HANDLING OF PROBLEMS WITH CALYPTE PRODUCTS Sample Clauses

HANDLING OF PROBLEMS WITH CALYPTE PRODUCTS. (a) COMPLAINTS AND REJECTIONS. Distributor will promptly notify Calypte if any Calypte Product is found, upon incoming inspection by Distributor, to be defective or to fail to meet Calypte's applicable written specifications or otherwise to be defective. Distributor and Calypte will discuss in good faith the resolution of any such problem, provided, however, that final resolution of any such problem will be at Calypte's sole discretion. If either of us receives any complaint regarding any Calypte Product from a third party, including without limitation a rejection by any of Distributor's customers of any Calypte Product or return by any customer of any Calypte Product to Distributor as a result of an alleged failure of such Calypte Product's performance, whichever of us receives the complaint will notify the other in writing as to such event within twenty-four (24) hours after receipt of such complaint, and will provide all information necessary to enable the other to comply with applicable regulatory requirements in a timely fashion. Distributor will be responsible for evaluating in detail all complaints from Distributor customers as to Calypte Products and will advise Calypte in writing of Distributor's findings. Calypte will attempt to assist Distributor in addressing any issues or alleged problems in Product performance which Distributor cannot remedy through Distributor's own technical support. Distributor also agrees to provide Calypte on a monthly basis a summary of all complaints that Distributor has received and if and how they were resolved. Calypte will provide to Distributor a form for this purpose, the design of which has been registered with the U.S. FDA. Product is not to be returned to Calypte unless or until Calypte provides to Distributor a Returned Goods Authorization number. If any Calypte Products are rejected because of quality problems associated with production, Calypte shall reimburse Distributor for all direct costs and expenses incurred by Distributor for such rejected products such as shipping expenses, product costs, handling, notification, testing or costs of destruction.
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Related to HANDLING OF PROBLEMS WITH CALYPTE PRODUCTS

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  • Contact with Customers and Suppliers Until the Closing Date, the Buyer shall not, and shall cause its Affiliates and direct its other Representatives not to, contact or communicate with the employees, customers, suppliers, distributors or licensors of the Acquired Entities, or any other Persons having a business relationship with the Acquired Entities, concerning the transactions contemplated hereby or any of the foregoing relationships without the prior written consent of the Seller.

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  • Communications with Regulatory Authorities During the Collaboration Term, Xencor shall provide MorphoSys with reasonable advance notice of any meeting or substantive telephone conference with any Regulatory Authority relating to any Licensed Antibody and/or Licensed Product. MorphoSys shall have the right to attend and observe (but not participate actively in) any material meeting or material conference call with any Regulatory Authority regarding any of MorphoSys (or its Affiliate’s or Sublicensee’s) Licensed Antibody and/or Licensed Products. In addition, Xencor shall promptly furnish to MorphoSys copies of all correspondence that Xencor (or its Affiliate) receives from, or submits to, any Regulatory Authority (including contact reports concerning conversations or substantive meetings) relating to any Licensed Antibody and/or Licensed Product. Xencor shall also provide to MorphoSys any meeting minutes that reflect material communications with any Regulatory Authority regarding a Licensed Antibody and/or Licensed Product. Subject to the provisions of Section 2.2(c)(ii), MorphoSys shall provide in its MorphoSys Annual Development Reports to Xencor, and through JDC discussion, information regarding its (or its Affiliate’s or, to the extent permitted by the Sublicense, Sublicensee’s) interactions with Regulatory Authorities with respect to all Licensed Antibodies and/or Licensed Products in its respective Territory. In addition, to the extent permitted by law and subject to Section 3.6, Xencor may participate in communications and meetings with any Regulatory Authority to the extent the name and/or then-current Xencor logo is used on the drug product label and such labeling is being discussed in such communication or meeting. Notwithstanding MorphoSys’ obligations under this Article 3, MorphoSys shall not be required to share with Xencor any information which MorphoSys is not permitted to share with Xencor under the applicable laws or regulations of the Securities & Exchange Commission or other regulatory body of the US or elsewhere.

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