Civil Aeronautical Product definition

Civil Aeronautical Product means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon.
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Civil Aeronautical Product means any civil aircraft, aircraft engine, or aircraft propeller or sub-assembly, appliance, or part, installed or to be installed thereon.
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Civil Aeronautical Product. (herein also referred to as “product”) means each civil aircraft, aircraft engine, or propeller.
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Examples of Civil Aeronautical Product in a sentence

  • On the other hand, a simple formula (17) was derived for eSI(k) based on combinatorial arguments.

  • The approved manufacturer of a New Civil Aeronautical Product other than a complete aircraft being exported will provide a statement or declaration on the Authorised Release Certificate (Airworthiness Approval Tag) of its certification in respect of subparagraph7.2.2.1 of the TIP, including the identification of any exception from the identified approved type design or notified directives and requirements of the Importing Party.

  • MaintenanceThe performance of inspection, overhaul, repair, preservation, or the replacement of parts, appliances, or components with the exception of pre-flight inspection of a Civil Aeronautical Product to assure the continued airworthiness of that product; and includes the embodiment of Modifications; but does not include the design of Repairs and Modifications.

  • Importing Party” means the Party to which a Civil Aeronautical Product is imported; 2.

  • The Exporting Party shall, in respect of Civil Aeronautical Products designed or manufactured under its jurisdiction, determine any appropriate action necessary to correct any unsafe condition of the type design that may be discovered after a Civil Aeronautical Product is placed in service, including any actions in respect of components designed and/or manufactured by a supplier under contract to a prime contractor in the territory under the Exporting Party's jurisdiction.

  • This Committee shall include representatives from each Party responsible at managerial level for: 2.1.1.1. Civil Aeronautical Product certification; 2.1.1.2. production, where different from persons covered by subparagraph 2.1.1.1.; 2.1.1.3. certification regulations and standards and‌ 2.1.1.4. internal standardisation inspections or quality control systems.

  • The Parties may also accept approvals, licences or other documents issued by a third country as a form of recognition of compliance that a Civil Aeronautical Product, organisation, or person complies with the applicable requirements set out in laws and regulations of that third country.

  • That any Civil Aeronautical Product under the jurisdiction of the other Party found any serious defects or un-airworthy condition shall be reported to the other Party, the type certificate holder, and customer.

  • That the release of Civil Aeronautical Product is in conformity with applicable legislative and regulatory requirements; e.

  • This Committee shall include representatives from each Party responsible at managerial level for: Civil Aeronautical Product certification; production, where different from persons covered by subparagraph 2.1.1(a) of this Procedure; certification regulations and standards and internal standardisation inspections or quality control systems.


More Definitions of Civil Aeronautical Product

Civil Aeronautical Product or “product” means each civil aircraft, aircraft engine, or propeller.
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Civil Aeronautical Product means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon.‌
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Civil Aeronautical Product or “product” means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon. (Ref. BASA Executive Agreement dated 2000)
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Civil Aeronautical Product or “Product” means each civil aircraft, aircraft engine or propeller.
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Civil Aeronautical Product. (herein also referred to as “product”) is confined from the definition contained in the Bilateral Aviation Safety Agreement to mean any civil aircraft, aircraft engine or propeller.
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Civil Aeronautical Product or “product” means each civil aircraft, aircraft
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Related to Civil Aeronautical Product

  • 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.

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

  • 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;

  • Aerosol product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • Aeronautical authorities means, in the case of the People’s Republic of China, the General Administration of Civil Aviation of China, or any person or agency authorized to perform any function presently exercised by the said Administration; and in the case of the Republic of South Africa, the Minister responsible for civil aviation or any person or agency authorized to perform any particular function provided for in this Agreement.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Reference biological product means the single biological product licensed pursuant to 42 U.S.C.

  • Final Product means a product that is not used in producing other products and is built and intended for use outdoors, provided the final product has not deteriorated or has otherwise become a potential source of contaminants.

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Commercial Product means any such product as defined in FAR 2.101.

  • Interchangeable biological product means a biological product that the U.S. Food and Drug Administration has:

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • aerodrome means a defined area on land or water (including any buildings, installations and equipment) intended to be used either wholly or in part for the arrival, departure and surface movement of aircraft;

  • 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.

  • Tobacco products means cigars, cigarettes, cheroots, stogies, periques, granulated, plug cut, crimp cut, ready rubbed, and other smoking tobacco, snuff, snuff flour, moist snuff, cavendish, ping and twist tobacco, fine-cut and other chewing tobaccos, shorts, refuse scraps, clippings, cuttings and sweepings of tobacco, and other kinds and forms of tobacco, prepared in such manner as to be suitable for chewing or smoking in a pipe or otherwise, or both for chewing and smoking.

  • Drug addiction means a disease characterized by a

  • Direction-indicator lamp means the lamp used to indicate to other road-users that the driver intends to change direction to the right or to the left;

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.

  • 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.