FUNCTIONAL DESIGN Sample Clauses

FUNCTIONAL DESIGN. 2.1 APPROACH For Field Activities (FA) created by City CSR: The following diagram illustrates the processes involved in the creation of the flat file that is interfaced to each Hauler. FDS – Create Download Staging This process looks for all field orders that are marked for extraction (a field order gets marked for extraction when it is first created if its dispatch group is dispatchable). For each record found, the system creates a field order download staging record. Each download staging record is marked with a batch control ID & run number when it’s created. • The batch control ID comes from the field order’s dispatch group. This ID corresponds with a specific extraction method. • The run number is the batch control ID’s current run number. FDL – Create Download Flat File This process reads all download staging records marked with a given batch control ID & run number, and creates the flat files for the Haulers. This process is re-runnable and the flat-files can be reproduced at any time. The no. of files created in each run is dependant on the distinct Distributor Ids (Haulers) for the batch and run number being processed. The file structure is as follows: PeopleSoft RM Field Name Structure Comments FA_ID AN (10) The Field Activity ID in PeopleSoft Revenue Management FA_TYPE_CD AN (8) The Field Activity type code FA_DESCR AN (30) The corresponding FA Description. SP_ID AN (10) The Service Point ID associated to the Field Activity SP_TYPE_CD AN (8) The SP Type Code for the SP_ID that is referenced on the FA. Since the same FA Type can be used across all services, the combination of the FA Description with the SP Type Code will indicate for which service the activity is being performed for. EXTRACT_DTTM DATE (26) CI_FO.EXTRACT_DTTM SCHED_DT DATE (10) CI_FO.SCHED_DT SCHED_TM TIME (15) CI_FO.SCHED_TM FA_STATUS_FLG AN (2) “P”  Pending INSTRUCTIONS AN (254) For applicable FA Types, the current and new Multi- Information will be transferred. This is only applicable for single-row SFDs or Yard Trimming/Street Sweeping Service. For e.g. multi-row SDF and MFDs, the user (City CSR) is required to manually input the instruction for the Hauler. PeopleSoft RM Field Name Structure Comments DESCR254 AN (254) Additional Comments. PREM_ID AN (10) CI_PREM.PREM_ID CU_LEGACY_SLN AN (50) Legacy Service Location Number CI_PREM_GEO.GEO_VAL Where GEO_TYPE_CD = ‘SLN’ (only populate if available) CU_APN AN (50) Current Parcel Number CU_SVC_ADDRESS AN (150) Custom Field. Servic...
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FUNCTIONAL DESIGN. A detailed functional design specification for the Network Status System will ensure that any reasonable requirements of BDB are met within the constraints of the CTI TOC system. SCHEDULE 4 SERVICES PROVIDED BY CTI GENERAL QUALITY CTI's operation is governed by a quality management system that is accredited to ISO 9001. As far as possible, CTI expects suppliers to operate under similar quality arrangements. CTI staff are chosen with appropriate skills and are kept up to date with training, as needed, in new techniques and systems. SAFETY CTI's internal Safety Policy (the "Safety Policy") fulfils the company's legal requirement under the Health and Safety at Work Xxx 0000. The Safety Policy is carried out through a series of Company Safety Instructions under the auspices of a full-time Company Safety Adviser (CSA). All staff receive relevant training to carry out their jobs in accordance with the Safety Policy. Such training is under continual review.
FUNCTIONAL DESIGN. The term “Functional Design” means a written description, usually in technical language, setting forth the specifications for a computer program or configuration of a computer system that implements the Requirements.
FUNCTIONAL DESIGN. 2.1 APPROACH For Field Activities (FA) created by City CSR: The following diagram illustrates the processes involved in the creation of the flat file that is interfaced to each Hauler. FDS – Create Download Staging This process looks for all field orders that are marked for extraction (a field order gets marked for extraction when it is first created if its dispatch group is dispatchable). For each record found, the system creates a field order download staging record. Each download staging record is marked with a batch control ID & run number when it’s created. • The batch control ID comes from the field order’s dispatch group. This ID corresponds with a specific extraction method. • The run number is the batch control ID’s current run number. FDL – Create Download Flat File This process reads all download staging records marked with a given batch control ID & run number, and creates the flat files for the Haulers. This process is re-runnable and the flat-files can be reproduced at any time. The no. of files created in each run is dependant on the distinct Distributor Ids (Haulers) for the batch and run number being processed. The file structure is as follows: PeopleSoft RM Field Name Structure Comments FA_ID AN (10) The Field Activity ID in PeopleSoft Revenue Management FA_TYPE_CD AN (8) The Field Activity type code FA_DESCR AN (30) The corresponding FA Description. SP_ID AN (10) The Service Point ID associated to the Field Activity
FUNCTIONAL DESIGN. Contractor shall develop and provide a comprehensive Functional Design Document (FDD) to Agency. Contractor shall maintain components of the design throughout the course of the Project and updated when any System design changes occur. The Contractor shall conduct a walkthrough of the FDD with the Oregon Votes Steering Committee and the External QA Consultant to validate the contents of the FDD. The FDD must incorporate all information from the design sessions and all Functional Requirements. Deliverable(s) and Acceptance Criteria Contractor shall provide the following:
FUNCTIONAL DESIGN. Complete functional design layout for the proposed improvements. The primary focus will be on development of roadway geometrics, identify existing and proposed utility locations, identify existing and proposed right-of-way needs, and develop a general staging concept to construct the improvements. The work to be performed by the Consultant under the Functional Design phase shall consist of the following tasks: Task 1 - Develop Design Criteria The Consultant will summarize and submit to the City design criteria used to develop the project. Criteria will conform to the City, Iowa DOT, SUDAS, and AASHTO design standards. The criteria to be addressed include: • Functional classification and design typeDesign speed and Regulatory speed • Design vehicles for intersection design • Widths of travel lanes, parking areas, and right-of-way • Preferred Clear Zone • Acceptable Clear Zone • Provisions for pedestrians and/or bicycles • Street lighting requirementsUtility corridor locations Prepare a brief technical memorandum documenting the proposed criteria. The memorandum will be reviewed, revised, and approved by the City prior to proceeding with subsequent tasks. Task 2 - Develop Typical Sections Develop typical sections for the mainline street improvements. This task includes lane widths, curb section/type, sidewalk widths, right-of-way widths, pavement types, and clear-zones. This task does not include pavement and subgrade design. This task also includes identifying potential storm sewer, sanitary sewer, water main, fiber optics, and other utility locations in the development of the typical sections. Detailed design calculations and capacity analysis for storm sewer, water main, or sanitary sewer is not included as part of this task. It is anticipated that three (3) typical cross sections will be developed for West First Street that includes widening to the north, widening to the south, or a symmetrical widening about the centerline of the existing roadway. Typical cross sections will also be developed for each of the side street connections. Task 3 - Develop Functional Geometrics Develop functional geometrics that includes intersection return radii, sidewalk locations, and driveway locations for the project. Included as part of this task is turning design vehicle templates at the intersections.

