Laboratory Report Sample Clauses

Laboratory Report. Confidentiality Notice: This Asbestos Survey Report is intended only for the use of the individual or entity addressed, and may contain information that is privileged, confidential, and exempt from disclosure under applicable law. If you are not the intended recipient or responsible for delivering this report to the intended recipient, you are hereby notified that any dissemination, distribution, or copying of this report, in whole or in part, is prohibited. If you have received this report in error, please notify us immediately. Thank you.
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Laboratory Report. Have the laboratory send the original test report directly to the Department's Representative with copies of the test results to the Contractor. Issue the reports no later than ten (10) calendar days after the representative samples are collected. • Include the following minimum information in each report: Identity of the waste stream(s) analyzed, the number of samples collected and tested, dates of sampling and testing, laboratory test procedures utilized, the names and signatures of the individuals collecting the samples and conducting the laboratory tests, and an interpretation of the test results. Include copies of the chain-of-custody forms in the documentation. • Prepare the Waste Characterization Data Sheet (WCDS) and provide to the Department's Representative for review and signature. Once approved, submit the original WCDS to the Department.
Sample 1
Laboratory Report. MassLabs agrees to deliver a copy of the original laboratory report in a timely manner to Medivolve. For clarity shipping or transportation time shall not be included in this turn time. The laboratory test report will include at a minimum: patient's name, date of birth, date of collection, date of report, test name, test result, laboratory name and address.
Sample 1
Laboratory Report. Note: There should be no limitations or restrictions on the report preventing the City from relying on the data and the report must be acceptable to the City of Burnaby’s Engineering Department. This document provides information on typical decommissioning methods that are suitable for use by industry during or following environmental and / or geotechnical site work.
Sample 1
Laboratory Report. Standard (PDF Laboratory Report) A Level 2 Laboratory Report shall be the standard PDF laboratory report for all analyses. The Level 2 Laboratory Report shall be e-mailed to the applicable Water Boards Project Manager and the SWAMP or Water Boards QA Officer (via OIMA- Xxxxxxxx@xxxxxxxxxxx.xx.xxx). The Level 2 Laboratory Report, whether generated by the primary Contractor or a subcontracted laboratory, shall include the following information: a. Case narrative b. Requestor c. Project Code/Region/Program d. COC form(s) (including initial sample submission and any interlaboratory transfers) e. Sample ID/number f. Date and time samples were collected g. Date and time samples were received by the laboratory
Sample 1

Related to Laboratory Report

  • Drug-Free Workplace Certification As required by Executive Order No. 90-5 dated April 12, 1990, issued by the Governor of Indiana, the Company hereby covenants and agrees to make a good faith effort to provide and maintain a drug-free workplace at the Project Location. The Company will give written notice to the IEDC within ten (10) days after receiving actual notice that the Company, or an employee of the Company in the State of Indiana, has been convicted of a criminal drug violation occurring in the workplace. False certification or violation of this certification may result in sanctions including, but not limited to, suspension of payments under the Agreement, termination of the Agreement and/or debarment of contracting opportunities with the State for up to three (3) years. In addition to the provisions of the above paragraph, if the total amount set forth in the Agreement is in excess of $25,000.00, the Company agrees that it will provide a drug-free workplace by: A. Publishing and providing to all of its employees a statement notifying them that the unlawful manufacture, distribution, dispensing, possession or use of a controlled substance is prohibited in the Company’s workplace, and specifying the actions that will be taken against employees for violations of such prohibition;

  • Research Use Reporting To assure adherence to NIH GDS Policy, the PI agrees to provide annual Progress Updates as part of the annual Project Renewal or Project Close-out processes, prior to the expiration of the one (1) year data access period. The PI who is seeking Renewal or Close-out of a project agree to complete the appropriate online forms and provide specific information such as how the data have been used, including publications or presentations that resulted from the use of the requested dataset(s), a summary of any plans for future research use (if the PI is seeking renewal), any violations of the terms of access described within this Agreement and the implemented remediation, and information on any downstream intellectual property generated from the data. The PI also may include general comments regarding suggestions for improving the data access process in general. Information provided in the progress updates helps NIH evaluate program activities and may be considered by the NIH GDS governance committees as part of NIH’s effort to provide ongoing stewardship of data sharing activities subject to the NIH GDS Policy.

  • 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.

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