Greece | BCH-NR5-GR-301175 | Fifth National Report on the Implementation of the Cartagena Protocol on Biosafety

Article 2 – General provisions

Article 2 requires each Party to take the necessary and appropriate legal, administrative and other measures to implement its obligations under the Protocol

7. Has your country introduced the necessary national measures for the implementation of the Protocol?

National measures are partially in place

EN

8. Which specific instruments are in place for the implementation of national biosafety measures? (select all that apply)

One or more national biosafety laws
One or more national biosafety regulations
Other laws, regulations or guidelines that indirectly apply to biosafety

Please provide further information on the instruments in place:

Greece ratified the Cartagena Protocol by law (No 3233) in 2004. A number of Joint Ministerial Decisions have also been issued to regulate biosafety matters. Greece also abides by EU legislature on biosafety. In particular, Greece is a member of the European Union and adopts EU legislation on GMOs. EU Regulations have immediate effect while Directives are transposed into national legislation by using national legal instruments (commonly in the form of Ministerial Decisions). Main pieces of legislation include: - Directive 2001/18/EC of 12 March 2001 on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC, covering the field testing of GMOs and the placing on the market of GMOs as well as products containing or consisting of GMOs, e.g. for cultivation, import or processing into industrial products. - Regulation (EC) No 1829/2003 of 22 September 2003 on genetically modified food and feed, covering the placing on the market of GMOs intended for food or feed and of food or feed products containing, consisting of or produced from GMOs. - Regulation (EC) No 1830/2003 of 22 September 2003 concerning the traceability and labelling of genetically modified organisms and the traceability of food and feed products produced from genetically modified organisms. - Regulation (EC) No 1946/2003 of 15 July 2003 on transboundary movements of genetically modified organisms covers exports of GMOs to third countries and unintentional movements of GMOs. - Regulation (EC) No 641/2004 of 6 April 2004 on detailed rules for the implementation of Regulation (EC) No 1829/2003 as regards the application for the authorization of new genetically modified food and feed, the notification of existing products and adventitious or technically unavoidable presence of genetically modified material which has benefited from a favourable risk evaluation. - Directive 2009/41/EC of the European Parliament and of the Council of 6 May 2009 on the contained use of genetically modified micro-organisms. - Commission Regulation 619/2011 of 24 June 2011 laying down the methods of sampling and analysis for the official control of feed as regards the presence of genetically modified material for which an authorization procedure is pending or the authorization of which has expired. - Commission Implementing Regulation (EU) No 503/2013 of 3 April 2013 on applications for authorization of genetically modified food and feed in accordance with Regulation (EC) No 1829/2003 of the European Parliament and of the Council and amending Commission Regulations (EC) No 641/2004 and (EC) No 1981/2006. - Directive (EU) 2015/412 of the European Parliament and of the Council of 11 March 2015 amending Directive 2001/18/EC as regards the possibility for the Member States to restrict or prohibit the cultivation of GMOs in their territory. More information on the content of these legislative acts is available at: http://ec.europa.eu/food/plant/gmo/new/legislation/index_en.htm (http://ec.europa.eu/food/plant/gmo/new/legislation/index_en.htm). Please take also into consideration the Commission Implementing Decision (EU) 2016/321 of 3 March 2016 adjusting the geographical scope of the authorisation for cultivation of genetically modified maize (Zea mays L.) MON 810 (MON-ØØ81Ø-6) (notified under document C(2016) 1231) (Text with EEA relevance)

EN

9. Has your country integrated biosafety in national sectoral and cross-sectoral strategies, action plans, programmes, policies or legislation?

Yes

EN

10. Does your country have resources for biosafety from national budgets?

No

EN

Are these resources adequate:

11. Does your country have qualified staff to administer functions directly related to biosafety?

Yes

EN

12. If you answered Yes to question 11, how many qualified staff members are in place whose functions are directly related to biosafety?

5 to 9

EN

Is this number adequate:

No

EN

13. Please use the space below to provide further details on the implementation of Article 2 in your country:

EN

Article 5 – Pharmaceuticals

14. Does your country regulate the transboundary movement, handling or use of living modified organisms (LMOs) which are pharmaceuticals for humans?

Yes

EN

15. Please use the space below to provide further details on the implementation of Article 5 in your country:

The EU medicine legislation makes provision for placing medicinal products on the market, if the latter have received a marketing authorization, granted either by the European Commission or by a member state. As regards medicinal products containing or consisting of GMOs, the assessment for a marketing authorization must include an environmental risk assessment in line with the requirements of Directive 2001/18/EC. Regulation 1946/2003 mirrors the provisions of the Protocol as regards exports of pharmaceuticals.

