DATA PATHS Clause Samples

The DATA PATHS clause defines how data is transmitted, routed, or accessed within a system or between parties. It typically specifies the technical or logical routes that data will follow, such as through specific servers, networks, or storage locations, and may outline requirements for encryption or security along these paths. By clearly delineating the permitted or required data pathways, this clause helps ensure data integrity, security, and compliance with relevant regulations, thereby reducing the risk of unauthorized access or data breaches.
DATA PATHS. Decrypted DT Data shall not be available on outputs other than those specified in the Compliance Rules. Within a Licensed Product that includes Sink Functions, Decrypted Type 2 Audio DT Data, Decrypted Type 3 Audio DT Data, and the video portion of Decrypted DT Data, shall not be present on any user-accessible buses in analog or unencrypted, compressed form.
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DATA PATHS. Decrypted DT Data shall not be available on outputs other than those specified in the Compliance Rules. Within a Licensed Product that includes Sink Functions, Decrypted Type 2 Audio DT Data, Decrypted Type 3 Audio DT Data, and the video portion of Decrypted DT Data, shall not be present on any user-accessible buses in analog or unencrypted, compressed form. 2.1 A “user accessible bus” means (a) an internal analog connector that: (i) is designed and incorporated for the purpose of permitting end user upgrades or access or (ii) otherwise readily facilitates end user access or (b) a data bus that is designed for end user upgrades or access, such as an implementation of a smartcard, PCMCIA, Cardbus, or PCI that has standard sockets or otherwise readily facilitates end user access. A “user accessible bus” does not include memory buses, CPU buses, or similar portions of a device’s internal architecture that do not permit access to content in a form useable by end users. Clause 2.1(a) should be interpreted and applied so as to allow Adopter to design and manufacture its products to incorporate means, such as test points, used by Adopter or professionals to analyze or repair products; but not to provide a pretext for inducing consumers to obtain ready and unobstructed access to internal analog connectors. Without limiting the foregoing, with respect to clause 2.1(a), an internal analog connector shall be presumed to not “readily facilitate end user access” if (i) such connector and the video signal formats or levels of signals provided to such connector, are of a type not generally compatible with the accessible connections on consumer products, (ii) such access would create a risk of product damage, or (iii) such access would result in physical evidence that such access had occurred and would void any product warranty. 2.2 Licensed Products that use Common Device Keys or are manufactured after December 31, 2006, shall be clearly designed such that when the video portion of uncompressed, Decrypted DT Data with a resolution greater than a Constrained Image is transmitted over a User Accessible Bus, such Decrypted DT Data are reasonably secure from unauthorized interception by using either Widely Available Tools or Specialized Tools, except with difficulty, other than Circumvention Devices. The level of difficulty applicable to Widely Available Tools is such that a typical consumer should not be able to use Widely Available Tools, with or without instructions, to i...
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DATA PATHS. Decrypted AACS Content shall not be available on outputs other than those specified in the Compliance Rules.
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DATA PATHS. Decrypted SVR Data shall not be available on outputs other than those specified in the Compliance Rules. Within a Licensed Product, the Decrypted SVR Data shall not be present on any user-accessible buses in analog or unencrypted, compressed form.
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DATA PATHS. Decrypted HDCP Content shall not be available on outputs other than those specified in the Compliance Rules. Within a Display Device or Repeater, Decrypted HDCP Content shall not be present on any user-accessible buses in analog form or in unencrypted, compressed form. Adopter is cautioned that, when it is deemed technically feasible to do so, Licensor may revise these Robustness Rules to require that uncompressed Decrypted HDCP Content will be re-encrypted or otherwise protected before it is transmitted over such buses.‌‌‌‌‌‌‌ 2.1 A “user accessible bus” means a data bus that is designed for end user upgrades or access such as an implementation of smartcard, PCMCIA, Cardbus or PCI that has standard sockets or otherwise readily facilitates end user access, but not memory buses, CPU buses, and similar portions of a device’s internal architecture.
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Related to DATA PATHS

  • Background Data The Disclosing Party's Background Data, if any, will be identified in a separate technical document.

