QUALITY AUDITING Sample Clauses

QUALITY AUDITING. We may request to carry out random quality audits on the work carried out on your Installation both during and after the completion of the Repair Visit. Bord Gáis Energy will notify you by telephone of any such request.
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QUALITY AUDITING. ‌ 7.1.1 Not later than 90 days after the Effective Date, or at an alternate time accepted by the City in the Submittal Schedule and Register, Design-Builder shall submit to the City the Quality Audit Plans. Design-Builder shall submit to the City updated Quality Audit Plans at 12 month intervals thereafter. 7.1.2 Each Quality Audit Plan shall: (a) contain an auditing process that is capable of identifying Nonconformities, necessary Corrective Actions and Preventive Actions and facilitate continuous improvement; and (b) detail the Quality Audits that Design-Builder shall conduct on its own processes and those of the Subcontractors, the planned dates of such Quality Audits, and the conditions or circumstances which could give rise to an unscheduled Quality Audit. 7.1.3 Design-Builder shall provide the following advance notice to the City’s Representative prior to the start of any Quality Audit, or any change to the planned date for a Quality Audit: (a) at least 5 Business Days for Quality Audits performed in Alberta; (b) at least 14 days for Quality Audits performed outside of Alberta but within North America; and (c) at least 30 days for Quality Audits performed outside of North America. The notice shall describe the scope and objectives of the applicable Quality Audit. Quality Audits must be scheduled or rescheduled to meet the notice requirements outlined in this Section 7.13.
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QUALITY AUDITING. 9.1 Thera, or any other Person designated by Thera subject to the confidentiality provisions of this Agreement or similar provisions of a confidentiality agreement executed with Bachem, shall be allowed to conduct Audits of Bachem facilities. Thera shall send a request to schedule an Audit with Bachem at least [Redacted: Term] prior to the proposed Audit date. Thera, or any Person designated by Thera, shall be permitted to conduct [Redacted: Amount] Audit per Calendar Year, unless an Audit discovers a problem or unsatisfactory conditions. In the event an Audit discovers a problem or unsatisfactory conditions, Thera, or any Person designated by Thera, shall be entitled to proceed with as many Audits as it deems necessary upon reasonable prior written notice to Bachem until such problem or unsatisfactory conditions are solved. For the purposes of this Section, “Audit” shall mean a Bachem audit involving the audit and inspection of all elements and systems of the manufacturing process of the Active Ingredient and of Bachem’s records of the elements and systems of the manufacturing process.
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QUALITY AUDITING. 7.1.1 Not later than 90 days after the Effective Date, or at an alternate time accepted by the City in the Submittal Schedule and Register, Project Co shall submit to the City the Quality Audit Plans. Project Co shall submit to the City updated Quality Audit Plans at 12 month intervals thereafter. 7.1.2 Each Quality Audit Plan shall: (a) contain an auditing process that is capable of identifying Nonconformities, necessary Corrective Actions and Preventive Actions and facilitate continuous improvement; and (b) detail the Quality Audits that Project Co shall conduct on its own processes and those of the Subcontractors, the planned dates of such Quality Audits, and the conditions or circumstances which could give rise to an unscheduled Quality Audit. 7.1.3 Project Co shall provide the following advance notice to the City’s Representative prior to the start of any Quality Audit, or any change to the planned date for a Quality Audit: (a) at least 5 Business Days for Quality Audits performed in Alberta; (b) at least 14 days for Quality Audits performed in the rest of North America; and (c) at least 30 days for Quality Audits performed outside of North America. The notice shall describe the scope and objectives of the applicable Quality Audit.
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QUALITY AUDITING. 6.1.1 Not later than 90 days after the Effective Date, Project Co shall submit the Quality Audit Plans to the City’s Representative in accordance with the Review Procedure. Project Co shall submit updated Quality Audit Plans to the City’s Representative, in accordance with the Review Procedure, at 12 month intervals thereafter. 6.1.2 Project Co shall provide the following advance notice to the City’s Representative prior to the start of any Quality Audit, or any change to the planned date for a Quality Audit: (a) at least 7 Business Days for Quality Audits performed in Alberta; (b) at least 14 days for Quality Audits performed in the rest of North America; and (c) at least 30 days for Quality Audits performed outside of North America. The notice shall describe the scope and objectives of the applicable Quality Audit.
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QUALITY AUDITING. 6.1 Thera, or any other Person designated by Thera subject to the confidentiality provisions of this Agreement or similar provisions of a confidentiality agreement executed with Bachem, shall be allowed to conduct audits of Bachem facilities in accordance with the terms of the Quality Agreement. 6.2 Any dispute of the audit responses relating to the quality systems of Bachem that cannot be resolved by the Parties in accordance with the Quality Agreement will be submitted to arbitration pursuant to the terms of Section 14. Until settlement of a dispute, Thera shall be entitled to have Lots of Active Ingredient manufactured by another supplier without being in breach of any provision of this Agreement. In the event the arbitration ruling is entirely in favour of the Bachem position, the entire quantity of Active Ingredient ordered and delivered by another supplier shall be added to the Minimum Purchase Obligation of Thera hereunder during the Calendar Year in which the ruling was issued if the ruling is issued on or before June 30 and during the following Calendar Year if the ruling is issued after June 30.
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Related to QUALITY AUDITING

  • Quality Assurance The parties endorse the underlying principles of the Company’s Quality Management System, which seeks to ensure that its services are provided in a manner which best conforms to the requirements of the contract with its customer. This requires the Company to establish and maintain, implement, train and continuously improve its procedures and processes, and the employees to follow the procedures, document their compliance and participate in the improvement process. In particular, this will require employees to regularly and reliably fill out documentation and checklists to signify that work has been carried out in accordance with the customer’s specific requirements. Where necessary, training will be provided in these activities.

  • Quality Assurance Program An employee shall be entitled to leave of absence without loss of earnings from her or his regularly scheduled working hours for the purpose of writing examinations required by the College of Nurses of Ontario arising out of the Quality Assurance Program.

  • Research Use Reporting To assure adherence to NIH GDS Policy, the PI agrees to provide annual Progress Updates as part of the annual Project Renewal or Project Close-out processes, prior to the expiration of the one (1) year data access period. The PI who is seeking Renewal or Close-out of a project agree to complete the appropriate online forms and provide specific information such as how the data have been used, including publications or presentations that resulted from the use of the requested dataset(s), a summary of any plans for future research use (if the PI is seeking renewal), any violations of the terms of access described within this Agreement and the implemented remediation, and information on any downstream intellectual property generated from the data. The PI also may include general comments regarding suggestions for improving the data access process in general. Information provided in the progress updates helps NIH evaluate program activities and may be considered by the NIH GDS governance committees as part of NIH’s effort to provide ongoing stewardship of data sharing activities subject to the NIH GDS Policy.

  • Office of Inspector General Investigative Findings Expert Review In accordance with Senate Bill 799, Acts 2021, 87th Leg., R.S., if Texas Government Code, Section 531.102(m-1)(2) (eff. Apr. 1, 2025, Section 544.0106, pursuant to House Bill 4611, Acts 2023, 88th Leg., R.S.) is applicable to this Contract, Contractor affirms that it possesses the necessary occupational licenses and experience.

  • OIG INSPECTION, AUDIT, AND REVIEW RIGHTS ‌ In addition to any other rights OIG may have by statute, regulation, or contract, OIG or its duly authorized representative(s) may conduct interviews, examine or request copies of ▇▇▇▇▇▇’▇ books, records, and other documents and supporting materials and/or conduct on-site reviews of any of ▇▇▇▇▇▇’▇ locations for the purpose of verifying and evaluating: (a) ▇▇▇▇▇▇’▇ compliance with the terms of this IA and (b) ▇▇▇▇▇▇’▇ compliance with the requirements of the Federal health care programs. The documentation described above shall be made available by ▇▇▇▇▇▇ to OIG or its duly authorized representative(s) at all reasonable times for inspection, audit, and/or reproduction. Furthermore, for purposes of this provision, OIG or its duly authorized representative(s) may interview ▇▇▇▇▇▇ and any of ▇▇▇▇▇▇’▇ employees or contractors who consent to be interviewed at the individual’s place of business during normal business hours or at such other place and time as may be mutually agreed upon between the individual and OIG. ▇▇▇▇▇▇ shall assist OIG or its duly authorized representative(s) in contacting and arranging interviews with such individuals upon OIG’s request. ▇▇▇▇▇▇’▇ employees and contractors may elect to be interviewed with or without a representative of ▇▇▇▇▇▇ present.