EN

Article 6 – Transit and contained use

16. Does your country regulate the transit of LMOs?

Yes

EN

17. Does your country regulate the contained use of LMOs?

Yes

EN

18. Has your country taken a decision concerning the import of LMOs for contained use?

No

EN

19. Please use the space below to provide further details on the implementation of Article 6 in your country:

Regulation (EC) No 1946/2003 addresses transboundary movement of GMOs aiming to ensure coherent implementation of the provisions of the Cartagena Protocol in the EU. It establishes rules for the transit of GMOs and for the transboundary movement of GMOs intended for contained use, in line with the provisions of the Cartagena Protocol. - Contained use: Directive 2009/41/EC of the European Parliament and of the Council of 6 May 2009 on the contained use of genetically modified micro-organisms. - Transit: According to Article 13 of Regulation (EC) No 1946/2003, the exporter shall ensure notification of the transit of GMOs to Parties that have taken the decision to regulate transit of GMOs through their territory and have informed the BCH of this decision. Transit procedures through the EU (and therefore through Greece as an EU Member State) are regulated by the EU transport legislation and the Customs Code.

EN

Articles 7 to 10: Advance informed agreement (AIA) and intentional introduction of LMOs into the environment

20. Has your country established legal requirements for exporters under its jurisdiction to notify in writing the competent national authority of the Party of import prior to the intentional transboundary movement of an LMO that falls within the scope of the AIA procedure?

Yes

EN

21. Has your country established legal requirements for the accuracy of information contained in the notification provided by exporters under its jurisdiction?

No

EN

22. In the current reporting period, has your country received a notification regarding intentional transboundary movements of LMOs for intentional introduction into the environment?

No

EN

23. If you answered Yes to question 22, did the notification(s) contain complete information (at a minimum the information specified in Annex I to the Cartagena Protocol on Biosafety)?

24. If you answered Yes to question 22, has your country acknowledged receipt of the notification(s) to the notifier within ninety days of receipt?

25. If you answered Yes to question 22, has your country informed the following of its decision(s):

a. The notifier?

b. The Biosafety Clearing-House (BCH)?

26. In the current reporting period, has your country taken a decision in response to the notification(s) regarding intentional transboundary movements of LMOs for intentional introduction into the environment?

No

EN

Please specify how many

EN

27. If you answered Yes to question 26, what percentage of your country’s decisions fall into the following categories?

Were the reasons for the conditions provided?

Were the reasons for the prohibition provided?

28. If you answered Yes to question 26, how many LMOs has your country approved for import for intentional introduction into the environment?

29. If you answered under question 28 that LMOs were approved, have these LMOs actually been imported into your country?

No

EN

30. Please use the space below to provide further details on the implementation of Articles 7 to 10 in your country, including measures in case of lack of scientific certainty on potential adverse effects of LMOs for intentional introduction to the environment:

Greece is a member of the European Union and follows the established procedures. The EU applies its domestic legislative framework instead of the advanced informed agreement procedure of the Protocol. This framework is compatible with the provisions of the Protocol. The EU domestic legislative framework is built on a range of legislative measures described above. A company intending to market a GMO in the EU for intentional introduction into the environment must first obtain an authorization to this end. The authorization procedure for placing the GMO on the market involves all Member States, as authorized products are granted free movement throughout the territory of the EU. That means that Greece is not taking decision alone, but decisions are taken at the EU level. The so-called "notification" or "application" submitted by the interested company must include a full evaluation of potential risks to human and animal health and the environment. It is only after this decision is finally adopted on the basis of a prior risk assessment that the company can proceed with the marketing of the GMO in the EU. A person or a company who wishes to introduce GMOs into the environment for experimental purposes must first obtain written authorization from the competent national authority of the Member State within whose territory the experimental release is to take place. Hence, the authorization procedure is simpler than the one referred above. The authorization is given on the basis of an assessment of the risks presented by the GMO –or GMOs- for the environment and human health. No authorizations were issued by Greece during the reporting period.

EN

Article 11 – Procedure for living modified organisms intended for direct use as food or feed, or for processing (LMOs-FFP)

31. Does your country have law(s), regulation(s) or administrative measures for decision-making regarding domestic use, including placing on the market, of LMOs that may be subject to transboundary movement for direct use as food or feed, or for processing?

Yes

EN

32. Has your country established legal requirements for the accuracy of information to be provided by the applicant regarding the domestic use, including placing on the market, of LMOs that may be subject to transboundary movement for direct use as food or feed, or for processing?

