparagraph 1 This Regulation establishes rules to be complied with by medical devices
Amendment 223 #
Proposal for a regulation Article 1 – paragraph 1 – subparagraph 2 For the purposes of this Regulation, medical devices
Amendment 239 #
Proposal for a regulation Article 2 – paragraph 1 – subparagraph 1 – point 2 (2) ‘accessory to a medical device’ means an article which
Amendment 241 #
Proposal for a regulation Article 2 – paragraph 1 – subparagraph 1 – point 2 a (new) (2a) ‘device for aesthetic purposes’ means any instrument, apparatus, appliance, software, implant, material, substance or other article, intended by the manufacturer to be used, alone or in combination, for the purposes of modifying the physical appearance of human beings, without any therapeutic or reconstructive intent, by implanting it in the human body, attaching it to the surface of the eye or using it to induce a tissue or cell reaction on external or non- external parts of the human body. Tattooing products and piercings shall not be considered devices for aesthetic purposes.
Amendment 301 #
Proposal for a regulation Article 8 – paragraph 6 – subparagraph 1 Proportionate to the risk class and the type of device, manufacturers of devices, other than custom-made devices, shall institute and keep up to date a systematic procedure to collect and review experience gained from their devices placed on the market or put into service and to apply any necessary corrective action, hereinafter referred to as ‘post-market surveillance plan’. Post-market surveillance assessments and reports shall be drawn up by independent bodies. The post-
Amendment 305 #
Proposal for a regulation Article 8 – paragraph 6 – subparagraph 2 If in the course of the post-market surveillance a need for corrective action is identified, the manufacturer shall implement the appropriate measures, including immediate notification to the European Databank on Medical Devices (Eudamed) established by means of Commission Decision 2010/227/EU of 19 April 2010.
Amendment 336 #
Proposal for a regulation Article 12 – paragraph 4 4. Distributors who consider or have reason to believe that a device which they have made available on the market is not in conformity with this Regulation shall immediately inform the manufacturer and, where applicable, his authorised representative and the importer and make sure, within the scope of their respective activities, that the necessary corrective action to bring that device into conformity, withdraw or recall it, if appropriate, is taken. Where the device presents a risk, they shall also immediately inform the competent authorities of the Member States in which they made the device available, giving details, in particular, of the non- compliance and of any corrective action taken.
Amendment 449 #
Proposal for a regulation Article 24 – paragraph 8 – point e a (new) (ea) the compatibility with the other traceability systems used by actors working in the field of medical devices.
Amendment 457 #
Proposal for a regulation Article 26 – paragraph 1 1. In the case of devices classified as class III and implantable devices, other than custom-made or investigational devices, the manufacturer shall draw up a
Amendment 475 #
Proposal for a regulation Article 27 – paragraph 4 4. All the information collated and processed by Eudamed shall be accessible to the Member States and to the Commission. The information shall be accessible to notified bodies, economic operators, sponsors, health professionals and the public to the extent defined in the provisions referred to in paragraph 2.
Amendment 505 #
Proposal for a regulation Article 33 – paragraph 9 9. Where no objection is raised in accordance with paragraph 7 or where the MDCG or the Commission, after having been consulted in accordance with paragraph 8, is of the opinion that the notification may be accepted fully or partially, the Commission shall publish the notification accordingly. The Commission shall also enter information on the notification of the notified body into the electronic system provided for in Article 27(2)(e). That information shall be accompanied by the final assessment report of the national authority responsible for notified bodies, the opinion of the joint assessment team and the recommendation of the MDCG, as referred to in this article. The information held in the electronic system shall be accessible to the Member States and the Commission.
Amendment 512 #
Proposal for a regulation Article 35 – paragraph 3 3. At least once a year, the national authority responsible for notified bodies shall assess whether each notified body under its responsibility still satisfies the requirements set out in Annex VI
Amendment 515 #
Proposal for a regulation Article 35 – paragraph 4 4. Three years after notification of a notified body, and again every third year thereafter, the assessment to determine whether the notified body still satisfies the requirements set out in Annex VI shall be conducted by the national authority responsible for notified bodies of the Member State in which the body is established and a joint assessment team designated in accordance with the procedure described in Article 32(3) and (4). At the request of the Commission or of a Member State, the MDCG may initiate the assessment process described in this paragraph at any time when there is reasonable concern about the ongoing compliance of a notified body or a subsidiary or subcontractor of a notified body with the requirements set out in Annex VI.
Amendment 519 #
Proposal for a regulation Article 35 – paragraph 5 a (new) 5a. Every year, the notified bodies shall forward an annual activity report setting out the information referred to in Annex VI, point 5 to the competent authority under which they come and to the Commission, which shall forward it to the MDCG.
