Cartagena Protocol definition

Cartagena Protocol means the Cartagena Protocol on Biodiversity to the Convention adopted at Montreal in January 2000 and any subsequent amendments thereto;
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Cartagena Protocol means the Cartagena Protocol on Biosafety to the Convention on Biological Diversity adopted at Montreal in January 2000;
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Cartagena Protocol means the Cartagena Protocol on Biosafety to the Convention on Biological Diversity, adopted in Montreal, Canada, by the Conference of the Parties to the Convention on January 29, 2000.
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Examples of Cartagena Protocol in a sentence

  • Work Plan of the Intergovernmental Committee for the Cartagena Protocol on Biosafety272.

  • With respect to paragraph 2 of article 6 bis, how the requirements made in accordance with the provisions of annex I bis are complementary to and mutually supportive of the Party’s national biosafety framework and consistent with the objectives of the Cartagena Protocol on Biosafety to the Convention on Biodiversity.

  • Korea ratified the Cartagena Protocol on Biosafety (CPB) on October 2, 2007.

  • Cartagena Protocol on Biosafety to the Convention on Biological Diversity.

  • See the Convention on Biological Diversity and its Cartagena Protocol on Biosafety.

  • The GEF will support thematic projects addressing some of the specific provisions of the Cartagena Protocol.

  • The Cartagena Protocol on Biosafety (CPB) seeks to ensure an adequate level of protection in the field of the safe transfer, handling, and use of living modified organisms resulting from modern biotechnology that may have adverse effects on biological diversity.

  • This proposal shall, in particular, include appropriate measures to implement the procedures laid down in the Cartagena Protocol and, in accordance with the Protocol, require Community exporters to ensure that all requirements of the Advance Informed Agreement Procedure, as set out in Articles 7 to 10, 12 and 14 of the Cartagena Protocol, are fulfilled.

  • The Recipient shall carry out Parts 1.1, 1.3, 1.4, 2, 3.1(b), 3.2, 3.3 and 4(ii) of the Project pursuant to its obligations under, and in accordance with environmental safeguards and international good practice and standards consistent with those of, the Cartagena Protocol on Biosafety.

  • Production of, or trade in, living genetically modified organisms can only take place if permission has been obtained from the importing country and all requirements of the Cartagena Protocol have been met.


More Definitions of Cartagena Protocol

Cartagena Protocol means the Protocol on Biosafety under the Convention on Biological Diversity;
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Cartagena Protocol means the Cartagena Protocol on Biosafety to the Convention on Biodiversity that entered into force on September 11, 2003.
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Cartagena Protocol means the Cartagena Protocol on Biosafety and set out as the First Schedule;
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Cartagena Protocol means Cartagena Protocol on Biosafety to the Biodiversity Convention, done at Montreal on 29 January 2000 and ratified by the Parliament of Georgia under its Resolution “On the Accession of Georgia to the Cartagena Protocol to the Convention of Biological Diversity” of 26 September 2008;
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Cartagena Protocol means the Cartagena Protocol on Biosafety of the United
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Cartagena Protocol means the Cartagena Protocol on Biosafety to the Convention on Biological Diversity;
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Related to Cartagena Protocol

  • Kyoto Protocol means the protocol to the UNFCCC adopted at the Third Conference of the Parties to the UNFCCC in Kyoto, Japan on 11 December 1997 as may be amended;

  • Protocol means, in respect of any category of object and associated rights to which this Convention applies, the Protocol in respect of that category of object and associated rights;

  • Step therapy protocol means a protocol or program that establishes the specific

  • MFDA means the Mutual Fund Dealers Association of Canada;

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.

  • Protocols means written directions and orders, consistent with the department’s standard of care, that are to be followed by an emergency medical care provider in emergency and nonemergency situations. Protocols must be approved by the service program’s medical director and address the care of both adult and pediatric patients.

  • Collaborative pharmacy practice agreement means a written and signed

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Manufacturing Process means any process for—

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

  • technical specification means, with respect to any Software, the document setting forth the technical specifications for such Software and included in the Statement of Work.

  • Technical Specifications means the detailed requirements for the Work furnished by the Architect and set forth in Book 3 of the Contract Documents.

  • Aircraft Protocol means the official English language text of the Protocol to the Convention on International Interests in Mobile Equipment on Matters Specific to Aircraft Equipment, adopted on November 16, 2001, at a diplomatic conference in Cape Town, South Africa, and all amendments, supplements, and revisions thereto (and from and after the effective date of the Cape Town Treaty in the relevant country, means when referring to the Aircraft Protocol with respect to that country, the Aircraft Protocol as in effect in such country, unless otherwise indicated).

  • API means American Petroleum Institute.

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.