Reagents bioMérieux’s reagents are intended for in vitro use. The compliance of the reagents with the specifications indicated on the package insert is guaranteed until expiry date.
Reagents. (a) bioMérieux’s reagents are intended for in vitro use. bioMérieux warrants that reagents shall conform in all material respects to the specifications indicated in the package insert until their expiry date.
(b) Subject to Condition 10.6, if:
(i) the Buyer gives notice in writing to the Sales Administration Department of bioMérieux within a reasonable time of discovery that some or all of the Goods do not comply with the warranty set out in Condition 10.1(a); and
(ii) bioMérieux is given a reasonable opportunity of examining such Goods; and
(iii) the Buyer (only if asked to do so by bioMérieux) returns such Goods to bioMérieux’s place of business at bioMérieux’s cost, bioMérieux shall, at its option, repair or replace the defective Goods, or refund the value of the defective Goods in full.
Reagents. (a) Buyer hereby covenants that it and each of its Affiliates will not (a) transfer to the United States or sell within the United States any (i) Products or (ii) other goods that (1) contain or are derivate of cell lines subject to paragraph 4 of the Consent Decree or (2) contain any Reagents supplied by Seller and its Affiliates that have not been created within the United States or (3) contain the Reagent 84165 S Pan-1; Hollow Fiber Harvest (“Prohibited Goods”) and (b) will use best efforts to prevent its representatives, agents, successors and assigns from transferring Prohibited Goods to or selling Prohibited Goods in the United States (including by the immediate termination or expiration of sales to distributors to the extent necessary to comply herewith); provided, however, that solely in the case of Products or other goods that contain any Reagents supplied by Seller and its Affiliates that have been created within the United States (other than Reagent 84165 S Pan-1; Hollow Fiber Harvest) this covenant shall not prohibit the transfer to or sale of such Products or other goods if (A) the FDA has first provided confirmation reasonably satisfactory to Seller that transfer or sale in the United States is acceptable to the FDA or (B) the restrictions imposed upon Seller with respect to a particular Prohibited Good under the Consent Decree has expired, lapsed or otherwise terminated. Buyer further acknowledges that because a breach, or failure to comply with, this Section 6.5(a) will cause irreparable injury to Seller for which there is no adequate remedy by Law and the exact amount of which will be difficult to ascertain, if Buyer, or any Affiliate, representative, agent successor or assign thereof, should in any way breach, or fail to comply with, the terms of this Section 6.5(a), Seller shall be immediately entitled to an injunction restraining such Person(s) from any such breach or failure, without the necessity of proving injury or damages or engaging in the alternative dispute resolution process set forth in the Asset Purchase Agreement. Resort of any such remedy provided for by Law shall not preclude or bar the concurrent or subsequent employment of any other appropriate remedy or remedies, or preclude the recover by Seller of monetary damages and compensation.
(b) Buyer acknowledges and agrees that (i) those Reagents manufactured by Seller and its Affiliates outside of the United States are not manufactured in accordance with FDA standards and Se...
