Research area Sample Clauses

Research area. The two villages where the research took place, Muluy and Rantau Layung (see Chapters 2 and 3), are located in the western part of Gunung Lumut and in two sub-districts in the kabupaten (regency or district) of Paser, in the province of East Kalimantan, (see figure 3.1).
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Research area the Western Wadden Sea This thesis focuses on the western part of the Dutch Wadden Sea and the former location of the Texel Roads in particular, with the Burgzand area at its centre. Historically, this is where ships were loaded and unloaded, primarily for the Amsterdam market.61 Much about the geological development of the Western Wadden Sea area has already been described in a series of publications, of which De Convexe Kustboog (the ‘Convex Coastal Arch’), by Xxxx Xxxxxxx, from 1999,62 deserves specific mention. Intensive archaeological research has also been done on the Texel Roads, mainly by government archaeologists, who have focused on the many well-preserved shipwrecks that have been discovered over the decades.63 Historians have paid special attention to the role of this area in the Golden Age and the Dutch East India Company (Vereenigde Oostindische Compagnie or VOC).64 However, the importance of the area as a roadstead is much greater and stretches over a longer period of time. It was not only used by ships going to the East and West Indies, but also by warships, merchant ships heading for or returning from the Baltic and elsewhere, and it functioned as such from at least the sixteenth to the twentieth century.
Research area. Development of a “reference case library” that advances a standard set of inputs of meteorology and land-use data, as well as different project facility types and traffic volumes. Such a library could serve as guidance and as a QA/QC check for future analyses. As part of an air quality analysis, meteorology and land use classes are needed to complete the final step: dispersion modeling. Gathering and inputting the necessary information is both confusing and time consuming. In many cases, depending upon the project facility type, inputs are similar in nature and could allow either a partially completed input file to be used directly or a comparison to established value ranges as a quality control measure. Each data type is discussed in detail below.
Research area. Application of the draft PA and TSD for CO to development of state-specific PAs for CO. This will identify and address issues with development and implementation of PAs from the template to be used by state DOTs. The research would encompass the entire process of PA development, from start to implementation. Lessons learned from this research could also be used to inform the process of state-specific PA development and implementation for MSATs and PM. As mentioned above, in addition to the five research areas related to PM and MSATs, a logical extension of Task 78 would be implementation of the phase 1 results to state-specific PAs for CO hot- spot analyses. Upon successful completion of such Task 78 extension research, similar work could be performed for any state DOT that would benefit from having a state-specific PA in place for CO hot- spot analysis. It is envisioned that most state DOTs would gain benefit by updating any CO analysis procedures they currently have in place. The following description outlines the concept of the proposed Task 78 extension research. The NCHRP 25-25 Task 78 study (2015) successfully developed templates for a PA and associated TSD that are designed to be implemented by state DOTs to streamline project-level air quality analyses for CO. The proposed study is for a pilot program that would apply the NCHRP templates for two or three state DOTS, starting from the beginning of the analysis process, making revisions to the templates as needed (e.g., to cover additional project types and/or configurations, and to use state-specific modeling inputs), and continuing through necessary approvals and subsequent execution with FHWA for each state DOT in the pilot program. Lessons learned in this initiative would inform and assist the subsequent implementation of the templates (with any revisions as appropriate) for state DOTs across the nation.
Research area. Research for this chapter was largely conducted between 2005 and 2007 in the cities of Balikpapan and Samarinda, and the districts of Kutai Kertanegara, East Kutai, Penajam North Paser, and Paser, where sawmills and industries were visited during this period. The flow of ironwood raw material, which comes from diverse areas, districts and municipalities, is complex.
Research area. The research area will consist of a process development lab of 750 square feet, a recovery area of 200 square feet, a centrifuge area of 200 square feet, fermentation area of 1,000 square feet, a microbial lab of 200 square feet, a refrigerated storage area of 200 square feet, and a quality assurance area of 1,000 square feet.

Related to Research area

  • Research Collaboration Upon FibroGen’s request, the Parties will discuss conducting a research program funded by AstraZeneca and directed toward franchise enhancement and lifecycle management for HIF Compounds or other topics that the Parties determine relevant to the Products and the Field. Upon agreement on the terms of such research program, the Parties will enter into a separate agreement or amend this Agreement accordingly.

  • Research Program 2.1 University will use reasonable efforts to conduct the Research Program described in Attachment A which is hereby incorporated in full by reference (“Research Program”), and will furnish the facilities necessary to carry out said Research Program. The Research Program will be under the direction of _____________________ (“Principal Investigator”), or his or her successor as mutually agreed to by the Parties and will be con­ducted by the Principal Investigator at the University.

  • Research Plan The Parties recognize that the Research Plan describes the collaborative research and development activities they will undertake and that interim research goals set forth in the Research Plan are good faith guidelines. Should events occur that require modification of these goals, then by mutual agreement the Parties can modify them through an amendment, according to Paragraph 13.6.

