Preparatory Phase Sample Clauses

Preparatory Phase. This phase shall be performed prior to beginning work on each definable feature of work, after all required plans/documents/materials are approved/accepted, and after copies are at the work site. This phase shall include: a. A review of each paragraph of applicable specifications. b. A review of the contract drawings. c. A check to assure that all materials and/or equipment have been tested, submitted, and approved. d. Review of provisions that have been made to provide required control inspection and testing. e. Examination of the work area to assure that all required preliminary work has been completed and is in compliance with the contract. f. A physical examination of required materials, equipment, and sample work to assure that they are on hand, conform to approved shop drawings or submitted data, and are properly stored. g. Discussion of procedures for controlling quality of the work including repetitive deficiencies. Document construction tolerances and workmanship standards for that feature of work. h. Discussion of the initial control phase.
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Preparatory Phase. All the evaluators will be aware of the input necessary to perform the cognitive walkthrough inspection, namely: the user population, the tasks, the action sequence for each task, and the interface. 1) User population: Who will be the users of the system? The target group of Miraculous-Life (defined to be 65 +), is the big group of healthy elderly or with light related physical or cognitive ageing related degradations who live alone at home and can find pleasure and relief in getting help or stimulation to carry out their daily activities. The users don’t necessarily have background knowledge or particular skills on technology.
Preparatory Phase. Between 2012 and 2014, four meetings of the focal points appointed by the governments of the signatory countries of the Declaration on the application of Principle 10 of the Rio Declaration on Environment and Development in Latin America and the Caribbean were held (see table I.1). 3 A/CONF.216/13. First meeting (Santiago, 2012) Road map Second meeting (Guadalajara, Mexico, April 2013) Plan of action to 2014 Third meeting (Lima, October 2013) Lima Vision Priority lines of action for capacity-building and cooperation Fourth meeting (Santiago, November 2014) San Xxxx Content Santiago Decision Beginning of negotiation phase At these meetings, the countries adopted the following foundational documents: (a) Road map (2012) The road map launched a process aimed at strengthening dialogue and regional cooperation and developing a regional instrument on rights of access to environmental information, participation and justice. It defined the instrument’s main principles and objectives. (b) Plan of action to 2014 (2013) The plan of action set forth the tasks to be accomplished up to 2014 to implement the Declaration on the application of Principle 10 of the Rio Declaration on Environment and Development in Latin America and the Caribbean. It included specific tasks, objectives, actions to be taken, resources and expected outcomes. The coordination of the process, including the establishment of working groups, and the modalities for the participation of stakeholders were defined. (c) Lima Vision for a regional instrument on access rights relating to the environment (2013) The Lima Vision outlined the importance and benefits of access rights and established the values and principles of the future regional instrument. (d) Priority lines of action for 2014 (2014) The priority lines of action established seven priorities for the working group on capacity-building and cooperation for 2014. These included the identification of best practices, the organization of regional and national capacity-building activities and the development of educational materials and training resources, among others. (e) San Xxxx Content (2014) The San Xxxx Content consisted of an annotated index of topics to be considered in the negotiation of the regional instrument on access rights in environmental matters. (f) Santiago Decision (2014) The Santiago Decision formally initiated the negotiations on the regional instrument, established a negotiating committee and requested the preparation of a prel...
Preparatory Phase. Case studies and testing (Oct–Dec 2011)
Preparatory Phase. Notify the Contracting Officer or designated representative at least 2 working days in advance of each preparatory phase. Conduct the preparatory phase with the superintendent and the xxxxxxx responsible for the definable feature of work. Document the results of the preparatory phase actions in the Contractor Daily Quality Control Report. Perform the following prior to beginning work on each definable feature of work: a) Review each paragraph of the applicable specification sections. b) Review the contract drawings. c) Verify that appropriate shop drawings and submittals for materials and equipment have been submitted and approved. Verify receipt of approved factory test results, when required. d) Review the testing plan and ensure that provisions have been made to provide the required QC testing. e) Examine the work area to ensure that the required preliminary work has been completed. f) Examine the required materials and equipment, and sample work to ensure that materials and equipment are on hand and conform to the approved shop drawings and submitted data. g) Review the safety plan and appropriate activity hazard analysis to ensure that applicable safety requirements are met, and that required material safety data sheets (MSDS) are submitted. h) Discuss construction methods.
