Scope of Work 1 Sample Clauses

Scope of Work 1. The Contractor shall perform the following if operating as a direct Title V program; for a Title V contracted program the Contractor shall ensure that the subcontractor shall perform the following: a. Implement statutory provisions of the Title V SCSEP in accordance with all applicable laws and regulations [OAA, Public Law 89-73, 20 CFR Part 641 – April 9, 2004, and 29 CFR Part 89; WIA, Public Law 105-220), Regulations section 121(b)(1)(B)(vi), 29 U.S.C. 2841 (b)(1)(B)(vi) and 29 CFR Part 662 Subpart B §§ 662.200 through 662.280 and Parts 660-671; The Jobs for Veterans Act (Public Law 107-288) (2002) (38 U.S.C. 4215); the Title V SCSEP Manual as issued by the Department, and any other subsequent memos, bulletins, or similar instructions issued during the term of this Agreement by DoL;
Sample 1
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Scope of Work 1. 1 Principal Investigator shall perform the Study at Institution in strict compliance with the terms and conditions of this Agreement, any written instructions from Sponsor and/or Medpace, all generally accepted standards of Good Clinical Practice, the Protocol, and with all applicable local laws and regulations governing the performance of clinical investigations. The Study location will not be changed without Medpace’s prior written consent. 1.2 Prior to the start of Study, Medpace/Sponsor will obtain any and all necessary approvals of the applicable regulatory authorities and Ethics Committees. 1.3 Institution agrees to provide the Investigator with free access to the Institution’s applicable subject population to recruit the number of subjects set forth in the Investigator Responsibilities Section below to participate in the Study, and will facilitate the proper performance of the Study. 1.4 Sponsor or its designee will provide Institution with sufficient quantities of Study Drug for use in the Study at no cost to Institution. Institution and Investigator agree that the Study Drug and all equipment provided by the Sponsor may only be used for the purposes of the Study, and shall only be used in accordance with the Protocol and any written instructions of the Sponsor. 1.5 Institution represents that neither Investigator nor Institution are a citizen or resident of the United States, or a corporation or partnership that is and has been treated as a U.S. corporation or U.S. partnership, and that all payments Institution VZHLEDEM K TOMU, ŽE společnost Medpace má zájem, aby se zdravotnické zařízení podílelo na provádění studie v souladu s protokolem a podmínkami této smlouvy a zdravotnické zařízení má zájem podílet se na provádění studie v souladu s protokolem a podmínkami této smlouvy. PROTO, s ohledem na výše uvedené a vzájemných ujednání a příslibů vyjádřených v této smlouvě a řádnou a hodnotnou odměnou, jejíž přijetí a přiměřenost se tímto potvrzuje, było xxxxxxxxx xxxxxxxx xxxxxxxx xxxxxxxxxxx: 0 XXXXXX XXXXX 1.1 Zkoušející bude provádět studii ve zdravotnickém zařízení v přísném souladu s podmínkami této smlouvy, písemnými pokyny od zadavatele nebo společnosti Medpace, všemi obecně přijímanými standardy správné klinické praxe, protokolem a všemi platnými místními zákony a předpisy upravujícími provádění klinických hodnocneí. Místo studie nebude změněno, pokud k tomu společnost Medpace nedá předem písemný souhlas. 1.2 Společnost Medpace/zadavatel obstar...
Sample 1
Scope of Work 1. 1 Institution shall perform the Study in strict compliance with (a) the terms and conditions of this Agreement, (b) any written instructions from Sponsor and/or Medpace, (c) the 1996 version of the Declaration of Helsinki or such other version as is subsequently adopted by the European Union, (d) the Protocol, (e) all generally accepted standards of good clinical practice (including the Guideline for Good Clinical Practice of the International Conference on Harmonisation of Technical Requirements for the Registration of Pharmaceuticals for Human Use (“ICH-GCP”)), (f) all applicable laws and regulations including, without limitation, those governing the performance of clinical investigations and data protection and privacy, and (g) . The Study will be conducted solely at the facilities of Institution. The Study location will not be changed without Sponsor and Medpace’s prior written consent. zadavatelem najata pro řízení a správu této studie, mimo jiné včetně vyjednání a uzavření této smlouvy; a VZHLEDEM K TOMU, ŽE zadavatel je v EU zastupován společností Medpace Finland OY, se sídlem na adrese Xxxxxxxxxxxx 0, 00000, Xxxxxxxx, Finsko; a to v souladu s čl. 19 směrnice EU 2001/20/ES; VZHLEDEM K TOMU, ŽE si společnost Medpace přeje, aby se poskytovatel zdravotních služeb zúčastnil provádění klinické studie v souladu s protokolem a podmínkami této smlouvy, a poskytovatel zdravotních služeb se chce zúčastnit provádění klinické studie v souladu s protokolem a podmínkami této smlouvy. PROTO, s ohledem na výše uvedené skutečnosti, vzájemná ujednání a přísliby vyjádřené v této smlouvě a řádnou a hodnotnou odměnou, jejíž přijetí a přiměřenost se tímto potvrzuje, bylo smluvními stranami ujednáno následující: 1 ROZSAHPRACÍ 1.1 Zdravotnické zařízení bude provádět studii v přísném souladu s (a) podmínkami této smlouvy, (b) písemnými pokyny zadavatele a/nebo společnosti Medpace, (c) xxxxx Helsinské deklarace z roku 1996 nebo jinou xxxxx, kterou Evropská unie přijme později, (d) protokolem, (e) všemi obecně uznávanými standardy správné klinické praxe (včetně pokynů pro správnou klinickou praxi Mezinárodní konference pro harmonizaci technických požadavků pro registraci léčivých přípravků pro humánní použití (xxxx xxx „ICH-GCP“)), (f) veškerými platnými zákony a předpisy, mimo jiné těmi, které upravují provádění klinických hodnocení a ochrany údajů a soukromí, a (g) Studie bude prováděna výhradně v prostorách zdravotnického zařízení. Místo provádění studie nebude měněno bez ...
Sample 1
