Product Notices. Company shall monitor adverse event and other failure reports or complaints and promptly advise Saint Luke’s of information indicating a significant trend of adverse events, consumer or practitioner complaints, or failures or injuries related to the use of the Products. Company agrees to send all Product notices (inclusive of notices of any changes affecting the Products and notices of new products) to Saint Luke’s. Company will promptly provide Saint Luke’s (via letter, e-mail or other similar form of communication) with any and all information regarding any routine backorders of Products, Product changes, Product packaging changes, safety announcements, and clinical information regarding Products. Company shall immediately provide Saint Luke’s with a copy of all communications from Company and/or the FDA advising of a recall, request for a recall, market withdrawal, safety alert, or a non-routine issue of Product availability (e.g. significant backorders of Products). Company shall provide Saint Luke’s with written notice of any Class I recall, whether voluntary or initiated by the FDA, affecting any of the Products within twenty-four (24) hours of Company’s receipt of any such request for a recall, or shorter period of time provided in the recall strategy. Company shall reimburse Saint Luke’s for any costs actually incurred by Saint Luke’s in complying with any recall instructions and processes provided by Company. In addition, Company shall, at no additional cost to Saint Luke’s, replace any such Products which are the subject of a recall with Company products which have been approved by Saint Luke’s as being clinically equivalent to the recalled products.
12.3.1 In the event Products are required to be modified to comply with any regulatory or safety standards imposed or implemented for such Product, Company shall, for Products previously purchased by Saint Luke’s hereunder, at no cost to Saint Luke’s provide hardware modifications necessary for the Products to meet all such regulatory requirements or shall exchange the Products for new Products that comply with the new requirements.
Product Notices. A. Any notice given under this Agreement shall be in writing and will be effective when delivered personally or deposited in the mail, postage prepaid and addressed to the parties at their respective addresses set forth below, or at any new address subsequently designated in writing by either party to the other: If to Seller: If to Buyer: APEX PC SOLUTIONS, INC. COMPAQ COMPUTER CORPORATION 0000 000XX XXXXXX, XX P.O. BOX 692000 XXXXXXX, XX 00000 20555 S.H. 249 XXXXXXX, XXXXX 00000-0000 ATTN.: XXXXX SlRIANNI ATTN.: XXXX XXXXXXXX with a copy to: COMPAQ COMPUTER CORPORATION P.O. BOX 692000 20555 S.H. 249 XXXXXXX, XX 00000-0000 ATTN.: Division Counsel-Operations
Product Notices. Creative shall reproduce, and shall not remove, any copyright, trademark or other proprietary rights notices included in the Licensed Products. Creative shall not make any representations or warranties concerning the Licensed Products, except as set forth in End User Documentation and other materials provided by Licensor or as otherwise approved in writing by Licensor.
Product Notices. The Geotab Buyer agrees to review and ensure compliance with any and all applicable product warning, recall or similar notices which are intended for Geotab end users of the Geotab products or services made available on our the Geotab website; specifically, xxxxx://xxx.xxxxxx.xxx SELLER IN NO EVENT SHALL HAVE ANY LIABILITY WHATSOEVER FOR PAYMENT OF INCIDENTAL, CONSEQUENTIAL, INDIRECT OR SPECIAL DAMAGES, INCLUDING BUT NOT LMITED TO DAMAGES FOR LOSS OF PROFIT OR DAMAGES RESULTING FROM PERSONAL INJURY OR DEATH OR DAMAGE TO, OR LOSS OF USE OF ANY PROPERTY, INCLUDING BUT NOT LMITED TO ANY PRODUCT SOLD HEREUNDER. WIRELESS TERMS
Product Notices. Company shall monitor adverse event and other failure reports or complaints and promptly advise Saint Luke’s of information indicating a significant trend of adverse events, consumer or practitioner complaints, or failures or injuries related to the use of the Equipment. Company agrees to send all Equipment notices (inclusive of notices of any changes affecting the Equipment and notices of new Equipment) to Saint Luke’s. Company will promptly provide Saint Luke’s (via letter, e-mail or other similar form of communication) with any and all information regarding any routine backorders of Equipment, Equipment changes, Equipment packaging changes, safety announcements, and clinical information regarding Equipment. Company shall immediately provide Saint Luke’s with a copy of all communications from Company and/or the FDA advising of a recall, request for a recall, market withdrawal, safety alert, or a non-routine issue of Equipment availability (e.g. significant backorders of Equipment). Company shall provide Saint Luke’s with written notice of any Class I recall, whether voluntary or initiated by the FDA, affecting any of the Equipment within twenty-four (24) hours of Company’s receipt of any such request for a recall, or shorter period of time provided in the recall strategy. Company shall reimburse Saint Luke’s for any costs actually incurred by Saint Luke’s in complying with any recall instructions and processes provided by Company. In addition, Company shall, at no additional cost to Saint Luke’s, replace any such Equipment which are the subject of a recall with Company Equipment which has been approved by Saint Luke’s as being clinically equivalent to the recalled Equipment.
