Licensed Certification Mark definition

Licensed Certification Mark means the Certification Mark identified in the Certificate and Licence;
Licensed Certification Mark means the specific Certification Mark licensed pursuant to this Certification Mark License Agreement;

Examples of Licensed Certification Mark in a sentence

  • The costs and benefits of such proceedings will be borne by Xxxxxxxx as owner of the Logo and Licensed Certification Mark.

  • You will not, at any time, whether during or after termination of this Agreement, use Bonsucro Logo and/or Licensed Certification Mark as part of your corporate, business or trading name or style nor will you apply for or obtain registration of the Logo and/or Licensed Certification Mark or any confusingly similar mark or logo for any goods or services in any country of the world.

  • You agree to use the Logo & Licensed Certification Mark (and any associated claims wording) only in the manner outlined in Xxxxxxxx’s Claims & Labelling Rules (as may be amended from time to time), and if for any other use, in the manner approved in advance and in writing by Xxxxxxxx.

  • Ensure that any claims wording associated with the Logo and/or Licensed Certification Mark is approved in writing by Xxxxxxxx in advance.

  • You acknowledge that any goodwill or other interests or rights that arise as a result of your use of the Logo and/or Licensed Certification Mark or any other intellectual property rights, as expressly permitted under this Agreement or any other agreement between the Parties, shall inure solely to the benefit of Bonsucro and you hereby assign and convey such goodwill and other interests and rights to Bonsucro without the payment of any consideration.

  • Xxxxxxxx will in its absolute discretion decide whether any proceedings will be instituted or defended in relation to the Logo and/or Licensed Certification Mark and will have the exclusive conduct of any such proceedings.

  • Upon termination of this Agreement, you shall fully and as promptly as reasonably practicable cease all use of the Logo and/or Licensed Certification Mark, and shall, at the option of Bonsucro, as promptly as reasonably practicable, destroy all materials related to such Logo and/or Licensed Certification Mark, and certify to Bonsucro such destruction.

  • The issue of the Licence does not restrict QCS(E)’s right to use or license the use of the Licensed Certification Mark to any other person.

  • You agree to use the Licensed Certification Mark (and any associated claims wording) only in the manner outlined in Xxxxxxxx’s Claims & Labelling Document (as may be amended from time to time), and if for any other use, in the manner approved in advance and in writing by Xxxxxxxx.

  • Ensure that any claims wording associated with the Licensed Certification Mark is approved in writing by Xxxxxxxx in advance.

Related to Licensed Certification Mark

  • certification mark means a mark used in connection with the goods or services of a person other than the certifier to indicate geographic origin, material, mode of manufacture, quality, accuracy, or other characteristics of the goods or services or to indicate that the work or labor on the goods or services was performed by members of a union or other organization.

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval (but excluding Pricing Approval) in any particular jurisdiction other than the U.S.

  • Client Application means an application developed by Licensee that a) utilizes the Runtime Product, b) is installed fully on an end user’s machine, with all report processing local to that machine, and c) adds significant and primary functionality to the Runtime Product.

  • Licensed Application means an Application that (a) meets and complies with all of the Documentation and Program Requirements, and (b) has been selected and digitally signed by Apple for distribution, and includes any additional permitted functionality, content or services provided by You from within an Application using the In-App Purchase API.

  • Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Patent Application means an application for patent protection for a CRADA Subject Invention with the United States Patent and Trademark Office (“U.S.P.T.O.”) or the corresponding patent-issuing authority of another nation.

  • Non-Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Instructional materials means relevant instructional

  • Cannabis production establishment agent registration card means a registration card that the department issues that:

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • Instructional material means instructional content that is provided to a student, regardless of its format, including printed or representational materials, audio-visual materials, and materials in electronic or digital formats (such as materials accessible through the Internet). The term does not include academic tests or academic assessments.

  • Development Application means the development application identified in Item 5 of Schedule 1 and includes all plans, reports models, photomontages, material boards (as amended supplemented) submitted to the consent authority before the determination of that Development Application.

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.

  • Diagnostic source assembly means the tube housing assembly with a beam-limiting device attached.

  • Brand Name Specification means a specification limited to one or more items by manufacturers’ names or catalogue number.

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Federal work authorization program means any of the electronic verification of work authorization programs operated by the United States Department of Homeland Security or any equivalent federal work authorization program operated by the United States Department of Homeland Security to verify information of newly hired employees, pursuant to the Immigration Reform and Control Act of 1986 (IRCA), D.L. 99-603.

  • L/C Application means an application and agreement for the issuance or amendment of a Letter of Credit in the form from time to time in use by the L/C Issuer.

  • DMF means a drug master file and all equivalents, and related proprietary dossiers, in any country or jurisdiction in the Territory (including any active substance master file in the EMA) for API submitted or to be submitted by a Party to Regulatory Authorities.

  • Contractor Materials means Materials owned or developed prior to the provision of the Work, or developed by Contractor independently from the provision of the Work and without use of the JBE Materials or Confidential Information.

  • Central Contractor Registration (CCR) database means the primary Government repository for Contractor information required for the conduct of business with the Government.

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

  • Commercial applicator means a person who, by contract or for hire, engages in the

  • Biosimilar Application has the meaning set forth in Section 7.3.3.

  • 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.

  • Pharmacist preceptor or “preceptor” means a pharmacist licensed to practice pharmacy whose license is current and in good standing. Preceptors shall meet the conditions and requirements of rule 657—4.9(155A). No pharmacist shall serve as a preceptor while the pharmacist’s license to practice pharmacy is the subject of disciplinary sanction by a pharmacist licensing authority.