Cyprus | BCH-NR3-CY-109475 | Third National Report on the Implementation of the Cartagena Protocol on Biosafety | Biosafety Clearing-House

Loading...
Third National Report on the Implementation of the Cartagena Protocol on Biosafety (NR3)
  |  
BCH-NR3-CY-109475-1   |   PDF   |   Print   |  
last updated: 01 Dec 2015
General Information


Department of Agriculture (MARDE), Agricultural Research Institute (MARDE), State General Laboratory (Ministry of Health), Medical & Public Health Services (MoH), Pharmaceutical Services (MoH), Department of Labor Inspection (Ministry of Labor & Social Insurance)
EN

01 Oct 2011
30 Sep 2015
Party to the Cartagena Protocol on Biosafety
Yes
EN
Article 2 – General provisions
A domestic regulatory framework is fully in place
EN
2003
EN
  • One or more national biosafety laws
  • One or more national biosafety regulations
  • One or more sets of biosafety guidelines
  • Other laws, regulations or guidelines that indirectly apply to biosafety
No
EN
Yes
EN
Less than 5
EN
Partially
EN
Cyprus as a member of the EU adopts the EU legislation on genetically modified organisms (GMOs). The main legal instruments of the EU include the following directives and regulations on which Cyprus bases its national legal framework:<br />Directive 2009/41/EC on the contained use of genetically modified microorganisms<br />Directive 2001/18/EC 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.<br />Regulation (EC) No 1946/2003 on transboundary movements of genetically modified organisms.<br />Regulation (EC) No 1829/2003 on genetically modified food and feed.<br />Regulation (EC) No 1830/2003 concerning the traceability and labelling of genetically modified organisms and the traceability of food and feed products produced from genetically modified organisms.<br />Regulation (EC) No 641/2004 on detailed rules for the implementation of Regulation (EC) No 1829/2003 as regards the application for the authorisation 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.
EN
Article 5 - Pharmaceuticals
Yes
EN
No
EN
EU pharmaceutical legislation provides that a medicinal product may only be placed on the market in the EU if it has received a marketing authorisation, granted either by the Commission or by a member state. As regards to medicinal products containing or consisting of GMOs, the assessment for a marketing authorisation must include an environmental risk assessment in line with the requirements of Directive 2001/18/EC.<br />Regulation 1946/2003 mirrors the provisions of the Protocol as regards exports of pharmaceuticals. Cyprus has not had a case of transboundary movement of LMO pharmaceuticals and has not granted a marketing authorisation.
EN
Article 6 – Transit and Contained use
Yes
EN
Yes
EN
No
EN
Cyprus as a member of the EU, adopts the EU legislation into national laws and regulations. However, Cyprus has not had any cases of contained use of LMOs.<br />Contained use:<br />Directive 2009/41/EC on the contained use of genetically modified microorganisms<br />Placing on the EU market:<br />Directive 2001/18/EC <br />Regulation (EC) No 1829/2003<br />Regulation (EC) No 1830/2003<br />Regulation (EC) No 641/2004 on detailed rules for the implementation of Regulation (EC) No 1829/2003.<br />Exports third countries. No exports from Cyprus to third countries or vice versa.<br />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.
EN
Articles 7 to 10 – Advance Informed Agreement (AIA) and intentional introduction of LMOs into the environment
Yes
EN
Yes
EN
Yes
EN
Yes
EN
Yes
EN
No
EN
No
EN
None
EN
None
EN
The EU applies its domestic legislative framework instead of the Protocol's advanced informed agreement procedure. This framework is compatible with the provisions of the Protocol. Cyprus follows the procedures set by the EU.
EN
Article 11 – Procedure for living modified organisms intended for direct use as food or feed, or for processing (LMOs-FFP)
Yes
EN
Yes
EN
No
EN
No
EN
No
EN
No
EN
The EU has developed a comprehensive legal framework on GMOs, which also addresses the import of GMOs intended for direct use for food or feed, or for 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. With regard to the decisions taken for placing on the market of LMOsFFP, it has to be noted that those decisions are taken for the whole European<br />territory and not by the MS individually.
EN
Article 12 – Review of decision
No
EN
No
EN
No
EN
None
EN
No further comments
EN
Article 13 – Simplified procedure
No
EN
No
EN
None
EN