Reagents. All remaining reagents stored at 2-8C, -20C and -80C. Reagents for KBRV201 include expression vectors for production of intact KBRV201 antibody by transient transfection of mammalian cell lines. All KBAB401 hybridoma and LCL cell lines (uncharacterized) Kenta Biotech, Schlieren, CH All remaining human PBLS stored in LN2 and all patient sera stored at -20C (see document “Freezer Content”). LA55 fusion partner cell line (RCB) Kenta Biotech, Schlieren, CH HL60 phagocytic cell line Kexxx Xxxxxxx, Xxxxxxxxx, XX X00-0 XBV secreting cell line Kenta Biotech, Schlieren, CH EL4-B5 murine feeder cell line Kenta Biotech, Schlieren, CH Patients PBL Kenta Biotech, Schlieren, CH Commercially available cell lines (Jurkat, HEK293, etc.) Kenta Biotech, Schlieren, CH See list of LN2 storage tank Kenta Biotech, Schlieren, CH Kenta Biotech, Schlieren, CH All remaining reagents stored at 2-8C, -20C and -80C (see document “Freezer Content”), including clinical isolates of viruses (RSV) and bacteria (P. aeruginosa, S. aureus, A. baumannii); Patients sera and clinical isolates (BAL, ETA and sputum) from all research activities. · ORION Clinical Services Limited, 7 Xxxx Xxxx, Xxxxxx, Xxxxxxx XX0 0XX · Xxxxxx Clinical Services Switzerland, Stxxxxxxxxxx 00, 0000 Xxxxxxxxx / Xxxxxxxxxxx · Cenduit LLC, Chelsea Place, 1000 Xxxxxx Xxxx, Suite 301, Durham, NC 27703, USA · Eurofins Medinet B.X., Xxxxxxxxx 00, 0000 XX, Xxxxx, xxx Xxxxxxxxxxx ORION Amendment No 5 to Work Order 001 expected Amendment No 4 to Work Order 001 Mar 27, 2013 Amendment No 3 to Work Order 001 Mar 26, 2013 Amendment No 2 to Work Order 001 Feb 1, 2013 Amendment No 1 to Work Order 001 Feb 1, 2013 Work Order 001 Feb 1, 2012 Master Study Agreement Dec 8, 2011 Xxxxxx Order 7, Vers. 2; FCS No 205523, Quote relabeling May 21, 2012 Order 1, Vers. 2; FCS No 207727, Quote LN2 storage, back ups May 14, 2012 Order 4, Vers. 2; FCS No 205523, Quote Logistics Feb 1, 2012 Order 6, Vers. 1; FCS No 205523, Quote Label- and Packaging Jan 31, 2012 Responsibilities Agreement (GMP) Nov 18, 2010 Cenduit IRT Change Order Pricing Mar 27, 2012 Individual Project Agreement Feb 24, 2012 IRT Pricing Proposal Feb 15, 2012 Master Project Agreement Dec 20, 2011 Eurofins Change Order 1 to Study Agreement Apr 11, 2012 Study Agreement Dec 20, 2011 Clinical Sites Cliniques Universitaires St Luc, 10 avenue Hippocrate, 1200 Brussels, Belgium Jun 12 Clinique Saxxx-Xxxxxx 0, Xxxxxx Xxxxx Xxxxxxx, 1340 Ottignies, Belgium Jun 12 University Hospital of Liege, ...
Reagents. Any service calls necessitated by poor quality reagent in the circumstances set out in this clause 6 will not be covered by the annual service fee payable by the Customer to Xxxxxxx Xxxxxxx in accordance with clause 4 of this Agreement. Where a problem occurs as a result of the poor quality of a reagent that has not been supplied by Xxxxxxx Xxxxxxx in circumstances where:
(a) Xxxxxxx Xxxxxxx’x quality control evaluation of the reagent proves the poor quality of the reagent; and
(b) Xxxxxxx Xxxxxxx has established that there is no malfunction of the Equipment, the Customer shall incur the cost of service calls resulting from such problem.
Reagents. Isis shall charge the Collaboration Funds for Reagent ASO Compounds provided to Lilly by Isis under the Reagent Provision Program at the Isis HTS Standard Cost or Isis RTS Standard Cost, as applicable, in accordance with the provisions of Section 9.1.1.
Reagents. Phosphate-buffered saline (PBS) Periodate Lysine Phosphate (PLP) Cell lysis buffer Neutralization buffer
Reagents. Subject to the terms and conditions of this Agreement, including but not limited to this Section 5.4 and Exhibit C, Illumina hereby appoints CareDx as its non-exclusive distributor for the re-Sale of Illumina [...***...] Reagents during the Term for use in the Licensed Field only, subject to the following additional restrictions on CareDx and any third parties that are re-Selling or using Illumina [...***...] Reagents purchased under this Agreement:
Reagents. Where a problem occurs as a result of the poor quality of a reagent not supplied by Bio-Strategy as proven by Bio- Strategy’s quality control evaluation of the reagent and where it is identified by Bio-Strategy that there is no malfunction of the Equipment the Customer shall incur the cost of service calls resulting from such problem.
Reagents. (a) All Intellectual Property Rights in the Reagents remain at all times vested in the Third Party Contractor.
(b) The Recipient must only use the Reagents in accordance with this Agreement.
(c) The Recipient must not, and must ensure that its Recipient Personnel do not, modify the Reagents.