Amendment 521 #
Proposal for a regulation Article 36 – paragraph 2 – subparagraph 2 The national authority responsible for notified bodies shall immediately inform the Commission
Amendment 523 #
Proposal for a regulation Article 36 – paragraph 4 4. The national authority responsible for notified bodies shall assess whether the reasons which gave rise to the
Amendment 524 #
Proposal for a regulation Article 36 – paragraph 4 4. The national authority responsible for notified bodies shall assess whether the reasons which gave rise to the change to the notification have an impact on the certificates issued by the notified body and, within three months after having notified the changes to the notification, shall submit a report on its findings to the Commission and the other Member States. Where necessary to ensure the safety of devices on the market, that authority shall instruct the notified body to suspend or withdraw, within a reasonable period of time determined by the authority, any certificates which were unduly issued. If the notified body fails to do so within the determined period of time, or has ceased its activity, the national authority responsible for notified bodies itself shall suspend or withdraw the certificates unduly issued. With a view to ascertaining whether the reasons for the suspension, restriction or withdrawal of the notification have implications for the certificates issued, the national authority responsible shall ask the relevant manufacturers to supply evidence of conformity at notification, and the manufacturers shall have 30 days in which to respond to that request.
Amendment 625 #
Proposal for a regulation Article 53 – paragraph 2 2. When setting up the electronic system referred in paragraph 1, the Commission shall ensure that it is interoperable with the EU database for clinical trials on medicinal products for human use set up in accordance with Article […] of Regulation (EU) No […/…] and the European Databank on Medical Devices (Eudamed) established under Commission Decision 2010/227/EU. With the exception of the information referred to in Article 52, the information collated and processed in the electronic system shall be accessible only to the Member States and to the Commission.
Amendment 636 #
Proposal for a regulation Article 61 – paragraph 3 – subparagraph 1 The Member States shall take all appropriate measures to encourage healthcare professionals including doctors and pharmacists, users and patients to report to their competent authorities suspected serious incidents referred to in point (a) of paragraph 1. They shall record such reports centrally at national level. Where a competent authority of a Member State obtains such reports, it shall take the necessary steps to ensure that the manufacturer of the device concerned is informed of the incident. The manufacturer shall ensure the appropriate follow-up.
Amendment 668 #
Proposal for a regulation Article 67 a (new) Amendment 788 #
Proposal for a regulation Annex 1 – part III – point 19 – point 19.1 – paragraph 1 – point d (d) Labels shall be provided in a human- readable format
source: PE-510.765
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| 30 |
2012/0305(COD) Fluorinated greenhouse gases
2013/04/05
ENVI
30 amendments...
Amendment 60 #
Proposal for a regulation Recital 3 (3) A Commission report on the application, effects and adequacy of Regulation (EC) No 842/2006 concluded that the current
Amendment 63 #
Proposal for a regulation Recital 4 (4) The Commission’s report also concluded that more can be done to reduce emissions of fluorinated greenhouse gases in the Union, in particular by avoiding the use of those gases where there are safe and energy efficient alternative technologies with no impact or a lower impact on the climate.
Amendment 66 #
Proposal for a regulation Recital 5 a (new) (5a) Comprehensive data acquisition is necessary in order to monitor progress towards achieving the objectives relating to the reduction of emissions of fluorinated greenhouse gases. The obligation to establish and maintain records of equipment that contains such gases should, therefore, also apply to electrical switchgear and other equipment covered by this Regulation.
Amendment 67 #
Proposal for a regulation Recital 7 (7) Given that there are suitable alternatives, the current ban on using sulphur hexafluoride in magnesium die- casting and the recycling of magnesium die-casting alloys should be extended to facilities that use less than 850 kg per year. Similarly, with an appropriate transitional period, the use of refrigerants with
Amendment 70 #
Proposal for a regulation Recital 8 (8) Additional bans on the placing on the market of new equipment for refrigeration, air-conditioning and fire protection that operate using specific fluorinated greenhouse gases should be introduced where suitable alternatives to the use of those substances are available. In the light of future technical developments and the availability of cost-efficient alternatives to the use of fluorinated greenhouse gases, the Commission should be empowered to include other products and equipment
Amendment 81 #
Proposal for a regulation Recital 18 (18) The Commission should continuously monitor the effects of reducing the placing on the market of hydrofluorocarbons, including the effect of reduction on the supply for appliances where the use of hydrofluorocarbons would result in lower life-cycle emissions than if an alternative technology was used The monitoring should also ensure the early detection of health or safety concerns, due to negative impacts on the availability of medicinal products. A comprehensive review should be carried out
Amendment 93 #
Proposal for a regulation Article 1 – paragraph 1 – point 4 (4) ‘operator’ means the natural or legal person
Amendment 100 #
Proposal for a regulation Article 1 – paragraph 1 – point 15 a (new) (15a) ‘refrigerated van’ means a vehicle with a mass of less than 3.5 tonnes that is designed and constructed primarily to carry goods and that is equipped with a refrigeration unit;
Amendment 101 #
Proposal for a regulation Article 1 – paragraph 1 – point 16 a (new) (16a) ‘container’ means an intermodal transport unit that is designed and constructed primarily to carry goods and that is equipped with a refrigeration unit;
Amendment 112 #
Proposal for a regulation Article 2 – paragraph 1 a (new) 1a. All measures which are technically and economically feasible shall be taken to minimise leaks of fluorinated gases.
