BETA


2018/2568(RSP) Resolution on the draft Commission implementing decision renewing the authorisation for the placing on the market of products containing, consisting of, or produced from genetically modified maize 59122 (DAS-59122-7)

Progress: Procedure completed

RoleCommitteeRapporteurShadows
Lead ENVI PIETIKÄINEN Sirpa (icon: PPE PPE), BALAS Guillaume (icon: S&D S&D), MAZURONIS Valentinas (icon: ALDE ALDE), STAES Bart (icon: Verts/ALE Verts/ALE), EVI Eleonora (icon: EFDD EFDD)
Lead committee dossier:
Legal Basis:
RoP 112-p2

Events

2018/07/23
   EC - Commission response to text adopted in plenary
Documents
2018/03/01
   EP - Motion for a resolution
Documents
2018/03/01
   EP - Results of vote in Parliament
2018/03/01
   EP - Decision by Parliament
Details

The European Parliament adopted by 405 votes to 205, with 25 abstentions, a resolution objecting to the draft Commission implementing decision renewing the authorisation for the placing on the market of products containing, consisting of, or produced from genetically modified maize 59122 (DAS-59122-7) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council on genetically modified food and feed.

On 19 July 2016, Pioneer Overseas Corporation and Dow AgroSciences Ltd. jointly submitted an application for the renewal of the authorisation for the placing on the market of foods and feed containing, consisting of, or produced from genetically modified (GM) maize 59122 .

GM maize 59122 expresses proteins conferring resistance to coleopteran insect pests belonging to the genus Diabrotica such as larvae of western corn rootworm and the PAT protein which confers tolerance to glufosinate containing herbicides .

Although the European Food Safety Authority (EFSA) adopted a favourable opinion to renew the authorisation, many critical comments were submitted by Member States in relation to the first EFSA opinion during the three-month consultation period relating to:

that ‘the monitoring conducted for GM maize 59122 is unable to provide meaningful results for the current assessment and to resolve uncertainties associated with the risk assessment conducted prior to authorisation, e.g. as regards exposure of the environment’; that ‘the monitoring approach implemented for GM maize 59122 is not in line with requirements of Annex VII of Directive 2001/18/EC’ .

Other areas of concern are: (i) the fact that several studies demonstrate that the immunogenicity of Cry proteins in mice have not been submitted by the applicant; (ii) the residues from spraying with glufosinate were not assessed; (iii) the fact that residues from the spraying of complementary herbicides could be expected to be present in the crops.

Members considered that it would be unacceptable from a food safety perspective, as well as highly inconsistent, to authorise the import of a glufosinate tolerant GM maize given that the authorisation for the use of glufosinate in the Union expires on 31 July 2018 due to its reproductive toxicity.

On the basis of these considerations, Parliament considered that the Commission’s implementing decision is not compatible with Union law which requires the provision of the basis for ensuring a high level of protection of human life and health, animal health and welfare, the environment and consumer interests, while ensuring the effective functioning of the internal market.

As a result, Parliament asked the Commission to withdraw its draft implementing decision.

On a procedural level , Members recalled that since the entry into force of authorisation procedure for GMOs, authorisation decisions have been adopted by the Commission without the support of the Standing Committee on the Food Chain and Animal Health.

The return of the dossier to the Commission for final decision, which is very much the exception for the procedure as a whole, has become the norm for decision-making on genetically modified food and feed authorisations. This practice has also been deplored by Commission President Juncker as not being democratic .

Parliament called on the Commission to suspend any implementing decision regarding applications for authorisation of genetically modified organisms until the authorisation procedure has been revised in such a way so as to address the shortcomings of the current procedure.

It also called on it to advance work on the Commission proposal amending Regulation (EU) No 182/2011 as a matter of urgency and to ensure that, inter alia, if no opinion is delivered by the Food Chain and Animal Health Standing Committee with respect to GMOs approvals, either for cultivation or for food and feed, the Commission will withdraw the proposal.

Lastly, the Commission is called on not to authorise the import of any genetically modified plant for food or feed uses which has been made tolerant to a complementary herbicide which is banned, or which will be banned in the near future, in the Union.