Related to FUNCTIONAL DESIGN

  • DTC DIRECT REGISTRATION SYSTEM AND PROFILE MODIFICATION SYSTEM (a) Notwithstanding the provisions of Section 2.4 of the Deposit Agreement, the parties acknowledge that DTC’s Direct Registration System (“DRS”) and Profile Modification System (“Profile”) apply to the American Depositary Shares upon acceptance thereof to DRS by DTC. DRS is the system administered by DTC that facilitates interchange between registered holding of uncertificated securities and holding of security entitlements in those securities through DTC and a DTC participant. Profile is a required feature of DRS that allows a DTC participant, claiming to act on behalf of an Owner of American Depositary Shares, to direct the Depositary to register a transfer of those American Depositary Shares to DTC or its nominee and to deliver those American Depositary Shares to the DTC account of that DTC participant without receipt by the Depositary of prior authorization from the Owner to register that transfer.

  • Recognition of the U.S. Special Resolution Regimes (a) In the event that any Underwriter that is a Covered Entity becomes subject to a proceeding under a U.S. Special Resolution Regime, the transfer from such Underwriter of this Agreement, and any interest and obligation in or under this Agreement, will be effective to the same extent as the transfer would be effective under the U.S. Special Resolution Regime if this Agreement, and any such interest and obligation, were governed by the laws of the United States or a state of the United States.

  • Outside Services Consultant shall not use the service of any other person, entity, or organization in the performance of Consultant’s duties without the prior written consent of an officer of the Company. Should the Company consent to the use by Consultant of the services of any other person, entity, or organization, no information regarding the services to be performed under this Agreement shall be disclosed to that person, entity, or organization until such person, entity, or organization has executed an agreement to protect the confidentiality of the Company’s Confidential Information (as defined in Article 5) and the Company’s absolute and complete ownership of all right, title, and interest in the work performed under this Agreement.

  • Recognition of U.S. Special Resolution Regimes (i) In the event a Covered Party becomes subject to a proceeding under a U.S. Special Resolution Regime, the transfer of this Agreement (and any interest and obligation in or under, and any property securing, this Agreement) from such Covered Party will be effective to the same extent as the transfer would be effective under the U.S. Special Resolution Regime if this Agreement (and any interest and obligation in or under, and any property securing, this Agreement) were governed by the laws of the United States or a State of the United States.

  • 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, Registration Statement, the Pricing Disclosure Package or the Prospectus were and, if still pending, are being conducted in all material respects in accordance with applicable laws, rules, regulations and policies of the Food and Drug Administration of the U.S. Department of Health and Human Services (the “FDA”) or any committee thereof or of any other U.S. or foreign government or drug or medical device regulatory agency, or health care facility Institutional Review Board; 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 materially inconsistent with, or otherwise call into question, the results described or referred to in the Registration Statement, the Pricing Disclosure Package or the Prospectus; for such studies that have been or are being conducted, the Company and its subsidiaries have made all such filings and obtained all such approvals as may be required by foreign government or drug or medical device regulatory agencies, or foreign health care facility Institutional Review Boards; and no investigational new drug application filed by or on behalf of the Company or any of its subsidiaries with the FDA has been terminated or suspended by the FDA, and neither the FDA nor any applicable foreign regulatory agency has commenced, or, to the knowledge of the Company, threatened to initiate, any action to place a clinical hold order on, or otherwise terminate, delay or suspend, any proposed or ongoing studies conducted or proposed to be conducted by or on behalf of the Company or any of its subsidiaries.

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