Protocol I definition

Protocol I means Protocol I to the MARPOL Convention.
Protocol I means the Protocol Additional to the Geneva Conventions of 12 August 1949, and Relating to the Protection of Victims of International Armed Conflicts, done at Geneva on 8 June 1977;
Protocol I means the Protocol on Non-detectable Fragments (Protocol I), 10 October 1980, set out in the Second Schedule;

Examples of Protocol I in a sentence

  • While the United States is not party to Protocol I, the plurality noted that many authorities regard it as customary international law.

  • Customs duties and charges having equivalent effect on imports shall be abolished in accordance with the provisions of Protocol I to this Agreement.

  • In case of error by the competent authorities in the proper management of the preferential system of export, and in particular in the application of the provisions of Protocol I, where this error leads to consequences in terms of import duties, the Party facing such consequences may request the CARIFORUM-EC Trade and Development Committee to examine the possibilities of adopting all appropriate measures with a view to resolving the situation.

  • The Parties to this Agreement shall mutually allocate concessions set forth in Protocol I in accordance with the provisions of this Chapter.

  • This Chapter shall apply to trade in all products between the Parties except where otherwise provided in this Chapter or in Protocol I.

  • For the purposes of this Chapter, "originating" means qualifying under the rules of origin set out in Protocol I.

  • In fact, in the debates at the Geneva Conference of 1974–1977 very few delegates commented on the proposal to introduce in the draft Additional Protocol I a provision similar to common Article 1 of the Geneva Conven- tions.

  • This section does not apply in relation to prescribed incidents that occur in the sea near a State, the Jervis Bay Territory or an external Territory to the extent that a law of that State or Territory makes provision giving effect to Protocol I to the Convention in relation to those prescribed incidents.

  • For the purposes of this Chapter, ‘originating’ means qualifying under the rules of origin set out in Protocol I to this Agreement.

  • As demonstrated by Vorobyov (2010a), systems with equal disk and stellar masses are short-lived and quickly evolve into binary/multiple systems with disk masses consider- ably smaller than those of the stars.


More Definitions of Protocol I

Protocol I means the Protocol Additional to the Geneva Conventions of 12 August 1949, and relating to the Protection of Victims of International Armed Conflicts (Protocol I), done at Geneva on 8 June 1977, a copy of which Protocol (including Annex 1 to that Protocol) is set out in Schedule 5;
Protocol I means Protocol I (reports on incidents involving harmful substances) to the MARPOL Convention;
Protocol I means the Protocol Additional to the Geneva Conventions of 12th August, 1949, and relating to the Protection of Victims of Non-International Armed Conflicts done at Geneva on 8th June , 1977.”
Protocol I. ’ means the Protocol Additional to the Geneva Conventions of 12 August 1f4f, and relating to the Protection of Victims of International Armed Conflicts (Protocol I), done at Geneva on 10 June 1f77, a copy of which Protocol (including Annex 1 to that Protocol) is set out in Schedule 5;

Related to Protocol I

  • 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

  • Study means the investigation to be conducted in accordance with the Protocol.

  • 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.

  • Manufacturing Know-How means all information, techniques, inventions, discoveries, improvements, practices, methods, knowledge, skill, experience and other technology, whether or not patentable or copyrightable, and any copyrights based thereon, relating to or necessary or useful for the production, purification, packaging, storage and transportation of Collaboration Products, including without limitation specifications, acceptance criteria, manufacturing batch records, standard operating procedures, engineering plans, installation, operation and process qualification protocols for equipment, validation records, master files submitted to the FDA, process validation reports, environmental monitoring processes, test data including pharmacological, toxicological and clinical test data, cost data and employee training materials.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or more pharmacists have jointly agreed, on a voluntary basis, to work in conjunction with one or more practitioners under protocol whereby the pharmacist may perform certain pharmaceutical care functions authorized by the practitioner or practitioners under certain specified conditions or limitations.

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.

  • Manufacturing Process means any process for—

  • Phase I Clinical Trial means the first study of a Product in humans the primary purpose of which is the determination of safety and which may include the determination of pharmacokinetic and/or pharmacodynamic profiles in healthy individuals or patients.

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Collaborative pharmacy practice agreement means a written and signed