Data Quality Improvement Plan definition

Data Quality Improvement Plan means a plan as set out in Section 3.3 to ensure appropriate progress is made by the Provider to improve the information that it provides to the Commissioner in terms of quality, accuracy, timeliness and completeness and shall include agreed milestones for the assessment of progress against which the withholding under clause 29 (Information Requirements) is assessed;
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Data Quality Improvement Plan or “DQIP” means a plan setting out specific data and information improvements to be achieved by the Provider in accordance with the timescales in such plan completed on the basis of and appended at Schedule 5 Part 4;
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Data Quality Improvement Plan. Standard NHS Multilateral Contrac VERSION AT 3rd December 2012 means a plan to ensure appropriate progress is made by the Provider to improve the information that it provides to the Commissioner in terms of quality, accuracy, timeliness and completeness, and shall include agreed milestones for the assessment of progress, against t for Mental Health and Learning Disability Services 84 which the withholding under clause 29 (Information Requirements) is assessed;
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Examples of Data Quality Improvement Plan in a sentence

  • Data Quality Improvement Plan (DQIP): Refers to a documented plan to improve Data Quality using improvement strategies recommended by EPCH.

  • For consistent issues with Data Timeliness, providers may be directed to create a Data Quality Improvement Plan (DQIP).

  • Where a provider will need time to make adjustments to move to use of any new data sets, a Data Quality Improvement Plan should be agreed locally to describe how the transition will be managed and over what period.

  • Data input sources will be agreed, and a Data Quality Improvement Plan will set out the measures needed to improve data and address gaps.

  • Data Quality Improvement Plan For areas where the local program does not reach “Superior” standards, a data quality improvement plan must be completed to describe the problem identified and a plan for correction.

  • For persistent data quality issues, AKHMIS-participating organizations may be contacted by the AK CoC to discuss the implementation of a Data Quality Improvement Plan (DQIP) (see 8.3 Data Quality Improvement Plan) for the project(s).

  • An action plan document12, which was provided to IPRO to help with the creation of the National Data Quality Improvement Plan.

  • Failure to establish such facts results in the matter proceeding to the merits.

  • Where appropriate, report of progress against milestones in Data Quality Improvement Plan [DN: Frequency, format and method for delivery to be determined locally as part of the plan].

  • The samples annealed for 12 hours displayed an enhanced OSL sensi- tivity compared to that found for shorter times, typically by a factor of 2-3.

Related to Data Quality Improvement Plan

  • Quality Improvement means a focus on activities to improve performance above minimum standards and reasonably expected levels of performance, quality and practice.

  • Quality improvement organization or “QIO” shall mean the organization that performs medical peer review of Medicaid claims, including review of validity of hospital diagnosis and procedure coding information; completeness, adequacy and quality of care; appropriateness of admission, discharge and transfer; and appropriateness of prospective payment outlier cases. These activities undertaken by the QIO may be included in a contractual relationship with the Iowa Medicaid enterprise.

  • Quality system means documented organizational procedures and policies: internal audits of those policies and procedures: management review and recommendation for quality improvement.”

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • health and safety specification means a site, activity or project specific document prepared by the client pertaining to all health and safety requirements related to construction work;

  • Project Implementation Manual or “PIM” means the manual setting out the measures required for the implementation of the Project, as the same may be amended from time to time, subject to prior approval of the Association;

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Energy efficiency improvement means equipment, devices, or materials intended to decrease energy consumption, including, but not limited to, all of the following:

  • site development plan means a dimensioned plan drawn to scale that indicates details of the proposed land development, including the site layout, positioning of buildings and structures, property access, building designs and landscaping;

  • Infrastructure improvement means permanent infrastructure that is essential for the public health and safety or that:

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • Quality Assurance Program means the overall quality program and associated activities including the Department’s Quality Assurance, Design-Builder Quality Control, the Contract’s quality requirements for design and construction to assure compliance with Department Specifications and procedures.

  • Spatial Planning and Land Use Management Act means the Spatial Planning and Land Use Management Act, 2013 (Act 16 of 2013);

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • High Quality Waters means all state waters, except:

  • Brand Name Specification means a specification limited to one or more items by manufacturers’ names or catalogue number.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Development Plan has the meaning set forth in Section 3.2.

  • Quality Assurance Plan or “QAP” shall have the meaning set forth in Clause 11.2;

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Nuclear fuel cycle-related research and development activities means those activities which are specifically related to any process or system development aspect of any of the following: - conversion of nuclear material, - enrichment of nuclear material, - nuclear fuel fabrication, - reactors, - critical facilities, - reprocessing of nuclear fuel, - processing (not including repackaging or conditioning not involving the separation of elements, for storage or disposal) of intermediate or high-level waste containing plutonium, high enriched uranium or uranium-233, but do not include activities related to theoretical or basic scientific research or to research and development on industrial radioisotope applications, medical, hydrological and agricultural applications, health and environmental effects and improved maintenance.

  • Basic Comprehensive User Guide means the Ministry document titled Basic Comprehensive Certificates of Approval (Air) User Guide” dated April 2004 as amended.

  • Drug use test means a scientifically substantiated method to test for the presence of illegal or performance-enhancing drugs or the metabolites thereof in a person’s urine.

  • Ambient air quality standard means an established concentration, exposure time, and frequency of occurrence of air contaminant(s) in the ambient air which shall not be exceeded.