Product Labeling Sample Clauses

Product Labeling. The labeling of all Licensed Products sold or offered for sale under this Agreement shall expressly state that the Licensed Product is manufactured under a license from the Medicines Patent Pool.
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Product Labeling. Licensee shall expressly state on the labeling of all Products sold or offered for sale under this Agreement that the Product “is manufactured under a license from Gilead Sciences Limited.”
Product Labeling. All product labels for Products shall include the names and logos of both Xxxxxx and Enanta, to the extent consistent with the Applicable Laws of any country in which Products are sold.
Product Labeling. The Products supplied to Purchaser will include Purchaser’s NDC number and be packaged in labeling and artwork approved by Purchaser to indicate Purchaser as a distributor of the Product. In order for Purchaser to include in the Product Label Purchaser Trademarks or similar changes indicating Purchaser as a distributor of the Product; (a) upon Purchaser’s request, Seller shall provide Purchaser with the Label artwork and text in electronic format, (b) Purchaser may update such artwork and text to include Purchaser Trademarks and such other similar changes as desired by Purchaser to indicate Purchaser as a distributor of the Product, and (c) Purchaser’s costs in connection with the foregoing shall be at its sole expense. Thereafter, Seller shall make all necessary arrangements, at its expense (except as provided in Section 6.2.1 above), to have changed Labels or Labeling printed and shall provide printer’s proofs to Purchaser for Purchaser’s review. Purchaser shall, within two (2) weeks of receipt of said printer’s proofs, provide written notice to Seller of Purchaser’s approval of such proofs in the form submitted by Seller (which approval shall not be unreasonably conditioned, withheld or delayed) or with such corrections thereto (in Purchaser’s reasonable judgment) as included in Purchaser’s notice. Thereafter, Seller shall incorporate in such Labels and Labeling Purchaser’s requested corrections thereto, if any, and shall supply Purchaser with examples of such Product Labels and Labeling for Purchaser’s regulatory filings; provided, however, that, if Seller shall not agree with Purchaser’s requested corrections, Purchaser and Seller shall consult in good faith to reach a resolution mutually agreeable to Purchaser and Seller. Confidential treatment has been requested for portions of this exhibit. The copy filed herewith omits the information subject to the confidentiality request. Omissions are designated as [***]. A complete version of this exhibit has been filed separately with the Securities and Exchange Commission.
Product Labeling. Artelo shall be solely responsible for the preparing, updating and maintaining product labeling in connection with commercialization of the Products and in compliance with all applicable laws and regulations. Such labeling may include but is not limited to text and graphical contents of printed labels and labeling components, including but not necessarily limited to healthcare professional leaflets or inserts, patient leaflets or inserts, and cartons.
Product Labeling. Unless otherwise agreed to by GRELAN, all labeling for Venture Products GR shall recognize that such products are distributed under license from GRELAN. Unless otherwise agreed to by BIONUMERIK, all labeling for Venture Products BN shall recognize that such products are distributed under license from BIONUMERIK. One or more of KI PHARMA, GRELAN and BIONUMERIK may be named on labeling for specified Venture Products as may be agreed from time to time by all the parties hereto.
Product Labeling. (a) Hospira shall label the Product in accordance with the Product Specifications using content provided by Theravance. Theravance shall control the content and type of all labeling and packaging (and any changes or supplements thereto) for the Product and shall have the responsibility, at Theravance’s expense, for: (i) ensuring such content is compliant with Regulatory Approval and all Applicable Law; and (ii) any changes or supplements to such content, including the expense of securing any approvals required by any applicable Regulatory Authority for any such changes or supplements. Hospira shall be responsible for obtaining such labels (and any changes or supplements thereto) in accordance with content specified by Theravance.
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Product Labeling. All GSI Products shall be sold under the GSI name and logo which will be the predominant branding element. Both parties acknowledge and agree that the presence of PKI's "PerkinElmer" brand will facilitate market recognition, credibility and customer communications. Accordingly, PKI shall cooperate with GSI to design and produce a subordinated brand label for GSI Products distributed outside Core Markets (eg. "in partnership with PerkinElmer) and a miniature brand label (eg. "Perkxx Xxxxx xxxbal alliance partner) for use in Core Markets. PE shall bear all of its own costs and expenses incurred in connection with such design activity and GSI shall bear its own cost in connection with production activities.
Product Labeling. Each Product shall bear a label and be contained in an outer package and/or carton and, if applicable, be accompanied by a package insert, which label, outer package and/or carton and/or package insert shall comply with all applicable regulatory requirements in the Territory and shall clearly carry a legend indicating that the Product was developed as a result of the research of Licensor. The label shall include the appropriate patent number of the appropriate Patent in accordance with the applicable requirements in the Territory.
Product Labeling. The parties acknowledge that the Products sold in the Territory shall bear labels which prominently display the name of Ethicon or its designated Affiliate. Focal agrees that it shall provide such reasonable cooperation and assistance to Ethicon as shall be necessary for Ethicon to obtain any CE marking in its own name for any of the Products to the extent necessary either (A) to enable the Products to include the labeling set forth in the preceding sentence, or (B) to enable Ethicon to effectively market the Products in the E.U. (as shall be mutually agreed upon by the parties).
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