Quality Standards and Control Sample Clauses

Quality Standards and Control. (a) The parties acknowledge that the Trademarks licensed hereunder have established valuable goodwill and that it is important to the parties that this valuable goodwill and reputation be preserved. Accordingly, the parties agree that the products with which the Licensed Trademarks are used by a party or its Affiliates, as Licensee, shall for the term of the respective Trademark license meet quality standards that are substantially equivalent to or higher than those standards maintained by Kraft Foods Inc. and its Subsidiaries immediately prior to the Distribution Date. Each party covenants and agrees that all of its and its Affiliates’ activities in connection with such Trademarks licensed to it by the other party will be conducted in conformity with all applicable Laws. In case a Licensed Trademark is used as an ingredient indicator on the packaging of a certain product, the Licensee shall purchase the indicated ingredient(s) from the Licensor or one of its Affiliates, or from a company designated and approved by the Licensor or one of its Affiliates.
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Quality Standards and Control. Licensee, on behalf of itself and its subsidiaries, represents, warrants and covenants that at all times during the term of this Agreement any advertising and promotional materials shall be used in accordance with such quality standards and specification as may be established by Licensor and communicated to Licensee from time to time, or upon which the Parties may agree from time to time (the “Quality Standards”) and any Applicable Requirements, and Licensee and its subsidiaries shall not use the Trademarks in a way that diminishes or is detrimental to Licensor’s rights in the Trademarks or the goodwill associated therewith (the “Goodwill”). Licensee and its subsidiaries shall not produce or use any advertising or promotional materials (including materials for websites) bearing the Trademarks other than those which are substantially the same as those in existence as of the date of this Agreement without obtaining the prior written approval of Licensor, such approval not to be unreasonably withheld or delayed.
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Quality Standards and Control. Licensee agrees that use of the Marks by Licensee in association with any products or services (the “Products” and “Services”) will meet or surpass the standards set by Licensor and conveyed to Licensee from time to time for the character and quality of such Products and Services.
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Quality Standards and Control. 7.1 KCI agrees that the Licensed Products shall be of high quality and of such style, appearance, and distinctiveness as will preserve and protect the prestige of the Licensed Marks and the goodwill represented and symbolized thereby; that such Licensed Products will be manufactured, packaged, marketed, advertised, promoted, distributed and sold in accordance with applicable laws and the directions which may be communicated by Hampton from time to time under this Agreement; and that KCI shall not deviate from the quality, standards and manufacturing specifications of the Licensed Products unless it obtains prior written consent from Hampton. As stated above, the LPAG shall govern the approval and regulation of the quality of the Licensed Products under this Agreement. Further, KCI agrees to market, advertise and promote the Licensed Products using such high standards that will preserve and protect the prestige of the Licensed Marks.
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Quality Standards and Control. 2.1 Each LICENSEE covenants that it will ensure that the Licensed Products and Licensed Use are maintained at a level of a quality at least equal to the quality maintained by CULLIGAN immediately prior to the Effective Date hereof (the “Quality Standards”).
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Quality Standards and Control. (a) Licensee agrees to comply fully both with the terms of this Agreement and with all such requirements for the use of the Intellectual Properties as Licensor may communicate to Licensee, from time to time, in its discretion. Should Licensor wish to make any changes to previously approved goods and services, it shall submit, at its own expense, a sample of the changed goods or services in the same manner for Licensee’s written approval prior to any advertising, sale or distribution.
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Quality Standards and Control 
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Related to Quality Standards and Control

  • Quality Standards Each Party agrees that the nature and quality of its products and services supplied in connection with the other Party's Marks will conform to quality standards set by the other Party. Each Party agrees to supply the other Party, upon request, with a reasonable number of samples of any Materials publicly disseminated by such Party which utilize the other Party's Marks. Each Party will comply with all applicable laws, regulations, and customs and obtain any required government approvals pertaining to use of the other Party's marks.