Preparatory Phase. Consensus/will building: There was a consensus/will building session with facility leaders before discussion on initiating QI activities. The purpose of consensus building was to activate leaders, establish readiness for QA/QI processes and to orient them on scope of work for the QI team that will be established. Establish and strengthen the QI team at health facilities: Support will be provided to facilities to establish Quality Improvement Team/QIT/. Primary hospitals have QI teams but they are not functional and it is an opportunity to strengthen and revitalize the team. The health centers have used their performance monitoring team/PMT/ as QI team with some modification to include major/key functions of the health center. Baseline assessment: The project conducted self-assessment baseline clinical auditing using comprehensive MNH self-assessment tool composed of set standards and criteria related to MNH service delivery. In the primary hospital, the project supported the QI team using the clinical audit tool developed by FMOH for hospitals. Health centers were assessed using modified self-assessment clinical audit tool that considers major clinical areas, health post linkage and community linkage including CSC and baseline data on KPI. The national MNH self-assessment clinical audit tool aimed at establishing a baseline data of which subsequent progresses will be measured and compared against the baseline data. Data for the last six months on selected MNH service indicators was collected as indicated below for all the facilities to serve as a baseline data to track improvement going forward. Table: The results of self- assessment clinical audits were: Region Zone/cluster Woreda Health facility Result (%) Amhara North Gondar Tacharmachiho Sanja PHL 22.2 Sanja HC 20.5 Musiebamb 7.7 North Wollo Wadla Wadla PHL 35.0 Xxxx XX 17.9 Hamusit HC 20.5 Oromia Ambo Guder Guder PHL 80.4 Xxxxx XX 24.0 Gorosole 33.0 Xxxxx Xxxxx Olenchiti PHL 70.5 Godedhera HC 18.0 Olenchite HC 13.0 Tigray Mekele HIntalo wajirat Adigudem PHL 85.0 Hewane HC 44.0 Debub HC 46.0 After the clinical audit self-assessment, the project supported the QITs on gap analysis, prioritization of identified problems, and the development of post assessment comprehensive QI action plans.
Preparatory Phase. This covers the period of employment from the date of commencement of your employment with the Employing Organisation until you successfully complete the Induction and Refresher assessments. During the preparatory phase you agree not to enter any other paid or voluntary employment or engagement without prior agreement in writing from your Employing Organisation. For the preparatory phase, until you complete the I&R assessments, the Employing Organisation agrees to pay you an International GP Programme salary of £3,000 per month. This is the net figure. Those working in London will be paid an additional weighting. The preparatory phase is to be completed within the Employing Organisation or another wider NHS placement. A wider NHS placement that meets the learning needs of the participant could be accommodated via a secondment arrangement. The preparatory phase will comprise of undertaking shadowing, training and other exercises required to produce familiarisation with the processes, procedures and approaches relating to primary care and other interlinking NHS and non NHS organisations, ensuring you are sufficiently prepared to undertake the I&R assessments and commence the I&R scheme period. Where the Employing Organisation is not an individual practice, the Employing Organisation agree that you will not work in isolation or across multiple sites for the duration of the Preparatory Phase. Where the Employing Organisation has multiple sites, you will be based at one primary practice and working across sites will only be allowable as part of the agreed training and development programme with you. At all times on-site senior clinical support will be available to you. The anticipated length of the preparatory phase is agreed between you, your Clinical Supervisor and your Educational Supervisor, as specified in Appendix A. For the completion of the preparatory phase and progression to I&R scheme phase, you must be able to evidence completion of the required preparatory work and successfully undertaking the I&R assessments, which include two ‘multiple-choice questions’ (MCQ) exams and if appropriate the ‘simulated surgery’. These assessments must be undertaken in accordance with Health Education England guidelines. During the preparatory phase, if you wish to cease employment with the Employing Organisation and withdraw from the International GP Recruitment Programme you should discuss this firstly with your Clinical Supervisor and/or Educational Supervisor. You...
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Preparatory Phase. The Steering Committee (SC) was created. Finalisation of the Final Project Proposal (FPP) was ensured. According to the project outline the analysis of employers´ requirements was supposed to be carried out. Considering to time- demandingness of the activity and shortened time of the preparatory phase, the activity will be carried out in Activity 2. In order to select study and vocational fields for realisation of pilot activities, the Analysis of current situation within the system of educational fields in selected groups of fields was prepared (in Annex 17). On the base of the analysis results activities were specified. Comments of NCP were incorporated. Activities of the project partner were specified, working meetings with partners representatives (1 business trip, e-mail and phone consultations) were realised. The partner provided professional and counselling activities at the stage of processing Final Project Proposal. The updating of EHB methodology for employers´ requirements analysis and training of experts from SR will be carried out in Activity 2. Activities were ensured 1. by own skilled manpower in permanent employment (free of charge), 2. manpower hired only for purpose of the project (working groups), 3. consultants from Switzerland and 4. externally.

