Preliminary Research Sample Clauses

Preliminary Research. Includes various historic documents as: as-built plans, for the existing bridge and approach roadway, right of way, geology, maintenance etc. COUNTY will assist in this effort to the limit of COUNTY records.
AutoNDA by SimpleDocs
Preliminary Research. DHA will obtain pertinent existing information from local, state, and federal agencies related to this project. The County will deliver any additional project information available to DHA at the kick-off meeting.
Preliminary Research. The second step in developing a project agree- ment involves a preliminary review of historical materials related to the site. Extensive informa- tion may be found in park files and in a variety of cultural and natural resources databases, such as the Cultural Landscapes Inventory, the List of Classified Structures, the Cultural Sites Inventory, natural resource inventories, and geographical information system databases. When reviewing historic materials, it is neces- sary to determine whether additional research is required to fully address the management objectives for the project. This step is critical for providing fundamental background informa- tion and clarifying what is known about the landscape and what additional information is needed. It is important to recognize that this research is quantitative but not extensive; research is conducted to identify and evaluate the adequacy of primary and secondary sources and collections, and to gather preliminary site information, ensuring the project agreement’s accuracy and completeness. Site Visit The final step in preparing a project agreement is a site visit. The site visit provides a prelimi- nary assessment of the landscape characteristics P R O J E C T A G R E E M E N T 3 Project Agreement for CLR Understand existing conditions in relation to management issues Determine level of investigation for the existing conditions investigation Identify the information that already exists Identify the information that needs to be added Determine level of investigation for the historical research List of specific issues and questions to be addressed by CLR Site Visit Preliminary assessment of landscape character- istics and associated features and conditions Preliminary Research Review of park files and archives Project Initiation Meeting between park and technical staff Outcome Process for Preparing a Project Agreement Activity Product and associated features, as well as the physical condition of the landscape. The site visit may take the form of a windshield survey or walk-through. It is preferable to be accompanied by someone who is knowledgeable about the site and the salient issues to be addressed in the CLR. The purpose of the visit is to understand management issues and existing conditions so that the project agreement can accurately reflect the required level of effort. Summary Although a project agreement directs and organizes the scope and content of a CLR, the agreement is not a static document. Becaus...
Preliminary Research. Includes various historic documents such as: as-built plans for the existing bridge and approach roadway, right-of-way, utilities, geology, maintenance, etc. The City will assist in this effort to the limit of City records. Field Investigation – Includes data gathering on the part of City and Quincy leading to the completion of the various reports and forms required for the funding, permitting, right-of-way acquisition and construction of the project. Task 1.2 – Coordination Point of Contact – Quincy’s Project Manager will be the single point of contact for maintaining liaison and coordination throughout the project with the City’s Project Manager and other team leaders. Project Data – City will provide available project data to Quincy.
Preliminary Research. ‌ As mentioned previously, this work builds upon the groundwork laid in [10], which describes a methodology to represent a system described in LSAT using automata. The definition of the system elements, namely, for resources, actions, activities, and sequences, used in this work is taken from [10]. Activity instantiation is an important concept with regards to this work. By definition, an instance of an activity in a sequence is the occurrence number of the activity in the given sequence. The instance number is usually denoted using superscript. To illustrate, consider the sequence ω in which activities ActA, ActB, ActA are executed sequentially. Then, ω = Act1 ; Act1 ; Act2 . Here, the first and second instances of ActA A A are denoted by Act1 and Act2 respectively. Since there is only one instance of ActB, it B is denoted by Act1 . [10] also explains how multiple instances of the same activity can be executed simultaneously. Subsequently, the steps to represent the behaviour of the system using activity, claiming and availability automata are also detailed (It is to be noted that the automata defining the peripheral behaviour have not been considered as part of the system behaviour as part of this research. Only the impact of introducing dependencies between actions of different activities are focused on). The activity automaton for an activity instance contains as edges the constituent actions of the activity while incorporating the dependencies between the actions as defined in the activity definition. The claiming automaton for a given resource defines the order in which a particular resource is claimed by different activities for a given activity sequence. Finally, the availability automata for a resource ensures that a resource can be claimed only when it is available or has been released by another resource. The activity, claiming and availability automata together describe the behavior of the system for a given sequence to which user-defined requirements are added for synthesis. 2 Implementation‌ In this section, a few methods are discussed to find activity sequences that can fulfil a set of given requirements. The LSAT specification elements are defined as per [10]. Furthermore, the following points are assumptions and definitions relevant to the implementation of the defined methods. L • The maximum length of the possible activity sequences ( ) is defined by the user. The length of a sequence (l) is defined as the number of activity instances in...