  • Quality Requirements Performance Indicator Heading Indicator (specific) Threshold Method of Measurement Frequency of monitoring Consequence of Breach QUALITY Patient Safety - Incidents I1 Number of incidents Adverse incidents include the following: clinical or non clinical adverse events that have potential to cause avoidable harm to a patient, including medical errors or adverse events related to medical devices or other equipment. Clinical or non- clinical accidents, accidental injuries to staff and members of the public, verbal, physical or psychological abuse or harassment, unusual or dangerous occurrences, damage to trust property, plant or equipment, fire or flood, security, theft or loss, near misses are identified as any event where under different circumstances significant injury or loss may have occurred Number of recorded incidents in the contract month Monthly Remedial Action Plan brought to Performance Meeting following breach; action under Module C Clause 32 if needed I2 Number of Sis Definition of SUI according to trust policy and national guidance Number of Serious Untoward Incidents reported in contract month Monthly Remedial Action Plan brought to Performance Meeting following breach; action under Module C Clause 32 if needed S1 Percentage of eligible staff received child safeguarding training at level 2 (as identified in LSCB training strategy) 95% Number received training/ Number of identified staff requiring training Monthly S2 Percentage of eligible staff received adult safeguarding awareness training at level 2 ( as identified in K&M Safeguarding Vulnerable Adults training strategy) 95% Number of staff trained/ Number of identified staff requiring training Monthly

  • Quality Specifications SANMINA-SCI shall comply with the quality specifications set forth in its Quality Manual, incorporated by reference herein, a copy of which is available from SANMINA-SCI upon request.

  • Service Level Standards In addition to all other requirements in this Agreement, and in accordance with the Best Claims Practices & Estimating Guidelines, Vendor shall use reasonable and good faith efforts to meet the Service Level Standards set forth below.

  • Clinical Data and Regulatory Compliance The preclinical tests and clinical trials, and other studies (collectively, “studies”) that are described in, or the results of which are referred to in, Registration Statement, the Pricing Disclosure Package or the Prospectus were and, if still pending, are being conducted in all material respects in accordance with applicable laws, rules, regulations and policies of the Food and Drug Administration of the U.S. Department of Health and Human Services (the “FDA”) or any committee thereof or of any other U.S. or foreign government or drug or medical device regulatory agency, or health care facility Institutional Review Board; each description of the results of such studies is accurate and complete in all material respects and fairly presents the data derived from such studies, and the Company and its subsidiaries have no knowledge of any other studies the results of which are materially inconsistent with, or otherwise call into question, the results described or referred to in the Registration Statement, the Pricing Disclosure Package or the Prospectus; for such studies that have been or are being conducted, the Company and its subsidiaries have made all such filings and obtained all such approvals as may be required by foreign government or drug or medical device regulatory agencies, or foreign health care facility Institutional Review Boards; and no investigational new drug application filed by or on behalf of the Company or any of its subsidiaries with the FDA has been terminated or suspended by the FDA, and neither the FDA nor any applicable foreign regulatory agency has commenced, or, to the knowledge of the Company, threatened to initiate, any action to place a clinical hold order on, or otherwise terminate, delay or suspend, any proposed or ongoing studies conducted or proposed to be conducted by or on behalf of the Company or any of its subsidiaries.

  • Technical Specifications The Technical Specifications furnished on the CD are intended to establish the standards for quality, performance and technical requirements for all labor, workmanship, material, methods and equipment necessary to complete the Work. When specifications and drawings are provided or referenced by the County, these are to be considered part of the Scope of Work, and to be specifically documented in the Detailed Scope of Work. For convenience, the County supplied specifications, if any, and the Technical Specifications furnished on the CD.

  • Technical Requirements 2.7.4.1 The NID shall provide an accessible point of interconnection and shall maintain a connection to ground.

  • Service Standards We provide the Services materially in accordance with the features and functionalities set out in the Specification Documents. We will use commercially reasonable efforts to make the Services available to you subject to operational requirements including maintenance and security.

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