Labelling and Packaging definition

Labelling and Packaging means labelling and packaging of the Drug Product, including insertion of materials such as patient inserts, patient medication guides, professional inserts and any other written, printed or graphic materials accompanying the Product considered to be part of the Finished Drug Product, and its handling, storage, quality control, quality assurance, testing and related activities of the Product in connection with the foregoing.
Labelling and Packaging means labelling and packaging of the Drug Product, including insertion of materials such as patient inserts, patient medication guides, professional inserts and any other written, printed or graphic materials accompanying the Product considered to be part of the Finished Drug Product, and its handling, storage, quality control, quality assurance, serialization, anti-counterfeiting measures, testing and related activities of the Product in connection with the foregoing.

Examples of Labelling and Packaging in a sentence

  • CLP = Classification, Labelling and Packaging of substances and mixtures.

  • Labelling and Packaging On dispatch of any consignment of the Goods the Contractor shall send the Authority an advice note specifying the means of transport, the place and date of dispatch, the number of packages and their weight and volume.

  • Abbreviations: ADR: European agreement concerning the international carriage of dangerous goods by Road.CLP: Classification, Labelling and Packaging IMDG: International Maritime Dangerous Goods.

  • Reg number 30702Not applicable Other regulations:According to 13 December 2014, No:29204, “Ministry of Environment and Urbanization; Regu- lation on Safety data sheets regarding hazardous substances and mixtures; Part I”.Regulation on Classification, Labelling and Packaging of Substances and Mixtures.

  • CLASSIFICATION according to Regulation EC 1272/2008 Classification, Labelling and Packaging Not classified.

  • Attachment D – Delivery Specification 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 forth in Attachment E (“Thermal Shipper”).

  • For the Agency to draw conclusions that all nuclear material remained in peaceful nuclear activities,60 it must verify the non-diversion of declared nuclear material and also provide assurances as to the absence of undeclared nuclear material and activities in a State.

  • Finally, the conference version of the mini-grids notes was discussed in a gender session at the joint CIF-ESMAP Mini-Grids event14 in Myanmar in February 2017 featuring CIF AU, Tide India, and an independent consultant.

  • In accordance with the European Communities Registration Evaluation Authorisation and Restriction of Chemicals (REACH) and Classification, Labelling and Packaging (CLP) Regulations, the Supplier shall provide the Purchaser with the relevant up to date EU version of the Safety Data Sheet(s) (“the Sheets”) for any hazardous substance(s) it is supplying.

  • Therefore, sodium bicarbonate is not classified according to EU Directive 67/548/EEC or EU Classification, Regulation, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.

Related to Labelling and 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.

  • 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;

  • Packaging Materials means the packaging materials for any of the Products, including product labels, packaging inserts, external packaging and similar materials.

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

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

  • 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.

  • API means American Petroleum Institute.

  • 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.

  • 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.

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

  • 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.

  • 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:

  • Labeler means an entity or person that receives prescription

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

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Training Materials means any and all materials, documentation, notebooks, forms, diagrams, manuals and other written materials and tangible objects, describing how to maintain the Facilities, including any corrections, improvements and enhancements thereto to the Bloom Systems which are delivered by Operator to Owner, but excluding any data and reports delivered to Owner.

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

  • CEMS means continuous emissions monitoring system.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Marketing Material means (a) customary bank books, information memoranda and other information packages regarding the business, operations, financial condition, projections and prospects of the Companies and their Subsidiaries, including all information relating to the transactions contemplated hereunder and (b) a customary “road show presentation” and a preliminary and final offering memorandum or private placement memorandum that is suitable for use in a customary “high-yield road show”, in each case required in connection with the Financing.

  • Manufacturing Process means any process for—

  • 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.

  • 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.

  • Label means a display of written, printed, or graphic matter upon the immediate container of any

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

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