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. 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. 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. 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. 7.1 SUBSTITUTIONS. SWD may, from time to time and without notice to GOA, make substitutions and modifications to the Products, provided such substitutions and modifications will not materially affect the form, fit, functions, features or performance of the Products.
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.
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. During the Term of this Agreement, Manufacturer shall not, and Licensor 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 Licensee. A “Material Change” is defined as any change that:
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:
