Labelling and Packaging Specifications definition

Labelling and Packaging Specifications shall have the meaning set forth in Section 2.4(e).
Labelling and Packaging Specifications shall have the meaning set forth in Section 2.4(h). 1.30. “Latent Defect” means a defect causing the Product to not conform to the applicable Specifications that Purchaser can show was present at the time of Pfizer´s delivery of the Product to Purchaser and which could not have been detected by Purchaser, its designee, or their Personnel at delivery through diligent inspection. 1.31. “Law/s” means, collectively, all applicable national and local laws, common laws, statutes, ordinances, codes, rules, regulations, orders, decrees or other pronouncements of any Government, administrative or judicial authority having the effect of law. 1.32. “Losses” shall have the meaning set forth in Section 8.1. 1.33. “Marketing Authorization” means the marketing authorization, or such other permission having similar effect, in respect of the Product granted by INVIMA- Instituto Nacional de Vigilancia de Medicamentos y Alimentos, as amended or varied by INVIMA- Instituto Nacional de Vigilancia de Medicamentos y Alimentos from time to time, that allows the Product to be placed on the market in Colombia according to Law. 1.34. “Non-Complying Product” shall have the meaning set forth in Section 4.4(a). información o datos técnicos o de otro tipo fabricación e ingeniería y dibujos técnicos, incluidos los derechos de propiedad exclusivos sobre cualquiera de los anteriores; y (b) las marcas registradas, solicitudes de registro de marcas, marcas sin registrar, imágenes comerciales, derechos de autor, conocimientos especializados, patentes, solicitudes de registro de patente y todas y cualesquiera disposiciones provisionales, divisiones, prolongaciones, prolongaciones parciales, prórrogas, sustituciones, renovaciones, registros, revalidaciones, reexpediciones o adiciones, incluyendo certificados complementarios de protección a las antedichas patentes y solicitudes de registro de patente y a todas las contrapartes extranjeras de esas patentes y solicitudes de registro de patente. 1.29. "Especificaciones de Empaque y Rotulado" tendrá el significado asignado en la Sección 2.4.(h). 1.30. "Defecto Latente" significa un defecto que hace que el Producto no se ajuste a las Especificaciones aplicables y que el Comprador pueda demostrar que existía en el momento de la entrega del Producto por parte de Pfizer y que no pudo ser detectado por el Comprador, su designado o su Personal mediante una inspección diligente en el momento de la entrega. 1.31. "Leyes" significan, colectivamente, todaslas...
Labelling and Packaging Specifications shall have the meaning set forth in Section 2.4(e). 1.30.“Latent Defect” means a defect causing the Product to not conform to the applicable Specifications that Purchaser can show was present at the time of delivery of the Product to Purchaser and which could not have been detected by Purchaser, its designee, or their Personnel at delivery through diligent inspection. 1.31.“Law/s” means, collectively, all applicable national and local laws, common laws, statutes, ordinances, codes, rules, regulations, orders, decrees or other pronouncements of any Government, administrative or judicial authority having the effect of law. 1.21."Instalaciones" significan los sitios de fabricación de Pfizer ubicados en Kalamazoo (Michigan) y Puurs (Bélgica) y dos sitios de fabricación de BioNTech, en Mainz e Xxxx Xxxxxxxxx (Alemania) o cualquier otro sitio de fabricación usado por Pfizer (o sus Filiales y/o BioNTech) para la fabricación del Producto suministrado bajo el presente. 1.22."Causal de Fuerza Mayor" tendrá el significado asignado en la Sección 12.8. 1.23."Formatos" tendrá el significado asignado en la Sección 12.12. 1.24."Gobierno" significa todos los niveles y subdivisiones administrativas (p.ej., local, regional, nacional, provincial, federal, administrativo, legislativo o ejecutivo) de Chile. 1.25."CCI" tendrá el significado asignado en la Sección 12.2. 1.26."Reclamos Indemnizados" tendrá el significado asignado en la Sección 8.2. 1.27."Parte Indemnizada" tendrá el significado asignado en la Sección 8.

Examples of Labelling and Packaging Specifications in a sentence

  • However, the assignmentx[1] = new A();is legal only if type A is a subtype of type B.

  • SANTE/2020/C3/043 - SI2.838335 to the special conditions and the general conditions of this APA and the following Annexes and Attachments: Attachment 1 – Specifications Attachment 2 – Delivery Documentation Attachment 3 – Delivery Specification Attachment 4 – Labelling and Packaging Specifications Attachment 5 – Return and Disposal of Product Materials which form an integral part of this APA.

