Field Laboratory Clause Samples

Field Laboratory. Developer shall provide a Type C field laboratory in Indiana and in Kentucky. The field laboratory shall be as specified in Department Standard Specifications 628.02(f). In addition to the provisions of Section 628.02(f) Developer shall provide hot and cold running water (potable). Developer does not need to include telephone lines or telephones in the field laboratory.
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Field Laboratory. The contractor shall arrange to provide fully furnished and adequately equipped field laboratory with adequate qualified technical staff. Preferably to located adjacent to the site of Engineer- in – charge and provided amenities like water supply, electric supply etc.The laboratory equipment shall confirm IS specifications and MOST specifications. It shall be considered as incidental to the work, and no extra payment will be made what so ever will not be made for the same.
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Field Laboratory. Design-Build Contractor shall provide for IFA’s use, one Type C field laboratory as specified in Department Standard Specifications 628.02(f). In addition to the provisions of Section 628.02(f) Design-Build Contractor shall provide hot and cold running water (potable), and a portable cook stove for drying samples and with propane in containers of suitable size to be transported to the jobsite. Design-Build Contractor does not need to include telephone lines or telephones in the field laboratory.
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Field Laboratory. The contractor shall establish a Field Laboratory for the various field tests for items like concrete cubes, cement, aggregates, sand, bitumen & bitumen products, soil, field density etc. A site laboratory of min. 5.0 m. x 7.0 m. area with platform etc. shall be constructed as directed by the Engineer. A contractor shall appoint experienced Laboratory Technician to carryout various tests at site. He shall carry out various tests and submit reports and maintain registers as per BIS formats. Besides list of all resources required with scheduled date of start and date of completion of all items of work. The laboratory must have the following equipments :- Sl. No. Equipments Requirements 1. Slump Cone 6 Nos. 2. Cube Moulds for concrete 24 Sets. 4. Cement testing equipment soundness accelerated (initial and final setting, fineness, compressive test equipment, etc.) 1 Set 5. Oven 1 No. 6. Cube Testing Machine (Electrically operated) Capacity 250 T. 1 No. 7. Weigh Balance (Digital) 2 Nos. 8. Laboratory balance to weight up to 20 kg. With 1 No. Sl. No. Equipments Requirements sensitivity of 10 gm 9. Laboratory balance of 2 kg. Capacity and sensitivity of 1 gm 1 No. 10. IS Sieves (For Coarse & Fine Aggregates) murum 2 set (each) 11. Glass measuring cylinders 12 Nos.
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Field Laboratory. If indicated, provide a laboratory for materials and soils testing. Set up the indicated field laboratory in an acceptable weatherproof building or trailer situated in an acceptable location. Supply a gravity or pressure potable water system having at least a 100-gallon capacity and connected to a service sink with a faucet and acceptable outside drain. Do not drain or discharge wastewater into the surrounding environment; use a container of sufficient size to collect all drained or discharged wastewater and transport and dispose of wastewater at an approved site for handling such wastewater. Equip the field laboratory as specified in Table A.
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Field Laboratory. The Contractor shall provide and maintain adequately equipped Field Laboratory as required for Site Control on the Quality of Material and the Works. It shall have a minimum of 40 Sqm Area. The Field Laboratory shall be located as directed by the Employer or his approved Representative. It shall be provided with Amenities like Water Supply, Electric Supply, etc. The Laboratory will have all Services, Furniture, Equipments, etc. Minimum of the following Items shall be provided in the Field Laboratory. Any Additional Items as required for Testing / Evaluation in line with the Standard Procedures and Codal Provisions shall also be provided.
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Field Laboratory. Post excavation artifact and sample processing and analysis are a major component of all archaeological excavation projects. These analytical and clerical activities can often add months to an excavation budget to ensure a site is adequately documented and interpreted. For this Project we sought to minimize this expense by establishing a well- equipped field laboratory with academically-trained archaeologists to handle all artifact recovery, documentation and analysis/cataloging immediately upon identification of a new find. Based on a comparable project using traditional post-field laboratory analysis – this Project would have been expected to have required a further 5-6 months with a crew of at least six to process and analyze the finds/samples. Using the Field Lab approach, a staff of four was required for 3 months to recheck field identifications, enter artifacts into the Province’s artifact database and ensure artifacts were prepared for curation/study. While providing better field results, this approach also resulted in a savings of between 40% and 60% when compared to the projected processing cost using traditional post- field cataloging and analysis.
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Field Laboratory. The contractor shall arrange to provide fully furnished and adequately equipped field laboratory with adequate qualified technical staff. Preferably to located adjacent to the site of Engineer- in – charge and provided amenities like water supply, electric supply etc.The laboratory equipment shall confirm IS specifications and MOST specifications. It shall be considered as incidental to the work, and no extra payment will be made what so ever will not be made for the same. After completion of work laboratory equipments will be the property of the contractor. After completion of work, the contractor shall clean all site by dismantling site office / laboratory and by removing all the debris from the site of wor
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Related to Field Laboratory

  • Laboratory Testing All laboratories selected by UPS Freight for analyzing Controlled Substances Testing will be HHS certified.

  • Laboratory a. Drug tests shall be conducted by laboratories licensed and approved by SAMSHA which comply with the American Occupational Medical Association (AOMA) ethical standards. Upon advance notice, the parties retain the right to inspect the laboratory to determine conformity with the standards described in this policy. The laboratory will only test for drugs identified in this policy. The City shall bear the cost of all required testing unless otherwise specified herein. b. Tests for all controlled substances, except alcohol, shall be by oral fluid testing and shall consist of two procedures, a screen test and, if that is positive, a confirmation test. c. To be considered positive for reporting by the laboratory to the City, both samples must be tested separately in separate batches and must also show positive results on the confirmatory test. d. In the event of a positive test, the testing laboratory will perform an automatic confirmation test on the original specimen at no cost to the Covered Employee. In addition, the testing laboratory shall preserve a sufficient specimen to permit an independent re-testing at the Covered Employee’s request and expense. The same, or any other, approved laboratory may conduct re-tests. The laboratory shall endeavor to notify the designated MRO of positive drug, alcohol, or adulterant tests results within five (5) working days after receipt of the specimen.