Scope of Work 1. 1 Parties shall perform the Study in strict compliance with the terms and conditions of this Agreement, any written instructions from Sponsor and/or Medpace, all generally accepted standards of Good Clinical Practice, the Protocol, and with all applicable laws and regulations governing the performance of clinical investigations. The Study location will not be changed without Medpace’s prior written consent. 1.2 Institution and Principal Investigator have the right to reject Sponsor´s or Medpace instructions that will be in contradiction with laws, Protocol, regulatory approval, Ethic Committee’s approval, good clinical practice or any instruction that, after reasonable consideration, can result in unreasonable increase of risk to subject’s health and welfare or risk of damages to Institution property; if such instructions may result in an increase of the budget VZHLEDEM K TOMU, ŽE společnost Medpace je smluvní výzkumnou organizací, která byla zadavatelem najata pro řízení a správu této studie, mimo jiné včetně vyjednání a uzavření této smlouvy; a VZHLEDEM K TOMU, ŽE si společnost Medpace přeje, aby se v souladu s protokolem a podmínkami této smlouvy na provádění studie podíleli i poskytovatel zdravotních služeb a hlavní zkoušející, a poskytovatel zdravotních služeb a hlavní zkoušející si přejí podílet se na provádění studie v souladu s protokolem a podmínkami této smlouvy. PROTO, s ohledem na výše uvedené skutečnosti, vzájemná ujednání a přísliby vyjádřené v této smlouvě a řádnou a hodnotnou odměnou, jejíž přijetí a přiměřenost se tímto potvrzuje, bylo smluvními stranami ujednáno následující: 1 ROZSAH PRACÍ 1.1 Smluvní strany budou provádět studii v přísném souladu s podmínkami této smlouvy, odpovídajícími písemnými pokyny zadavatele a/nebo společnosti Medpace, všemi obecně přijímanými standardy správné klinické praxe, protokolem a všemi příslušnými zákony a předpisy upravujícími provádění klinického výzkumu. Místo provádění studie nebude měněno bez předchozího písemného souhlasu společnosti Medpace. 1.2 Poskytovatel zdravotnických služeb a zkoušející jsou oprávněni odmítnout plnění pokynů zadavatele a/nebo společnosti Medpace a nebudou vázáni povinností tyto pokyny plnit, pokud jsou tyto v rozporu s právními předpisy, Protokolem, povolením Státního ústavu pro kontrolu léčiv SÚKL) nebo souhlasným stanoviskem příslušných etických komisí, správnou klinickou praxí, nebo lze odůvodněně předpokládat, že jejich plnění by představovalo neúměrné zvýšení zdravotníh...
Sample 1
Scope of Work 1. 1.1. 1.1.2. To supply new multi-process welding equipment After welding equipment are functional, provide operational training on 8 operators.
Sample 1
Scope of Work 1. 1 Institution and Principal Investigator shall perform the Study at Institution in strict compliance with the terms and conditions of this Agreement, any written instructions from Sponsor and/or Medpace, all generally accepted standards of Good Clinical Practice, the Protocol, and with all applicable laws and regulations of the Czech Republic, governing the performance of clinical investigations. The Study location will not be changed without Medpace’s prior written consent. 1.2 Prior to the start of Study, Medpace/Sponsor will obtain any and all necessary approvals of the applicable regulatory authorities and central Ethics Committee. If applicable Principal Investigator shall be responsible for submissions to Institution’s local Ethics Committee. 1.3 Institution agrees to provide the Principal Investigator with free access to the Institution’s applicable subject population to recruit the number of subjects set forth in the Principal Investigator Responsibilities Section below to participate in the Study, and will facilitate the proper performance of the Study. 1.4 Study Drug shall be shipped to Institution´s pharmacy. Institution is obligated to ensure that Study Drug is stored separately from other drugs and medications and Institution also assures that preparation, control, storage and handover of Study Drug shall be conducted in compliance with Protocol, applicable laws of Czech Republic and Good clinical practice and in compliance with instruction from IRS office code LEK-12. Principal Investigator represents that he will collect Study Drug from the Institution´s pharmacy in compliance with Protocol. 1.5 Sponsor or its designee will provide Institution with sufficient quantities of Study Drug for use in the Study at no cost to Institution. Institution and Principal Investigator agree that the Study Drug and all equipment provided by the Sponsor may only be used for the purposes of the Study, and shall only be PROTO, s ohledem na výše uvedené skutečnosti, vzájemná ujednání a přísliby vyjádřené v této smlouvě a řádnou a hodnotnou odměnou, jejíž přijetí a přiměřenost se tímto potvrzuje, bylo smluvními stranami ujednáno následující: 1 ROZSAH PRACÍ 1.1 Poskytovatel zdravotních služeb a hlavní zkoušející budou provádět studii na pracovištích poskytovatele zdravotních služeb v přísném souladu s podmínkami této smlouvy, jakýmikoliv písemnými pokyny zadavatele a/nebo společnosti Medpace, všemi obecně přijímanými standardy správné klinické praxe, protokolem a ...
Sample 1
Scope of Work 1. 3.2.1, is deleted and replaced as follows: Assess compliance with Deliverables, Performance Measures, or other associated requirements in accordance with the monitoring activities set forth in the Contract
Sample 1
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Scope of Work 1. 3.2.5 Addressing Deficiencies is hereby added to the Contract: To the extent that Deficiencies are identified in the Contractor’s performance and notwithstanding other remedies available under this Contract, the Agency may require the Contractor to develop and comply with a plan acceptable to the Agency to resolve the Deficiencies.
Sample 1
Scope of Work 1 
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Related to Scope of Work 1

