Common use of Preparation of Laboratory Report - Positive Test Specimens Clause in Contracts

Preparation of Laboratory Report - Positive Test Specimens. In the event that a specimen is found to be positive by the GC/MS process, the Laboratory shall prepare a written report. The original report shall be retained by the Laboratory. One copy, along with the sealed pre-test Declaration Form, shall be sent to the Medical Review Officer. The laboratory report shall contain the following information: 1. Employee confidential test identification number. 2. The drug identified. 3. The initial screening method. 4. The date screened. 5. The screening analyst's name. 6. The printed output from the immunoassay screening instrument pertaining to the batch of samples which includes the positive sample. That output will include the data from the relevant standards, blanks, quality control samples, and positive sample. 7. The confirmation method. 8. The date confirmed. 9. The confirming analyst's name and signature. 10. The graphs and reports pertaining to the gas chromatographmass spectrometer analysis of the relevant batch of samples and associated controls and quantitative standards. 11. The name and signature of the reviewing laboratory supervisor.

Preparation of Laboratory Report - Positive Test Specimens. In the event that a specimen is found to be positive by the GC/MS processconfirmatory test, the Laboratory shall prepare a written report. The original report shall be retained by the Laboratory. One copy, along with the sealed pre-test Declaration Form, shall be sent to the Medical Review Officer. The laboratory report shall contain the following information: 1. Employee confidential test identification number. 2. The drug identified. 3. The initial screening method. 4. The date screened. 5. The screening analyst's name. 6. The printed output from the immunoassay screening instrument pertaining to the batch of samples which includes the positive sample. That output will include the data from the relevant standards, blanks, quality control samples, and positive sample. 76. The confirmation method. 87. The date confirmed. 98. The confirming analyst's name and signature. 109. The graphs and reports pertaining to the gas chromatographmass spectrometer analysis confirmatory test of the relevant batch of samples and associated controls and quantitative standards. 1110. The name and signature of the reviewing laboratory supervisor. 11. Collection Log Sheet. Following confirmation, all positive urine samples are to be frozen and retained for a minimum of two (2) years by the Laboratory.

Preparation of Laboratory Report - Positive Test Specimens. In the event that a specimen is found to be positive by the GC/MS processconfirmatory test, the Laboratory shall prepare a written report. The original report shall be retained by the Laboratory. One copy, along with the sealed pre-test Declaration Form, shall be sent to the Medical Review Officer. The laboratory report shall contain the following information: 1. Employee confidential test identification number. 2. The drug identified. 3. The initial screening method. 4. The date screened. 5. The screening analyst's name. 6. The printed output from the immunoassay screening instrument pertaining to the batch of samples which includes the positive sample. That output will include the data from the relevant standards, blanks, quality control samples, and positive sample. 7. The confirmation method. 8. The date confirmed. 9. The confirming analyst's name and signature. 10. The graphs and reports pertaining to the gas chromatographmass chromatograph mass spectrometer analysis of the relevant batch of samples and associated controls and quantitative standards. 11. The name and signature of the reviewing laboratory supervisor.