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time. (b) The Supplier shall not change any process, material, component, packaging or manufacturing location without the Purchaser’s express prior written approval.

  • Clinical 1.1 Provides comprehensive evidence based nursing care and individual case management to a specific group of patients/clients including assessment, intervention and evaluation. 1.2 Undertakes clinical shifts at the direction of senior staff and the Nursing Director including participation on the on-call/after-hours/weekend roster if required. 1.3 Responsible and accountable for patient safety and quality of care through planning, coordinating, performing, facilitating, and evaluating the delivery of patient care relating to a particular group of patients, clients or staff in the practice setting. 1.4 Monitors, reviews and reports upon the standard of nursing practice to ensure that colleagues are working within the scope of nursing practice, following appropriate clinical pathways, policies, procedures and adopting a risk management approach in patient care delivery. 1.5 Participates in ▇▇▇▇ rounds/case conferences as appropriate. 1.6 Educates patients/carers in post discharge management and organises discharge summaries/referrals to other services, as appropriate. 1.7 Supports and liaises with patients, carers, colleagues, medical, nursing, allied health, support staff, external agencies and the private sector to provide coordinated multidisciplinary care. 1.8 Completes clinical documentation and undertakes other administrative/management tasks as required. 1.9 Participates in departmental and other meetings as required to meet organisational and service objectives. 1.10 Develops and seeks to implement change utilising expert clinical knowledge through research and evidence based best practice. 1.11 Monitors and maintains availability of consumable stock. 1.12 Complies with and demonstrates a positive commitment to Regulations, Acts and Policies relevant to nursing including the Code of Ethics for Nurses in Australia, the Code of Conduct for Nurses in Australia, the National Competency Standards for the Registered Nurse and the Poisons Act 2014 and Medicines and Poisons Regulations 2016. 1.13 Promotes and participates in team building and decision making. 1.14 Responsible for the clinical supervision of nurses at Level 1 and/or Enrolled Nurses/ Assistants in Nursing under their supervision.

  • Manufacturing Technology Transfer Except as provided in Section 4.3(f)(iii)(1) and Section 6.10, with respect to any Collaboration Product (or LGC Reserved Product, if applicable) for which LGC (or its Affiliate) performed CMC Development or CMC Manufacturing, if (a) Cue does not elect for LGC to perform CMC Step 2, CMC Step 3, or CMC Step 4 (or with respect to LGC Reserved Products, upon completion of CMC Step 1), or (b) upon failure of the Parties to reach agreement with respect to a Clinical Supply Agreement or a Commercial Supply Agreement or (c) [***] under this Agreement and does not cure such breach within [***] days (provided, that if such breach is not reasonably capable of cure within such [***] day period, then such cure period shall be automatically extended for an additional [***] day period as long as LGC continues to use diligent efforts to cure such breach in accordance with a reasonable cure plan and if such breach is not reasonably capable of cure within such combined [***] day period, then Cue shall reasonably consider consenting to any extension of such cure period as long as LGC continues to use diligent efforts to cure such breach in accordance with a reasonable cure plan), as applicable, then, in each case upon the written request of Cue, LGC shall use Commercially Reasonable Efforts to make a technology transfer to an Approved CMO the Manufacturing processes (including materials and such other information) but solely as is necessary to enable the Manufacture of such Collaboration Product (including the Collaboration Compound therein) (or LGC Reserved Product, including the LGC Reserved Compound therein, if applicable) by such Approved CMO to comparable biochemical structure, quality and purity as that Manufactured by LGC or its Affiliate or CMO, provided that neither Cue, LGC or any Third Party shall perform such a technology transfer to any CMO [***] without LGC’s consent, not to be unreasonably withheld, conditioned or delayed if LGC has approved the CMO to manufacture Collaboration Products (or LGC Reserved Products, if applicable). LGC shall conduct such technology transfer as soon as reasonably practicable after receiving such written notice, using good faith efforts to support supply needed to achieve timelines in the Cue Territory Development Plan (or Cue’s development plan for LGC Reserved Products, if applicable) or Cue Territory Commercialization Plan, as applicable. LGC shall conduct the first technology transfer for each Collaboration Product (or LGC Reserved Products, if applicable) [***] (provided that [***]) for a period of up to [***] months from the date Cue or its designee has provided notice it is ready to receive the technology transfer, provided, that such [***] month period [***]. After the expiration of the initial such [***] month period for a Collaboration Product (or LGC Reserved Products, if applicable), if required to complete the technology transfer to enable the Manufacture of such Collaboration Product (including the Collaboration Compound therein) (or LGC Reserved Product, including the LGC Reserved Compound therein, if applicable) by such Approved CMO to comparable biochemical structure, quality and purity as that Manufactured by LGC, LGC shall continue to provide support to Cue for up to an additional [***] period for up to [***] hours at the FTE Rate and thereafter at [***]. Thereafter, LGC will also provide [***] for such Collaboration Product (or LGC Reserved Products, if applicable). Neither Cue nor its Affiliates or Cue Collaborators shall reverse engineer any materials provided hereunder by LGC. Notwithstanding anything in this Agreement to the contrary, LGC’s CMC information may only be shared with an Approved CMO.