Yes

EN

33. In the current reporting period, how many decisions has your country taken regarding domestic use, including placing on the market, of LMOs that may be subject to transboundary movement for direct use as food or feed, or for processing?

None

EN

34. Does your country have law(s), regulation(s) or administrative measures for decision-making regarding the import of LMOs for direct use as food or feed, or for processing?

Yes

EN

35. In the current reporting period, how many decisions has your country taken regarding the import of LMOs for direct use as food or feed, or for processing?

None

EN

36. Please use the space below to provide further details on the implementation of Article 11 in your country, including measures in case of lack of scientific certainty on potential adverse effects of LMOs that may be subject to transboundary movement for direct use as food or feed, or for processing:

The EU has developed a comprehensive legal framework on GMOs, which also addresses the import of LMOs intended for direct use for food, feed or processing. The EU has declared, with reference to Article 14.4 of the Cartagena Protocol, that it relies on its existing legislative framework for intentional movements of GMOs within the EU and for imports of GMOs into the EU. For instance, Regulation (EU) 2017/625 of the European Parliament and of the Council of 15 March 2017 deals with official controls and other official activities performed to ensure the application of food and feed law, rules on animal health and welfare, plant health and plant protection products. With regard to the decisions taken for placing on the market of LMOs-FFP, it has to be noted that those decisions are taken for the whole European territory and not by the MS individually, so with that consideration, Greece has not taken any decision individually.

EN

Article 12 – Review of decisions

37. Has your country established a mechanism for the review and change of a decision regarding an intentional transboundary movement of LMOs?

No

EN

38. In the current reporting period, has your country reviewed and/or changed a decision regarding an intentional transboundary movement of an LMO?

No

EN

39. If you answered Yes to question 38, how many decisions were reviewed and/or changed?

40. If you answered Yes to question 38, were any of the reviews triggered by a request from the Party of export or the notifier?

41. If you answered Yes to question 40, did your country provide a response within ninety days setting out the reasons for the decision?

42. If you answered Yes to question 38, were any of the reviews initiated by your country as the Party of import?

43. If you answered Yes to question 42, did your country, within thirty days, set out the reasons for the decision and inform:

a. The notifier?

b. The BCH?

44. Please use the space below to provide further details on the implementation of Article 12 in your country:

EN

Article 13 – Simplified procedure

45. Has your country established a mechanism for the application of the simplified procedure regarding an intentional transboundary movement of LMOs?

No

EN

46. In the current reporting period, has your country applied the simplified procedure?

No

EN

47. If you answered Yes to question 46, for how many LMOs has your country applied the simplified procedure?

48. If you answered Yes to question 46, has your country informed the Parties through the BCH of the cases where the simplified procedure was applied?

49. Please use the space below to provide further details on the implementation of Article 13 in your country:

EN

Article 14 – Bilateral, regional and multilateral agreements and arrangements

50. How many bilateral, regional or multilateral agreements or arrangements relevant to biosafety has your country established with other Parties/non-Parties?

None

EN

51. If you answered under question 50 that agreements or arrangements were established, please provide a brief description of their scope and objective:

EN

52. Please use the space below to provide further details on the implementation of Article 14 in your country:

EN

Articles 15 & 16 – Risk assessment and risk management

53. Does the domestic regulatory framework of your country require risk assessments of LMOs to be conducted?

Yes

EN

To which LMOs does this requirement apply (select all that apply):

For imports of LMOs for intentional introduction into the environment
For imports of LMOs intended for direct use as food or feed, or for processing
For decisions regarding domestic use, including placing on the market, of LMOs that may be subject to transboundary movements for direct use as food or feed, or for processing
For imports of LMOs for contained use
Other (“Determination of measures and conditions for the deliberate release of genetically modified organisms into the environment, in compliance with the provisions of Directive 2001/18/EC ‘on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC’ of 12 March 2001 of the European Communities,” as well as the amendments to the aforementioned decision, and more specifically Joint Ministerial Decisions (JMDs) No. 2775/128098/2017 (Government Gazette B’ 4287) and No. 1371/99270 (Government Gazette B’ 1865).)

54. Has your country established a mechanism to conduct risk assessments prior to taking decisions regarding LMOs?

Yes

EN

Conducting risk assessment or risk management

55. In the current reporting period, has your country conducted any kind of risk assessment of LMOs, including for contained use, field trials, commercial purposes, direct use as food, feed, or for processing?

No

EN

56. If you answered Yes to question 55, how many risk assessments were conducted?

57. If you answered Yes to question 55, please indicate the scope of the risk assessments (select all that apply):

58. If you answered Yes to question 55, were risk assessments conducted for all decisions taken on LMOs for intentional introduction into the environment or on domestic use of LMOs that may be subject to transboundary movement for direct use as food or feed, or for processing?

