Quality Reports Sample Clauses

Quality Reports. ACO Contract Exhibit Number Name of Report Deliverable Frequency Target System QR-01 QR-01 QM/QI Program Description/Workplan Report needs to be submitted as per Appendix B, Quality Improvement Goals. Annually OnBase QR-02 QR-02 CAHPS Reports (Submission of full CAHPS Report) CAHPS Reports (Submission of full CAHPS Report as well Member-level and aggregate data made available via NCQA submission process) Annually OnBase QR-03 QR-03 External Research Project Notification External Research Project Notification Ad-Hoc OnBase QR-04 QR-04 External Audit/Accreditation External Accreditation (Submission of NCQA accreditation report and associated results) Ad-Hoc OnBase QR-05 QR-05 HEDIS IDSS Report HEDIS IDSS Report (Submission in Excel and CSV formats). Annually OnBase QR-06 QR-06 HEDIS Member Level Data Annually Email QR-07 QR-07 Clinical Quality Measures Annually Quality Vendor QR-08 QR-08 Supplemental Data for Clinical Quality and Health Equity Measures Supplemental data files (Format for submission determined and communicated by MassHealth’s Comprehensive Quality Measure Vendor (CQMV). Annually Inter- change QR-09 QR-09 Validation of Performance Measures Performance Measure Data (Format for submission determined and communicated by External Quality Review Organization). Annually EQRO QR-10 QR-10 Performance Improvement Projects Performance Improvement Project Reports (Format for submission determined by and communicated by External Quality Review Organization). Bi-Annually EQRO ACO Contract Exhibit Number Name of Report Deliverable Frequency Target System QR-11 QR-11 Serious Reportable Events (SREs) and Provider Preventable Conditions (PPCs) Serious Reportable Events (SREs) and Provider Preventable Conditions (PPCs) (including Health care Acquired Conditions (HCACs) and Other Provider Preventable Conditions (OPPCs) Submission using EOHHS developed template). Notification: Within 30 calendar days of occurrence OnBase QR-12 QR-12 Summary of Serious Reportable Events (SREs) and Provider Preventable Conditions (PPCs) Summary of Serious Reportable Events (SREs) and Provider Preventable Conditions (PPCs) (Submission using EOHHS- developed template). Annually OnBase The Contractor shall provide to each Enrollee each of the ACO Covered Services listed below in an amount, duration, and scope that is Medically Necessary (as defined in Section 1 of this Contract), provided that the Contractor is not obligated to provide any ACO Covered Service in excess of any service ...

Quality Reports. 3.9.1. CM shall provide a report to MFR on a monthly basis containing mutually agreed upon quality information and metrics. The report shall be provided no later than the 10th calendar day of each month with information current to the last calendar day of the preceding month.

Quality Reports. The Supplier will provide Alliance with weekly quality summaries regarding the manufacture of the Products, which summaries will include end of line yield and audit yield for units produced. Such summaries shall also identify manufacturing defects and corrective action taken. Alliance shall determine the detail of the information and format for such quality reports.

Quality Reports. Woodbridge will provide to UFP out-turn quality reports related to Foam upon request. Woodbridge and UFP will share open quality books with one another and with Customers, if necessary.

Quality Reports. Supplier will provide, on a monthly basis, a quality assurance report, which will include a listing of all product related corrective and preventative action reports (CAPAs) issued globally for OEM Products (regardless of brand), and a detailed description of the root cause analysis of the reason for the report. Upon request, Supplier will provide GEMS-IT with additional information on any item that appears in the quality assurance report and participate in phone calls with GEMS-IT regarding the same. Supplier will provide, on a monthly basis, a report listing all RMAs issued globally for OEM Products, and a detailed description of the root cause analysis of the reason for the return. Supplier shall promptly respond to GEMS-IT’s reasonable inquiries regarding such RMAs and, if they involve GEMS-IT’s customers, the resolution of such RMAs.

Quality Reports. Submit the following reports in accordance with the approved Quality Plan and Quality Procedures.

Quality Reports. Supplier will provide, on a monthly basis, a quality assurance report, which will include a listing of all product related corrective and preventative action reports (CAPAs) issued globally for OEM Products or equivalent CSI-branded devices, and a detailed description of the root cause analysis of the reason for the report; notwithstanding the foregoing, Supplier does not need to provide any information concerning Powerheart AED G3 automatic or FirstSave AED G3 or any other Cardiac Science products that GEMS-IT does not market. Upon request, Supplier will provide GEMS-IT with additional information on any item that appears in the quality assurance report and participate in phone calls with GEMS-IT regarding the same. Supplier will provide, on a monthly basis, a report listing all RMAs issued globally for OEM Products that have been sold directly or indirectly by GEMS-IT, and a detailed description of the root cause analysis of the reason for the return. Supplier shall promptly respond to GEMS-IT’s inquiries regarding RMAs if they involve GEMS-IT’s customers and the resolution of such RMAs.”

Quality Reports. (a) As measured on a calendar quarter, LabAlliance shall meet or exceed the Service Standards. Within fifteen (15) days following each calendar quarter, LabAlliance shall provide the Alliance with a written report detailing each of the Service Standards and LabAlliance's performance with respect to such Service Standards during said calendar quarter (the "Quality Report"). Upon request of the Alliance, LabAlliance shall provide the Alliance with access to and copies of all information necessary to verify LabAlliance's performance with respect to the Service Standards. The Alliance's acceptance of a Quality report shall not be deemed a waiver of any of the Alliance's rights or remedies under this Agreement. (b) If the Quality Report indicates that for any particular Service Standard, the Service Standard has not been met for three (3) consecutive calendar quarters, then LabAlliance shall immediately develop a plan of corrective action in consultation with the Alliance. The plan shall be implemented within thirty (30) days following the end of the immediately preceding calendar quarter. LabAlliance shall provide a supplemental Quality Report as of the end of the second month of the calendar quarter in which the plan is implemented. If such supplemental Quality Report indicates that the corrective action plan has not resulted in the Service Standard being met, the Alliance shall have the termination rights set forth in Section 11 of this Agreement. (c) If the Quality Report indicates that for any particular Service Standard the results are more than 20% below the established Service Standard for that calendar quarter, then LabAlliance shall immediately develop a plan of corrective action in consultation with the Alliance. The Plan shall be implemented within twenty (20) days following the end of the immediately preceding calendar quarter. LabAlliance shall provide a supplemental Quality Report for the fifteen (15) day period immediately following the implementation of the corrective plan. Such report shall be delivered within three (3) days of the completion of such fifteen (15) day period. If such supplemental Quality Report indicates that the corrective action plan has not resulted in a correction and compliance with the Service Standard, the Alliance shall have the termination rights set forth in Section 11 of this Agreement.

Quality Reports. The Contractor must provide quality reports in writing to the Superintendent monthly at least 5 Working Days prior to each monthly project control group meeting as follows: (i) the quality assurance status of the Works (in reference to the Project Quality Plan); (ii) a description of any problems or defective work and the corrective action being undertaken; (iii) a list of all shop drawings approved by the design Consultants and/or the Superintendent during the period covered by the report and the name of the design Consultant or firm who or which approved the shop drawing; (iv) a list of all samples approved by the design Consultants during the period covered by the report; and (v) subject to the Superintendent approving otherwise, such approval not to be unreasonably withheld, a Consultant’s Certificate signed by each design Consultant confirming that as far as the Consultant is aware the construction accords in all material respects with the design or detailing any material non-conformance of construction of which the Consultant is aware as at the end of the period covered by the report and which has arisen or occurred since the last certificate or statement was signed by the relevant design Consultant.