Final Packaging definition

Final Packaging means the labeling and packaging to be used in connection with the Product labeled for use in the Field in the Territory, including the packaging of package inserts and components reasonably necessary for sale of the finished Product to the ultimate consumer.
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Final Packaging means the Labeling and packaging of Xxxxxx’x Generic Product in accordance with Applicable Law and Xxxxxx’x XXXX, including the package inserts and other components reasonably necessary for the sale or distribution of the Finished Product to the ultimate consumer.
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Final Packaging means the packaging and labelling of Bulk Drug Product to produce finished product, including the primary packaging, secondary packaging, insertion of package inserts necessary for sale of Licensed Product for the Initial Indication in each country in the Territory to the ultimate consumer, storage of the finished product until release for shipment, tertiary packaging of finished product in a form suitable for shipping and transportation of finished product under the specified conditions to Orion’s designated destinations.
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Examples of Final Packaging in a sentence

  • SCHERING will provide INDEVUS with timely notification of all significant deviations, notes to file, and other deficiencies that may reasonably be expected to impact the quality of the Finished Product, as well as all FDA correspondence regarding testing, Manufacture, Final Packaging, or Packing of the Finished Product.

  • Schering will maintain complete and accurate records and Documentation of all validation data, stability testing data, batch records, quality control and testing relating to the Substance and the Finished Product and the Manufacture, Final Packaging, labeling, testing and shipment thereof.

  • Records which include the information relating to the Manufacturing, Final Packaging and quality operation for each lot of Substance and Finished Product will be prepared by Schering at the time such operations occur.

  • Final Packaging and Packing for shipment shall be governed by Section 5.1 of the MSA which is hereby incorporated by reference herein, as if stated herein, in its entirety.

  • Indevus shall provide Schering with specifications for the FDA approved labeling, artwork, drawings and any additional Final Packaging which shall accompany Finished Product (and which shall be used by Schering solely for the Manufacture and supply to Indevus or Indevus’ designee of Finished Product pursuant to this Agreement) sufficient time in advance to enable Schering to Manufacture Finished Product in due time prior to the scheduled delivery to Indevus.

  • Unless the Parties otherwise agree in writing, Nycomed, in consultation with Acusphere, shall be responsible for packaging the Product for resale in the Territory in accordance with the Final Packaging Specifications and assuring that final packaging and labeling comply with all Applicable Laws where such Product is to be distributed for sale in the Territory.

  • Orion shall be solely responsible for Final Packaging, at its own cost and expense, and for ensuring that all Final Packaging, labels and labelling, including the package make-up, package inserts and other elements relating to packaging, labels and labelling, as well as all promotional materials, comply with all applicable laws and regulations in the Territory.

  • Xxxxx shall have the option to have Xxxx manufacture and supply Licensed Product in primary packaging and Final Packaging bearing two different and distinct trademarks, tradenames and/or tradedress (each, a “Brand”).

  • On receipt of the Product complying with the certification and packaging requirements in Section 2.3.1, LifeNet will insert the Product into the Final Packaging.

  • If orders are pending, the respective product is sent directly to the Final Packaging Area for Outward Processing.3. Physical placement on shelves: Based on the Put-list, the products are placed on the respective shelves.


More Definitions of Final Packaging

Final Packaging. SPECIFICATIONS" means the packaging specifications and the labeling specifications necessary for the resale of Product by Nycomed, its Affiliates or Partners within the Territory, as determined by Nycomed in consultation with Acusphere from time to time, and in compliance with Applicable Laws.
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Final Packaging means the labeling and packaging (as defined in the Act) of Finished Product, including product carton, package inserts, labels and associated components accompanying and necessary for use or sale of the Clinical Supplies or Finished Product in the Territory, as applicable.
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Final Packaging means the packaging and labeling of product in a form suitable for shipping and the transportation of Product under the specified conditions and to OCEANA’s designated destinations.
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Final Packaging means the labeling, packaging, storage and transportation of vials of BULK DRUG PRODUCT to produce FINISHED PRODUCT, including, without limitation, the packaging of package inserts and components reasonably necessary for sale of the FINISHED PRODUCT to the ultimate consumer, from the time of receipt of such vials of BULK DRUG PRODUCT through the time FINISHED PRODUCT is shipped to AVENTIS or its designees.
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Final Packaging means the exterior packaging and labeling of the Product conforming with the specifications set forth on EXHIBIT H hereto, including product inserts and tracking materials, and such additional labeling as is determined by LifeNet to be ---------- *** Indicates the omission of confidential material pursuant to the request for confidential treatment made in accordance with Rule 24b-2 under the Securities Exchange Act of 1934, as amended. The confidential material is being filed separately with the Securities and Exchange Commission. required by applicable Laws and Rules and placing Product in an appropriate container for shipping.
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Related to Final Packaging