59. If you answered Yes to question 55, have you considered:

a. other available scientific evidence, as referred to in Article 15 of the Protocol?

b. relevant traditional knowledge of indigenous peoples and local communities?

60. If you answered Yes or In some cases to question 59(b), was this information considered in a scientifically sound manner?

61. Has your country established appropriate mechanisms, measures and strategies to regulate and manage risks identified in the risk assessment of LMOs?

Yes

EN

62. Has your country taken appropriate measures to prevent unintentional transboundary movements of LMOs including such measures as requiring a risk assessment to be carried out prior to the first release of a LMO? ¹

Yes

EN

63. Has your country taken measures to ensure that any LMO, whether imported or locally developed, undergoes an appropriate period of observation that is commensurate with its life-cycle or generation time before it is put to its intended use?

Yes

EN

64. Has your country established a mechanism for monitoring potential effects of LMOs released into the environment?

Yes

EN

65. Does your country have measures to identify LMOs or specific traits that may have adverse effects on the conservation and sustainable use of biological diversity?

Yes

EN

66. Has your country had access to or used any resource materials, including guidance documents, for the purpose of conducting risk assessment or risk management, or for evaluating risk assessment reports submitted by notifiers?

a. Risk assessment:

Yes

EN

b. Risk management:

Yes

EN

67. If you answered Yes to question 66(a) or (b), is your country using the “Guidance on Risk Assessment of LMOs” (developed by the Online Forum and the AHTEG on Risk Assessment and Risk Management) ² for conducting risk assessment or risk management, or for evaluating risk assessment reports submitted by notifiers?

No

EN

68. Does your country have specific needs for further guidance on specific topics of risk assessment of LMOs?

No

EN

Capacity-building in risk assessment or risk management

69. Does your country have the capacity to detect, identify, assess the risk of and/or monitor LMOs or specific traits that may have adverse effects on the conservation and sustainable use of biological diversity, taking into account risks to human health?

a. Detect:

Yes

EN

b. Identify:

Yes

EN

c. Assess the risk:

Yes

EN

d. Monitor:

Yes

EN

70. In the current reporting period, how many people in your country have been trained in risk assessment, risk management and monitoring of LMOs?

a. Risk assessment:

1 to 9

EN

Is this number adequate:

No

EN

b. Risk management:

1 to 9

EN

Is this number adequate:

No

EN

c. Monitoring:

1 to 9

EN

Is this number adequate:

No

EN

71. Is your country using training material and/or technical guidance for training in risk assessment and risk management of LMOs?

Yes

EN

Which materials/guidance are being used

Other materials/guidance: ("Better Training for Safer Food" of the EU)

72. Please use the space below to provide further details on the implementation of Articles 15 and 16 in your country:

Greece, as a Member State of the EU, abides by the EU legislation. The risk assessment is carried out at EU level with active involvement of all Member States.

EN

Article 17 – Unintentional transboundary movements⁵ and emergency measures

⁵ In accordance with the operational definition adopted in decision CP-VIII/16, “‘Unintentional transboundary movement’ is a transboundary movement of a living modified organism that has inadvertently crossed the national borders of a Party where the living modified organism was released, and the requirements of Article 17 of the Protocol apply to such transboundary movements only if the living modified organism involved is likely to have significant adverse effects on the conservation and sustainable use of biological diversity, taking also into account risks to human health, in the affected or potentially affected States.”

73. Has your country established measures to notify affected or potentially affected States, the Biosafety Clearing-House and, where appropriate, relevant international organizations in case of a release under its jurisdiction that leads, or may lead, to an unintentional transboundary movement?

Yes

EN

74. In the current reporting period, how many releases of LMOs occurred under your country’s jurisdiction that led, or may have led, to an unintentional transboundary movement?

None

EN

75. If you answered under question 74 that a release occurred, has your country notified affected or potentially affected States, the Biosafety Clearing-House and, where appropriate, relevant international organizations?

76. In the current reporting period, how many times has your country become aware of an unintentional transboundary movement into its territory?

None

EN

77. Does your country have the capacity to take appropriate measures in response to unintentional transboundary movements?

Yes

EN

78. Please use the space below to provide further details on the implementation of Article 17 in your country:

Article 14 of Regulation 1946/2003 provides Member States with measures to prevent unintentional transboundary movement of GMOs and appropriate responses, including emergency measures.

EN

Article 18 – Handling, transport, packaging and identification

79. Has your country taken measures to require that LMOs that are subject to transboundary movement are handled, packaged and transported under conditions of safety, taking into account relevant international rules and standards?

