PDMP Data definition

PDMP Data means prescription history information maintained by the Oregon PDMP under ORS 431A.855 to 431A.900.
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PDMP Data means prescription history information reported and accessed through the PDMP, including through the PDMP System.
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PDMP Data means the information compiled and ana- lyzed by the PDMP system from dispensing data submitted to it by dispensers
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Examples of PDMP Data in a sentence

  • Without limiting the applicability of terms defined in law and rule, the following terms also apply to this Agreement: Affiliate means an entity directly or indirectly controlling, controlled by or under common control with Approved Entity and whose employees, agents, and contractors will access PDMP Data through Approved Entity’s Gateway Service connection.

  • Leveraging Prescription Drug Monitoring Program (PDMP) Data in Overdose Prevention and Response,” 2021.

  • Authorized User may use the PDMP System to send, receive, find, and use PDMP Data only for the purposes set forth in this Agreement and applicable law and rules.

  • The Approved Entity may use the PDMP System to send, receive, find, and use PDMP Data only for the purposes set forth in this Agreement and applicable law and rules.

  • Authorized User shall not nor may it permit any attempted or actual duplication, modification, adaptation, translation, reverse engineering, decompilation, disassembling or creation of a derivative work based on the PDMP System or PDMP Data except as specifically provided for under this Agreement.

  • Notes from the Field: NF 3.2 Project Lazarus: Using PDMP Data to Mobilize and Measure Community Drug Abuse Prevention.

  • Both States have issued guides that require daily reporting of opioid dispensing data: North Dakota PDMP Data Submission Dispenser Guide, March 2017; and Arizona Controlled Substance Prescription Monitoring Program, January 2017.

  • Clinical User Registration and Access of PDMP Data The first two requirements of the report rely on registration and user statistics as follows:I.

  • Riparian function and stream morphology can be negatively affected leading to losses in fisheries habitat and increases in fish mortality.

  • As between the Authority and the Approved Entity, the Approved Entity, its Affiliates, and their Authorized Users are solely responsible for all decisions and actions taken or not taken involving patient care and monitoring resulting from, or in any way related to, the use of the PDMP System or PDMP Data.


More Definitions of PDMP Data

PDMP Data means the electronic data and information collected, processed and generated by regional authorities as part of their Prescription Drug Monitoring Programs.
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PDMP Data means data that are collected, maintained, managed and disclosed by the PDMP.
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PDMP Data means controlled substance or prescription data. “The PDMP hub” means Bureau of Justice Assistance (“BJA”) designated PDMP data sharing system.
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Related to PDMP Data

  • GLO Data means any data or information owned by the GLO, including PII or SPI as defined below, that Provider creates, obtains, accesses (via records, systems, or otherwise), receives (from the GLO or on behalf of the GLO), or uses in the performance of the Contract or any documents related thereto.

  • UNICEF Data means any and all information or data in digital form or processed or held in digital form that

  • Study Data shall have the meaning set forth in Section 8.1.

  • System Data means data and data elements collected by the SaaS Software, SaaS Service or Licensor’s computer systems regarding configuration, environment, usage, performance, vulnerabilities and security of the SaaS Software or SaaS Service that may be used to generate logs, statistics and reports regarding performance, availability, integrity and security of the SaaS Software.

  • Licensee Data means, other than Resultant Data, information, data and other content, in any form or medium, that is collected, downloaded or otherwise received, directly or indirectly from Licensee or an Authorized User by or through the Services.

  • Product Data are illustrations, standard schedules, performance charts, instructions, brochures, diagrams, and other information furnished by the Contractor to illustrate materials or equipment for some portion of the Work.

