Chemical Inputs Procurement Sample Clauses

Chemical Inputs Procurement. REG, Inc. will be responsible for purchasing methanol, sodium methylate, hydrochloric acid, and caustic soda, together with such other chemical inputs as may be needed in the future. REG, Inc. will procure all basic chemical inputs necessary for production at the Biodiesel Facility; and will: • Perform due diligence requirements for investigation of suppliers of the chemical inputs; • Provide analysis and audit of chemical suppliers; • Purchase chemical inputs at competitive prices meeting specifications for use in the Biodiesel Facility; • Negotiate for discounts where obtainable on chemicals (with all applicable price discounts, rebates or other incentives passed through to Western Dubuque); • Procure adequate chemical inputs to meet production schedules for the Biodiesel Facility; • Provide analysis and audit of bulk transportation suppliers; and • Arrange for transportation, logistics, and scheduling services for chemical input deliveries by suppliers based upon competitive bidding, with local haulers having an equitable chance to bid.
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Chemical Inputs Procurement. REG Services will be responsible for purchasing methanol, sodium methylate, hydrochloric acid, and caustic soda, together with such other chemical inputs as may be needed in the future. REG Services will procure all basic chemical inputs necessary for production at the Biodiesel Facility; and will: · Perform due diligence requirements for investigation of suppliers of the chemical inputs; · Provide analysis and audit of chemical suppliers; · Purchase chemical inputs at competitive prices meeting specifications for use in the Biodiesel Facility; · Negotiate for discounts where obtainable on chemicals; · Procure adequate chemical inputs to meet production schedules for the Biodiesel Facility; · Provide analysis and audit of bulk transportation suppliers; and · Arrange for transportation, logistics, and scheduling services for chemical input deliveries by suppliers.
Sample 1Sample 2
Chemical Inputs Procurement. REG will use its best efforts to purchase methanol, sodium methylate, hydrochloric acid, and caustic soda, together with such other chemical inputs as may be needed in the future. REG will use its best efforts to: • Procure all basic chemical inputs necessary for production at the Biodiesel Facility; • Perform due diligence requirements for investigation of suppliers of the chemical inputs; • Provide analysis and audit of chemical suppliers; • Purchase chemical inputs at competitive prices meeting specifications for use in the Biodiesel Facility (with East Fork Biodiesel having the right to reject any chemical inputs not meeting specifications); • Negotiate for discounts where obtainable on chemicals; • Procure adequate chemical inputs to meet production schedules for the Biodiesel Facility; • Provide analysis and audit of bulk transportation suppliers; and • Arrange for transportation, logistics, and scheduling services for chemical input deliveries by suppliers.
Sample 1
Chemical Inputs Procurement. West Central will arrange for the purchase and procure all basic chemical inputs necessary or appropriate for production at the Biodiesel Facility, and will: • Perform due diligence requirements for investigation of suppliers of the chemical inputs; • Provide analysis and audit of chemical suppliers; • Purchase chemical inputs at competitive prices meeting specifications for use in the Biodiesel Facility; • Negotiate for discounts where obtainable on chemicals; • Procure adequate chemical inputs to meet production schedules for the Biodiesel Facility; • Provide analysis and audit of bulk transportation suppliers; and • Arrange for transportation, logistics, and scheduling services for chemical input deliveries by suppliers.
Sample 1
Chemical Inputs Procurement. West Central will be responsible for purchasing methanol, sodium methylate, hydrochloric acid, and caustic soda, together with such other chemical inputs as may be needed in the future. West Central will procure all basic chemical inputs necessary for production at the Biodiesel Facility; and will: • Perform due diligence requirements for investigation of suppliers of the chemical inputs; • Provide analysis and audit of chemical suppliers; • Purchase chemical inputs at competitive prices meeting specifications for use in the Biodiesel Facility; • Negotiate for discounts where obtainable on chemicals; • Procure adequate chemical inputs to meet production schedules for the Biodiesel Facility; • Provide analysis and audit of bulk transportation suppliers; and • Arrange for transportation, logistics, and scheduling services for chemical input deliveries by suppliers.
Sample 1
Chemical Inputs Procurement. West Central will initially be responsible for purchasing methanol, sodium methylate, hydrochloric acid, and caustic soda, together with such other chemical inputs as may be needed in the future. West Central will utilize its best efforts to procure all basic chemical inputs necessary for production at the Biodiesel Facility, and to: • Perform due diligence requirements for investigation of suppliers of the chemical inputs. • Provide analysis and audit of chemical suppliers. • Provide to Western Iowa Energy the specifications for chemical inputs being required of suppliers. • Purchase chemical inputs at competitive prices meeting specifications for use in the Biodiesel Facility. • Review on a monthly basis the average prices paid for chemical inputs by Western Iowa Energy, including comparisons to industry averages. • Negotiate for discounts where obtainable on chemicals. • Procure adequate chemical inputs to meet production schedules for the Biodiesel Facility. • Provide analysis and audit of bulk transportation suppliers. • Arrange for transportation, logistics, and scheduling services for chemical input deliveries by suppliers.
Sample 1

