Manufacturing Release definition

Manufacturing Release or “MR” refers to commencement of production of sellable, market-ready units. This is characterized by continuous or multi-batch production and a stable, reliable design. D&K Supply Agreement Final D&K Confidential Date Printed: 6/1/2017
Manufacturing Release means the date on which the applicable hardware and/or software has successfully completed Final Acceptance Testing, upon which date DIRECTV shall notify TiVo of such in writing.
Manufacturing Release means the version of TiVo Technology that (a) has passed TiVo's quality assurance tests [ * ]to be conducted by TiVo with respect to such TiVo Technology); (b) performs in all respects in accordance with the Post Build Test Criteria; (c) has been determined by TiVo to be suitable for use in and distribution to TiVo's consumer network using Personal Digital Recording Technology; and (d) would otherwise be available for distribution by TiVo through a general release as part of the TiVo Service.

Examples of Manufacturing Release in a sentence

  • Following the Manufacture of each Batch of Product, and upon written request as required, Immtech shall provide Par with properly completed copies of all Manufacturing Release Records, including Manufacturing and Packaging Batch records prepared in accordance with the Specifications.

  • Biogen shall notify Vir without undue delay if Biogen becomes aware that it will or has reason to believe that it may be unable to meet the previously estimated date for Manufacturing Release of the applicable Drug Substance or Drug Product.

  • At any time until [*]after the Manufacturing Release of the Version [*]Software, DIRECTV shall notify TiVo in writing if DIRECTV, at its discretion, will use the DIRECTV satellite-based push network for all TiVo push content and data [*]Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission.

  • At any time until [*] after the Manufacturing Release of the Version [*] Software, DIRECTV shall [*] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission.

  • DIRECTV shall have the right to terminate this Agreement if the Manufacturing Release of the Provo Receiver (with Version [*]Software) does not occur on or before [*] (as such date may be adjusted on a day-by-day basis for adjustments in the Manufacturing Release date pursuant to Section 2.1(a)).

  • Pursuant to the letter agreement of July 22, 2002, the first two sentences of Section 2.5 of the Development Agreement are deleted and replaced in their entirety with the following: “At DIRECTV’s request, TiVo shall develop the Two-Chip Receiver, for Manufacturing Release no later than [*].

  • Section 4.2 of the Marketing Agreement --------------------------- shall terminate as of the Manufacturing Release of the Version [*] Software (as provided in the Development Agreement).

  • TiVo and DIRECTV anticipate that the Provo Receiver will undergo Manufacturing Release (as defined below) no later than[*].

  • Notwithstanding the foregoing, following Manufacturing Release of the Version 3.1 Software (as defined in the Development Agreement), DIRECTV shall not have the right to (iv) for Prior Software Versions.

  • Further, following the Manufacturing Release of Version [*] Software, to the extent that any claim arises from such agreements for liabilities incurred after the assignment thereof, DIRECTV shall indemnify and hold TiVo harmless from such claim in accordance with the terms and conditions in Article VII.


More Definitions of Manufacturing Release

Manufacturing Release means Intuit's first release for manufacturing of any version of the Private Label Software or Retail Pro Software that provides capability for multiple retail sales locations.
Manufacturing Release has the meaning set forth in Section 2.9.

Related to Manufacturing Release

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Manufacturing Agreement has the meaning set forth in Section 2.6.

  • Manufacturing Technology means any and all patents, patent applications, Know-How, and all intellectual property rights associated therewith, and including all tangible embodiments thereof, that are necessary or useful for the manufacture of adeno- associated viruses, adeno-associated virus vectors, research or commercial reagents related thereto, Licensed Products, or other products, including manufacturing processes, technical information relating to the methods of manufacture, protocols, standard operating procedures, batch records, assays, formulations, quality control data, specifications, scale up, any and all improvements, modifications, and changes thereto, and any and all activities associated with such manufacture. Any and all chemistry, manufacturing, and controls (CMC), drug master files (DMFs), or similar materials provided to regulatory authorities and the information contained therein are deemed Manufacturing Technology.

  • Manufacturing Process means any process for—

  • 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.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • Quality Agreement has the meaning set forth in Section 9.6.

  • API means American Petroleum Institute.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Product Specific Terms means the terms applicable to a specific item of Licensed Software as set out in Schedule 2;

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • 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.

  • Manufacturing Site means a location where a manufacturing

  • NDA means a New Drug Application, as defined in the regulations promulgated by the United States Food and Drug Administration, or any foreign equivalent thereof.

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Supply Agreement has the meaning set forth in Section 7.1.

  • Development Plan has the meaning set forth in Section 3.2.

  • Clinical Supply Agreement shall have the meaning set forth in Section 7.2.

  • Bulk Product means Licensed Product supplied in a form other than Finished Product which can be converted into Finished Product.

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Milk product or "dairy product" means cottage cheese, dry curd cottage cheese, reduced fat cottage cheese, lowfat cottage cheese, cream, light cream, light whipping cream, heavy cream, heavy whipping cream, whipped cream, whipped light cream, sour cream, acidified sour cream, cultured sour cream, half-and-half, sour half-and-half, acidified sour half-and-half, cultured sour half-and-half, reconstituted or recombined milk and milk products, concentrated milk, concentrated milk products, skim milk, lowfat milk, frozen milk concentrate, flavored milk, eggnog, buttermilk, cultured milk, cultured lowfat milk, cultured skim milk, yogurt, lowfat yogurt, nonfat yogurt, acidified milk, acidified lowfat milk, acidified skim milk, low-sodium milk, low-sodium lowfat milk, low-sodium skim milk, lactose-reduced milk, lactose-reduced lowfat milk, lactose-reduced skim milk, aseptically processed and packaged milk, milk products with added safe and suitable microbial organisms, and any other milk product made by the addition or subtraction of milkfat or addition of safe and suitable optional ingredients for protein, vitamin, or mineral fortification. Unless a product is considered a milk product under this subdivision, milk product does not include dietary products, infant formula, ice cream or other desserts, cheese, or butter. Milk products include the following: