Value Engineering Studies Sample Clauses

Value Engineering Studies. The CM shall provide value engineering recommendations to the Owner and Designer for major construction components, including cost evaluations of alternative materials and systems.
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Value Engineering Studies. The CM shall provide value engineering recommendations to the Owner and Designer at the Schematic Design, Design Development and 75% of the Construction Drawings Phases for major construction components, including cost evaluations of alternative materials and systems. The 75% Construction Drawings Phase set shall be the basis for the PMGP.
Sample 1
Value Engineering Studies. The Consultant shall provide value engineering recommendations to the City and Designer on major construction components, including cost evaluations of alternative materials and systems. 1.3.4. Reporting
Sample 1
Value Engineering Studies. When required, the Consultant shall provide team staffing and support to conduct Value Engineering studies on projects, standards, specifications or processes. Minimum service requirements are as follows: I. Value Engineering studies may be required at one or more of the following project phases, as outlined in FDOT Procedure No. 000-000-000 A. Concepts - immediately following the development of a recommended concept or corridor analysis. B. Project Development and Environmental Studies (PD&E) - normally following the draft Preliminary Engineering Report, and prior to the public hearing, but may be held at other key times during the PD&E phase. C. Design – the desired time is following completion of Phase I (30%) design plans and prior to Phase II (60%) design plans, but can be held at other times during the projects design phase. D. Design/Build – Prior to the release of the Request for Proposal (RFP) Document. II. The consultant shall be available to conduct Value Engineering studies for a period of time to be established jointly by the Department’s State Value Engineer, District Value Engineer and the Consultant. The Consultant shall receive notice to proceed on each Value Engineering study prior to the start of the study. III. Services to be provided may involve any of the following, at the discretion of the Department’s State Value Engineer. A. A Value Engineering Team Leader with remaining team members comprised of personnel appointed by the Department. B. A Value Engineering Team Leader with remaining team members comprised of specialists provided by the Consultant and personnel appointed by the Department. C. A Value Engineering Team Leader with remaining team members comprised of specialists provided by the Consultant.
Sample 1
Value Engineering Studies. A. Participate in Value Engineering reviews at the level appropriate for the projects at the completion of the first draft of the Final Design Phase documents (approximately 60% completion) to assist in identifying ways to improve value to the owner or reduce the cost for the project. Provide cost estimates to quantify potential cost savings to reduce the overall cost for the Project. B. Assist OA in conducting a workshop to identify potential changes which could reduce the cost of the Project or increase the value of the Project by more than the cost of the changes. Present selected alternatives for more detailed evaluation. The detailed evaluation will consider cost, ability to implement the changes, technical analysis, and the impact of changes on the Project. Ideas that pass the technical and economic analysis, and merit incorporation into the design of the project, will be presented, in a draft report, as a proposal to the OPT for consideration. Incorporate responses of the OPT in the final report. C. Review and comment on deliverables which include draft and final value engineering recommendation reports.
Sample 1
Value Engineering Studies. If deemed necessary by the Owner, the CM shall provide value engineering recommendations to the Owner and Designer at the Schematic Design, Design Development and 75% of the Construction Drawings Phases for major construction components, including cost evaluations of alternative materials and systems. The Schematic Design Phase set shall be the basis for the Statement of Probable Construction Cost (“SPCC”).
Sample 1
Value Engineering Studies. The CM shall provide value engineering recommendations to the Owner and Designer at the Schematic Design, Design Development and 75% of the Construction Drawings Phases for major construction components, including cost evaluations of alternative materials and systems. Alternative building systems shall be analyzed at the Schematic Design Phase to compare costs, availability and sequencing. At a minimum, compare and contrast cost, availability and constructability issues for the following building systems: load bearing masonry; precast concrete walls and double tee roof; structural steel frame with masonry bracing/infill; rigid steel frame with light gauge framing infill and rainscreen envelope; and cold rolled framing, panelized system. Note that the Media Center Classroom additions may require different building systems to provide the most cost effective solution. The 75% Construction Drawings Phase set shall be the basis for the PMGP.
Sample 1
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Value Engineering Studies. Value Engineering (VE) studies shall be conducted on projects in accordance with Federal and State requirements and latest version of the AASHTO - Guidelines for Value Engineering. VE will be used to provide recommendations for: providing the needed functions safely, reliably, efficiently, and at the lowest overall cost; improving the value and quality of the project; and reducing the time to complete the project.
Sample 1

Related to Value Engineering Studies

  • Feasibility Study A feasibility study will identify the potential costs, service quality and other benefits which would result from contracting out the work in question. The cost analysis for the feasibility study shall not include the Employer’s indirect overhead costs for existing salaries or wages and benefits for administrative staff or for rent, equipment, utilities, and materials, except to the extent that such costs are attributable solely to performing the services to be contracted out. Upon completion of the feasibility study, the Employer agrees to furnish the Union with a copy if the feasibility study, the bid from the Apparent Successful Bidder and all pertinent information upon which the Employer based its decision to contract out the work including, but not limited to, the total cost savings the Employer anticipates. The Employer shall not go forward with contracting out the work in question if more than sixty percent (60%) of any projected savings resulting from the contracting out are attributable to lower employee wage and benefit costs.

