Use of Samples Sample Clauses

Use of Samples. Approved samples not destroyed in testing will be sent to the Owner’s Representative at the Project. Approved samples of hardware in good condition will be marked for identification and may be used in the Work. Materials and equipment incorporated in the Work must match the approved samples. Samples not destroyed in testing and not approved will be returned at the Private Entity’s expense if the Private Entity so requests in writing at the time of submission.
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Use of Samples. Impax shall procure, either itself or through CSO, that the Sales Force shall:
Use of Samples. Gateway reserves the right to use samples of goods provided under this purchase order for future quoting requirements for any third party.
Use of Samples. Omeros shall transfer to North Coast the sufficient or requested quantities of proteins, reagents, antibodies and/or other materials involved in the Services as specified in any Research Plan (“Samples”). Omeros shall provide all pertinent information known to Omeros regarding the Samples to the extent necessary for carrying out any Research Plan. North Coast shall be responsible for and bear the expense of obtaining any other chemicals, materials, equipment, animals and facilities needed to conduct the Services and produce the Deliverables. North Coast shall not use or analyze any Samples provided under this Agreement except as necessary to carry out the relevant Research Plan and shall not administer or permit the Samples to be administered to any person. After completion of the Services, North Coast shall either return the Samples to Omeros or dispose of the Samples, upon written request by Omeros and at Omeros’ risk and expense. North Coast accepts full responsibility for safe handling of all Samples or other compounds or materials used in the performance of the Services and shall be responsible for any loss or destruction of the Samples after delivery to North Coast.
Use of Samples. Omeros shall transfer to Affitech the sufficient or requested quantities of proteins, reagents and/or other materials involved in the Services as specified in the Initial Research Plan and any Additional Research Plan(s) (“Omeros Samples”). Omeros shall provide all pertinent information known to Omeros regarding the Omeros Samples to the extent necessary for carrying out the Initial Research Plan and any Additional Research Plan(s). Affitech shall be responsible for [†]. Affitech shall not use or analyze any Omeros Samples provided by Omeros under this Agreement except as necessary to carry out the Initial Research Plan or any Additional Research Plan(s) and shall not administer [†]. After completion of the Services, Affitech shall either return the Omeros Samples to Omeros or dispose of the Omeros Samples, upon written request by Omeros and at Omeros’ risk and expense. Affitech [†] of all Omeros Samples or other compounds or materials used in the performance of the Services and shall [†] of the Omeros Samples after delivery to Affitech.
Use of Samples. 3.1 Parties must use Samples only for purposes that are consistent with the consent obtained and in compliance with relevant laws and regulations.
Use of Samples. Product samples supplied by Santarus to Co-Promotion Partner shall be used by Co-Promotion Partner solely in making Product Calls in the Territory pursuant to this Agreement. Upon its receipt of Product samples, Co-Promotion Partner shall be responsible for accountability and compliance with the PDMA, and other applicable federal, state and local laws, rules and regulations relating to such samples or the distribution of same and shall be responsible for adherence by its sales representatives to such laws, rules and regulations. Santarus or its appointed agents shall have the right to audit the records and/or reports for the Product samples, as required to be kept by Co-Promotion Partner under the PDMA, during normal business hours, at convenient times and upon no less than five (5) calendar days' prior written notice.
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Use of Samples. During the Copromotion Period the Product samples supplied by King to Wyeth or to King’s sales representatives shall be used by Wyeth and King solely in making Detail calls to Physicians in the Territory pursuant to this Agreement. Upon its receipt of Product samples, Wyeth shall be responsible for accountability and compliance with the PDMA, and other applicable federal, state and local laws and regulations relating to such samples or the distribution of same. King shall be responsible for accountability and compliance with the PDMA, and other applicable federal, state and local laws and regulations relating to Product samples that King supplies for distribution by King’s sales representatives. Wyeth and King each shall be responsible for adherence by its respective sales representatives to such laws and regulations. Each Party or its appointed agents shall have the right to audit the records and/or reports for the Product samples, as required to be kept by the other Party under the PDMA, during normal business hours, at convenient times and upon no less than [***] prior notice, provided, however, that no such audit shall occur more than [***] after the end of the Copromotion Period. Pursuant to Section 11 of the Transition Plan, after the Copromotion Period Wyeth shall at King’s option and expense either return or destroy all of the Product samples in Wyeth’s, its Affiliates’ or its employees’ control.
Use of Samples. (a) Each party will be responsible for accountability and compliance with the PDMA, and other applicable federal, state, and local laws and regulations relating to such samples or the distribution of same. Inyx and King each will be responsible for adherence by its respective sales representatives to such laws and regulations. Each party or its appointed agents will have the right to audit the records and/or reports for the Products samples, as required to be kept by the other party under the PDMA, pursuant to the provisions of Article 10 of the Collaboration Agreement.
Use of Samples. The parties acknowledge that the Samples may contain one or more infectious agents and may have additional unknown and hazardous properties. Receiving Party shall use the Samples under appropriate containment conditions.
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