Related to Preparatory Phase

  • 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.

  • Preparatory Contract Negotiations Meetings Where operational requirements permit, the Employer will grant leave without pay to an employee to attend preparatory contract negotiations meetings.

  • 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.

  • 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.

  • Development Program RWJPRI shall be [**] and have [**] in consultation with the JDAC, to select LICENSED COMPOUNDS which shall then be designated PRODUCTS for further DEVELOPMENT by RWJPRI and marketing by ORTHO and its AFFILIATES. RWJPRI shall provide KOSAN with written notice of its decision to select a LICENSED COMPOUND for DEVELOPMENT. Once a PRODUCT has been selected for further DEVELOPMENT, RWJPRI, with the advice of the JDAC, shall have the [**] right to develop the PRODUCT through STAGES O, I, II and III and shall have the [**] right to prepare and file, and shall be the owner of, all applications for MARKETING AUTHORIZATION throughout the world. During such DEVELOPMENT efforts, KOSAN will assist RWJPRI as may be mutually agreed, at RWJPRI's expense, in chemical development, formulation development, production of labeled material and production of sufficient quantities of material for STAGE O and initial STAGE I studies. RWJPRI shall exercise diligent efforts, commensurate with the efforts it would normally exercise for products with similar potential sales volume and consistent with its overall business strategy, in developing such PRODUCT in accordance with the DEVELOPMENT PLAN established by RWJPRI. In the course of such efforts RWJPRI shall, either directly or through an AFFILIATE or SUBLICENSEE to which the license shall have been extended, take appropriate steps including the following: (i) in consultation with the JDAC, select certain LICENSED COMPOUNDS for STAGE O DEVELOPMENT; and (ii) establish and maintain a program reasonably designed, funded and resourced to obtain information adequate to enable the preparation and filing with an appropriate and properly empowered national regulatory authority all necessary documentation, data and [**] CERTAIN INFORMATION IN THIS EXHIBIT HAS BEEN OMITTED AND FILED SEPARATELY WITH THE COMMISSION. CONFIDENTIAL TREATMENT HAS BEEN REQUESTED WITH RESPECT TO THE OMITTED PORTIONS. other evidence required for IND non-rejection to commence and conduct human clinical trials of such PRODUCT. (iii) proceed following IND non-rejection to commence PHASE I, II, and III clinical trials, associated studies and such other work which RWJPRI reasonably deems to be required for subsequent inclusion in filings for MARKETING AUTHORIZATION; (iv) after such submissions are filed prosecute such submissions and file all reasonably necessary, reports and respond to all reasonable requests from the pertinent regulatory, authorities for information, data, samples, tests and the like.

  • Design Development Phase INDICATE IN STATEMENT OF WORK “NOT APPLICABLE” IF SECTION IS NOT APPLICABLE 1.1.6.1. The ARCHITECT/ENGINEER shall prepare from the approved Schematic Design Studies, the Design Development Documents consisting of drawings (including at least architectural, landscaping, civil, structural, mechanical and electrical plans, building sections; and finish schedule), outline specifications following the Construction Specification Institute "CSI" Format and other necessary documents to fix and describe the size and character of the entire Project as to its site, structural, mechanical, and electrical systems, materials and other such essentials as may be appropriate, for and until approved by the State. 1.1.6.2. The ARCHITECT/ENGINEER shall conduct meetings with the State, Efficiency Vermont, and relevant members of the design team, to review the Design Development Documents for the purposes of furthering the energy efficiency objectives of the Project. 1.1.6.3. The ARCHITECT/ENGINEER shall prepare for the State a revised accounting of how the Project is responding to LEED criteria. 1.1.6.4. The ARCHITECT/ENGINEER shall submit to the State a revised Statement of Probable Construction Cost based thereon for and until approved by the State.

  • Production Phase contract period in which the Development and the Production are to be performed.

  • 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.

  • Project Plan Development of Project Plan Upon the Authorized User’s request, the Contractor must develop a Project Plan. This Project Plan may include Implementation personnel, installation timeframes, escalation procedures and an acceptance plan as appropriate for the Services requested. Specific requirements of the plan will be defined in the RFQ. In response to the RFQ, the Contractor must agree to furnish all labor and supervision necessary to successfully perform Services procured from this Lot. Project Plan Document The Contractor will provide to the Authorized User, a Project Plan that may contain the following items: • Name of the Project Manager, Contact Phone Numbers and E-Mail Address; • Names of the Project Team Members, Contact Phone Numbers and E-Mail Address; • A list of Implementation milestones based on the Authorized User’s desired installation date; • A list of responsibilities of the Authorized User during system Implementation; • A list of designated Contractor Authorized Personnel; • Escalation procedures including management personnel contact numbers; • Full and complete documentation of all Implementation work; • Samples of knowledge transfer documentation; and • When applicable, a list of all materials and supplies required to complete the Implementation described in the RFQ. Materials and Supplies Required to Complete Implementation In the event that there are items required to complete an Implementation, the Contractor may request the items be added to its Contract if the items meet the scope of the Contract. Negotiation of Final Project Plan If the Authorized User chooses to require a full Project Plan, the State further reserves the right for Authorized Users to negotiate the final Project Plan with the apparent RFQ awardee. Such negotiation must not substantively change the scope of the RFQ plan, but can alter timeframes or other incidental factors of the final Project Plan. The Authorized User will provide the Contractor a minimum of five (5) business days’ notice of the final negotiation date. The Authorized User reserves the right to move to the next responsible and responsive bidder if Contractor negotiations are unsuccessful.

  • Project Implementation The Borrower shall:

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