  • Details of the Labelling and Packaging Specifications (including any branding requirements) for both Primary and Secondary Packaging will be agreed by Xxxx Xxxxxxx and Customer before commencement of manufacturing of the Device.

  • Product Delivery, Storage & Handling Specifications Shipments will arrive in a long-distance thermal shipping container as provided by Pfizer in accordance with the Labelling and Packaging Specifications set f01th in Attachment E ("Thermal Shipper").

  • Details of the Labelling and Packaging Specifications (including any branding requirements) for both Primary and Secondary Packaging will be agreed by Owen Mumford and Customer before commencement of manufacturing of the Device.

Related to Labelling and Packaging Specifications

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • Contract Specifications means the principal trading terms in CFD (for example Spread, Swaps, Lot Size, Initial Margin, Necessary Margin, Hedged Margin, the minimum level for placing Stop Loss, Take Profit and Limit Orders, financing charges, charges etc) for each type of CFD as determined by the Company from time to time. The Contract Specifications appear on the Website.

  • Packaging Materials means art and mechanical formats for a Software Title including the retail packaging, end user instruction manual with end user license agreement and warranties, end user warnings, FPU media label, and any promotional inserts and other materials that are to be included in the retail packaging.

  • Technical Specifications A specification in a document defining the characteristics of a product or a service, such as the quality levels, the environmental and climate performance levels, the design for all needs, including accessibility for people with disabilities, and the evaluation of conformity, of product performance, of the use of the product, safety or dimensions, as well as requirements applicable to the product as regards the name by which it is sold, terminology, symbols, testing and test methods, packaging, marking or labelling, instructions for use, the production processes and methods at every stage in the life cycle of the supply or service, as well as the evaluation and conformity procedures;

  • Brand Name Specification means a specification limited to one or more items by manufacturers’ names or catalogue number.

  • labelling means any words, particulars, trade marks, brand name, pictorial matter or symbol relating to a food and placed on any packaging, document, notice, label, ring or collar accompanying or referring to such food;

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

  • Service Specifications means the following documents, as applicable to the Services under Your order: (a) the Oracle Cloud Hosting and Delivery Policies, the Program Documentation, the Oracle service descriptions, and the Data Processing Agreement described in this Schedule C; (b) Oracle’s privacy policies; and (c) any other Oracle documents that are referenced in or incorporated into Your order. The following do not apply to any non-Cloud Oracle service offerings acquired in Your order, such as professional services: the Oracle Cloud Hosting and Delivery Policies, Program Documentation, and the Data Processing Agreement. The following do not apply to any Oracle Software: the Oracle Cloud Hosting and Delivery Policies, Oracle service descriptions, and the Data Processing Agreement.

  • TENDER SPECIFICATIONS means the Scope of Work, Special Instructions / Conditions, Technical specifications/requirement , Appendices, Site Information and drawings pertaining to the work and any other relevant reference in the Tender Document for which the Bidder are required to submit their offer.

  • District Specifications means the specifications followed by the State Government in the area where the work is to be executed.

  • Specifications means the Specifications of the Works included in the Contract and any modification or addition made or approved by the Project Manager.

  • IS Specification means the Specification of latest edition with amendments, if any, up to time of receipt of tender by Corporation issued by the Bureau of Indian Standards as referred to in the specifications and / or work orders.

  • Functional Specifications means the descriptions of features and functions of the Application as expressly set forth in Quote.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Marketing Materials has the meaning ascribed thereto in NI 41-101;

  • Standard Specifications means a compilation in book form of specifica- tions approved for general application and repetitive use;

  • Manufacturing Process means any process for—

  • 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.

  • The Specification means the Specification annexed to or issued with G.T.C.C. and shall include the schedules & drawings attached thereto as well as all samples and pattern, if any.

  • API means the American Petroleum Institute.

  • Goods Specification means any specification for the Goods, including any related plans and drawings that is set out in the Purchase Order or otherwise agreed in writing by the Customer and the Supplier;

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • Service Specification means and include detailed description, statements to technical data, performance characteristics, and standards (Indian as well as) as applicable and as specified in the Contract as well as those specifications relating to Industry standards and codes applicable to the performance of the work, work performance quality and the specifications affecting the works or any additional specification required to be produced by the DCO to meet the design criteria.