Correction of Nonconformities Sample Clauses

Correction of Nonconformities. In consideration of the ELF and MF, and subject to the terms of this Agreement, upon written notification by Customer of a Nonconformity in the most current Release of the MPOWER Software or in the one prior Release immediately preceding the most current Release of the MPOWER Software, MPOWER will analyze the Nonconformity and notify Customer of its estimate of when and how such Nonconformity will be corrected or any Workaround provided and MPOWER. shall use commercially reasonable efforts to correct such Nonconformity in accordance with the procedures and priorities established in Exhibit 1 under Help Desk. Notwithstanding the prior sentence, MPOWER's sole obligation hereunder shall be limited to correcting identified and reproducible Nonconformities in the Shelf Version of the MPOWER Software in accordance with Section 4 herein and the relevant portions of Exhibit 1 which deal with Definitions, Support and Time Frame for Resolution of issues logged through the MPOWER Help Desk.
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Correction of Nonconformities. After Company receives a Rejection Notice, the Parties will meet and confer to agree in good faith upon the timing schedule by which Company will perform additional Services to remedy the nonconformities set forth in the Rejection Notice and the applicable additional charges associated therewith, if any. When Company remedies the nonconformities, Company will redeliver the deliverable to Client and Client will again review the deliverable for acceptance or rejection in accordance with this Section 3.
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Correction of Nonconformities. BMS shall promptly notify 3DP, in writing or by telephone (confirmed in writing), of any nonconformity in the 3DP Interfaces. 3DP will respond to and correct any confirmed nonconformities in the 3DP Interfaces within a reasonable time and as prioritized by the Program Directors.
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Correction of Nonconformities. After Company receives a Rejection Notice, the Parties will confer to agree in good faith upon (a) whether a nonconformity exists; (b) if so, the timing schedule by which Company will perform additional Services to remedy the nonconformities set forth in the Rejection Notice; and (c) the applicable additional charges associated therewith, if any. When Company remedies the nonconformities, Company will redeliver the Deliverable to Client and Client will again review the Deliverable for acceptance or rejection in accordance with this Section 3 and the time periods contained in Sections 3.2 and 3.3.
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Correction of Nonconformities. 3. Licensee shall notify ISO via entry into the AscendantOne online issue tracking system (‘Issues’) of Nonconformities. In addition, after logging Severity 1 Issues (only) in the online tracking system, Licensee will contact the ISO Help Desk via telephone to receive acknowledgement that the Issue has been received. In order for ISO replicate the Issue, Licensee shall prepare and provide to ISO process documentation, files, databases and all such other data to permit ISO to simulate conditions similar to that present when the Nonconformity was discovered. ISO shall act in good faith to initiate and prosecute corrective measures for Nonconformities involving the Product.
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Correction of Nonconformities. After GREEN DISTRICT MEDIA receives a Rejection Notice, the parties will meet and confer to agree in good faith upon the timing schedule by which GREEN DISTRICT MEDIA will perform additional Services to remedy the nonconformities set forth in the Rejection Notice and the applicable additional charges associated therewith, if any. When GREEN DISTRICT MEDIA remedies the nonconformities, GREEN DISTRICT MEDIA will redeliver the deliverable to Client and Client will again review the deliverable for acceptance or rejection in accordance with this Section 3.
Sample 1
Correction of Nonconformities. At Supplier’s expense, Supplier must Cure any Nonconformity within the Correction Period. If Supplier fails to Cure any Nonconformity within the Correction Period, CELLCENTRIC may give notice to Supplier that CELLCENTRIC reasonably believes that Supplier will not or cannot Cure, and demand assurances by a specific date of Supplier’s ability and willingness to Cure by a specific date. If Supplier fails to provide assurances reasonably satisfactory to CELLCENTRIC by the specified date, CELLCENTRIC may exercise its termination rights under Section 3.3 of this Agreement.
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Related to Correction of Nonconformities

  • Correction of Defects 35.1 The Engineer shall give notice to the Contractor of any Defects before the end of the Defects Liability Period, which begins at Completion and is defined in the Contract Data. The Defects Liability Period shall be extended for as long as Defects remain to be corrected.

  • Correction of Errors Contractor shall perform, at its own cost and expense and without reimbursement from the District, any work necessary to correct errors or omissions which are caused by the Contractor’s failure to comply with the standard of care required herein.

  • Latent Defects Notwithstanding anything to the contrary set forth herein, no acceptance, or deemed acceptance, by City pursuant to this Section shall be applicable with respect to any Latent Defects. An acceptance, or deemed acceptance, by City pursuant to this Section shall not mean that City has accepted, or the other party has been relieved of, responsibility for: (i) compliance with the Laws; (ii) the proper application of construction means or methods; or (iii) correcting any portion of the Project if it later is determined that any portion of the Project is inconsistent with the Final Documents and Drawings.

