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. 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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Examples of Final Packaging in a sentence

  • Specifically, your firm does not follow its SOP (b)(4) - "Quality Assurance of Final Packaging of Product," which requires that, before product can be packaged for shipment, the QA clerk must check the package labels against the work order and verify that the label is correct.

  • MS Processing - Final Packaging of Osseous Grafts Procedure, SOP 210-8009-4, Effective Date February 15, 2010, was identified as controlling the packaging of the DBM Putty device.

  • 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.

  • This applies to all manufacturing and support operations responsible for the manufacture of product, and shall apply to (but not be limited to): Design, Purchasing, Manufacturing, Testing, Final Packaging for Shipment, Customer Material Returns and Failure Analysis.Emphasis shall be placed on identifying the root cause and the prevention of recurrence of the nonconformance.

  • Again November is our most ac- tive month of the year in recruiting.

  • Indevus will provide to Schering its requirements for any additional units of Clinical Supplies at least six (6) months prior to anticipated delivery setting forth the quantity, amount of placebo (if any), the Final Packaging and the delivery time.

  • Using VR-Head-Mounted Displays (VR- HMDs), people can freely move their head and interact with the 3D environment and recognize subtle context shifts.

  • Checks to ensure that only the correctly printed materials are available in packaging lines are documented in QC Final Packaging Inspection and observed implemented at packaging line.

  • On or about 5/4/2023, the employer did not determine the combustibility hazards of materials used during the Dekon 139 production process such as but not limited to Unit 5: PFN2 - Drying Dekon, Unit 6 Sifting and Milling and Unit 7: Final Packaging) to protect employees from fire and explosion hazards of combustible dust.

  • Pick-list generation: Based on the orders to be delivered for the day, a Pick-list is generated by the IT system.2. Pick-up from shelves: The respective products from the Pick-list are picked up from the shelves as per the IT system entries and gathered together to move towards Final Packaging Area.3. Final packaging: The picked-up products are packed in Flipkart-branded boxes.


More Definitions of Final Packaging

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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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 related to the manufacture of a Compound, including planning, purchasing, manufacture, processing, compounding, storage, filling, packaging, waste disposal, labeling, leafleting, testing, quality assurance, sample retention, stability testing, release, dispatch and supply, as applicable.

  • 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 all items which are consumed in the execution of the Work, without being directly incorporated in the Work, such as fuel, electricity, water, POL, welding rods, electrodes and utilities.

  • 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 the 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

  • Drug store means a place whose principal business is, the

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority-approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • 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.

  • Technical Specifications means the detailed requirements for the Work furnished by the Architect and set forth in Book 3 of the Contract Documents.

  • 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.