Documents
2018/03/01
   EP - End of procedure in Parliament
2018/01/29
   EP - PIETIKÄINEN Sirpa (PPE) appointed as rapporteur in ENVI
2018/01/29
   EP - BALAS Guillaume (S&D) appointed as rapporteur in ENVI
2018/01/29
   EP - MAZURONIS Valentinas (ALDE) appointed as rapporteur in ENVI
2018/01/29
   EP - STAES Bart (Verts/ALE) appointed as rapporteur in ENVI
2018/01/29
   EP - EVI Eleonora (EFDD) appointed as rapporteur in ENVI

Documents

Votes

B8-0122/2018 - Résolution 01/03/2018 12:18:12.000 #

2018/03/01 Outcome: +: 405, -: 205, 0: 25
IT FR DE HU EL AT GB PT SE CY MT ES LV DK SK LU SI NL RO BG BE IE LT PL EE FI CZ HR
Total
45
61
83
16
19
17
59
19
18
6
6
48
7
13
11
5
7
22
28
15
20
8
10
48
4
13
17
9
icon: S&D S&D
163

Cyprus S&D

2

Malta S&D

3

Latvia S&D

1

Luxembourg S&D

For (1)

1

Netherlands S&D

3

Estonia S&D

For (1)

1
icon: Verts/ALE Verts/ALE
46

Italy Verts/ALE

For (1)

1

Hungary Verts/ALE

For (1)

1

Austria Verts/ALE

2

United Kingdom Verts/ALE

5

Spain Verts/ALE

3

Latvia Verts/ALE

1

Denmark Verts/ALE

For (1)

1

Luxembourg Verts/ALE

For (1)

1

Slovenia Verts/ALE

For (1)

1

Netherlands Verts/ALE

2

Belgium Verts/ALE

2

Lithuania Verts/ALE

For (1)

1

Estonia Verts/ALE

For (1)

1

Finland Verts/ALE

For (1)

1

Croatia Verts/ALE

For (1)

1
icon: GUE/NGL GUE/NGL
45

France GUE/NGL

1

United Kingdom GUE/NGL

1

Sweden GUE/NGL

For (1)

1

Cyprus GUE/NGL

2

Denmark GUE/NGL

For (1)

1

Netherlands GUE/NGL

3

Ireland GUE/NGL

3

Finland GUE/NGL

For (1)

1

Czechia GUE/NGL

2
icon: ENF ENF
27

Italy ENF

2

United Kingdom ENF

Abstain (1)

1

Netherlands ENF

3

Romania ENF

1

Poland ENF

2
icon: EFDD EFDD
34

Germany EFDD

Abstain (1)

1

Sweden EFDD

2

Poland EFDD

1
icon: NI NI
15

France NI

For (1)

Against (1)

2

Germany NI

2

Hungary NI

2

United Kingdom NI

For (1)

1

Denmark NI

1

Poland NI

Against (1)

2
icon: ECR ECR
58

Italy ECR

Against (1)

1

Germany ECR

For (1)

4

Greece ECR

For (1)

1

Cyprus ECR

1

Latvia ECR

For (1)

1

Slovakia ECR

Against (1)

2

Netherlands ECR

For (1)

1

Romania ECR

Against (1)

1

Bulgaria ECR

For (1)

Against (1)

2

Lithuania ECR

1

Finland ECR

Against (1)

2

Czechia ECR

2

Croatia ECR

Against (1)

1
icon: ALDE ALDE
58

Germany ALDE

For (1)

3

Austria ALDE

Against (1)

1

United Kingdom ALDE

Abstain (1)

1

Portugal ALDE

1

Sweden ALDE

2

Latvia ALDE

1

Denmark ALDE

3

Slovenia ALDE

Against (1)

1

Romania ALDE

Against (1)

3

Bulgaria ALDE

For (1)

4

Ireland ALDE

For (1)

1

Lithuania ALDE

3

Estonia ALDE

Against (1)

1

Croatia ALDE

2
icon: PPE PPE
188

United Kingdom PPE

2

Cyprus PPE

1

Latvia PPE

Against (1)

3

Denmark PPE

Against (1)

1

Luxembourg PPE

3

Belgium PPE

4

Estonia PPE

Against (1)

1

Finland PPE

3

History

(these mark the time of scraping, not the official date of the change)

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BOYLAN Lynn
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group
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  • date: 2018-03-01T00:00:00 docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=MOTION&reference=B8-2018-0122&language=EN title: B8-0122/2018 type: Motion for a resolution body: EP
  • date: 2018-07-23T00:00:00 docs: url: /oeil/spdoc.do?i=30818&j=0&l=en title: SP(2018)292 type: Commission response to text adopted in plenary
events
  • date: 2018-03-01T00:00:00 type: Results of vote in Parliament body: EP docs: url: https://oeil.secure.europarl.europa.eu/oeil/popups/sda.do?id=30818&l=en title: Results of vote in Parliament
  • date: 2018-03-01T00:00:00 type: Decision by Parliament, 1st reading/single reading body: EP docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P8-TA-2018-0051 title: T8-0051/2018 summary: The European Parliament adopted by 405 votes to 205, with 25 abstentions, a resolution objecting to the draft Commission implementing decision renewing the authorisation for the placing on the market of products containing, consisting of, or produced from genetically modified maize 59122 (DAS-59122-7) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council on genetically modified food and feed. On 19 July 2016, Pioneer Overseas Corporation and Dow AgroSciences Ltd. jointly submitted an application for the renewal of the authorisation for the placing on the market of foods and feed containing, consisting of, or produced from genetically modified (GM) maize 59122 . GM maize 59122 expresses proteins conferring resistance to coleopteran insect pests belonging to the genus Diabrotica such as larvae of western corn rootworm and the PAT protein which confers tolerance to glufosinate containing herbicides . Although the European Food Safety Authority (EFSA) adopted a favourable opinion to renew the authorisation, many critical comments were submitted by Member States in relation to the first EFSA opinion during the three-month consultation period relating to: that ‘the monitoring conducted for GM maize 59122 is unable to provide meaningful results for the current assessment and to resolve uncertainties associated with the risk assessment conducted prior to authorisation, e.g. as regards exposure of the environment’; that ‘the monitoring approach implemented for GM maize 59122 is not in line with requirements of Annex VII of Directive 2001/18/EC’ . Other areas of concern are: (i) the fact that several studies demonstrate that the immunogenicity of Cry proteins in mice have not been submitted by the applicant; (ii) the residues from spraying with glufosinate were not assessed; (iii) the fact that residues from the spraying of complementary herbicides could be expected to be present in the crops. Members considered that it would be unacceptable from a food safety perspective, as well as highly inconsistent, to authorise the import of a glufosinate tolerant GM maize given that the authorisation for the use of glufosinate in the Union expires on 31 July 2018 due to its reproductive toxicity. On the basis of these considerations, Parliament considered that the Commission’s implementing decision is not compatible with Union law which requires the provision of the basis for ensuring a high level of protection of human life and health, animal health and welfare, the environment and consumer interests, while ensuring the effective functioning of the internal market. As a result, Parliament asked the Commission to withdraw its draft implementing decision. On a procedural level , Members recalled that since the entry into force of authorisation procedure for GMOs, authorisation decisions have been adopted by the Commission without the support of the Standing Committee on the Food Chain and Animal Health. The return of the dossier to the Commission for final decision, which is very much the exception for the procedure as a whole, has become the norm for decision-making on genetically modified food and feed authorisations. This practice has also been deplored by Commission President Juncker as not being democratic . Parliament called on the Commission to suspend any implementing decision regarding applications for authorisation of genetically modified organisms until the authorisation procedure has been revised in such a way so as to address the shortcomings of the current procedure. It also called on it to advance work on the Commission proposal amending Regulation (EU) No 182/2011 as a matter of urgency and to ensure that, inter alia, if no opinion is delivered by the Food Chain and Animal Health Standing Committee with respect to GMOs approvals, either for cultivation or for food and feed, the Commission will withdraw the proposal. Lastly, the Commission is called on not to authorise the import of any genetically modified plant for food or feed uses which has been made tolerant to a complementary herbicide which is banned, or which will be banned in the near future, in the Union.
  • date: 2018-03-01T00:00:00 type: End of procedure in Parliament body: EP
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    • ENVI/8/12162
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    Rules of Procedure EP 112-p2
    procedure/legal_basis/0
    Rules of Procedure of the European Parliament EP 106-p2
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    • 3.10.09.06 Agro-genetics, GMOs
    New
    3.10.09.06
    Agro-genetics, GMOs
    procedure/title
    Old
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    New
    Resolution on the draft Commission implementing decision renewing the authorisation for the placing on the market of products containing, consisting of, or produced from genetically modified maize 59122 (DAS-59122-7)
    activities/0/docs/0/text
    • The European Parliament adopted by 405 votes to 205, with 25 abstentions, a resolution objecting to the draft Commission implementing decision renewing the authorisation for the placing on the market of products containing, consisting of, or produced from genetically modified maize 59122 (DAS-59122-7) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council on genetically modified food and feed.

