{"id":51327,"date":"2017-11-21T17:55:26","date_gmt":"2017-11-21T21:55:26","guid":{"rendered":"https:\/\/www.nationaldrugscreening.com\/?p=51327"},"modified":"2022-11-30T11:16:02","modified_gmt":"2022-11-30T16:16:02","slug":"dot-final-rule-for-employers","status":"publish","type":"post","link":"https:\/\/www.nationaldrugscreening.com\/blogs\/dot-final-rule-for-employers\/","title":{"rendered":"DOT Final Rule for Employers"},"content":{"rendered":"\n
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Thank you to attorney Tommy Eden of Constangy, Brooks, Smith & Prophete, LLP<\/a> for providing this great information for DOT regulated employers.  Tommy can be reached at teden@constangy.com<\/a>.<\/p>\n

2018 TO DO LIST FOR DOT EMPLOYERS<\/strong><\/p>\n

On November 13, 2017, the Department of Transportation (DOT<\/strong>)<\/a> published a final rule in the Federal Register (82 FR 52229) (much of this update is taken from the extremely well written release by ODAPC). The rule, among other items, added four semi-synthetic opioids (i.e., hydrocodone, oxycodone, hydromorphone, oxymorphone) to the testing panel for all DOT regulated employees including FMCSA, PHMSA, FAA, USCG, FRA and FTA.  It also added methylenedioxyamphetamine (MDA) as an initial test analyte and removed the testing for methylenedioxyethylamphetaime (MDEA).<\/p>\n

When is the final rule effective?<\/p>\n

The final rule is effective January 1, 2018.<\/p>\n

What does this mean for employees?<\/p>\n

In addition to DOT 5 panel, you will also be tested for four semi-synthetic opioids (i.e., hydrocodone, oxycodone, hydromorphone, oxymorphone). Some common names for these semi-synthetic opioids include OxyContin\u00ae, Percodan\u00ae, Percocet\u00ae, Vicodin\u00ae, Lortab\u00ae, Norco\u00ae, Dilaudid\u00ae, and Exalgo\u00ae. In addition, you will no longer be tested for MDEA.<\/p>\n

What does this mean for employers and Consortium\/Third Party Administrators (C\/TPA)?<\/p>\n

As an employer or C\/TPA, you will no longer be required to submit blind specimens to laboratories.<\/p>\n

What does this mean for urine collectors?<\/p>\n

The shy bladder process has been modified so that the collector will discard any specimen provided during the collection event when the employee does not provide a sufficient specimen by the end of the three hour wait period.<\/p>\n

What does this mean for laboratories?<\/p>\n

As an HHS-certified laboratory you will:<\/p>\n