Verification Product definition

Verification Product means either (i) a combination of a DVD Decryption Module with a (1) DVD Drive and (2) tape drive and/or hard disk and/or second DVD Drive into a single physical unit which is intended to facilitate the manufacture of CSS Compliant discs by allowing the contents of a DVD Disc to be compared to the unscrambled contents of a tape or hard disk based image or another DVD Disc, and which does not allow the transmission of any unscrambled content in digital or analog form to any external output or connection (“Type 1 Verifier”); or (ii) a combination of an Authenticator and Scrambler, with (1) a tape drive and/or DVD Drive and/or a hard disk, and (2) a second DVD Drive, and/or floppy disk drive into a single physical unit which is intended to facilitate the manufacture of CSS Compliant DVD Discs by allowing the scrambled contents of a DVD Disc to be compared to the scrambled contents of a tape or DVD Disc, and which does not allow the transmission of unscrambled content in digital or analog form to any external output or connection (“Type 2 Verifier”)
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Verification Product means any Product that employs or is in any way produced by the practice of an invention claimed in the Verification Patents (whether issued or pending), except claim #6 of the U.S. Verification Patent and the equivalent claim(s) in any foreign application, or any Product that would otherwise constitute infringement of any claims of the Verification Patents (whether issued or pending), except claim #6 of the U.S. Verification Patent and the equivalent claim(s) in any foreign application.
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Verification Product has the meaning set forth in the Recitals.
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Examples of Verification Product in a sentence

  • Licensee shall timely provide Licensor with the name and address of each person to whom a Verification Product is sold, leased, or otherwise made available.

  • Pursuant to the applicable Technical Specifications, Licensor shall disclose to Verification Product Manufacturers the following: (i) the Disc Key Recovery Logic; (ii) the Title Key Recovery Algorithm; (iii) the Content Scrambling Algorithm; (iv) the CSS Authentication Algorithm; (v) the Authentication Key, (vi) the control method of the Descrambler Module; and (vii) the control method of the Authenticator Module.

  • A Verification Product shall additionally conform to the CSS Procedural Specifications pertaining to Software Authentication and Descrambling set forth in Section 6.2.4.

  • In consideration for the provision set forth above, Client will pay Fidelity the amounts set forth in Attachment 1 attached hereto after the Implementation Date of the Signature Verification Product.

  • Swaminathan joined Williamson &Magor Group ( to which this Company belongs ) in 1982 as its Company Secretary.

  • Fidelity will run the update cycle for the Signature Verification Product [***].

  • Client agrees to accept full responsibility for the payment of all instruments, whether or not the instrument passed the scrutiny of the Signature Verification Product and Client will indemnify, defend and hold harmless Fidelity against any claim made by any person that is based on Fidelity’s providing access to and use of the Signature Verification Product.

  • Client acknowledges that Fidelity does not employ experts in detecting fraud and that use of the Signature Verification Product will not eliminate the risk or exposure to fraud that is inherent in Client’s business.

  • Client acknowledges that Fidelity does not employ experts in detecting fraud and that use of the Signature Verification Product will not eliminate the risk or exposure to fraud that is inherent in Client's business.

  • Some of our products, such as the Verification Product, require consent from the end-user.

Related to Verification Product

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

  • Collaboration Product means a pharmaceutical product containing or comprising Compound in any dosage form alone, or in combination with, one or more other pharmaceutically active ingredients, and any and all Improvements thereto.

  • Licensed Product means a product or part of a product in the Licensed Field of Use: (A) the making, using, importing or selling of which, absent this license, infringes, induces infringement, or contributes to infringement of a Licensed Patent; or (B) which is made with, uses or incorporates any Technology.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Approved Product means any water fitting, plumbing product, material or component which is the subject of an existing WRAS Approval;

  • Licensed Products means tangible materials which, in the course of manufacture, use, sale, or importation, would be within the scope of one or more claims of the Licensed Patent Rights that have not been held unpatentable, invalid or unenforceable by an unappealed or unappealable judgment of a court of competent jurisdiction.

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

  • Reference biological product means the single biological product licensed pursuant to 42 U.S.C.

  • Final Product means a reasonably homogenous cannabis product in its final packaged form created using the same standard operating procedures and the same formulation.

  • Diagnostic Product means any test or assay for diagnosing or detecting a disease, disorder, medical condition, or symptom.

  • 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:

  • Field means all fields of use.

  • Royalty Product means, either (a) an Alnylam Royalty Product, or (b) an Inex Royalty Product.

  • Batch means a specific quantity of Product that is intended to be of uniform character and quality, within specified limits, and is produced during the same cycle of Manufacture as defined by the applicable Batch Record.

  • Hemp product means the same as that term is defined in § 3.2-4112.

  • 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.

  • Royalty-Bearing Product means (a) any Product that is not a Co-Developed Product and (b) any Co-Developed Product to the extent sold outside of the Co-Development Territory.

  • Assay means a laboratory analysis of Crude Petroleum to include the following: A.P.I. Gravity, Reid vapor pressure, composition, pour point, water and sediment content, sulfur content, viscosity, distillation, hydrogen sulfide, flash/boiling point and other characteristics as may be required by Carrier.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

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

  • Licensed producer means an agent, broker, or reinsurance intermediary licensed pursuant to the applicable provision of the insurance law of any jurisdiction.

  • Product Inventory means all inventory of the Product owned by Seller or its Affiliates as of the Closing, including raw materials, work-in-process, bulk form drug and finished Product.

  • Drug sample means a unit of a prescription drug that is not intended to be sold and is intended to promote the sale of the drug.

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority‑approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.