Researcher Provided Data definition

Researcher Provided Data means any and all data provided by another approved MSSNG Database researcher other than Institution, the Researcher or the Research Team to AS for inclusion in the MSSNG Database.

Examples of Researcher Provided Data in a sentence

  • Institution and Researcher shall acknowledge the contribution of researchers who generated Researcher Provided Data used by Institution in any and all publications, written and oral presentations, media reports, interviews and disclosures that are permitted hereunder and that result from any and all analyses of such Researcher Provided Data, whether the same occur during the term of this DAA or afterwards, in accordance with guidelines in this DAA and the MSSNG Website.

  • The UPDM and its attendant documentation become Attachment C of this document, Data Permissions for Researcher Provided Data.

  • Researcher shall obtain and provide to CES any necessary approvals for the use of non- Census data used at CES from CES and from the data producers, as appropriate (See Attachment C: Data Permissions for Researcher Provided Data).

Related to Researcher Provided Data

  • Licensed Data means the data licensed by the LME to the Licensee set out in the Order Form and further defined in Schedule 1 (Licensed Data);

  • Service Provider Materials means all works of authorship, products and materials [including, but not limited to, data, diagrams, charts, reports, specifications, studies, inventions, software, software development tools, methodologies, ideas, methods, processes, concepts and techniques] owned by, or licensed to, the Service Provider prior to the Commencement Date or independently developed by the Service Provider outside the scope of this Agreement at no expense to Transnet, and used by the Service Provider in the performance of the Services;

  • Excluded Data None – All data that falls into the sets below will be shared Data Being Sent for Categories A (Clinicians & Prescribing professionals) in 6.3 of this agreement. Below data items are coded data and free text Demographics data Previous and Future Appointments Discharge Summaries Clinic Letters Diagnosis Chronic Problems Allergies Current Medications Immunisations Data Being Sent for Category B (Other clinically supervised staff providing direct care) in 6.3 of this agreement. Below data items are coded data only and exclude free text Demographics data Previous and Future Appointments Discharge Summaries Clinic Letters Diagnosis Chronic Problems Allergies Current Medications Immunisations Data Being Sent for Category C (Administrative Staff supporting direct care) in 6.3 of this agreement Demographics data Previous and Future Appointments Receiving Organisations for this data: London Borough of Xxxxxxx - Care City of London – Social Care London Borough of Newham – Social Care Receiving Data from Agreement Name : East London Patient Record (eLPR) Method for receiving Data : East London Patient Record using the Cerner HIE This following table represents which roles in Homerton University Hospital Community that will fall into Categories A, B and C in terms of viewing shared data from other organisations. Name Code Category A Category B Category C Biomedical Scientist Access Role A Clinical Practitioner Access Role A Health Professional Access Role A Midwife Access Role A Nurse Access Role A Privacy Officer A Medical secretaries B Clinical administrators B Receptionists C The Caldicott Guardian or equivalent for the Homerton University Hospital will authorise the sending of this data and the receiving of any reciprocal data by accepting or rejecting this agreement in the Data Controller Console. The Caldicott Guardian for each provider will be added via the Data Controller Console. Providers will need to notify xxxx.xxxxx@xxx.xxx if there is a change in Caldicott Guardian or if there are any other changes: See Appendix E for more detail on the role of the Caldicott Guardian with this tool Appendix A continued: Homerton University Hospital – Acute Sharing arrangements for east London Patient Record – HEALTH ONLY Agreement Name : East London Patient Record (eLPR) Method for Sending – East London Patient Record using the Cerner HIE Purpose for sharing data : Individual Care (or Direct Care)

  • 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;

  • Derived Data means data of any kind derived as a result (directly or indirectly) of the Data being Manipulated;

  • Development Data means any and all research data, pharmacology data, chemistry, manufacturing and control data, preclinical data, clinical data and all other documentation (including raw data) compiled, developed or generated with respect to the Compound or Product.

  • 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.

  • 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.

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

  • Research Materials means all tangible materials other than Subject Data first produced in the performance of this CRADA.

  • 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:

  • Restricted Data means data typically exempt from public disclosure requirements under the provisions of applicable state or federal law. Examples of restricted information are regulated and confidential data.

  • Third-Party Filer means an entity that submits a Product filing to the Commission on behalf of an Insurer.

  • 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.

  • Deidentified data means data that cannot reasonably be

  • 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.

  • Protected Data means Student Data and/or Teacher or Principal Data, to the extent applicable to the product or service actually being provided to the District by Vendor pursuant to the Master Agreement.

  • Third Party Materials means any materials and information, including documents, data, know-how, ideas, methodologies, specifications, software, content, and technology, in any form or media, in which any Person other than the State or Contractor owns any Intellectual Property Right, but excluding Open-Source Components.

  • Product Information has the meaning specified in Section 10.12(a).

  • Internet Service Provider (ISP) means an Enhanced Service Provider (ESP) that provides Internet Services.

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

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

  • 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).

  • Development Site means any parcel or lot on which exists or which is intended for building development other than the following:

  • Anonymized Data means any Customer Data, from which all identifying information has been removed so that the individual data or information of a customer cannot be associated with that customer without extraordinary effort.

  • Study Materials means all the materials and information created for the Study, or required to be submitted to the Sponsor including all data, results, Biological Samples, Case Report Forms (or their equivalent) in whatever form held, conclusions, discoveries, inventions, know-how and the like, whether patentable or not, relating to the Study, which are discovered or developed as a result of the Study, but excluding the Institution’s ordinary patient records.