GSK Data definition

GSK Data means all text, files, images, graphics, illustrations, information, data (including Personal Information or Personal Data, as that term is described in the Data Privacy Schedule), audio, video, photographs and any other content and materials, in any format, that is provided by or on behalf of GSK or obtained by Supplier or Supplier Personnel in connection with or the performance of Supplier’s obligations under this Agreement, including any derivatives of such data or information. GSK Data includes any such data or information that either (a) is created, generated, collected or Processed by Supplier Personnel in the performance of Supplier’s obligations under the Agreement, or (b) resides in, or runs on or through, the Supplier Environment, or is accessed through GSK’s information systems, as well as any output, copies, reproductions, improvements, modifications, adaptations, translations or other derivative works of, based on, derived from or otherwise using such data and information. For the avoidance of doubt, GSK Data: (i) includes all GSK Confidential Information, and (ii) excludes Supplier Confidential Information.
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GSK Data means any data or information of or concerning GSK or its Affiliates or other recipients of the Services that is provided to or obtained by Supplier or Supplier Personnel in connection with the negotiation and execution of the Agreement or the performance of Supplier’s obligations under the Agreement, including any such data and information that either (i) is created, generated, collected or Processed by Supplier Personnel in the performance of Supplier’s obligations under the Agreement, including data processing input and output, Service Level measurements, asset information, reports, third party service and product agreements, and Supplier’s charges to GSK, or(ii) resides in or is accessed through GSK’s Information Systems or Supplier’sInformation System; as well as any data and information derived from the foregoing. For the avoidance of doubt, GSK Data includes all GSK Confidential Information, GSK Critical and Sensitive Information, GSK Personal Information and GSK Sensitive Personal Information. 2.7 GSK Critical and Sensitive Information.
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GSK Data means all text, files, images, graphics, illustrations, information, data (including GSK Personal Information or personal data) , audio, video, photographs and any other content and materials, in any format, that is provided by or on behalf of GSK or obtained by Supplier or Supplier Personnel in connection with the performance of Supplier's obligations under the Agreement, including any data and information that is entered into or stored by or on behalf of GSK or derivatives of such data or information.
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Examples of GSK Data in a sentence

  • Supplier shall maintain software and hardware used to Process GSK Data at versions supported by the licensor or manufacturer, as applicable.

  • While providing the Services identified in a Service Order or Statement of Work to the Agreement, Supplier will maintain, and will comply at all times with, a comprehensive cyber security program of policies, standard operating procedures (“SOPs’) and controls governing the Processing, storage, transmission and security of GSK Data (the “CSP”).

  • The locations where Supplier will receive, maintain, Process, store, access or transmit GSK Data can not be changed without GSK consent.

  • The location where Supplier will receive, maintain, Process, store, access or transmit GSK Data is at GSK Premises.

  • Supplier will report to GSK by email to xxxx@xxx.xxx any verified accidental, unauthorized or unlawful use, loss, destruction, disclosure, access, corruption, modification, sale, rental or other Processing of any GSK Data (a “Security Breach”) within twenty-four (24) hours of Supplier’s verification.

  • GSK ACCESS.Supplier will make available upon GSK request security logs and other operational records pertaining to the access, storage, maintenance, Processing or destruction of GSK Data.

  • Mr. Auriol testified that “you need an odd number” of grooves, pointing to the three grooves in Figure 2 and explaining that “[i]f we only had two grooves, there was a chance that the rivet would rotate on itself inside the tube because the stem of the rivet might go inside one of the grooves.” Auriol Dep.

  • Supplier shall encrypt all GSK Data stored on any removal media or portable device.

  • Supplier shall maintain a continuous vendor risk management program that assesses all Subcontractors that access, store, process or transmit GSK Data for appropriate security controls and cyber security practices, and will only engage Subcontractors who demonstrate compliance with Supplier’s CSP or like standards to support the delivery of the Services.

  • Supplier will ensure that GSK Data and areas where GSK Data is Processed are physically secured against unauthorized access.


More Definitions of GSK Data

GSK Data means any data or information GSK or its Affiliates provides to or is obtained by the Company in connection with the Agreement or the performance of the Company’s obligations under the Agreement. Including any such data and information that either (i) is created, generated, collected or Processed by Contractor, including data processing input and output, asset information, reports, third party service and product agreements, and charges, or (ii) resides in or is accessed through GSK’s Information Systems; as well as any data and information derived from the foregoing. For the avoidance of doubt, GSK Data includes all GSK Confidential Information, GSK Critical and Sensitive Information, GSK Personal Information, GSK Sensitive Personal Information and GSK Content.
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GSK Data means any and all Data other than Eurand Data.
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Related to GSK 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;

  • 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).

  • 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.

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

  • 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.

  • 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.

  • 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);

  • 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.

  • 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:

  • Regulatory Materials means, with respect to a Licensed Product for any particular indication in any particular jurisdiction, regulatory applications and submissions (and any supplements or amendments thereto), and any notifications, communications, correspondence, registrations, drug master files, Regulatory Approvals and/or other filings made to, received from or otherwise conducted with a Regulatory Authority, including BLAs and INDs, as applicable, that relate to such Licensed Product in such jurisdiction. Regulatory Materials also include presentations, responses, and applications for Regulatory Approvals.

  • 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.

  • 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.

  • Third Party Data has the meaning set forth in Section 9.3(a).

  • Customer Materials any materials, data, information, software, equipment or other resources owned by or licensed to You and made available to Us pursuant to facilitating Your use of the Services, including Customer Data.

  • Third Party Materials means materials and information, in any form or medium, including any software, documents, data, content, specifications, products, equipment or components of or relating to the Services that are not proprietary to NCIT.

  • IP Materials has the meaning given to it in clause E8.1 (Intellectual Property Rights).

  • DXC Data means the content, information and data pertaining to DXC and/or DXC Customers that is submitted to or accessed by Supplier pursuant to this Agreement. DXC Data may include, but is not limited to the following, each of which is defined more fully herein, DXC Sensitive Information, Confidential Information, Personal Information, and Protected Health Information (PHI).

  • Technical Information means technical data or computer software, as those terms are defined in the clause at DFARS 252.227-7013, Rights in Technical Data-Non Commercial Items, regardless of whether or not the clause is incorporated in this solicitation or contract. Examples of technical information include research and engineering data, engineering drawings, and associated lists, specifications, standards, process sheets, manuals, technical reports, technical orders, catalog-item identifications, data sets, studies and analyses and related information, and computer software executable code and source code.

  • SAP Materials means any software, programs, tools, systems, data, or other materials made available by SAP or any other member of the SAP Group to Partner or to an End User (either directly or indirectly via Partner) prior to or in the course of the performance under any part of this Agreement including, but not limited to, the other SAP Products.

  • 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.

  • 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.

  • Licensed Materials means any materials that Executive utilizes for the benefit of the Company (or any Subsidiary thereof), or delivers to the Company or the Company’s Customers, which (a) do not constitute Work Product, (b) are created by Executive or of which Executive is otherwise in lawful possession and (c) Executive may lawfully utilize for the benefit of, or distribute to, the Company or the Company’s Customers.

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

  • Licensed Technology means the Licensed Patents and the Licensed Know-How.

  • APIs means SAP application programming interface and accompanying or related Documentation, source code, tools, executable applications, libraries, subroutines, widgets and other materials made available by SAP or through SAP tools or SAP Software Development Kit (and all derivative works or modifications thereof) to Provider that allow Provider to integrate the Provider Service with the Cloud Service, including any access code, authentication keys or similar mechanisms to enable access of the APIs.