  • Packaging means the assembly of components necessary to ensure compliance with the packaging requirements of these regulations. It may consist of one or more receptacles, absorbent materials, spacing structures, thermal insulation, radiation shielding, and devices for cooling or absorbing mechanical shocks. The vehicle, tie-down system, and auxiliary equipment may be designated as part of the packaging.

  • 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.

  • Child-resistant packaging means packaging that is designed or constructed to be significantly difficult for children under five years of age to open or obtain a toxic or harmful amount of the substance in the container within a reasonable time and not difficult for normal adults to use properly, but does not mean packaging that all children under five years of age cannot open or obtain a toxic or harmful amount of the substance in the container within a reasonable time.

  • Fabrication means making up data or results and recording or reporting them.

  • Manufacturing means all activities directed to sourcing of necessary raw materials, producing, processing, packaging, labeling, quality assurance testing, release of a Licensed Product or Licensed Product candidate, whether for Development or Commercialization. When used as a verb, “Manufacture” means to engage in Manufacturing.

  • Design flow means the average annual flow or average daily flow specified in an approved facilities plan or approved plans and specifications, the flow specified in a WPDES permit, or the flow required to meet performance standards.

  • Consumables means where the context permits, Digital Print Consumables, Inkjet Printing System Consumables and Prepress Consumables.

  • 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 Facility means buildings and structures, including machinery and equipment, the primary purpose of which is or will be the manufacture of tangible goods or materials or the processing of such goods or materials by physical or chemical change.

  • Packing means the activities required to wrap and protect an article, properly place the article in appropriate carton or box, and stow the article and its carton or box in a lift van of sufficient size and constructed in accordance with post specifications; includes obtaining customs clearances and required documentation for shipment, via surface or air as appropriate.

  • Batch means a specific quantity of Product that is intended to have uniform character and quality, within specified limits, and is produced according to a single manufacturing order during the same cycle of manufacture.

  • Remanufacturing means the activity of overhauling, retrofitting, fabricating, or repairing a product or its component parts for ultimate sale at retail.

  • APIs means SAP application programming interface and accompanying or related Documentation, source code, tools, executable applications, libraries, subroutines, widgets and other materials made available by SAP or through SAP tools or SAP Software Development Kit (and all derivative works or modifications thereof) to Provider that allow Provider to integrate the Provider Service with the Cloud Service, including any access code, authentication keys or similar mechanisms to enable access of the APIs.

  • Goods Specification any specification for the Goods including any relevant plans or drawings, that is agreed in writing by the Reseller and Voip-Unlimited.

  • Operational Flow Order means any directive issued to a Customer by KUB which requires the Customer to adjust Deliveries to KUB or deliveries of non-Firm gas to the Customer by KUB.

  • 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.

  • API means American Petroleum Institute.

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

  • Cartridge means a pleated or surface-type filter component with fixed dimensions that is designed to remove suspended particles from water flowing through the filter.

  • Labeling means all labels and other written, printed, or graphic matter on an article or any of its

  • Product Labeling means (a) the full prescribing information for the Product approved by the applicable Regulatory Authority, and (b) all labels and other written, printed or graphic information included in or placed upon any container, wrapper or package insert used with or for the Product.

  • 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.

  • Project Management Report means each report prepared in accordance with Section 4.02 of this Agreement;

  • Flexographic printing means the application of words, designs, and pictures to a substrate by means of a roll printing technique in which the pattern to be applied is raised above the printing roll and the image carrier is made of rubber or other elastomeric materials.

  • Certificate of Analysis means a document signed by an authorized representative of Manufacturer, describing Specifications for, and testing methods applied to, Product, and the results of testing.

  • Manufacturing Facilities means facilities engaged in the mechanical or chemical transformation of materials or substances into new products and shall include: