Clinical data repository definition

Clinical data repository means a real time database that consolidates data from a variety of clinical sources to present a unified view of a single patient and is used by a state-certified health information exchange service provider to enable health information exchange among health care providers that are not related health care entities as defined in section 144.291, subdivision 2, paragraph (j). This does not include clinical data that are submitted to the commissioner for public health purposes required or permitted by law, including any rules adopted by the commissioner.
Clinical data repository or “CDR” means the Washington State’s Health Information Exchange (HIE) service providing authorized access to integrated medical, dental, behavioral health, and social service support data for Apple Health enrollees.
Clinical data repository means Covisint’s real-time database that consolidates data from a variety of clinical sources to present a unified view of a single Patient.

Examples of Clinical data repository in a sentence

  • Place emitters or spray stakes directly into the container and make sure that water doesn’t spray out of the container and that the flow of water from the emitter or spray stake outlet is not hindered.

  • Figure 13 Information view: Repositories and interacting components Here we can see the major repositories where crucial information is stored:  The Clinical data repository, which stores de-identified clinical data originating from hospitals or clinical trials (through OBTIMA).

  • It is the responsibility of the HIE provider to select appropriate database system for development of Clinical data repository and expose APIs to get it accessed by various information systems participating in the information exchange/ for analytics/data query and further development or enhancement of the CDR output.

  • Accordingly, achieving true EMR functionality requires adding capabilities including: Clinical data repository (CDR), clinical decision support systems (CDSS), computerized practitioner order entry (CPOE), and other provider-centric information technologies (Carter, 2008).

  • ACSRC Auckland Cancer Society Research Centre AETMIS Agence d'Évaluation des Technologies et des Modes Intervention en Santé (Québec) ALARA As Low as Reasonably Achievable ANZSNM Australian and New Zealand Society of Nuclear Medicine C-11 Carbon -11 isotope CDR Clinical data repository CGPET Gamma camera PET.

  • Below we give two indicative examples, describing the information stored in the Clinical data repository and in the User repository.

  • In CHIC we will have the data flow as shown in Figure 13 in chapter 6.2. In this figure, we just describe that data from OBTIMA will pass through the security/pseudonymization framework and will be imported into the Clinical data repository of CHIC.


More Definitions of Clinical data repository

Clinical data repository means a real time database that consolidates data from a variety of clinical sources to present a unified view of a single patient and is used by a state-certified health information exchange service provider to enable health information exchange among health care providers that are not related health care entities as defined in section 144.291, subdivision 2, paragraph (j) (k). This does not

Related to Clinical data repository

  • WOSB Program Repository means a secure, Web-based application that collects, stores, and disseminates documents to the contracting community and SBA, which verify the eligibility of a business concern for a contract to be awarded under the WOSB Program.

  • Analytical x-ray system means a group of components utilizing x-rays to determine the elemental composition or to examine the microstructure of materials.

  • Clinical Data means the information concerning the safety or performance that is generated from the use of a device and that are sourced from the following:

  • trade repository means a legal person that centrally collects and maintains the records of derivatives;

  • 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.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Electronic Funds Transfer (EFT) indicator means a four-character suffix to the unique entity identifier. The suffix is assigned at the discretion of the commercial, nonprofit, or Government entity to establish additional System for Award Management records for identifying alternative EFT accounts (see subpart 32.11) for the same entity.

  • Batch means a specific quantity of Product that is intended to have uniform character and quality, within specified limits, and is produced according to a single manufacturing order during the same cycle of manufacture.

  • Authorized nuclear pharmacist means a pharmacist who:

  • Repository means each National Repository and each State Repository.

  • Diagnostic source assembly means the tube housing assembly with a beam-limiting device attached.

  • Database Management System (DBMS) A system of manual procedures and computer programs used to create, store and update the data required to provide Selective Routing and/or Automatic Location Identification for 911 systems. Day: A calendar day unless otherwise specified. Dedicated Transport: UNE transmission path between one of CenturyLink’s Wire Centers or switches and another of CenturyLink’s Wire Centers or switches within the same LATA and State that are dedicated to a particular customer or carrier. Default: A Party’s violation of any material term or condition of the Agreement, or refusal or failure in any material respect to properly perform its obligations under this Agreement, including the failure to make any undisputed payment when due. A Party shall also be deemed in Default upon such Party’s insolvency or the initiation of bankruptcy or receivership proceedings by or against the Party or the failure to obtain or maintain any certification(s) or authorization(s) from the Commission which are necessary or appropriate for a Party to exchange traffic or order any service, facility or arrangement under this Agreement, or notice from the Party that it has ceased doing business in this State or receipt of publicly available information that signifies the Party is no longer doing business in this State.

  • Electronic Subcontracting Reporting System (eSRS) means the Governmentwide, electronic, web-based system for small business subcontracting program reporting. The eSRS is located at http://www.esrs.gov.

  • 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.

  • Network Data Mover (NDM) or “Connect Direct” means the industry standard protocol for transferring information electrically.

  • 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.

  • Root Cause Analysis Report means a report addressing a problem or non-conformance, in order to get to the ‘root cause’ of the problem, which thereby assists in correcting or eliminating the cause, and prevent the problem from recurring.

  • Technical data means recorded information, regardless of the form or method of the recording, of a scientific or technical nature (including computer software documentation). The term does not include computer software or data incidental to contract administration, such as financial and/or management information.

  • Central Contractor Registration (CCR) database means the primary Government repository for Contractor information required for the conduct of business with the Government.

  • 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.

  • Database Management System (“DBMS”) is a computer process used to store, sort, manipulate and update the data required to provide Selective Routing and ALI.

  • Automated data acquisition and handling system or "DAHS" means that component of the continuous emission monitoring system, or other emissions monitoring system approved for use under section 11 of this rule, designed to interpret and convert individual output signals from pollutant concentration monitors, flow monitors, diluent gas monitors, and other component parts of the monitoring system to produce a continuous record of the measured parameters in the measurement units required by section 11 of this rule.

  • UNICEF Supply Website means UNICEF's public access webpage available athttp://www.unicef.org/supply/index_procurement_policies.html, as may be updated from time to time.

  • Data Log means a complete record of all Data Interchanged representing the Messages and their Associated Data between the parties;

  • Contractor Software means software which is proprietary to the Contractor, including software which is or will be used by the Contractor for the purposes of providing the Services.

  • Diagnostic x-ray system means an x-ray system designed for irradiation of any part of the human or animal body for the purpose of diagnosis or visualization.