The U.S. Department of Transportation is issuing a final rule to amend the Department’s Air Carrier Access Act (ACAA) regulation to improve the accessibility of lavatories on single-aisle aircraft. This final rule is intended to ensure that our air transportation system is safe and accessible to...
Appendix G to Part 40—SAP Equivalency Requirements for Certification Organizations
Experience: Minimum requirements are for three years of full-time supervised experience or 6,000 hours of supervised experience as an alcoholism and/or drug abuse counselor. The supervision must be...
Appendix I to Part 40—Alcohol Testing Form
The following form is the alcohol testing form required for use in the DOT alcohol testing program beginning January 1, 2011. Employers are authorized to use the form effective February 25, 2010.
[75 FR 8529, Feb...
Appendix J to Part 40
DOT Drug and Alcohol Testing Management Information System (MIS) Data Collection Form
The following form is the MIS Data Collection form required for use to report calendar year MIS data. The Instructions for this form are found at https://www....
Subpart F - Drug Testing Laboratories
§ 40.92 What is oral fluid validity testing, and are laboratories required to conduct it?
(a) Specimen validity testing is the evaluation of the specimen to determine if it is consistent with normal human oral fluid. The purpose of validity testing is...
Subpart F - Drug Testing Laboratories
§ 40.90 What criteria do laboratories use to establish that a urine specimen is invalid?
(a) As a laboratory, you must use the invalid test result criteria for the initial and confirmation testing as required by the HHS Mandatory Guidelines, and you...
Subpart F - Drug Testing Laboratories
§ 40.88 What criteria do laboratories use to establish that a urine specimen is dilute or substituted?
(a) As a laboratory, you must consider the primary specimen to be dilute when:
The creatinine concentration is greater than or...
Subpart F - Drug Testing Laboratories
§ 40.86 What is urine validity testing, and are laboratories required to conduct it?
(a) Specimen validity testing is the evaluation of the specimen to determine if it is consistent with normal human urine. The purpose of validity testing is to...
Subpart F - Drug Testing Laboratories
§ 40.84 How long does the laboratory retain specimens after testing?
(a) As a laboratory testing the primary specimen, you must retain a specimen that was reported with positive, adulterated, substituted, or invalid results for a minimum of one year....
Subpart F - Drug Testing Laboratories
§ 40.82 What drugs do laboratories test for?
As a laboratory, you must test for the following five drugs or classes of drugs in a DOT drug test. You must not test “DOT specimens” for any other drugs.
(a) Marijuana...