Laboratory Records Sample Clauses

Laboratory Records. Upon receipt of written request of the Union, accompanied by signed consent of the employee for release of record, a laboratory performing employee drug tests must furnish a completed record of the employee's identification assay(s) within three working days, unless the Union and lab make other arrangements. This record shall include evidence of a complete and unbroken chain of custody, all evaluable GC/MS data (including quality controls), and all reports furnished to the medical provider. The Union will provide a copy of all materials received pursuant to its request to the Employee Relations office. Quality Assurance Results of all quality assurance tests required under the DHHS guidelines shall be requested by the Employer from the participating laboratory in a timely manner, and disclosed to the Union upon receipt. A laboratory cited for any "false positive" on a quality assurance test shall not be allowed to perform services under this contract until the cause of the "false positive" identification is identified and corrected. Medical Review Officer Following forensic identification of a suspected unknown, all drug testing data relevant to that identification shall be evaluated by a Medical Review Officer (MRO) prior to becoming part of any fitness determination. In appropriate cases, the Employer may select a local forensic toxicologist or other expert to review the results of a drug test. The MRO shall follow evaluation procedures specified in appropriate federal guidelines.
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Laboratory Records. Synterys shall prepare and maintain detailed laboratory notebook records of all activities and work conducted in connection with each and every Project. Such notebook records may include electronic notebook records as determined by the Parties.
Laboratory Records. Please see the detailed laboratory records information attached in the Quality Assurance Project Manuals in Appendix C. Baseline and daily air samples to be analyzed by PCM will be collected by an LDEQ-accredited Contractor Supervisor and analyzed by AIHA Accredited staff within 24 hours of the close of each workday. The standard laboratory turnaround time for final clearance samples submitted to subcontract laboratory for analysis by TEM is 24 hours after receipt by the laboratory.
Laboratory Records. After any purchase by Omeros of the MOCA Technology in accordance with this Agreement, the Founders and Patobios shall deliver to Omeros all available original laboratory notebooks and scientific records, in true and complete form, pertaining to the conception, reduction to practice, testing, evaluation and use of the Assays and the MOCA Technology by the Founders and Patobios.
Laboratory Records. All relevant records shall be available for inspection by any employee who has been tested, upon the employee's request. All such records shall be available to the Union, with the employee's written consent, upon any grievance concerning the testing or any discipline resulting from testing.

Related to Laboratory Records

  • Inventory Records Each Loan Party keeps correct and accurate records itemizing and describing the type, quality, and quantity of its and its Subsidiaries’ Inventory and the book value thereof.

  • 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.

  • 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.

  • Development Records Each Party shall maintain complete, current and accurate records of all Development activities conducted by it hereunder, and all data and other information resulting from such activities. Such records shall fully and properly reflect all work done and results achieved in the performance of the Development activities in good scientific manner appropriate for regulatory and patent purposes. Each Party shall document all non-clinical studies and Clinical Trials in formal written study reports according to Applicable Laws and national and international guidelines (e.g., ICH, cGCP, cGLP, and cGMP).

  • Books, Records and Regulatory Filings (a) The Sub-Adviser agrees to maintain and to preserve for the applicable periods any such records as are required to be maintained by the Sub-Adviser with respect to the Fund by the 1940 Act and rules adopted thereunder, and by any other applicable laws, rules and regulations. The Sub-Adviser further agrees that all records that it maintains for the Fund are the property of the Fund and it will promptly surrender any of such records upon request; provided, however, that the Sub-Adviser may retain copies of such records for the applicable periods they are required by law to be retained, and thereafter shall destroy such records.

  • Project Records ‌ As further described below, Project records include but are not limited to Grantee, financial, and voucher records. All Project records must be retained for a period of three (3) years after final payment under this Grant. All Project records are subject to audit pursuant to Section P of this Grant Agreement. Upon completion of the third year of record retention, the Grantee shall submit all Project records to CARB. Hardcopy of electronic records are suitable. Acceptable forms of electronic media include hard drives, CDs, DVDs, and flash drives. Other forms of electronic media may be allowed based on prior written concurrence from CARB.

  • Education Records Educational Records are official records, files and data directly related to a student and maintained by the school or local education agency, including but not limited to, records encompassing all the material kept in the student’s cumulative folder, such as general identifying data, records of attendance and of academic work completed, records of achievement, and results of evaluative tests, health data, disciplinary status, test protocols and individualized education programs. For purposes of this DPA, Education Records are referred to as Student Data. Personally Identifiable Information (PII): The terms “Personally Identifiable Information” or “PII” has the same meaning as that found in U.C.A § 53E-9-301, and includes both direct identifiers (such as a student’s or other family member’s name, address, student number, or biometric number) and indirect identifiers (such as a student’s date of birth, place of birth, or mother’s maiden name). Indirect identifiers that constitute PII also include metadata or other information that, alone or in combination, is linked or linkable to a specific student that would allow a reasonable person in the school community, who does not have personal knowledge of the relevant circumstances, to identify the student with reasonable certainty. For purposes of this DPA, Personally Identifiable Information shall include the categories of information listed in the definition of Student Data.

  • Marking Records As of the Closing Date, Seller has caused the Computer File relating to the Contracts sold hereunder and concurrently reconveyed by Trust Depositor to the Trust and pledged by the Trust to the Indenture Trustee to be clearly and unambiguously marked to indicate that such Contracts constitute part of the Trust Corpus, are owned by the Trust and constitute security for the Notes.

  • Audits and Records 7.5.1 The Contractor agrees that the representatives of the Office of the City Auditor or other authorized representatives of the City shall have access to, and the right to audit, examine, or reproduce, any and all records of the Contractor related to the performance under this Contract. The Contractor shall retain all such records for a period of three (3) years after final payment on this Contract or until all audit and litigation matters that the City has brought to the attention of the Contractor are resolved, whichever is longer. The Contractor agrees to refund to the City any overpayments disclosed by any such audit.

  • Client Records 26.2.1 CONTRACTOR shall prepare and maintain accurate and complete records of clients served and dates and type of services provided under the terms of this Contract in a form acceptable to ADMINISTRATOR.

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