Preliminary Research. Prior to the study, some preliminary data were collected to inform the study design, understand the cultural context for the study and to identify ways to gain entrée into the study community. Preliminary data collection included a focus group discussion with key informants (e.g. educators, midwives, health workers, government officials, psychologists, and social workers) to inform participant recruitment, recommend culturally appropriate recruitment and entrée, and refine the scope of the topics covered in the in-depth interviews. We conducted four focus group discussions to develop the questions for the in-depth interview guide for the study with adolescent mothers. We conducted two of the four focus groups with adolescent girls ages 15 to 19 to discuss cultural norms surrounding dating, sexual health education, and teen pregnancy from the adolescent perspective to inform the wording of questions to account for linguistic variations across Kaqchikel communities and more commonly used terminology among adolescents; these focus grouped also helped refine the topics included in the in-depth interview guide. The other two focus groups were conducted with mothers of adolescent-age children to cover cultural norms of dating, sexual health education, and teen pregnancy from a mother´s perspective to provide context for the study and to develop questions for the interview guide. These preliminary data are not included in the data analysis for the study. Study Location This study took place in Sololá, Guatemala across ten municipalities where Kaqchikel is the dominant ethnic group, as demonstrated in Figure 1. The study was conducted in 2014 in collaboration with the Universidad del Xxxxx de Guatemala (UVG), Campus Altiplano, who contributed to the study design, hosted and supervised the research team, and facilitated connections to municipal government and community gatekeepers. Sololá is a department in the Western Highland of Guatemala that is home to approximately 450,000 residents, with 3 out of 5 residents living in rural communities. The population of Sololá are young with an average age of 18 years that experiences one of the highest adolescent fertility rates in the country. The average age of first childbirth being 20.3 years old [15]. The population is 94% indigenous comprising three indigenous ethnic groups: Kaqchikel (37%), Quiche (43%), and Tzutujil (16%) [15]. These three ethnic groups are geographically divided within the 19 municipalities in Solo...
Preliminary Research. CONSULTANT will obtain pertinent existing information from local, state, and federal agencies related to this project. The COUNTY will deliver any additional project information available to CONSULTANT at the kick-off meeting.
AutoNDA by SimpleDocs
Preliminary Research. The project regarding the collection of data concerning the cost of hip replacement implants carried out in the Xxxxxx-Romagna region took root from the research project whose aim was the “Analysis of cost-effectiveness in hip arthroprostheses operations”, launched in 2004, and also had the involvement of GRTS. As well, the Orthopaedic Prosthetic Implantology Register (RIPO) is situated at and managed by the Xxxxxx-Romagna Regional Authority and contains hip replacement implant data from 2001 to the present. The data held within the RIPO are collected from a form sent after each implant is performed by orthopaedic operating units of various health authorities. The collected data are then inserted into a database whose track record is defined and unmodified. This type of register permits the identification of the type of fixing of each implant, the product code that every producer assigns each single prosthetic component, the clinical information linked to the patient who has undergone the operation, whether it deals with primary implants or revisions. With this in mind, and using previously available flows of data, the next step was to define the set information needed in order to reach project objectives. The project is made up of several phases that are needed to collect, consolidate and integrate various types of data. The first phase involved analysing the dynamics when prosthetic elements are purchased by healthcare and hospital authorities in Xxxxxx-Romagna. Research was undertaken on a sample site, being a local health unit authority (AUSL) of the region in order to verify which purchasing and management methods were mainly used and how the cost data could be identified in a structured flow. The first obvious result was to single out as separate object the different hip replacement implants components dealt in the buying phase. Therefore, a search was made for the cost data concerning acetabular cups, acetabular inserts, femoral heads, stems and modular necks. Subsequently, other AUSLs were given a brief questionnaire so as to verify that the results obtained from the AUSL sample extended to the regional level. The following information was requested: • the most frequent types of negotiation when buying orthopaedic prostheses; • existence of eventual code systems at the health authority level, particularly relating to orthopaedic prostheses; • flow management flow of the concerned purchases and people in order to identify the representatives. the an...
Preliminary Research. XXXX and KHA will collect existing data, reports, and traffic studies relating to KHA’s previous work in preparing the SR 227 Operations Study prepared for, and approved by SLOCOG. XXXX and KHA will obtain pertinent existing information from local, state, and federal agencies related to this project. It is assumed the County will deliver additional project information available to the consultant at the kick-off meeting. Data Collection KHA will collect week-day peak-period intersection traffic counts for AM, afternoon school, and PM peak hours (six hours total at each intersection), at the following locations: • Aero Drive • Airport Drive • Farmhouse Lane • Fire Station Driveway (first driveway south of Farmhouse Lane) • Xxxxxxx Road KHA will collect 24-hour roadway segment volume counts at two locations. KHA will request signal timing data from the City of San Xxxx Obispo for the existing signal at Aero Drive. We assume the traffic data collected in June 2019 is valid and new traffic counts are not needed for the purpose of this study.

