Quality Indicators definition

Quality Indicators means an annual summary report against the quality indicators required as a condition of registration under the Act and National Act. Records means any document within the meaning of the Evidence Xxx 0000 (Vic) including: anything on which there is writing; anything on which there are marks, figures, symbols or perforations having a meaning for persons qualified to interpret them; anything from which sounds, images or writings can be reproduced with or without the aid of anything else; or a map, plan, drawing or photograph, and which is produced or created by the RTO under or in the course of performing its obligations under this VET Funding Contract. Recordkeeping means making and maintaining complete, accurate and reliable evidence of business transactions in the form of recorded information.
Quality Indicators means an annual summary report against the quality indicators required as a condition of registration under the Act and National Act. Records means any document within the meaning of the Evidence Xxx 0000 (Vic) including:
Quality Indicators means measurable variables relating to a specified clinical or health services delivery area that are reviewed over a period of time to monitor the process or outcome of care delivered in that area.

Examples of Quality Indicators in a sentence

  • A conceptual framework for the OECD Health Care Quality Indicators Project.

  • HCUP Quality Indicators, Methods, Version 1.1: Outcome, Utilization, and Access Measures for Quality Improvement.

  • The RTO must publish on its website a copy of its most recent Quality Indicators (or its successor).

  • HCUPnet includes statistics based on the AHRQ Quality Indicators (QIs) which have been applied to the HCUP NIS.

  • Measures include established indicators for clinical care (e.g., Healthcare Effectiveness Data and Information Set measures, Adult Core Quality Indicators) with identified measure stewards (e.g., National Quality Forum).

  • These reports incorporated many Prevention Quality Indicators, Inpatient Quality Indicators, and Patient Safety Indicators.

  • These measures, when complemented by the recent Expanded Behavioral Risk Factor Surveillance System and Prevention Quality Indicators, provide health indicators that can be potentially impacted in the short-term.

  • Connections for Quality The Provider must report publicly against Connections for Quality Indicators in accordance with any Guidelines.

  • The purpose of the facilitation guide is to assist discussion groups of charter school stakeholders in reviewing and developing a common understanding of the Maryland Public Charter School Quality Indicators and Standards as described in the Maryland Charter School Quality Standards Implementation Guides.

  • The IQSASA2 program calculates the observed or raw rates for the area-level Inpatient Quality Indicators, using the data derived in a previous step (IQSAS1).


More Definitions of Quality Indicators

Quality Indicators means financial and clinical quality measures including, but not limited to, those found in the Consolidated List of Performance Measures published by the Bureau of Primary Healthcare (BPHC).
Quality Indicators means the referral to measurable variables relating to a specific clinic or health services delivery area which are reviewed over a period of time to screen delivered health care and to monitor the process or outcome of care delivered in that clinical area.
Quality Indicators means the set of statutes and rules that affect the quality of services provided to clients. These statutes and rules determine the scope and content of actions that may be addressed through a plan of correction.
Quality Indicators means the set of statutes and rules that affect the quality of services provided to clients. These statutes and rules determine the scope and content of actions that may be addressed through a plan of correction. Monitoring of quality indicators shall be documented on a form provided by the Secretary. Quality indicators include the following:

Related to Quality Indicators

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

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

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • 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.

  • Mobile crisis outreach team means a crisis intervention service for minors or families of minors experiencing behavioral health or psychiatric emergencies.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.

  • Contract Specifications means the principal trading terms in CFD (for example Spread, Swaps, Lot Size, Initial Margin, Necessary Margin, Hedged Margin, the minimum level for placing Stop Loss, Take Profit and Limit Orders, financing charges, charges etc) for each type of CFD as determined by the Company from time to time.

  • Service Specifications means the following documents, as applicable to the Services under Your order:

  • 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.

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • Technical Specifications means the detailed requirements for the Work furnished by the Architect and set forth in Book 3 of the Contract Documents.

  • Quality Standards means the quality standards published by BSI British Standards, the National Standards Body of the United Kingdom, the International Organisation for Standardisation or other reputable or equivalent body, (and their successor bodies) that a skilled and experienced operator in the same type of industry or business sector as the Contractor would reasonably and ordinarily be expected to comply with, and as may be further detailed in the Specification.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Monitoring Indicator means a measure of HSP performance that may be monitored against provincial results or provincial targets, but for which no Performance Target is set;

  • Timelines means the dates set out in Appendix 2 hereto as may be amended by agreement between the Parties and Timeline shall mean any one of such dates.

  • Quality Management System means a set of interrelated or interacting elements that organisations use to direct and control how quality policies are implemented and quality objectives are achieved;

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

  • GMPs means all good manufacturing practices under Title 21 of the United States Code of Federal Regulations, as amended from time to time.

  • Functional Specifications means the descriptions of features and functions of the Application as expressly set forth in Quote.

  • Standard Specifications means a compilation in book form of specifica- tions approved for general application and repetitive use;

  • biodiversity means the variability among living organisms from all sources including, inter alia, terrestrial, marine and other aquatic ecosystems and the ecological complexes of which they are part; this includes diversity within species, between species and of ecosystems;

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • Manufacturing Process means any process for—

  • Manufacturing Site means a location where a manufacturing

  • 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.