  • Research Program Term The Research Program shall be conducted during the period of five years commencing as of the Agreement Date ("Research Program Term"). Upon not later than seventy-five (75) days' prior written notice JT may, in its sole judgment, terminate the Research Program at the end of the third (3/rd/) year and fourth (4/th/) year of the Research Program. The RMC may terminate the Research Program any time during the Research Program Term if it unanimously determines the Research Program is no longer scientifically useful or that all potential Products would not be commercially viable. In case of such an early termination by JT or the RMC, JT shall be exempt from any payment(s) under Section 10(a) that would have become due and payable after the effective date of such early termination. Following any termination of the Research Program (i) that occurs simultaneously with the termination of this Agreement in accordance with Section 13 (i.e., no compound or Lead Compound has been designated previously a Collaboration Lead Compound in accordance with Section 3(b) and no Independent Lead Compound is being developed in accordance with Section 3(m)) or (ii) that is followed at some future date by the termination by JT of Development or co-promotion of any Collaboration Lead Compound and/or Product pursuant to Sections 3(l) or 5(c), respectively, or development of an Independent Lead Compound in accordance with Section 3(m) (A) any licenses granted by Tularik to JT will terminate, (B) JT will grant to Tularik an exclusive, sublicensable, worldwide license, to make, use and sell compounds, Collaboration Lead Compounds or Products under JT's interest in Program Patents and Program Know-How and (C) under the terms and conditions to be separately agreed, JT will also grant to Tularik a nonexclusive, sublicensable, worldwide license under any JT Patent Rights and Know-How to the extent necessary to practice the license granted under the Program Patents and Program Know-How in (B) (including, with respect to compounds, a limited number of JT's library compounds approved by JT); provided, however, that in the event the Research Program terminates but the Agreement has not terminated with respect to designated Collaboration Lead Compounds, Independent Lead Compounds and/or Products as provided in Section 2(g)(ii), Sections 2(g)(A), (B) and (C) shall apply only to those compounds, Collaboration Lead Compounds, Independent Lead Compounds and Products for which Development or co-promotion shall have been terminated and/or to those compounds or Lead Compounds that have not been designated previously a Collaboration Lead Compound in accordance with Section 3(b) or an Independent Lead Compound in accordance with Section 3(m); provided further that in the event that JT elects to pursue a Discontinued Compound or a Non-Proposed Compound on or before the first anniversary of the expiration or termination of the Research Program Term pursuant to Section 3(b)(iii) or 3(b)(iv), respectively, Sections 2(g)(A), (B) and (C) shall not apply to such Discontinued Compound or Non-Proposed Compound until such time as JT shall have terminated the Development or co-promotion of such Discontinued Compound or Non- Proposed Compound. Tularik will then be free to pursue clinical development and registration of such compounds, Lead Compounds and/or Products without obligation to JT except as provided in Section 4(f) or Section 5(c), as appropriate.

  • Collaboration We believe joint effort toward common goals achieves trust and produces greater impact for L.A. County’s youngest children and their families.

  • Development Program A. Development activities to be undertaken (Please break activities into subunits with the date of completion of major milestones)

  • 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.

  • Research License Each Collaborator shall allow the other Collaborator to practice any of its Non- Subject Inventions for the purpose of performing the Cooperative Work. No license, express or implied, for commercial application(s) is granted to either Collaborator in Non-Subject Inventions by performing the Cooperative Work. For commercial application(s) of Non-Subject Inventions, a license must be obtained from the owner.

  • Research Term The Research Program will be carried out during the two (2) year period following the Effective Date, unless this Agreement is terminated in accordance with Article 13 (such period, as may be extended pursuant to this Section 3.2, being the “Research Term”). BMS shall have the option to extend the Research Term for three (3) additional one (1) year periods on a year-by-year basis after the initial two (2) year period. At least one hundred eighty (180) days prior to the scheduled expiration of the Research Term (i.e., the applicable anniversary of the Effective Date) BMS will provide Ambrx with a nonbinding, good faith indication of whether or not BMS intends to extend the Research Term. In order to exercise its option to extend the Research Term, BMS must provide Ambrx a written notice exercising BMS’ option to extend the Research Term at least ninety (90) days prior to the scheduled expiration of the Research Term (i.e., the applicable anniversary of the Effective Date). If BMS does not provide such written notice, the Research Term will end when scheduled (i.e., on the applicable anniversary of the Effective Date). For each extension of the Research Term, subject to Section 3.4, the JRC will prepare an update to the Research Plan which will include an updated Budget for the BMS-funded Ambrx FTEs to perform the work required under such Research Plan and the projected Third Party Costs.

  • Research Plans The Research Plan for the [***] Designated Target is attached as Schedule 2.2.3-1. Subsequent Research Plans agreed upon in accordance with Section 2.4.2.4 will be attached as additional sequentially numbered schedules (Schedule 2.2.3-2, Schedule 2.2.3-3, etc.).

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