Yes

EN

80. Has your country taken measures to require that documentation accompanying LMOs-FFP, in cases where the identity of the LMOs is not known, clearly identifies that they may contain LMOs and are not intended for intentional introduction into the environment, as well as a contact point for further information?

Yes

EN

81. Has your country taken measures to require that documentation accompanying LMOs-FFP, in cases where the identity of the LMOs is known, clearly identifies that they contain LMOs and are not intended for intentional introduction into the environment, as well as a contact point for further information?

Yes

EN

82. If you answered Yes or Yes, to some extent to question(s) 79, 80 and/or 81, what type of documentation accompanying LMOs does your country require?

Other

EN

Additional Information

Documentation specific to the genetic modification (e.g., GMOs identification, laboratory analysis, etc.)

EN

83. Has your country taken measures to require that documentation accompanying LMOs that are destined for contained use clearly identifies them as LMOs, and specifies any requirements for the safe handling, storage, transport and use, as well as the contact point for further information, including the name and address of the individual and institution to whom the LMO are consigned?

Yes

EN

84. If you answered Yes or Yes, to some extent to question 83, what type of documentation does your country require for the identification of LMOs that are destined for contained use?

Documentation specific to LMOs

EN

85. Has your country taken measures to require that documentation accompanying LMOs that are intended for intentional introduction into the environment of the Party of import clearly identifies them as living modified organisms; specifies the identity and relevant traits and/or characteristics, any requirements for the safe handling, storage, transport and use, the contact point for further information and, as appropriate, the name and address of the importer and exporter; and contains a declaration that the movement is in conformity with the requirements of the Cartagena Protocol applicable to the exporter?

Yes

EN

86. If you answered Yes or Yes, to some extent to question 85, what type of documentation does your country require for the identification of LMOs that are intended for intentional introduction into the environment?

Documentation specific to LMOs

EN

87. Does your country have the capacity to enforce the requirements of identification and documentation of LMOs?

Yes

EN

88. In the current reporting period, how many customs officers in your country have received training in the identification of LMOs?

None

EN

Is this number adequate:

89. Has your country established procedures for the sampling and detection of LMOs?

Yes

EN

90. Does your country have access to and use resource materials and detection methods to detect and identify LMOs?

a. access to resource materials and detection methods to detect and identify LMOs?

Yes

EN

b. use of resource materials and detection methods to detect and identify LMOs?

Yes

EN

91. Does your country have access to and use tools to detect and identify LMOs?

a. access to tools?

Yes

EN

b. use of tools?

Yes

EN

92. Does your country have access to and use certified reference materials necessary to detect and identify LMOs?

a. access to certified reference materials?

Yes

EN

b. use of certified reference materials?

Yes

EN

93. How many laboratory personnel in your country have received training in detection of LMOs?

10 to 49

EN

Is this number adequate:

Yes

EN

94. Does your country have reliable access to technical infrastructures, such as laboratories for the detection and identification of LMOs?

a. technical infrastructure for detection of LMOs?

Yes

EN

b. technical infrastructure for identification of LMOs

Yes

EN

95. How many laboratories in your country are certified for LMO detection?

5 to 9

EN

96. If you answered under question 95 that certified laboratories exist in your country, how many of them are currently operating in the field of the detection of LMOs?

5 to 9

EN

97. Please use the space below to provide further details on the implementation of Article 18 in your country:

Directive 2001/18/EC of the European Parliament and of the Council of 12 March 2001 on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC - Commission Declaration, Regulation (EC) No 1829/2003, Commission Implementing Regulation (EU) No 503/2013 of 3 April 2013 on applications for authorisation of genetically modified food and feed in accordance with Regulation (EC) No 1829/2003 of the European Parliament and of the Council and amending Commission Regulations (EC) No 641/2004 and (EC) No 1981/2006 Text with EEA relevance

EN

Article 19 – Competent national authorities and national focal points

98. In case your country has designated more than one competent national authority, has your country established a mechanism for the coordination of their actions prior to taking decisions regarding LMOs?

Yes

EN

99. Has your country established adequate institutional capacity to enable the competent national authority(ies) to perform the administrative functions required by the Cartagena Protocol on Biosafety?

Yes

EN

100. Has your country undertaken initiatives to strengthen collaboration among national focal points, competent national authority(ies) and other institutions on biosafety-related matters?

