Changes to Product Sample Clauses
The "Changes to Product" clause defines the process and conditions under which modifications can be made to the product specified in the agreement. Typically, this clause outlines who has the authority to request or approve changes, the procedures for documenting and implementing such changes, and any requirements for mutual consent or additional costs. For example, it may allow the supplier to update product specifications due to regulatory changes or technological improvements, provided the customer is notified in advance. The core function of this clause is to provide a clear framework for managing product updates or alterations, thereby reducing disputes and ensuring both parties are aware of their rights and obligations when changes occur.
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Changes to Product. If required by settlement or court order, or if deemed reasonably necessary in response to a Provider Covered Claim, Provider may: (a) obtain the right for Customer to continue using the Product; (b) replace or modify the affected component of the Product without materially reducing the general functionality of the Product; or (c) if neither (a) nor (b) are reasonable, terminate the affected Order Form and issue a pro-rated refund of prepaid fees for the remainder of the Subscription Period.
Changes to Product. SMART reserves the right to make substitutions and/or modifications in the Product specifications provided that (i) such substitutions and/or modifications do not cause a material adverse effect on the Product's overall performance, and (ii) WATCHGUARD has been notified thereof. WATCHGUARD reserves the right to specify modifications to the Product from time to time and, consistent with the Statement of Work, SMART agrees to incorporate such modifications. The parties shall negotiate in good faith any price, schedule and other business issues that result from such modifications.
Changes to Product. Supplier reserves the right, without any liability whatsoever, to modify any Product to the extent that such modification is mandated by a Regulatory Authority or, to the extent approved by Purchaser in writing prior to the implementation of such modification (which approval shall not be unreasonably withheld, conditioned or delayed), does not require additional or independent regulatory approval.
Changes to Product. Following Aphria Diamond’s Acceptance of a Purchase Order, Aphria Diamond will not make any change to any Products which are included in such Purchase Order or the production process in respect of any Products which are included in such Purchase Order unless: (i) such change is required by the Canadian Regulatory Authority or Applicable Laws and Aphria Diamond has provided reasonable detail to Aphria in respect of such change, including whether any such change would result in an increase or decrease in the purchase price of such Product (a “Required Change”); or (ii)(a) such change is proposed by Aphria Diamond in order to maintain or improve the quality of any Product; (b) Aphria Diamond has provided reasonable detail to Aphria in respect of such change, including whether any such change would result in an increase or decrease in the purchase price of such Product; and (c) Aphria Diamond has obtained the prior written consent of Aphria for such change, which consent may be withheld in Aphria’s sole discretion (an “Optional Change”). Upon adoption of any Required Change or any Optional Change, such Required Change or Optional Change, as the case may be, shall become part of the Specifications for such Product. Aphria shall solely bear the costs associated with any Required Change or any Optional Change.
Changes to Product. ABI shall notify SYNOVA in writing at least ninety (90) days prior to any proposed changes in its manufacturing procedures, materials, equipment used or processes, which effect Product fit, form or function. ABI has the absolute right to change the Product and to unilaterally amend the Specifications to reflect any such change; provided, however, SYNOVA may immediately cancel any outstanding purchase orders if such changes are unacceptable to SYNOVA. SYNOVA shall in no way modify, alter or change the Product. In addition, SYNOVA shall not repackage any Product unless ABI has agreed to such repackaging in writing and signed by ABI.
Changes to Product. BioPad shall notify Synova in writing at least sixty (60) days prior to any proposed changes in its manufacturing procedures, materials, equipment used or processes, which effect Licensed Product fit, form or function. BioPad shall not make any changes to any Licensed Product that would require a new, amended, or updated 510(k) registration with the FDA. Unless approved in advance by Synova, which approval will not be withheld unreasonably, BioPad shall not make any change to the Licensed Products that requires Synova to incur additional effort, cost, or expense or otherwise negatively impacts Synova. Without limiting the foregoing, if any change to BioPad's manufacturing procedures, materials, equipment used or processes, if implemented, likely would materially change any Licensed Product or Synova's rights or obligations under this Agreement, Synova shall have the right to terminate this Agreement immediately upon thirty (30) days' advance written notice to BioPad.
Changes to Product. SPECIFICATIONS
Changes to Product. 9.1 Any changes to the Product proposed by Philips shall be discussed and handled by the Parties as described in the Quality Agreement. Until execution of the Quality Agreement, the provisions of this clause 9 shall apply.
9.2 Philips shall be entitled to make changes to the Products to comply only with any applicable Laws. Without prejudice to the foregoing, it is understood and agreed that Customer (and not Philips) shall be responsible to notify Philips of any changes required to comply with any applicable Laws, as long as such applicable Laws concern the Products.
9.3 Customer may reasonably request and Philips may propose, in writing, that Philips makes a change to the method of packing, a change to the packaging, or the Products. Such request or proposal (as applicable) will include a description of the requested/proposed change sufficient to allow Philips, using commercially reasonable efforts, to evaluate the feasibility and impact on costs and other terms of such requested change, it being understood that Customer shall pay for any reasonable incremental and documented costs incurred by Philips in connection with such evaluation. All such changes are subject to Philips’s written approval (and in case of a change proposal by Philips, Customer’s written approval), which cannot unreasonably withheld, conditioned or delayed, it being understood that, if technically feasible and commercially reasonable, Philips shall make any changes required to comply with any applicable Laws upon Customer’s written request. Philips will not be obligated to agree or accept any such request for a change nor to proceed with the requested change until the Parties have mutually agreed upon the changes to the Product’s Specifications, the price, the implementation costs to be borne by Customer including, without limitation, development and other non-recurring expenses, the cost of inventory and materials that may become obsolete, and any other terms of this Agreement.
9.4 The incremental and documented costs of any changes (including any non-recurring costs such as development and re-engineering costs, as well as costs of changes to the tools used to manufacture the changed Products) shall be borne by Customer. All such charges will be charged to Customer at cost, without any additional markup.
Changes to Product. During the Term of this Agreement, Manufacturer shall not, and Oculus shall cause Manufacturer not to, implement any Material Changes (see definition below) relating to the Product for purposes of this Agreement without the prior written consent of More Pharma. A “Material Change” is defined as any change that:
Changes to Product. Supplier shall not make changes or alterations to Products supplied to Logitech or to any materials or processes that may directly or indirectly affect Products supplied to Logitech without prior written notification to, and acceptance from, the Logitech Quality Representative. This includes, but is not limited to, changes in Product design, manufacturing processes, test processes, quality control processes, and components or subassemblies used by Supplier or their sub-contractors. Any changes made by Supplier may require requalification of the Products as outlined in Section 3.0 below, Product Qualification, and Supplier shall be liable for all expenses incurred for Product requalification.