What does 49 CFR 40.87 (What validity tests must laboratories conduct on primary urine specimens?) require?
Generated guidance. Confirm the source and its applicability before you act. How we check sources.
As a motor-carrier owner, here is what 49 CFR 40.87 requires laboratories to do for validity testing on primary urine specimens:
* Creatinine Concentration: The lab must test the creatinine concentration on every primary specimen.
* Specific Gravity: If the creatinine concentration is found to be less than 20 mg/dL, the lab must also test the specific gravity.
* pH Levels: The lab must determine the pH of every primary specimen.
* Oxidizing Adulterants: The lab must run one or more validity tests for oxidizing adulterants on every primary specimen.
* Additional Tests: The lab must perform extra validity tests if they spot abnormal physical characteristics, see reactions/responses typical of an adulterant during drug tests (such as unusual responses or the non-recovery of internal standards), or encounter a possible unidentified interfering substance or adulterant.
* Invalid Specimens and MRO Contact: If the lab determines a specimen is invalid and HHS guidelines require it, the lab and the Medical Review Officer (MRO) must work together to decide if sending the primary specimen to another HHS-certified laboratory would help report a positive or adulterated result.
Ask X3