Amendment 139 #
Proposal for a regulation Article 3 – paragraph 1 – subparagraph 3 – point e e) refrigerat
Amendment 153 #
Proposal for a regulation Article 5 – paragraph 1 a (new) 1a. The persons carrying out the leak checks of the equipment referred to in Article 3(2)(a) shall on each occasion draw up a check report containing the following information: a) the type of equipment checked, its charge size, the type of greenhouse gas charged and the date of its entry into service; b) the type of work performed on the equipment and the date on which the check was carried out; c) any damage noted; d) the amount of fluorinated greenhouse gases added and the type of gas used; e) the quantity of fluorinated greenhouse gases recovered; f) whether the equipment has been decommissioned; g) the name of the operator and, in the case of the equipment referred to Article 3(1)(e), the vehicle or container identification number. The persons carrying out the leak checks shall keep a record containing the information listed in paragraph 1 and shall provide the operator with a copy of the check report. The operators of equipment containing the greenhouse gases referred to in Article 3(2)(a) shall keep all check reports throughout the life of the equipment concerned.
Amendment 155 #
Proposal for a regulation Article 5 – paragraph 1 – subparagraph 2 This paragraph shall apply to operators of electrical switchgear that contains SF6 and of the equipment referred to in Article 3(2)(b) and (c).
Amendment 159 #
Proposal for a regulation Article 5 – paragraph 2 – subparagraph 1 a (new) Unless the records referred to in paragraph 1a are kept in a database established by the competent authorities of the Member States, the persons carrying out the leak checks referred to in paragraph 1a shall keep the records for at least five years after the check was carried out.
Amendment 200 #
Proposal for a regulation Article 8 – paragraph 6 6. Member States shall notify the Commission of their training and certification programmes by 1 January 201
Amendment 212 #
Proposal for a regulation Article 9 – paragraph 3 3. The Commission shall be empowered to adopt delegated acts in accordance with Article 20 amending the list set out in Annex III to include other products and equipment that contain fluorinated greenhouse gases with a global warming potential of 150 or more, or that rely on them to work, if it has been established that alternatives to the use of fluorinated greenhouse gases or to the use of specific types of fluorinated greenhouse gases are available, and their use would result in lower overall greenhouse gas emissions
Amendment 234 #
Proposal for a regulation Article 11 – paragraph 3 – subparagraph 1 3. The use of fluorinated greenhouse gases, or of mixtures that contain fluorinated greenhouse gases, with a global warming potential of 2500 or more, to service or maintain refrigeration equipment with a charge size equivalent to 50 tonnes of CO2 or more, shall be prohibited from 1 January 2020.
Amendment 252 #
Proposal for a regulation Article 12 – paragraph 1 – subparagraph 1 1. From [dd/mm/yyyy] [insert date
Amendment 258 #
Proposal for a regulation Article 12 – paragraph 1 – subparagraph 2 Amendment 259 #
Proposal for a regulation Article 12 – paragraph 1 – subparagraph 2 a (new) The equipment referred to in Article 3(1)(e) shall be charged by persons certified in accordance with Article 8 in the Member State where the vehicle is registered and made available to the operator.
Amendment 303 #
Proposal for a regulation Article 19 – paragraph 3 – subparagraph 2 No later than
Amendment 306 #
Proposal for a regulation Article 19 – paragraph 3 – subparagraph 3 No later than
Amendment 314 #
Proposal for a regulation Article 20 – paragraph 2 2. The power to adopt delegated acts referred to in Articles 3(4), 7(2), 8(7), 9(3), 10(7), 13(
Amendment 315 #
Proposal for a regulation Article 20 – paragraph 3 3. The
Amendment 316 #
Proposal for a regulation Article 20 – paragraph 5 5. A delegated act adopted pursuant to Articles 3(4), 7(2), 8(7), 9(3), 10(7), 13(
Amendment 348 #
Proposal for a regulation Annex III – row 12 a (new) 12a. Air conditioning systems in category 1 January 2011 M1 and N1, class I vehicles type approved after 1 January 2011, and air conditioning systems for retrofitting to vehicles type approved after 1 January 2011 and which are designed to contain fluorinated greenhouse gases with a global warming potential higher than 150 as provided for in Directive 2006/40/EC1 ________________________ 1 Directive 2006/40/EC of the European Parliament and of the Council of 17 May 2006 relating to emissions from air- conditioning systems in motor vehicles and amending Council Directive 70/156/EEC, OJ L 161 of 14.6.2006, p. 12.