Related to Chemical Inputs Procurement

  • Manufacturing Intrexon shall have the option and, in the event it so elects, shall use Diligent Efforts, to perform any manufacturing activities in connection with the Aquaculture Program that relate to the Intrexon Materials, including through the use of a suitable Third Party contract manufacturer. To the extent that Intrexon so elects, Intrexon may request that AquaBounty and Intrexon establish and execute a separate manufacturing and supply agreement, which agreement will establish and govern the production, quality assurance, and regulatory activities associated with manufacture of Intrexon Materials. Except as provided in Section 4.1, any manufacturing undertaken by Intrexon pursuant to the preceding sentence shall be performed in exchange for cash payments equal to Intrexon’s Fully Loaded Cost in connection with such manufacturing, on terms to be negotiated by the Parties in good faith. In the event that Intrexon does not manufacture Intrexon Materials or bulk quantities of other components of AquaBounty Products, then Intrexon shall provide to AquaBounty or a contract manufacturer selected by AquaBounty and approved by Intrexon (such approval not to be unreasonably withheld) all Information Controlled by Intrexon that is (a) related to the manufacturing of such Intrexon Materials or bulk qualities of other components of AquaBounty Products for use in the Field and (b) reasonably necessary to enable AquaBounty or such contract manufacturer (as appropriate) for the sole purpose of manufacturing such Intrexon Materials or bulk quantities of other components of AquaBounty Products. The costs and expenses incurred by Intrexon in carrying out such transfer shall be borne by Intrexon. Any manufacturing Information transferred hereunder to AquaBounty or its contract manufacturer shall not be further transferred to any Third Party, including any Product Sublicensee, or any AquaBounty Affiliate without the prior written consent of Intrexon; provided, however, that Intrexon shall not unreasonably withhold such consent if necessary to permit AquaBounty to switch manufacturers.

  • Manufacturing License Subject to the terms of this Agreement, including without limitation Section 2.2, Theravance grants to GSK an exclusive license under the Theravance Patents and Theravance Know-How to make and have made API Compound or formulated Alliance Product in the Territory.

  • Product The term “

  • Raw Materials Lonza shall procure all required Raw Materials as well as consumables other than those Raw Materials that are Customer Materials. Customer shall be responsible for payment for all consumables and Raw Materials ordered or irrevocably committed to be procured by Lonza hereunder. Upon cancellation of any Batch or termination of the Agreement, all unused Raw Materials shall be paid for by Customer within [***] days of invoice and at Customer’s option will either be (a) held by Lonza for future use for the production of Product, (b) delivered to Customer, or (c) disposed of by Lonza.

  • Manufacturing Technology Transfer With respect to each Technology Transfer Product, upon AbbVie’s written request after the Inclusion Date for the Included Target to which such Technology Transfer Product is Directed, Morphic shall effect a full transfer to AbbVie or its designee (which designee may be an Affiliate or a Third Party manufacturer) of all Morphic Know-How and Joint Know-How relating to the then-current process for the Manufacture of such Technology Transfer Product (the “Manufacturing Process”) and to implement the Manufacturing Process at facilities designated by AbbVie (such transfer and implementation, as more fully described in this Section 5.3, the “Manufacturing Technology Transfer”). To assist with the Manufacturing Technology Transfer, Morphic will make its personnel reasonably available to AbbVie during normal business hours for up to [***] FTE hours with respect to each Included Target (in each case, free of charge to AbbVie) to transfer and implement the Manufacturing Process under this Section 5.3. Thereafter, if requested by AbbVie, Morphic shall continue to perform such obligations; provided, that AbbVie will reimburse Morphic for its full-time equivalent (FTE) costs (for clarity, in excess of [***] FTE hours) and any reasonable and verifiable out-of-pocket costs incurred in providing such assistance. CERTAIN CONFIDENTIAL INFORMATION CONTAINED IN THIS DOCUMENT, MARKED BY [***], HAS BEEN OMITTED BECAUSE IT IS NOT MATERIAL AND WOULD LIKELY CAUSE COMPETITIVE HARM TO THE COMPANY IF PUBLICLY DISCLOSED.