No

EN

101. Please use the space below to provide further details on the implementation of Article 19 in your country:

EN

Article 20 – Information-sharing and the Biosafety Clearing-House (BCH):

102. Please provide an overview of the status of the mandatory information provided by your country to the BCH by specifying for each category of information whether it is available ⁶ and whether it has been submitted to the BCH:

a. Existing legislation, regulations and guidelines for implementing the Protocol, as well as information required by Parties for the advance informed agreement procedure (Article 20, paragraph 3(a))

Information available and in the BCH

EN

b. Legislation, regulations and guidelines applicable to the import of LMOs intended for direct use as food or feed, or for processing (Article 11, paragraph 5)

Information available and in the BCH

EN

c. Bilateral, multilateral and regional agreements and arrangements (Article 14, paragraph 2, and Article 20, paragraph 3 (b))

Information available and in the BCH

EN

d. Contact details for competent national authorities (Article 19, paragraphs 2 and 3), national focal points (Article 19, paragraphs 1 and 3), and emergency contacts (Article 17, paragraph 3(e))

Information available and in the BCH

EN

e. Decisions regarding transit of LMOs (Article 6, paragraph 1)

Information not available

EN

f. Decisions regarding import of LMOs for contained use (Article 6, paragraph 2)

Information not available

EN

g. Notifications regarding the release under your country’s jurisdiction that leads, or may lead, to an unintentional transboundary movement of a LMO that is likely to have significant adverse effects on biological diversity (Article 17, paragraph 1)

Information not available

EN

h. Information concerning cases of illegal transboundary movements of LMOs (Article 25, paragraph 3)

Information not available

EN

i. Decisions regarding the importation of LMOs for intentional introduction into the environment (Article 10, paragraph 3)

Information not available

EN

j. Information on the application of domestic regulations to specific imports of LMOs (Article 14, paragraph 4)

Information not available

EN

k. Decisions regarding the domestic use of LMOs that may be subject to transboundary movement for direct use as food or feed, or for processing (Article 11, paragraph 1)

Information not available

EN

l. Decisions regarding the import of LMOs intended for direct use as food or feed, or for processing that are taken under domestic regulatory frameworks (Article 11, paragraph 4) or in accordance with Annex III to the Protocol (Article 11, paragraph 6)

Information not available

EN

m. Declarations regarding the framework to be used for LMOs intended for direct use as food or feed, or for processing (Article 11, paragraph 6)

Information not available

EN

n. Review and change of decisions regarding intentional transboundary movements of LMOs (Article 12, paragraph 1)

Information not available

EN

o. Cases where intentional transboundary movement may take place at the same time as the movement is notified to your country (Article 13, paragraph 1(a))

Information not available

EN

p. LMOs exempted from the advance informed agreement procedure (Article 13, paragraph 1(b))

Information not available

EN

q. Summaries of risk assessments or environmental reviews of LMOs generated by regulatory processes and relevant information regarding products thereof (Article 20, paragraph 3(c))

Information not available

EN

103. Please provide a brief explanation if you answered that the information is available but not in the BCH or only partially available in the BCH to any item under question 102:

EN

104. Has your country established a mechanism for the coordination among the BCH national focal point, the Cartagena Protocol national focal point, and the competent national authority(ies) for making information available to the BCH?

Yes, to some extent:

EN

Additional Information

Greece has appointed the same person as NFP for both the Cartagena Protocol and the BCH. This person has regular contants with other national competent authorities

EN

105. In the current reporting period, has your country used the information available in the BCH in its decision-making processes on LMOs?

Yes, always

EN

106. In the current reporting period, has your country experienced difficulties accessing or using the BCH?

No

EN

107. Does your country have a national biosafety clearing-house?

No

EN

108. Please use the space below to provide further details on the implementation of Article 20 in your country:

Greece has appointed the same person as NFP for both the Cartagena Protocol and the BCH

EN

Article 21 – Confidential information

109. Has your country established procedures to protect confidential information received under the Protocol?

Yes

EN

110. Does your country allow the notifier to identify information that is to be treated as confidential?

Yes, always

EN

111. Please use the space below to provide further details on the implementation of Article 21 in your country:

EN

Article 22 – Capacity-building

112. Does your country have predictable and reliable funding for its capacity-building needs for the effective implementation of the Protocol?

No

EN

113. Has your country received external support for the development and/or strengthening of human resources and institutional capacities in biosafety?

No

EN

114. If you answered Yes or Yes, to some extent to question 113, how was this support made available?

115. Has your country provided support to other Parties in the development and/or strengthening of human resources and institutional capacities in biosafety?

No

EN

116. If you answered Yes to question 115, how was this support made available?

117. In the current reporting period, has your country used its GEF STAR allocation for biosafety activities?

No

EN

118. In the current reporting period, has your country undertaken activities for the development and/or strengthening of human resources and institutional capacities in biosafety?

