Quality Certifications Clause Samples
Quality Certifications. Kanbay agrees to provide all information and supporting documentation reasonably requested by ▇.▇. ▇▇▇▇▇▇▇ regarding Kanbay's CMM assessments and ISO certifications. Kanbay further agrees to (i) provide audit reports related to the certifications and to update those reports as periodically requested by ▇.▇. ▇▇▇▇▇▇▇, but not more than once per year, (ii) make personnel available to discuss the certifications and audit reports with ▇.▇. ▇▇▇▇▇▇▇, and (iii) provide ▇.▇. ▇▇▇▇▇▇▇ with documentation reflecting any corrective measures taken to address problems identified in any audit.
Quality Certifications. Contractor is obliged to maintain the ISO 9001 and ISO 14001 certification. Manufacturing and testing will be according to agreed workmanship standards and the approved relevant drawings, supplied by Veraz.
Quality Certifications. Except as set forth in Section 4.11 of the Disclosure Schedule, all operations of the Business (a) are compliant, in all material respects, with all applicable FDA Quality System Regulations and FDA Establishment Registration and Listing requirements and (b) have achieved and maintained all applicable quality certifications including all required ISO (International Organization for Standardization) certifications. Section 4.11 of the Disclosure Schedule lists each ISO and quality certification applicable to the Business (and the holder thereof). There is no pending or, to the Knowledge of TEI Bio, threatened, Proceeding to audit, repeal, fail to renew or challenge any such certification.
Quality Certifications. Company will be responsible for manufacturing the Product and maintaining the quality requirements to preserve the permits, licenses and approvals necessary for the proper manufacture of the Product. Company will maintain all documentation relating to the manufacture and or quality control of the Product for the required periods by statute or regulation. Sgenia and Subco will have the right, during normal business hours to review such documentation at its expense, and Company will cooperate to make the documentation available. Additionally, Sgenia and Subco will have the right, during normal business hours, to have access to Company’s manufacturing facilities upon reasonable notice at any time during the manufacture of the Product and all related material and for quality audits, to observe the manufacture, packaging, labeling and storage of the Product. ii Samples. Sgenia and Subco may obtain samples of each batch of products, at their expense, equivalent to the cost to Company.
Quality Certifications. All operations of the Business (a) are compliant, in all material respects, with all applicable FDA Quality System Regulations and FDA Establishment Registration and Listing requirements and (b) have achieved and maintained all applicable quality certifications including all required ISO (International Organization for Standardization) certifications. Section 4.11 of the Disclosure Schedule lists each ISO and quality certification applicable to the Business (and the holder thereof). There is no pending or, to the Knowledge of TEI Med, threatened, Proceeding to audit, repeal, fail to renew or challenge any such certification.