      On 19 July 2016, Pioneer Overseas Corporation and Dow AgroSciences Ltd. jointly submitted an application for the renewal of the authorisation for the placing on the market of foods and feed containing, consisting of, or produced from genetically modified (GM) maize 59122.

      GM maize 59122 expresses proteins conferring resistance to coleopteran insect pests belonging to the genus Diabrotica such as larvae of western corn rootworm and the PAT protein which confers tolerance to glufosinate containing herbicides.

      Although the European Food Safety Authority (EFSA) adopted a favourable opinion to renew the authorisation, many critical comments were submitted by Member States in relation to the first EFSA opinion during the three-month consultation period relating to:

      • that ‘the monitoring conducted for GM maize 59122 is unable to provide meaningful results for the current assessment and to resolve uncertainties associated with the risk assessment conducted prior to authorisation, e.g. as regards exposure of the environment’;
      • that ‘the monitoring approach implemented for GM maize 59122 is not in line with requirements of Annex VII of Directive 2001/18/EC’.

      Other areas of concern are: (i) the fact that several studies demonstrate that the immunogenicity of Cry proteins in mice have not been submitted by the applicant; (ii) the residues from spraying with glufosinate were not assessed; (iii) the fact that residues from the spraying of complementary herbicides could be expected to be present in the crops.

      Members considered that it would be unacceptable from a food safety perspective, as well as highly inconsistent, to authorise the import of a glufosinate tolerant GM maize given that the authorisation for the use of glufosinate in the Union expires on 31 July 2018 due to its reproductive toxicity.

      On the basis of these considerations, Parliament considered that the Commission’s implementing decision is not compatible with Union law which requires the provision of the basis for ensuring a high level of protection of human life and health, animal health and welfare, the environment and consumer interests, while ensuring the effective functioning of the internal market.

      As a result, Parliament asked the Commission to withdraw its draft implementing decision.

      On a procedural level, Members recalled that since the entry into force of authorisation procedure for GMOs, authorisation decisions have been adopted by the Commission without the support of the Standing Committee on the Food Chain and Animal Health.

      The return of the dossier to the Commission for final decision, which is very much the exception for the procedure as a whole, has become the norm for decision-making on genetically modified food and feed authorisations. This practice has also been deplored by Commission President Juncker as not being democratic.

      Parliament called on the Commission to suspend any implementing decision regarding applications for authorisation of genetically modified organisms until the authorisation procedure has been revised in such a way so as to address the shortcomings of the current procedure.

      It also called on it to advance work on the Commission proposal amending Regulation (EU) No 182/2011 as a matter of urgency and to ensure that, inter alia, if no opinion is delivered by the Food Chain and Animal Health Standing Committee with respect to GMOs approvals, either for cultivation or for food and feed, the Commission will withdraw the proposal.

      Lastly, the Commission is called on not to authorise the import of any genetically modified plant for food or feed uses which has been made tolerant to a complementary herbicide which is banned, or which will be banned in the near future, in the Union.

    activities/0/docs
    • url: http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P8-TA-2018-0051 type: Decision by Parliament, 1st reading/single reading title: T8-0051/2018
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    • body: EP responsible: True committee: ENVI date: 2018-01-29T00:00:00 2018-01-29T00:00:00 2018-01-29T00:00:00 2018-01-29T00:00:00 2018-01-29T00:00:00 2018-01-29T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: EPP name: PIETIKÄINEN Sirpa group: S&D name: BALAS Guillaume group: ALDE name: MAZURONIS Valentinas group: GUE/NGL name: BOYLAN Lynn group: Verts/ALE name: STAES Bart group: EFD name: EVI Eleonora
    links
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      3.10.09.06 Agro-genetics, GMOs