  • Data Use Each party may use Connected Account Data in accordance with this Agreement and the consent (if any) each obtains from each Connected Account. This consent includes, as to Stripe, consent it receives via the Connected Account Agreement.

  • Clinical Data and Regulatory Compliance The preclinical tests and clinical trials, and other studies (collectively, “studies”) that are described in, or the results of which are referred to in, the Registration Statement or the Prospectus were and, if still pending, are being conducted in all material respects in accordance with the protocols, procedures and controls designed and approved for such studies and with standard medical and scientific research procedures; each description of the results of such studies is accurate and complete in all material respects and fairly presents the data derived from such studies, and the Company and its subsidiaries have no knowledge of any other studies the results of which are inconsistent with, or otherwise call into question, the results described or referred to in the Registration Statement or the Prospectus; the Company and its subsidiaries have made all such filings and obtained all such approvals as may be required by the Food and Drug Administration of the U.S. Department of Health and Human Services or any committee thereof or from any other U.S. or foreign government or drug or medical device regulatory agency, or health care facility Institutional Review Board (collectively, the “Regulatory Agencies”); neither the Company nor any of its subsidiaries has received any notice of, or correspondence from, any Regulatory Agency requiring the termination, suspension or modification of any clinical trials that are described or referred to in the Registration Statement or the Prospectus; and the Company and its subsidiaries have each operated and currently are in compliance in all material respects with all applicable rules, regulations and policies of the Regulatory Agencies.

  • Technology Access Contractor expressly acknowledges that state funds may not be expended in connection with the purchase of an automated information system unless that system meets certain statutory requirements relating to accessibility by persons with visual impairments. Accordingly, Contractor represents and warrants to System Agency that the technology provided to System Agency for purchase (if applicable under this Contract or any related Solicitation) is capable, either by virtue of features included within the technology or because it is readily adaptable by use with other technology, of: • providing equivalent access for effective use by both visual and non-visual means; • presenting information, including prompts used for interactive communications, in formats intended for non-visual use; and • being integrated into networks for obtaining, retrieving, and disseminating information used by individuals who are not blind or visually impaired. For purposes of this Section, the phrase “equivalent access” means a substantially similar ability to communicate with or make use of the technology, either directly by features incorporated within the technology or by other reasonable means such as assistive devices or services which would constitute reasonable accommodations under the Americans With Disabilities Act or similar state or federal laws. Examples of methods by which equivalent access may be provided include, but are not limited to, keyboard alternatives to mouse commands and other means of navigating graphical displays, and customizable display appearance. In accordance with Section 2157.005 of the Texas Government Code, the Technology Access Clause contract provision remains in effect for any contract entered into before September 1, 2006.

  • Research Use The Requester agrees that if access is approved, (1) the PI named in the DAR and (2) those named in the “Senior/Key Person Profile” section of the DAR, including the Information Technology Director and any trainee, employee, or contractor1 working on the proposed research project under the direct oversight of these individuals, shall become Approved Users of the requested dataset(s). Research use will occur solely in connection with the approved research project described in the DAR, which includes a 1-2 paragraph description of the proposed research (i.e., a Research Use Statement). Investigators interested in using Cloud Computing for data storage and analysis must request permission to use Cloud Computing in the DAR and identify the Cloud Service Provider (CSP) or providers and/or Private Cloud System (PCS) that they propose to use. They must also submit a Cloud Computing Use Statement as part of the DAR that describes the type of service and how it will be used to carry out the proposed research as described in the Research Use Statement. If the Approved Users plan to collaborate with investigators outside the Requester, the investigators at each external site must submit an independent DAR using the same project title and Research Use Statement, and if using the cloud, Cloud Computing Use Statement. New uses of these data outside those described in the DAR will require submission of a new DAR; modifications to the research project will require submission of an amendment to this application (e.g., adding or deleting Requester Collaborators from the Requester, adding datasets to an approved project). Access to the requested dataset(s) is granted for a period of one (1) year, with the option to renew access or close-out a project at the end of that year. Submitting Investigator(s), or their collaborators, who provided the data or samples used to generate controlled-access datasets subject to the NIH GDS Policy and who have Institutional Review Board (IRB) approval and who meet any other study specific terms of access, are exempt from the limitation on the scope of the research use as defined in the DAR.