12.2.1 In the event Equipment is required to be modified to comply with any regulatory or safety standards imposed or implemented for such Equipment, Company shall, for Equipment previously purchased by Saint Luke’s hereunder, at no cost to Saint Luke’s provide hardware modifications necessary for the Equipment to meet all such regulatory requirements or shall exchange the Equipment for new Equipment that comply with the new requirements.
Product Notices. Seller agrees to send all Product notices (including without limitation recall notices and product availability notices), as well as notices of any other changes affecting the Products and notices of new Products, to each Participating Member with copies to Purchasing Partners. Seller shall provide Purchasing Partners written notice of any Class I FDA recall affecting any of the Products within three (3) business days of Seller’s receipt of any such recall. Seller shall provide Purchasing Partners written notice of any Class II or Class III FDA recall affecting any of the Products within five (5) business days of Seller’s receipt of any such recall. Further, Seller agrees to promptly notify Purchasing Partners and each Participating Member of any problems in the manufacture or production of any Products that affects Product quality and of any back-order situation that might affect Seller’s ability to meet Seller’s obligations under this Agreement. Upon Purchasing Partners’ request, Seller shall provide Purchasing Partners summaries of any FDA Form 483, regulatory letter, and/or warning letter relating to the Products and Seller’s response thereto.
Product Notices. 17.1. Any notice given under this Agreement shall be in writing and will be effective (i) when delivered, if delivered in person, (ii) during the business hour of receipt (or the next business hour if not received during a normal business hour), if by telecopy or (iii) 3 business days after depositing same in the U.S. mail, postage prepaid and addressed to Smart Modular at the address set forth below or to such other address as Smart Modular may specify to Compaq in accordance with this Section 17.1 or to Compaq at the address set forth below or at such other address as Compaq may specify to Smart Modular in accordance with this Section 17.1: If to Compaq: If to Smart Modular: ATTN.: Division Counsel — Operations Associate General Counsel
17.2. For the purpose of this Agreement Table 5: Contacts shall be used for determining point of contact. Table 5: Contacts Memory component pricing Order Processing / Verification Supplier allocation / weighted average price Product pricing Product qualification Approval for partial shipments Approved Vendor List Adjust Product Schedule Approval for spot market purchases Product Transportation Supplier commitments Customs Waiver for non-AVL product usage Invoice Reconciliation New Product Information (Spec, BOM, artwork, etc.) Smart Program Reviews DRAM Program Reviews
Product Notices. All uses by Kiniksa of the Existing Product Trademarks owned by Regeneron shall be accompanied by a statement that the Existing Product Trademark is a registered trademark of Regeneron.
Product Notices. 15.1. Any notice given under this Agreement shall be in writing and will be effective (i) when delivered, if delivered in person, (ii) during the business hour of receipt (or the next business hour if not received during a normal business hour), if by telecopy or (iii) 5 days after depositing same in the U.S. mail, postage prepaid and addressed to Seller at the address for notice specified on Exhibit A or such other address as Seller may specify to Buyer in accordance with this Section 15.1 or to Buyer at the address set forth below or at such other address as Buyer may specify to Seller in accordance with this Section 15.1: If to Buyer: COMPAQ COMPUTER CORPORATION P.O. XXX 000000 X.X. 000 XXXXXXX, XXXXX 00000-0000 ATTN: Patrxxx Xxxxxxx with a copy to: COMPAQ COMPUTER CORPORATION P.O. XXX 000000 X.X. 000 XXXXXXX, XX 00000-0000 ATTN: Division Counsel-Operations
Product Notices. Seller agrees to send all Product notices, as well as notices of any other changes affecting the Product(s) and notices of new products, to each Premier Member with copies to Purchasing Partners.