  • Scope of Work The Contractor has overall responsibility for and shall provide and furnish all materials, equipment, tools and labor as necessary or reasonably inferable to complete the Work, or any phase of the Work, in accordance with the Owner’s requirements and the terms of the Contract Documents.

  • Scope of Works CHAPTER III

  • 000 SCOPE OF WORK 5.100 The scope of this Agreement covers all work of a maintenance, repair and renovation nature, assigned by the Owner to the Company and performed by the employees of the Company covered by this Agreement, within the limits of the Owner's plant site.

  • General Scope of Work The Scope of Work and projected level of effort required for these SERVICES is described in Exhibit “A” attached hereto and by this reference made a part of this AGREEMENT. The General Scope of Work was developed utilizing performance based contracting methodologies.

  • Detailed Scope of Work The complete description of services to be provided by the Contractor under an individual Job Order. Developed by the Contractor, after the Joint Scope Meeting and submitted for approval to the County Project Manager.

  • Scope of Work and Deliverables 9.1 Background and Scope

  • Work Order (s) means a detailed scope of work for a Service required by Transnet, including timeframes, Deliverable, Fees and costs for the supply of the Service to Transnet, which may be appended to this Agreement from time to time.

  • Statement of Work The Contractor shall provide the services and staff, and otherwise do all things necessary for or incidental to the performance of work, as set forth below:

  • Services Rendered/Scope of Work The Contractor shall, in a satisfactory and proper manner as determined by the Authority, render the services described in Exhibit A, which is attached and made a part of this Agreement.

  • OF WORK The normal hours of work for an employee are not a guarantee of work per day or per week, or a guarantee of days of work per week. The normal hours of work shall be seven and one-half (7%) hours per day, and seventy-five (75) hours in any period. The normal daily tour shall consist of seven and one-half hours, exclusive of a one-half hour unpaid meal period. Employees shall be entitled to a fifteen (15) minute paid break during each half of the normal daily tour, at a time designated by the Employer. Employees required for reporting purposes shall remain at work for a period of up to fifteen (15) minutes which shall be unpaid. Should the reporting time extend beyond fifteen ( I 5) minutes however, the entire period shall be considered for the purposes of payment. Requests for change in posted work schedules must be submitted in writing and by the employee willing to exchange days off or shifts and are subject to the discretion of the Administrator or her designate. In any event, it is understood that such a change initiated by the employee and approved by the Employer shall not result in overtime compensation or payment or any other claims on the Employer by an employee under the terms of this t Where there is a change to Daylight Savings from Standard Time or vice-versa, an employee who is scheduled and works a full shift shall be paid for a seven and one-half (7.5) hour tour rather than the actual hours worked. The Employer will endeavour to accommodate requests by employees for specific days off and also requests for changes in posted time schedules once the schedule has been posted. Shift schedules shall be posted two (2) weeks in advance and shall cover a minimum of a four (4) week period. The following shall apply to full-time employees: During each pay period, two (2) consecutive days off will be scheduled. Schedules may provide for more than (5) consecutive days of work, but not more than seven (7) consecutive days of work without days off, as long as four (4) days off are scheduled in each fourteen (14) day period. Except as outlined below, meal time of one-half hour shall be scheduled away from the floor during the employee's shift whether day, evening or night. Where there is only one registered employee on duty, it is recognized that this is not possible. Should an employee be recalled to duty during meal time, additional time shall be provided later in the shift.

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