REQUIRED COMSATCOM COMPLEX SOLUTION TYPES Clause Samples

REQUIRED COMSATCOM COMPLEX SOLUTION TYPES. C.2.3.1 COMSATCOM Complex Solutions include, but are not limited to, any combination of bandwidth, throughput, terminals, other user equipment, teleports, terrestrial tail circuits, networks, other terrestrial infrastructure, integration and engineering services, and installation, operations, and maintenance. C.2.3.2 The Contractor solutions shall meet the Information Assurance, Responsiveness, Portability, Flexibility/Optimization, Capacity, Coverage, Net Ready (Interoperability), Network Monitoring (Net Ops), Electro Magnetic Interference (EMI) / Radio Frequency Interference (RFI) Identification, Characterization, and Geo-location, and Security requirements outlined in Section C.2.4 as assigned by the Ordering Activity on a Task Order basis. C.2.3.3 The Contractor shall have the capability to deploy the necessary terminals, teleports, terrestrial tail circuits, networks, Integration Services, Engineering Services, Licensing, Network Management, Operations & Maintenance, and Training required by the Ordering Activity. The Contractor must provide documentation required to conduct Security Assessments and obtain a Security Authorization.4 C.2.3.4 The Contractor shall provide the necessary capabilities and deliver solutions of the scope herein, in response to requirements aligning with the COMSATCOM Complex Solution types described in C.2.3.4.1 through C.2.3.4.9. Additionally, content/solution types/applications (e.g., broadcast technology) that is connected to a satellite network may be considered in-scope if the majority of the solution is satellite-orientated.
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Related to REQUIRED COMSATCOM COMPLEX SOLUTION TYPES

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  • 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.

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