  • Commercialization License Subject to the terms of this Agreement, including without limitation Section 2.2 and Theravance's Co-Promotion rights in Section 5.3.2, Theravance hereby grants to GSK, and GSK accepts, an exclusive license under the Theravance Patents and Theravance Know-How to make, have made, use, sell, offer for sale and import Alliance Products in the Territory.

  • Formation; Composition Each Party will initially appoint [***] representatives to the JCC, with each representative having knowledge and expertise in the commercialization of products similar to the Regional Licensed Products and having sufficient seniority within the applicable Party to make decisions arising within the scope of the JCC’s responsibilities. The JCC may change its size from time to time by mutual consent of its members, provided that the JCC will consist at all times of an equal number of representatives of each of Surface and Novartis. Each Party may replace its JCC representatives at any time upon written notice to the other Party. The JCC may invite non-members to participate in the discussions and meetings of the JCC, provided that such participants have no voting authority at the JCC and are bound under written obligation of confidentiality no less protective of the Parties’ Confidential Information than those set forth in this Agreement. The JCC will be co-chaired, with one chairperson designated by Surface and [***] designated by Novartis, whose responsibilities will include conducting meetings, including, when feasible, ensuring that objectives for each meeting are set and achieved. Responsibility for running each meeting of the JCC will alternate between the chairpersons from meeting-to-meeting, with Novartis’s chairperson running the first meeting. CERTAIN CONFIDENTIAL PORTIONS OF THIS EXHIBIT WERE OMITTED AND REPLACED WITH “[***]”. A COMPLETE VERSION OF THIS EXHIBIT HAS BEEN FILED SEPARATELY WITH THE SECRETARY OF THE SECURITIES AND EXCHANGE COMMISSION PURSUANT TO AN APPLICATION REQUESTING CONFIDENTIAL TREATMENT PURSUANT TO RULE 406 PROMULGATED UNDER THE SECURITIES ACT OF 1933, AS AMENDED.

  • Information Systems Acquisition Development and Maintenance a. Client Data – Client Data will only be used by State Street for the purposes specified in this Agreement.

  • Manufacturing Services Jabil will manufacture the Product in accordance with the Specifications and any applicable Build Schedules. Jabil will reply to each proposed Build Schedule that is submitted in accordance with the terms of this Agreement by notifying Company of its acceptance or rejection within three (3) business days of receipt of any proposed Build Schedule. In the event of Jabil’s rejection of a proposed Build Schedule, Jabil’s notice of rejection will specify the basis for such rejection. When requested by Company, and subject to appropriate fee and cost adjustments, Jabil will provide Additional Services for existing or future Product manufactured by Jabil. Company shall be solely responsible for the sufficiency and adequacy of the Specifications [***].

  • API A. Reliant shall supply to Cardinal Health for Manufacturing and Packaging, at Reliant’s sole cost, the API and applicable reference standards in quantities sufficient to meet Reliant’s requirements for each Product as further set forth in Article 4. Prior to delivery of any of the API or reference standard to Cardinal Health for Manufacturing and Packaging, Reliant shall provide to Cardinal Health a copy of the API Material Safety Data Sheet (“MSDS”), as amended, and any subsequent revisions thereto. Reliant shall supply the API, reference standards, and Certificate of Analysis FOB the Facility no later than thirty (30) days before the scheduled Manufacture Date upon which such API will be used by Cardinal Health. Upon receipt of the API, Cardinal Health shall conduct identification testing of the API. Cardinal Health shall use the API solely and exclusively for Manufacturing and Packaging under this Agreement. The maximum volume of API that Reliant supplies to Cardinal Health shall not exceed the amount reflected in the Firm Commitment and the next six (6) months of the Rolling Forecast.

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