As an MRO you have an important and indispensable role in the DOT drug testing process. You act as an independent and impartial 'gatekeeper' and you advocate for the accuracy and integrity of the drug testing process. Your quality assurance reviews of the drug testing process strengthen...
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...
--- Reminder ---
The Revised Federal Drug Testing Custody and Control Form
must be used beginning August 30th, 2021[1]
Important Dates
We will conform to the dates HHS has...
DOT Drug Testing: After January 1, 2018 – Still a 5-Panel
The DOT testing at HHS-certified laboratories is a 5-panel drug test regimen. As of January 1, 2018, the ‘Opiates’ category was renamed ‘Opioids’:
Marijuana (THC)CocaineAmphetaminesOpioidsPhencyclidine (PCP)Under ‘...