No

EN

119. If you answered Yes or Yes, to some extent to question 118, in which of the following areas were these activities undertaken (select all that apply)?

120. If you answered Yes or Yes, to some extent to question 118, did your country use capacity-building materials, including online resources, for the development and/or strengthening of capacity-building?

121. In the current reporting period, has your country carried out a capacity-building needs assessment?

No

EN

122. Does your country still have capacity-building needs?

Yes

EN

123. If you answered Yes to question 122, which of the following areas still need capacity-building (select all that apply)?

Institutional capacity and human resources
Integration of biosafety in cross-sectoral and sectoral legislation, policies and institutions (mainstreaming biosafety)
Risk assessment and other scientific and technical expertise
Risk management
Public awareness, participation and education in biosafety
Information exchange and data management, including participation in the Biosafety Clearing-House
Scientific, technical and institutional collaboration at subregional, regional and international levels
Technology transfer
Sampling, detection and identification of LMOs
Socioeconomic considerations
Implementation of the documentation requirements for handling, transport, packaging and identification
Handling of confidential information
Measures to address unintentional and/or illegal transboundary movements of LMOs
Scientific biosafety research relating to LMOs
Taking into account risks to human health
Liability and redress

124. If you answered Yes to question 122, has your country prioritized its capacity-building needs?

No

EN

125. Does your country have in place a functional national mechanism for coordinating biosafety capacity-building initiatives?

No

EN

126. Please use the space below to provide further details on the implementation of Article 22 in your country, including further details about your experience in accessing GEF funds:

EN

Article 23 – Public awareness and participation

127. Is biosafety public awareness, education and/or participation addressed in legislation or policy in your country?

Yes, to some extent:

EN

Additional Information

Mainly through the public education system

EN

128. Has your country established a mechanism to ensure public access to information on LMOs?

No

EN

129. Has your country established a mechanism to facilitate and promote public participation, including consultation, in the decision-making process regarding LMOs?

No

EN

130. Has your country informed the public about existing modalities for public participation in the decision-making process regarding LMOs?

No

EN

131. In the current reporting period, how many times has your country consulted the public in the decision-making process regarding LMOs?

None (decisions taken without consultation)

EN

132. In the current reporting period, has your country made the results of decisions regarding LMOs available to the public?

No

EN

133. Has your country informed the public about the means to access the Biosafety Clearing-House?

No

EN

134. Has biosafety been addressed or integrated in educational and training programmes in your country?

Yes

EN

135. Does your country have in place a national communication strategy on biosafety?

No

EN

136. Does your country have any awareness and outreach programmes on biosafety?

No

EN

137. Does your country currently have a national biosafety website?

No

EN

138. In the current reporting period, has your country accessed resource materials for facilitating and promoting public awareness, education and participation in biosafety?

No

EN

139. Please use the space below to provide further details on the implementation of Article 23 in your country:

EN

Article 24 – Non-Parties

140. Has your country entered into any bilateral, regional, or multilateral agreement(s) with non-Parties regarding transboundary movements of LMOs?

No

EN

141. In the current reporting period, has your country imported LMOs from a non-Party?

No

EN

142. In the current reporting period, has your country exported LMOs to a non-Party?

No

EN

143. If you answered Yes to question 141 and/or 142, were the transboundary movements of LMOs consistent with the objective of the Cartagena Protocol on Biosafety?

144. Please use the space below to provide further details on the implementation of Article 24 in your country:

EN

Article 25 – Illegal transboundary movements ⁷

⁷ In accordance with the operational definition adopted in decision CP-VIII/16, “‘Illegal transboundary movement’ is a transboundary movement of living modified organisms carried out in contravention of the domestic measures to implement the Protocol that have been adopted by the Party concerned”

145. Has your country adopted domestic measures aimed at preventing and/or penalizing transboundary movements of LMOs carried out in contravention of its domestic measures to implement the Cartagena Protocol?

Yes

EN

146. In the current reporting period, how many cases of illegal transboundary movements of LMOs has your country become aware of?

None

EN

147. If you indicated under question 146 that your country became aware of cases of illegal transboundary movements, has the origin of the LMO(s) been established?

148. Please use the space below to provide further details on the implementation of Article 25 in your country:

EN

Article 26 – Socio-economic considerations

149. Does your country have any specific approaches or requirements that facilitate how socioeconomic considerations should be taken into account in LMO decision-making?

Yes

EN

150. Has your country used resource materials for taking socioeconomic considerations into account?

No

EN

151. In the current reporting period, have socioeconomic considerations arising from the impact of LMOs been taken into account in decision-making?

