Laboratory Duties Clause Samples

Laboratory Duties. Level I Duties:
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Laboratory Duties. 1. Cooperate with the Commissioner and the Contractor. 2. Provide qualified personnel promptly on notice. 3. Perform specified inspections, sampling and testing of materials and methods of construction. 4. Comply with specified standards and other recognized authorities and as specified. 5. Ascertain compliance with requirements of the Contract Documents. 6. Promptly notify the Commissioner and the Contractor of irregularity or deficiency of Work, which are observed during performance of services. 7. Perform additional services as required. 8. Promptly submit two (2) written copies and one (1) electronic copy of the report for each test to the Commissioner. Transmit to the Commissioner within three (3) workdays after each test is completed. Each report for each type of test shall be consecutively numbered. Each report shall include: a. Date issued. b. Project title and number. c. Testing laboratory name and address. d. Name and signature of inspector. e. Date of inspection or sampling. f. Record of temperature and weather. g. Date of test. h. Identification of product and Specification section. i. Location of Project. j. Type of inspection or test. k. Results of test. l. Observations regarding compliance with the Contract Documents. 9. Laboratory is not authorized to: a. Release, revoke, alter or enlarge on requirements of the Contract Documents. b. Approve or accept any portion of the Work.
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Laboratory Duties. Cooperate with A/E, ODR and Contractor. Upon notice, provide qualified personnel to perform required tests and inspections. In performing tests and inspections, Laboratory shall: 1. Comply with specified standards. Comply with building code requirements for "Special Inspection" whether or not such inspections are specified herein. 2. Ascertain compliance of materials with requirements of Contract Documents. If the material furnished and/or work performed fails to meet requirements of Contract Documents, laboratory inspector shall promptly notify the Contractor, A/E and the ODR of such failure. 3. Promptly notify ODR, Contractor and A/E of observed irregularities or deficiencies in the Work. 4. A representative of the Owner's testing laboratory, who has reviewed and is familiar with the Project and Specifications, shall participate in all preconstruction conferences. The testing firm shall coordinate material testing and inspection requirements with the Contractor and its Subcontractors consistent with the planned construction schedule. The laboratory personnel shall attend, throughout the course of the Project, such conferences as may be required or requested to address quality control issues. 5. Laboratory personnel shall inspect and/or test materials, assemblies, specimens, and work performed, including design mixes, methods and techniques and furnish report(s) to the A/E and the ODR of the progress thereof.
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Related to Laboratory Duties

  • Research Use The Requester agrees that if access is approved, (1) the PI named in the DAR and (2) those named in the “Senior/Key Person Profile” section of the DAR, including the Information Technology Director and any trainee, employee, or contractor1 working on the proposed research project under the direct oversight of these individuals, shall become Approved Users of the requested dataset(s). Research use will occur solely in connection with the approved research project described in the DAR, which includes a 1-2 paragraph description of the proposed research (i.e., a Research Use Statement). Investigators interested in using Cloud Computing for data storage and analysis must request permission to use Cloud Computing in the DAR and identify the Cloud Service Provider (CSP) or providers and/or Private Cloud System (PCS) that they propose to use. They must also submit a Cloud Computing Use Statement as part of the DAR that describes the type of service and how it will be used to carry out the proposed research as described in the Research Use Statement. If the Approved Users plan to collaborate with investigators outside the Requester, the investigators at each external site must submit an independent DAR using the same project title and Research Use Statement, and if using the cloud, Cloud Computing Use Statement. New uses of these data outside those described in the DAR will require submission of a new DAR; modifications to the research project will require submission of an amendment to this application (e.g., adding or deleting Requester Collaborators from the Requester, adding datasets to an approved project). Access to the requested dataset(s) is granted for a period of one (1) year, with the option to renew access or close-out a project at the end of that year. Submitting Investigator(s), or their collaborators, who provided the data or samples used to generate controlled-access datasets subject to the NIH GDS Policy and who have Institutional Review Board (IRB) approval and who meet any other study specific terms of access, are exempt from the limitation on the scope of the research use as defined in the DAR.

  • Laboratory Services Covered Services include prescribed diagnostic clinical and anatomic pathological laboratory services and materials when authorized by a Member's PCP and HPN’s Managed Care Program.

  • Diagnostic Services Procedures ordered by a recognized Provider because of specific symptoms to diagnose a specific condition or disease. Some examples include, but are not limited to:

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

  • 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.