  • Notification of Material Events The Company, during the period when the Prospectus is (or but for the exemption in Rule 172 would be) required to be delivered under the 1933 Act or the 1934 Act, shall notify the Representatives of the occurrence of any material events respecting its (including those of the Operating Partnership) activities, affairs or condition, financial or otherwise, if, but only if, as a result of any such event it is necessary, in the opinion of counsel, to amend or supplement the Prospectus in order to make the Prospectus not misleading in the light of the circumstances existing at the time it is (or but for the exemption in Rule 172 would be) delivered to a purchaser, and the Company will forthwith supply such information as shall be necessary in the opinion of counsel to the Company and the Underwriters for the Company to prepare any necessary amendment or supplement to the Prospectus so that, as so amended or supplemented, the Prospectus will not contain an untrue statement of a material fact or omit to state a material fact necessary in order to make the statements therein, in the light of the circumstances existing at the time it is (or but for the exemption in Rule 172 would be) delivered to a purchaser, not misleading.

  • Supply of Materials The following materials will be supplied by the department Name of Materials Rate. Place of delivery 1.

  • Corrections There may be information on the Site that contains typographical errors, inaccuracies, or omissions, including descriptions, pricing, availability, and various other information. We reserve the right to correct any errors, inaccuracies, or omissions and to change or update the information on the Site at any time, without prior notice.

  • Notification of Material Changes The Advisor also agrees to give the Company prior written notice of any proposed material change in its Trading Approach and agrees not to make any material change in such Trading Approach (as applied to the Company) over the objection of the Company, it being understood that the Advisor shall be free to institute non-material changes in its Trading Approach (as applied to the Company) without prior written notification. Without limiting the generality of the foregoing, refinements to the Advisor’s Trading Approach and the deletion (but not the addition) of Commodities (other than the addition of Commodities then being traded (i) on organized domestic commodities exchanges, (ii) on foreign commodities exchanges recognized by the Commodity Futures Trading Commission (the “CFTC”) as providing customer protections comparable to those provided on domestic exchanges or (iii) in the interbank foreign currency market) to or from the Advisor’s Trading Approach, shall not be deemed a material change in the Advisor’s Trading Approach, and prior approval of the Company shall not be required therefor. The utilization of forward markets in addition to those enumerated in the Advisor’s Disclosure Document attached hereto as Exhibit C would be deemed a material change to the Advisor’s Trading Approach and prior approval shall be required therefor. Subject to adequate assurances of confidentiality, the Advisor agrees that it will discuss with the Company upon request any trading methods, programs, systems or strategies used by it for trading customer accounts which differ from the Trading Approach used for the Company, provided that nothing contained in this Agreement shall require the Advisor to disclose what it deems to be proprietary or confidential information.

  • Non-Conforming Product If Reliant notifies Cardinal Health during the Review Period that the Manufacturing Sample does not conform to the warranty set forth in Section 13.1 and Cardinal Health agrees with Client’s determination, Client shall not be responsible to pay for such batch (the “Defective Product”), and Cardinal Health shall, at Reliant’s option, either (A) replace any Batch of non-conforming Product, or (B) credit any payments made by Reliant for such Batch. If Cardinal Health does not agree with Reliant’s determination that such Product fails to meet the warranty set forth in Section 13.1, then after reasonable efforts to resolve the disagreement, the Parties shall cause a mutually acceptable independent third party to review records, test data and to perform comparative tests and/or analyses on the Manufacturing Sample. The results of the independent review shall be final and binding. Unless otherwise agreed to by the Parties in writing, the costs associated with such testing and review shall be borne by the non-prevailing Party. THE OBLIGATION OF CARDINAL HEALTH TO (A) REPLACE DEFECTIVE PRODUCT IN ACCORDANCE WITH THE SPECIFICATIONS OR CREDIT PAYMENTS MADE BY RELIANT FOR DEFECTIVE PRODUCT AND (B) REIMBURSE RELIANT FOR API LOST IN THE DEFECTIVE BATCH, SUBJECT TO THE LIMITATIONS IN ARTICLE 15.1, SHALL BE RELIANT’S SOLE AND EXCLUSIVE REMEDY (WITHOUT PREJUDICE TO ANY INDEMNIFICATION OBLIGATIONS UNDER SECTION 14.1 OR THE OBLIGATIONS OF SECTION 10.6 (RECALL)) UNDER THIS ARTICLE FOR DEFECTIVE PRODUCT AND IS IN LIEU OF ANY OTHER WARRANTY, EXPRESS OR IMPLIED.

  • Defective Product Seller must guarantee a return for all defective products. a) Goods rejected by Buyer for whatever reason shall be held, transported and/or stored at Seller’s sole expense. Seller shall promptly reimburse Buyer for any such expenses. B) Defective product purchase COD will be returned COD to Seller or COD check will be cancelled, at Buyer’s discretion. c) Seller is responsible for all costs associated RoHS noncompliance returns and will accept a full return for all parts not meeting RoHS compliance criteria if necessary. d) Seller is 100% responsible for all monetary and/or rework costs associated with product failures in addition to any further cost whatsoever associated with product failures. e) If suspect parts/counterfeit parts are furnished under this agreement such parts shall be impounded by Buyer. Buyer may provide a sample batch Supplier for verification and authentication. In addition, Buyer reserves the right to send such items to the appropriate manufacturer and appropriate authorities for investigation. f) Seller shall be liable for all costs relating to impound, investigation, removal, or replacement of suspect/counterfeit parts.

  • Return of Materials at Termination In the event of any termination or cessation of his employment with Employer for any reason, Employee shall promptly deliver to Employer all documents, data and other information derived from or otherwise pertaining to Confidential Information. Employee shall not take or retain any documents or other information, or any reproduction or excerpt thereof, containing any Confidential Information.

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