  • Client Data means personal data of data subjects, such as your employees, associates or partners, that is provided to S&P Global Ratings during the provision by S&P Global Ratings of the Services to you, such as name, job title, name of employer, office email address, office physical address, internet protocol address, office telephone number and language selection (and excludes special categories of personal data);

  • Research Data means documents in a digital form, other than scientific publications, which are collected or produced in the course of scientific research activities and are used as evidence in the research process, or are commonly accepted in the research community as necessary to validate research findings and results;

  • Patient Data means any electronic data, information or material about a Patient entered into the Software.

  • Customer Data means any content, materials, data and information that Authorized Users enter into the production system of a Cloud Service or that Customer derives from its use of and stores in the Cloud Service (e.g. Customer-specific reports). Customer Data and its derivatives will not include SAP’s Confidential Information.

  • input data means data provided to or directly acquired by an AI system on the basis of which the system produces an output;

  • Development Data means all non-clinical, clinical, technical, chemical, safety, and scientific data and information and other results, including relevant laboratory notebook information, screening data, and synthesis schemes, including descriptions in any form, data and other information, in each case, that is generated by or resulting from or in connection with the conduct of Development of Products, to the extent that the same are Controlled by or in Adapt’s or its Affiliates’ or Adapt’s Commercial Sublicensees’ possession, and may be disclosed to Lightlake without violating any obligation under Applicable Law.

  • Sensitive Data means information that is protected against unwarranted disclosure, to include Personally Identifiable Information (PII), Protected Health Information (PHI) or other private/confidential data, as specifically determined by the State. Sensitive Data includes information about an individual that (1) can be used to distinguish or trace an individual‘s identity, such as name, social security number, date and place of birth, mother‘s maiden name, or biometric records; (2) is linked or linkable to an individual, such as medical, educational, financial, and employment information; (3) falls within the definition of “personal information” under Md. Code Ann., Com. Law § 14-3501(d); or (4) falls within the definition of “personal information" under Md. Code Ann., State Govt. § 10-1301(c).

  • Raw Data means the primary quantitative and empirical data first collected from experiments and clinical trials conducted within the scope of this CRADA.

  • End User Data means any information or data of any kind that personally identifies (or that can be used, together with other information or data, to personally identify) an End User.

  • Health data means data related to the state of physical or mental health of the data principal and includes records regarding the past, present or future state of the health of such data principal, data collected in the course of registration for, or provision of health services, data associating the data principal to the provision of specific health services.

  • Subject Data As used in this section, “subject data” means recorded information, whether or not copyrighted, that is delivered or specified to be delivered as required by the Underlying Agreement. Examples of subject data include, but are not limited to computer software, standards, specifications, engineering drawings and associated lists, process sheets, manuals, technical reports, catalog item identifications, and related information, but do not include financial reports, cost analyses, or other similar information used for performance or administration of the Underlying Agreement.

  • 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:

  • User Data means any Personal Data or other data or information collected by or on behalf of the Company or any of its Subsidiaries from users of any Company Product or website of the Company or any of its Subsidiaries.

  • Pseudonymous data means personal data that cannot be attributed to a specific natural person

  • Regulatory Data means any and all research data, pharmacology data, chemistry, manufacturing, and control data, preclinical data, clinical data or all other documentation submitted, or required to be submitted, to Regulatory Authorities in association with regulatory filings for the Product in the Field (including any Drug Master Files (DMFs), Chemistry, Manufacturing and Control (“CMC”) data, or similar documentation).

  • Vendor Data means any and all information, data and documentation to be provided by Subcontractor/Supplier and its Subcontractors/Suppliers under this Order.

  • Company Data means all data collected, generated, or received in connection with the marketing, delivery, or use of any Company Product, including Personal Data.

  • Project Data means all proprietary data of the Project generated out of the Project operations and transactions, documents and related information including but not restricted to user data which the Bidder obtains, possesses or processes in the context of providing the Services to the users pursuant to this RFP including the SLA;

  • Detailed manufacturing or process data means technical data that describe the steps, sequences, and conditions of manufacturing, processing or assembly used by the manufacturer to produce an item or component or to perform a process.

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.