Amendment 349 #
Proposal for a regulation Annex III – row 12 b (new) 12b. Air conditioning systems for the 1 January 2017 fitting or retrofitting of all category M1 and N1, class I vehicles and which are designed to contain fluorinated greenhouses gases with a global warming potential higher than 150 as provided for in Directive 2006/40/EC1 ______________________ 1 Directive 2006/40/EC of the European Parliament and of the Council of 17 May 2006 relating to emissions from air- conditioning systems in motor vehicles and amending Council Directive 70/156/EEC, OJ L 161 of 14.6.2006, p. 12.
Amendment 414 #
Proposal for a regulation Annex VII – point 1 – point a a) the total
source: PE-508.030
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| 4 |
2012/0337(COD) General Union Environment Action Programme to 2020: 'Living well, within the limits of our planet'
2013/03/27
ENVI
4 amendments...
Amendment 258 #
Proposal for a decision Annex 1 – point 37 37. There is also considerable potential for improving waste management in the EU to make better use of resources, open up new markets, create new jobs and reduce dependence on imports of raw materials, while having lower impacts on the environment. Each year in the EU, 2.7 billion tonnes of waste are produced, of which 98 million tonnes is hazardous. On average, only 40 % of solid waste is re- used or recycled. There are no reliable figures for liquid waste, but the percentage recycled is clearly very small. The rest goes to landfill or incineration. In some Member States, more than 70 % of waste is recycled, showing how waste could be used as one of the EU’s key resources. At the same time, many Member States landfill over 75 % of their municipal waste.
Amendment 267 #
Proposal for a decision Annex 1 – point 38 38. Turning waste into a resource, as called for in the Resource Efficiency Roadmap, requires the full implementation of EU waste legislation across the EU, based on strict application of the waste hierarchy and covering different types of waste. With regard to liquid waste, the collection of used fats at source, before they are discharged into wastewater networks, must be made a priority. Additional efforts are needed to: reduce per capita waste generation in absolute terms, limit energy recovery to non-recyclable materials, phase out landfilling, ensure high quality recycling, and develop markets for secondary raw materials. Hazardous waste will need to be managed so as to minimise significant adverse effects on human health and the environment, as agreed at the Rio+20 Summit. To achieve this, market- based instruments that privilege prevention, recycling and re-use should be applied much more systematically across the EU. Barriers facing recycling activities in the EU internal market should be removed and existing prevention, re-use, recycling, recovery and landfill diversion targets reviewed so as to move towards a ‘circular’ economy, with a cascading use of resources and residual waste close to zero.
Amendment 274 #
Proposal for a decision Annex 1 – point 39 39. Resource efficiency in the water sector will also be tackled as a priority to help deliver good water status. Even though droughts and water scarcity are affecting more and more parts of Europe, an estimated 20-40 % of Europe’s available water is still being wasted, for instance, through leakages in the distribution system. According to available modelling, there is still considerable scope for improving water efficiency in the EU. Moreover, rising demand and the impacts of climate change are expected to increase the pressure on Europe’s water resources significantly. Against this background, the Union and Member States should take action to ensure water abstraction respects available renewable water resource limits by 2020, including by improving water efficiency through the use of market mechanisms such as water pricing that reflects the true value of water. Progress will be facilitated by accelerated demonstration and rolling out of innovative technologies, systems and business models building on the Strategic Implementation Plan of the European Innovation Partnership on Water. Separating used fats at source, before they are discharged into wastewater networks, and subsequently collecting and recycling them, must become a water treatment policy priority.
Amendment 323 #
Proposal for a decision Annex 1 – point 41 – subparagraph 2 - point f (f) Improving water efficiency by setting targets at river basin level, as well as for wastewater recycling, and using market mechanisms, such as water pricing.
source: PE-508.027
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| 2 |
2012/0366(COD) Tobacco and related products: manufacture, presentation and sale. Approximation of Member States legislation
2013/05/14
ENVI
1 amendments...
Amendment 948 #
Proposal for a directive Article 14 – paragraph 2 – point g 2012/0366(COD) Article 14(2)(g) (g) the intended shipment route
source: PE-510.719
2013/05/21
ENVI
1 amendments...
Amendment 938 #
Proposal for a directive Article 14 – paragraph 1 1. Member States shall ensure that all unit packets of tobacco products shall be marked with a unique identifier. In order to ensure their integrity, unique and secure identifiers shall be irremovably printed/affixed, indelible and in no way hidden or interrupted in any form, including through tax stamps and price marks, or by the opening of the packet. In relation to products manufactured outside the Union the obligations laid down in this Article apply only to those destined to or placed on the Union market.
source: PE-510.718
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