FDC Film definition

FDC Film means films used in FUJI DRI-CHEM system applicable to the tests listed in Schedules A and B.
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Examples of FDC Film in a sentence

  • For example, the T'Sou-ke project is modeling energy autonomy for other Aboriginal communities by installing PV (Kimmett, 2009).

  • FUJI shall have the right, with respect to any FDC Film supplied to EXIGENT under this Agreement which becomes or is likely to become the subject of such claim or legal action, to replace or modify such FDC Film, or in case injunction is granted by court or FDC to withhold further shipment of such FDC Film.

  • The FDC Film applicable to the tests in Sodium, Potassium and Chloride shall be supplied to EXIGENT by FUJI in a slide form on which such FDC Film is mounted.

  • EXIGENT shall make best efforts to develop and complete EXIGENT POCT System which incorporates FDC Film and/or FUJI Technology supplied hereunder in accordance with the time schedule provided in Schedule H.

  • The terms and conditions for supply of FDC Film to be required for marketing of EXIGENT POCT System shall be separately agreed upon between the parties hereto.

  • FUJI shall have the right, with respect to any FDC Film supplied to CARESIDE under this Agreement which becomes or is likely to become the subject of such claim or legal action, to replace or modify such FDC Film, or in case injunction is granted by court or FTC to withhold further shipment of such FDC Film.

  • Except as otherwise agreed upon by and between the parties hereto, all payments for FDC Film supplied to CARESIDE by FUJI hereunder shall be made in Japanese Yen, and shall be remitted, within forty-five (45) days of the custom clearance of FDC Film, by bank-to-bank telegraphic transfer to FUJI's account with such bank in Tokyo as designated by FUJI.

  • The purchase prices of FDC Film shall be as listed in Schedule D, which are indicated on the basis of CIF Los Angeles Airport.

Related to FDC Film

  • Drug Master File or “DMF” is described in 21 C.F.R. Part 314.420. A DMF is a submission to the FDA that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.

  • Master File has the meaning set forth in the CAISO Tariff.

  • Manufacturing Know-How means, with respect to the Product or any Variant thereof, the technology, data, designs, processes, methods, specifications and other know-how used in connection with the formulation, manufacture, labeling, packaging, quality control, release testing, and production of the Product, and all ingredients used therein and portions thereof.

  • Product Know-How means Know-How

  • CREFC® Intellectual Property Royalty License Fee With respect to each Mortgage Loan (including any REO Mortgage Loan) and for any Distribution Date, the amount accrued during the related Interest Accrual Period at the CREFC® Intellectual Property Royalty License Fee Rate on, in the case of the initial Distribution Date, the Cut-Off Date Balance of such Mortgage Loan and, in the case of any subsequent Distribution Date, the Stated Principal Balance of such Mortgage Loan as of the close of business on the Distribution Date in the related Interest Accrual Period; provided that such amounts shall be computed for the same period and on the same interest accrual basis respecting which any related interest payment due or deemed due on the related Mortgage Loan is computed and shall be prorated for partial periods. For the avoidance of doubt, the CREFC® Intellectual Property Royalty License Fee shall be payable from the Lower-Tier REMIC.

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

  • DMF means any drug master file filed with the FDA, and any equivalent filing in other countries or regulatory jurisdictions.

  • CREFC® Intellectual Property Royalty License Fee Rate With respect to each Mortgage Loan, a rate equal to 0.0005% per annum.

  • Investigational Product means the Study Drug identified above and the control material, as further detailed in the Protocol;

  • Biologics License Application or “BLA” means, with respect to a country or extra-national territory, a request for permission to introduce, distribute, sell or market a biologic product in such country or some or all of such extra-national territory, including pursuant to 21 CFR 601.2 in the U.S.

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • 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.