  • Development Phase contractual phase initiated with the approval of ANP for the Development Plan and which is extended during the Production Phase while investments in xxxxx, equipment, and facilities for the Production of Oil and Gas according to the Best Practices of the Oil Industry are required.

  • Studies The clinical, pre-clinical and other studies and tests conducted by or on behalf of or sponsored by the Company or its subsidiaries that are described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus were and, if still pending, are being conducted in accordance in all material respects with all statutes, laws, rules and regulations, as applicable (including, without limitation, those administered by the FDA or by any foreign, federal, state or local governmental or regulatory authority performing functions similar to those performed by the FDA). The descriptions of the results of such studies and tests that are described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus are accurate and complete in all material respects and fairly present the published data derived from such studies and tests, and each of the Company and its subsidiaries has no knowledge of other studies or tests 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 and the Prospectus. Except as described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, neither the Company nor its subsidiaries has received any notices or other correspondence from the FDA or any other foreign, federal, state or local governmental or regulatory authority performing functions similar to those performed by the FDA with respect to any ongoing clinical or pre-clinical studies or tests requiring the termination or suspension of such studies or tests. For the avoidance of doubt, the Company makes no representation or warranty that the results of any studies, tests or preclinical or clinical trials conducted by or on behalf of the Company will be sufficient to obtain governmental approval from the FDA or any foreign, state or local governmental body exercising comparable authority.

  • Development Diligence Pfizer will use its Commercially Reasonable Efforts to Develop and seek Regulatory Approval for [ * ] Product [ * ] in the Field [ * ]. Pfizer will [ * ] with respect to the Development or Regulatory Approval of Products under this Agreement.

  • Clinical Studies The animal and other preclinical studies and clinical trials conducted by the Company or on behalf of the Company were, and, if still pending are, to the Company’s knowledge, being conducted in all material respects in compliance with all Applicable Laws and in accordance with experimental protocols, procedures and controls generally used by qualified experts in the preclinical study and clinical trials of new drugs and biologics as applied to comparable products to those being developed by the Company; the descriptions of the results of such preclinical studies and clinical trials contained in the Registration Statement and the Prospectus are accurate and complete in all material respects, and, except as set forth in the Registration Statement and the Prospectus, the Company has no knowledge of any other clinical trials or preclinical studies, the results of which reasonably call into question the clinical trial or preclinical study results described or referred to in the Registration Statement and the Prospectus when viewed in the context in which such results are described; and the Company has not received any written notices or correspondence from the FDA, the EMA, or any other domestic or foreign governmental agency requiring the termination, suspension or modification of any preclinical studies or clinical trials conducted by or on behalf of the Company that are described in the Registration Statement and the Prospectus or the results of which are referred to in the Registration Statement and the Prospectus.

  • Development Plan document specifying the work program, schedule, and relevant investments required for the Development and the Production of a Discovery or set of Discoveries of Oil and Gas in the Concession Area, including its abandonment.

  • Development Work The Support Standards do not include development work either (i) on software not licensed from CentralSquare or (ii) development work for enhancements or features that are outside the documented functionality of the Solutions, except such work as may be specifically purchased and outlined in Exhibit 1. CentralSquare retains all Intellectual Property Rights in development work performed and Customer may request consulting and development work from CentralSquare as a separate billable service.

  • Study An application for leave of absence for professional study must be supported by a written statement indicating what study or research is to be undertaken, or, if applicable, what subjects are to be studied and at what institutions.

  • Development Activities The Development activities referred to in item “b” of paragraph 3.1 include: studies and projects of implementation of the Production facilities; drilling and completion of the Producing and injection xxxxx; and installation of equipment and vessels for extraction, collection, Treatment, storage, and transfer of Oil and Gas. The installation referred to in item “c” includes, but is not limited to, offshore platforms, pipelines, Oil and Gas Treatment plants, equipment and facilities for measurement of the inspected Production, wellhead equipment, production pipes, flow lines, tanks, and other facilities exclusively intended for extraction, as well as oil and gas pipelines for Production Outflow and their respective compressor and pumping stations.

  • Research Project The findings of any research project, which would change the provisions of this Agreement will not be implemented until such changes are negotiated and agreed to by the parties.

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