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49 CFR 40.90

§ 40.90 What criteria do laboratories use to establish that a urine specimen is invalid?

United States · 49 CFR — Transportation · Status: effective

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49 CFR 40.90, § 40.90 What criteria do laboratories use to establish that a urine specimen is invalid?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/255235
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(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 must use two separate aliquots—one for the initial test and another for the confirmation test. (b) As a laboratory, for a specimen having an invalid result for one of the reasons outlined in the HHS Mandatory Guidelines, you must contact the MRO to discuss whether sending the specimen to another HHS certified laboratory for testing would be useful in being able to report a positive or adulterated result. (c) As a laboratory, you must report invalid results in accordance with the invalid test result criteria as required by the HHS Guidelines and provide the numerical value that supports the invalid result, where appropriate, such as pH. (d) As a laboratory, you must report the reason a test result is invalid.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.