Related to Preliminary Research

  • Design Development Phase INDICATE IN STATEMENT OF WORK “NOT APPLICABLE” IF SECTION IS NOT APPLICABLE

  • Phase II A small portion of the work for the Phase II modifications to the Plattsburgh Substation will be performed by Transmission Owner, and the remainder will be performed by Clinton and Xxxxxxxxx. A detailed definition of the specific scope for Transmission Owner and Clinton and Xxxxxxxxx including interface points shall be defined during the design phase and, as such documents become available, copies will be delivered to the NYISO, Transmission Owner, Noble Altona Windpark, LLC and Marble River, LLC. The full scope includes the installation of wave traps, CCVT’s and modifications and/or additions to relaying on the MWP-1 and MWP- 2 lines. These lines will be reconfigured at the completion of Phase II to connect to Xxxxx and Xxxxxxx Substations on MWP-1 and the Xxxx Substation on MWP-2. Clinton and Xxxxxxxxx will design the upgrades and purchase the materials based on the outline specification that was prepared and issued by Transmission Owner. The work to be performed by Clinton and Xxxxxxxxx will include both the materials for the exterior and interior installations and items for Transmission Owner installation inside the control building in existing relay panels and communication racks. In addition, Clinton and Xxxxxxxxx will be responsible for the exterior and interior construction work and will provide construction management services in coordination with Transmission Owner. The civil design for the foundations and the electrical design for the cable runs to the control room will be designed by, as approved by Transmission Owner, and installed under the supervision and control of Clinton and Xxxxxxxxx. The equipment will be selected and procured in accordance with the specifications developed during the detailed engineering phase, copies of which shall be furnished to the NYISO, Transmission Owner, Noble Altona Windpark, LLC and Marble River, LLC. The construction of the foundations, structures, wave traps, CCTV and cable runs into the control building to the termination cabinets will be completed by Clinton and Xxxxxxxxx. The work at the Plattsburgh Substation will be installed under Transmission Owner’s CPP-1. Transmission Owner will provide Protection and Controls Engineering, install and terminate wiring from the termination cabinets to the control panels and relays, install relays and equipment in the existing panels, and will commission such work inside the 230kV control building. Transmission Owner will develop the communications protocols and data flow over the circuits.

  • 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.

  • Project Planning GOVERNMENTAL APPROVALS; ENVIRONMENTAL COMPLIANCE; PUBLIC INFORMATION 30 4.1 Planning and Engineering Activities 30 4.2 Site Conditions 30 4.3 Governmental Approvals 30 4.4 Environmental Compliance 34 4.5 Community Outreach and Public Information 35

  • PHASE is a distinct portion of the Work to be provided under this Agreement, as specified in the Statement Of Work.

  • Design Review Consumer shall provide Holy Cross an electrical one-line diagram and a relaying and metering one-line diagram prior to completion of detailed designs, unless the Consumer is installing a packaged system that is pre-certified to IEEE 1547.1 and UL 1741 standards. Packaged systems pre-certified under IEEE Standard 1547.1 and UL Standard 1741 will not require a relaying and metering one-line diagram. The submitted application and diagrams will be processed, reviewed, and acted upon in accordance with the Holy Cross Interconnection Policy.

  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMEA, Health Canada and other comparable drug and medical device (including diagnostic product) regulatory agencies outside of the United States to which they are subject; the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Disclosure Package and the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement, the Time of Sale Disclosure Package or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMEA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.

  • PROFESSIONAL DEVELOPMENT AND EDUCATIONAL IMPROVEMENT A. The Board agrees to implement the following:

  • 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.

  • Technology Research Analyst Job# 1810 General Characteristics Maintains a strong understanding of the enterprise’s IT systems and architectures. Assists in the analysis of the requirements for the enterprise and applying emerging technologies to support long-term business objectives. Responsible for researching, collecting, and disseminating information on emerging technologies and key learnings throughout the enterprise. Researches and recommends changes to foundation architecture. Supports research projects to identify and evaluate emerging technologies. Interfaces with users and staff to evaluate possible implementation of the new technology in the enterprise, consistent with the goal of improving existing systems and technologies and in meeting the needs of the business. Analyzes and researches process of deployment and assists in this process.

Time is Money Join Law Insider Premium to draft better contracts faster.