Cyprus has not made use of the simplified procedure for imports of LMOs as specified in Article 13.
EN
Article 14 – Bilateral, regional and multilateral agreements and arrangements
No
EN
Cyprus has not entered into any bilateral, regional or multilateral agreements or arrangements as per Article 14(1).
EN
Articles 15 & 16 – Risk Assessment and Risk Management
No
EN
One or more
EN
One or more
EN
One or more
EN
No
EN
No
EN
No
EN
n/a
EN
Yes
EN
Yes
EN
Yes
EN
Yes
EN
Yes
EN
Yes
EN
Yes
EN
Yes
EN
Yes
EN
No
EN
Yes
EN
Yes
EN
Yes
EN
Art.15- Cyprus as a Member State of the EU follows the legal framework of the EU. The risk assessment is done at EU level, with an active involvement of all Member States, including Cyprus.<br /><br />Art.16- The legislative framework of the EU, provides that the environmental risk assessment should be conducted with a view to identifying if there is a need for risk management and if so, the most appropriate methods to be used as well as a risk management strategy to be defined. In cases of limited data availability particular appropriate risk management has to be considered to prevent adverse effects on human health and the environment.
EN
Article 17 – Unintentional transboundary movements and emergency measures
Yes
EN
Yes
EN
Yes
EN
Never
EN
Article 14 of Regulation 1946/2003 provides for measures to prevent unintentional transboundary movement of GMOs and appropriate responses, including emergency measures.
EN
Article 18 – Handling, transport, packaging and identification
Yes
EN
Yes
EN
Yes
EN
Existing types of documentation
EN
Yes
EN
Existing types of documentation
EN
Yes
EN
Existing types of documentation
EN
Yes
EN
Yes
EN
One or more
EN
Yes
EN
One or more
EN
Yes
EN
One or more
EN
One or more
EN
The EU has developed a comprehensive legal framework on GMOs, which also addresses the issues of handling, transport, packaging and identification requirement covered by Article 18. Cyprus abides by this framework.
EN
Article 19 – Competent National Authorities and National Focal Points
Yes
EN
Yes, to some extent
EN
Human resource is limited
EN
No further details
EN
Article 20 – Information Sharing and the Biosafety Clearing-House (BCH)
Information available but only partially available in the BCH
EN
Information available but only partially available in the BCH
EN
Information not available
EN
Information available but only partially available in the BCH
EN
Information not available
EN
Information available but not in the BCH
EN
Information not available
EN
Information not available
EN
Information available but not in the BCH
EN
Information available but not in the BCH
EN
Information available but not in the BCH
EN
Information available but not in the BCH
EN
Information available but not in the BCH
EN
Information not available
EN
Information not available
EN
Information not available
EN
Information not available
EN
No
EN
No
EN
Yes, in some cases
EN
No
EN
No
EN
None
EN
None
EN
Cyprus is not yet actively participating in the BCH, mainly due to limited human resources.
EN
Article 21 – Confidential information
Yes
EN
Yes, always
EN
No further comments
EN
Article 22 – Capacity-building
No
EN
No
EN
No
EN
No
EN
No
EN
No
EN
Yes, a few
EN
  • Human resources capacity development and training
  • Risk assessment and other scientific and technical expertise
  • Risk management
  • Information exchange and data management including participation in the Biosafety Clearing-House
  • Scientific, technical and institutional collaboration at subregional, regional and international levels
  • Scientific biosafety research relating to LMOs
No
EN
No
EN
None
EN
No
EN
No further comments
EN
Article 23 – Public awareness and participation
Yes, to some extent
EN
No
EN
No
EN
No
EN
None
EN
Yes, to some extent
EN
Yes
EN
Yes
EN
Yes, to some extent
EN
  • Mailing lists
  • 5B6177DD-5E5E-434E-8CB7-D63D67D5EBED (Case-by-case)
Mailing lists
EN
No
EN
None
EN
None
EN
No
EN
Never
EN
EU legislation on GMOs promotes public awareness and participation as an integral part of its regulatory framework.
EN
Article 24 – Non-Parties
No
EN
No
EN
No
EN
No further comments.
EN
Article 25 – Illegal transboundary movements
Yes
EN
Yes
EN
Never
EN
No further comments.
EN
Article 26 – Socio-economic considerations
No
EN
Not applicable
EN
None
EN
Yes, to some extent
EN
Article 27 – Liability and Redress
Yes
EN
No
EN
No
EN
The Supplementary Protocol has not yet been turned into national law.
EN
Article 28 – Financial Mechanism and Resources
Less than 5,000 USD
EN
Article 33 – Monitoring and reporting
Yes
EN
Yes
EN
Yes
EN
Other information
Comments on reporting format