Not applicable (no decisions were taken)

EN

152. Please use the space below to provide further details on the implementation of Article 26 in your country:

EN

Article 28 – Financial mechanism and resources

153. In the current reporting period, how much funding (in the equivalent of US dollars) has your country mobilized to support implementation of the Cartagena Protocol beyond the regular national budgetary allocation?

None

EN

Article 33 – Monitoring and reporting

Article 33 requires Parties to monitor the implementation of its obligations under the Cartagena Protocol and to report to the Conference of the Parties serving as the meeting of the Parties to the Cartagena Protocol on measures taken to implement the Protocol.

154. Does your country have in place a system to monitor and enforce the implementation of the Cartagena Protocol?

Yes

EN

Cooperation

Goal B.4 of the Implementation Plan for the Cartagena Protocol addresses cooperation and coordination on biosafety issues at the national, regional and international levels. Questions related to this goal are presented below, including questions related to cooperation under different provisions of the Protocol.

155. In the current period, has your country cooperated with other Parties in:

a. exchange of scientific, technical and institutional knowledge;

No

EN

b. identifying LMOs or specific traits that may have adverse effects on the conservation and sustainable use of biological diversity? (Article 16(5)).

No

EN

c. research and information exchange on any socioeconomics impacts of LMOs? (Article 26(2))

No

EN

Does this include research and information exchange on socioeconomic impacts of LMOs on indigenous peoples and local communities?

d. public awareness, education and participation? (Article 23(1)(a))

No

EN

e. strengthening capacities for the implementation of the Protocol?

No

EN

156. In the current reporting period, has your country engaged in bilateral, regional or multilateral activities for the implementation of the Protocol?

No

EN

157. Does your country have mechanisms in place for involving indigenous peoples and local communities and relevant stakeholders from different sectors in the implementation of the Protocol?

a. mechanisms for involving indigenous peoples and local communities

No

EN

b. mechanisms for involving relevant stakeholders from different sectors

No

EN

158. Please use the space below to provide further details on biosafety cooperation in your country:

EN

Nagoya – Kuala Lumpur Supplementary Protocol on Liability and Redress

Parties to the Cartagena Protocol that are not yet Party to the Supplementary Protocol are also invited to respond to the questions below

159. Is your country a Party to the Nagoya – Kuala Lumpur Supplementary Protocol on Liability and Redress?

No

EN

Is there any national process in place towards becoming a Party to the Supplementary Protocol?

No

EN

160. Has your country introduced the necessary measures for the implementation of the Supplementary Protocol?

No measures have yet been taken

EN

161. Which instruments are in place for the implementation of the Supplementary Protocol (select all that apply)?

No instruments are in place

Please provide further information on the instruments in place:

EN

162. Does your country have administrative or legal instruments that require response measures to be taken:

a. In case of damage resulting from LMOs?

Yes

EN

b. In case there is sufficient likelihood that damage will result if response measures are not taken?

Yes

EN

163. If you answered Yes to question 162a, do these instruments impose requirements on an operator (select all that apply)?

Yes, the operator must inform the competent authority of the damage

164. If you answered Yes to question 162a, do these instruments require the operator to take response measures to avoid damage?

Yes

EN

165. If you answered Yes to question 162a or 162b, do these instruments provide for a definition of “operator”?

Yes

EN

166. If you answered Yes to question 165, which of the following could be an ‘operator’ (select all that apply)?

Permit holder
Person who placed the LMO on the market
Developer
Producer
Notifier
Exporter
Importer
Carrier
Supplier

167. Has a competent authority been identified for carrying out the functions set out in the Supplementary Protocol?

No

EN

168. If you answered Yes to question 167, what measures may the competent authority take (select all that apply)?

169. Does your country have measures in place to provide for financial security for damage resulting from LMOs?

No

EN

170. If you answered Yes to question 169, what type of financial security measures are in place (select all that apply)?

171. Does your country have rules and procedures on civil liability that address damage resulting from LMOs, or has such damage been recognized in court rulings (select all that apply)?

No

172. Have there been any occurrences of damage resulting from LMOs in your country?

No

EN

173. If you answered Yes to question 172, have response measures been taken?

174. Please use the space below to provide further details on any activities undertaken in your country towards the implementation of the Nagoya – Kuala Lumpur Supplementary Protocol on Liability and Redress:

EN

Other information

175. Please use this field to provide any other information on issues related to national implementation of the Cartagena Protocol and the Supplementary Protocol, including any obstacles or impediments encountered:

EN

Comments on reporting format

176. Please use this field to provide any information on difficulties that you have encountered in filling in this report, and suggestions for its improvement:

EN

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