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.
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. 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. 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.
