Quality Assurance Responsibilities Sample Clauses
The Quality Assurance Responsibilities clause defines the obligations of parties to maintain and verify the quality of goods or services provided under the agreement. Typically, it outlines specific standards or procedures that must be followed, such as regular inspections, testing protocols, or documentation requirements to ensure compliance with agreed-upon quality benchmarks. This clause serves to ensure that deliverables consistently meet the required standards, thereby reducing the risk of defects and disputes over quality.
Quality Assurance Responsibilities. Supplier agrees that, in order to expedite the acceptance of Products by Distributor’s Quality Assurance and/or Regulatory departments, that Distributor will, at Supplier’s expense, implement Quality Assurance and/or Regulatory programs and/or personnel into the Supplier’s manufacturing facilities. Supplier grants Distributor the right to conduct Quality Assurance and/or Regulatory audits (based on Distributor’s Quality Assurance standards, which at all times shall incorporate applicable FDA and GMP requirements) using Distributor’s personnel, Supplier’s personnel and/or independent consultants on a quarterly basis or more frequent spot basis. Supplier agrees that Supplier will cure any curable deficiencies within ten (10) days of written notice by Distributor of any such Quality Assurance and/or Regulatory audits and commence curing all other curable deficiencies that are curable but not reasonably subject of cure within 10 days. Supplier agrees to credit Distributor’s account in the amount of Five Thousand Dollars (US$5,000.00) per day for every calendar day that any deficiencies remain uncured following the ten (10) day written notice period described above. Similarly, following Clearance Distributor agrees to credit Supplier’s account in the amount of Five Thousand Dollars (US$5,000.00) per day for every calendar day that any deficiencies imposed by the FDA on Distributor and relating to Distributor’s obligations under this Agreement remain uncured following the 10-day period commencing on the later of the date of Distributor’s receipt of notice thereof from the FDA or the date imposed by the FDA for cure or compliance.
Quality Assurance Responsibilities. Quality Assurance Responsibilities
(1) Develop a quality assurance program, subject to County review and Approval, and Implement, Operate, Manage, and Maintain such quality assurance program at County’s direction, in order to promote performance of the Services at a high level of quality, focusing on measuring and improving reliability, speed, cost effectiveness, and customer satisfaction.
(2) Write and Implement, Operate, Manage, and Maintain procedures and measurements, subject to County review and Approval, on all quality assurance activities associated with the Services.
(3) Employ quality metrics and procedures that are consistent with similar standards in County peer group and/or in the provision of professional services that are similar to the Services.
(4) Comply with a published quality assurance program, with adequate internal controls and verification activities.
(5) Allow County to perform audits that focus on Supplier’s adherence to its quality assurance procedures and standards; on the metrics gathered to support quality assurance activities; and on Supplier’s efforts to improve overall quality. Supplier shall cooperate fully and assist County with any such audits.
Quality Assurance Responsibilities. 33BQuality Assurance Responsibilities