Quality Control Information Clause Samples
Quality Control Information. Upon the reasonable request of Wats▇▇, ▇▇▇▇▇▇ ▇▇▇ll provide Wats▇▇ ▇▇▇h such information, including analytical and manufacturing documentation, requested by Wats▇▇ ▇▇▇arding quality control of Active Ingredient supplied hereunder.
Quality Control Information. Upon the reasonable request of either IRC or Trinity, the other party shall provide the requesting party with such information, including analytical and manufacturing documentation, requested by the requesting party relating to quality control of the Product; provided, however, the requesting party shall treat all such information disclosed pursuant to this Section 6.5.3 as confidential information subject to the provisions of Article 10 below.
Quality Control Information. Upon the reasonable request of Chiron, Gen-Probe shall provide Chiron with such reasonable information, including analytical and manufacturing documentation, requested by Chiron regarding quality control of the Products. Chiron shall treat all such information disclosed pursuant to this Section as confidential information of Gen-Probe subject to the provisions of Article 8 below.
Quality Control Information. Upon the reasonable request of Novartis, Gen-Probe shall provide Novartis with such reasonable information, including analytical and manufacturing documentation, requested by Novartis regarding quality control, stability data and shipping validation for Products. Novartis shall treat all such information disclosed pursuant to this Section as confidential information of Gen-Probe subject to the provisions of ARTICLE 7 below.
Quality Control Information. ISTA shall assure the quality level of the Product and Product In Final Form, whether manufactured by it or by an ISTA Contract Manufacturer(s), through the use of a formal quality assurance program in conformance with reasonable industry standards. Such program shall require ISTA or the ISTA Contract Manufacturer(s) to prepare and maintain written records sufficient to enable Otsuka to trace the history of each lot of Product and Product In Final Form delivered to Otsuka hereunder. Upon the reasonable request of Otsuka, ISTA shall provide Otsuka with such information, including analytical and manufacturing documentation, requested by Otsuka regarding quality control of the Product and Product In Final Form supplied hereunder and which ISTA shall maintain in accordance with applicable laws and regulations.
Quality Control Information. Hercon shall perform quality control tests to ensure that the Clinical Trial Products are produced in accordance with GMP and all applicable laws and regulations, including the U.S. Federal Food, Drug and Cosmetic Act, 21 U.S.C. §301 et seq. and regulations promulgated thereunder, and conform to the Product Specifications. Upon the written request of CTI, Hercon shall provide CTI with the results of such quality control tests and such other information, including other analytical and manufacturing documentation, reasonably requested by CTI, regarding quality control of the Clinical Trial Products supplied hereunder. Hercon shall notify CTI as soon as practicable after Hercon identifies any manufacturing or testing deviations, and shall provide CTI with complete records of any investigations, reports and the like pertaining to such deviations.
Quality Control Information. Upon the reasonable request of Biosite, ▇▇▇▇▇▇▇ shall provide Biosite with such information, including analytical and manufacturing documentation, requested by Biosite regarding quality control of the BNP Assays supplied under this Agreement. Biosite shall treat all such information disclosed pursuant to this Section 4.4 as confidential information of ▇▇▇▇▇▇▇ subject to the provisions of Section 7 (Confidentiality).
Quality Control Information. Ista shall assure the quality level of the Finished Product, whether manufactured by it or by an Approved Third Party Contractor, through the use of a formal quality assurance program in conformance with reasonable industry standards. Such program shall require Ista or the Approved Third Party Contractor to prepare and maintain written records sufficient to enable Allergan to trace the history of each Finished Product lot delivered to Allergan hereunder. Upon the reasonable request of Allergan, Ista shall provide Allergan with such information, including analytical and manufacturing documentation, requested by Allergan regarding quality control of the Finished Product supplied hereunder and which Ista shall maintain in accordance with applicable laws and regulations.