Labelling Sample Clauses

Labelling. 1. Products imported from one Party by the other Party in accordance with this Agreement shall meet the requirements on labelling set out in the laws and regulations of the other Party listed in Annexes III and IV. Those products may bear the Union's organic logo, the Chilean organic logo or both logos, as set out in the relevant laws and regulations, provided that they comply with the labelling requirements for the respective logo or for both logos. 2. The Parties undertake to avoid any misuse of the terms referring to organic production, including derivatives or diminutives such as ‘bio’ and ‘eco’, in relation to products that are covered by the recognition of equivalence referred to in Article 3. 3. The Parties undertake to protect the Union's organic logo and the Chilean organic logo set out in the relevant laws and regulations against any misuse or imitation. The Parties shall ensure that the Union's organic logo and the Chilean organic logo are used only for the labelling, advertising or commercial documents of products complying with the laws and regulations listed in Annexes III and IV.

Labelling. A label shall be permanently affixed on each container with at least the following information: name of the manufacturer, serial number, date of manufacture, MFP, NWP, type of fuel (e.g. "

Labelling. The distributor, on behalf of the selected vendor agrees that all supplies of articles should invariably contain the following information on its label and the carton. One information should not be overlapped by any other information needed to be furnished. The label should contain : a. Name of the item as approved b. CMS Cat. No. c. Manufacturing date/Import date for the imported items. d. Expiry Date. (where applicable) e. Name & address of Registered Office of Manufacturers and place of manufacture. f. Manufacturing License Number. (where applicable) g. Batch Number (where applicable) h. Month and Year of supply. i. The label & Carton must invariably marked “W B. GOVT SUPPLY : NOT FOR SALE”. j. All Surgical items quoted/supplied by the tenderer must conform to IS /BIS/CE/USFDA. Pacemker must conform to CE & US FDA norms. In case of Drugs items quoted /supplied by tenderer MUST CONFORM TO IP, BP, or USP norms and N.F.I. –III specification as noted against the item(s) in catalogue as applicable. k. The MRP and Trade Name will not be allowed to be printed in any pack. This will lead to cancellation of candidature straightaway. However, for excisable products, insertion of writing of Govt MRP is allowed as per provision laid down in the order of the Central Excise dept. However, for imported items, trade/brand name may be allowed in addition to the generic name.

Labelling. The distributor, on behalf of the selected vendor agrees that all supplies of articles in equipment section should invariably contain the following information on its label and the carton. One information should not be overlapped by any other information needed to be furnished. The label should contain : a. Name of the item as approved b. CMS Cat. No. c. Manufacturing date. d. Expiry Date. e. Name & address of Registered Office of Manufacturers and place of manufacture. f. Manufacturing License Number.

Labelling. StemCell shall label and package the Product prior to shipment using such packaging and labelling in accordance with the Product Specifications relating to the labelling of Product as approved by Oxford and included in Schedule “C”.

Labelling. (a) POLYPEPTIDE shall label each container of bulk drug substance according to the Specification including manufacturer name, name of product, product code, storage temperature, expiration date (if available), and quantity and number of containers. Each container will carry a caution statement as required by the applicable regulations in the country of shipping, transit and destination. INTRABIOTICS reserves the right to review and approve the master sample of the bulk drug container labels prior to their use. (b) Each container will contain a status label such as "IN QUARANTINE" or "RELEASED" etc. (c) Copies of labels used to label the bulk container will be kept as part of the batch record.

Labelling. Is a conformity marking issued by a notified body after examining the technical design of a product and verifying that the technical design of the product meets the requirements of the applicable technical regulations of the GSO member states.

Labelling. All supplies of articles in drugs section should invariably contain the following information on its label and the carton. One information should not be overlapped by any other information needed to be furnished. a. Pharmacopoeia name. b. Manufacturing date. c. Expiry Date. d. Name & address of Registered Office of Manufacturers and place of manufacture. e. Manufacturing Licence Number.

Labelling. 1. The labelling requirements of goods and services are subject to the provisions of this chapter. 2. Each Party shall apply its relevant labelling requirements under this chapter. 3. The Parties shall develop common labelling requirements. the proposals made by each Party shall be evaluated by the Sub-Committee on measures related to standardization in packaging and labelling and packaging, in accordance with paragraph 5 of article 14. 4. The Sub-Committee measures relating to standardization in packaging and labelling and packaging may work and make recommendations on: a) The establishment of a common system of symbols and pictograms to the Parties; b) Definitions and terminology; c) Submission of information, including language, measurement systems, ingredients and sizes; or d) Other matters.