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;
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Examples of Cartagena Protocol in a sentence

  • Implementing the national and, when in place, regional institutional, legal and regulatory biosafety framework in Member States which have ratified the Cartagena Protocol, in both cases through support to inform, sensitize, and strengthen the capacities of the stakeholders.


More Definitions of Cartagena Protocol

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 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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Cartagena Protocol means the Protocol on Biosafety under the Convention on Biological Diversity;
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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 and set out as the First Schedule;
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Cartagena Protocol means the Cartagena Protocol on Biosafety of the United
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Related to Cartagena Protocol

  • 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;

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • 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.

  • 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.

  • technical specification means a document that prescribes technical requirements to be fulfilled by a product, process or service;

  • API means the American Petroleum Institute.