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  1. 49 CFR Part 40 - §40.385 Who bears the burden of proof in a PIE proceeding?

    49 CFR Part 40 - §40.385 Who bears the burden of proof in a PIE proceeding?

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  2. 49 CFR Part 40 - §40.403 Must a service agent notify its clients when the Department issues a PIE?

    49 CFR Part 40 - §40.403 Must a service agent notify its clients when the Department issues a PIE?

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  3. 49 CFR Part 40: §40.3 What Do The Terms Used In This Part Mean?

    49 CFR Part 40: §40.3 What Do The Terms Used In This Part Mean?

  4. 49 CFR Part 40 - Subpart F—Drug Testing Laboratories

    49 CFR Part 40 - Subpart F—Drug Testing Laboratories

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  5. 49 CFR Part 40 Subpart G—Medical Review Officers and the Verification Process

    49 CFR Part 40 Subpart G—Medical Review Officers and the Verification Process

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  6. 49 CFR Part 40 Subpart H—Split Specimen Tests

    49 CFR Part 40 Subpart H—Split Specimen Tests

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  7. 49 CFR Part 40 Subpart I—Problems in Drug Tests

    49 CFR Part 40 Subpart I—Problems in Drug Tests

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  8. 49 CFR Part 40 Subpart K—Testing Sites, Forms, Equipment and Supplies Used in Alcohol Testing

    49 CFR Part 40 Subpart K—Testing Sites, Forms, Equipment and Supplies Used in Alcohol Testing

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  9. 49 CFR Part 40 Subpart M—Alcohol Confirmation Tests

    49 CFR Part 40 Subpart M—Alcohol Confirmation Tests

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  10. Saliva/Oral Fluid Specimen Collector Training (Non-DOT )

    Saliva/Oral Fluid Specimen Collector Training (Non-DOT )

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  11. Truthzilla Podcast - #004 - Good Covid Fearing Americans

    Truthzilla Podcast - #004 - Good Covid Fearing Americans

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  12. 49 CFR Part 40: Part A Administrative Provisions - Who Does This Regulation Cover?

    49 CFR Part 40: Part A Administrative Provisions - Who Does This Regulation Cover?

  13. 49 CFR Part 40: §40.71 How Does The Collector Prepare The Specimens?

    49 CFR Part 40: §40.71 How Does The Collector Prepare The Specimens?

  14. 49 CFR Part 40: §40.67 When and How Is a Direct Observed Collection Conducted?

    49 CFR Part 40: §40.67 When and How Is a Direct Observed Collection Conducted?

  15. 49 CFR Part 40: §40.69 How Is a Monitored Collection Conducted?

    49 CFR Part 40: §40.69 How Is a Monitored Collection Conducted?

  16. 49 CFR Part 40 - §40.87 What Are The Cutoff Concentrations For Drug Tests?

    49 CFR Part 40 - §40.87 What Are The Cutoff Concentrations For Drug Tests?

  17. 49 CFR Part 40 - §40.83 How Do Laboratories Process Incoming Specimens?

    49 CFR Part 40 - §40.83 How Do Laboratories Process Incoming Specimens?

  18. 49 CFR Part 40 - §40.85 What Drugs Do Laboratories Test For?

    49 CFR Part 40 - §40.85 What Drugs Do Laboratories Test For?

  19. 49 CFR Part 40: §40.113 Where Is Other Information Concerning Laboratories Found In This Regulation?

    49 CFR Part 40: §40.113 Where Is Other Information Concerning Laboratories Found In This Regulation?

  20. 49 CFR Part 40 - §40.101 What Relationship May a Laboratory Have With An MRO?

    49 CFR Part 40 - §40.101 What Relationship May a Laboratory Have With An MRO?

  21. 49 CFR Part 40 - §40.125 What Relationship May An MRO Have With a Laboratory?

    49 CFR Part 40 - §40.125 What Relationship May An MRO Have With a Laboratory?

  22. 49 CFR Part 40 - §40.91 What Validity Tests Must Laboratories Conduct On Primary Specimens?

    49 CFR Part 40 - §40.91 What Validity Tests Must Laboratories Conduct On Primary Specimens?

  23. 49 CFR Part 40 - §40.107 Who May Inspect Laboratories?

    49 CFR Part 40 - §40.107 Who May Inspect Laboratories?

  24. 49 CFR Part 40 - §40.97 What Do Laboratories Report And How Do They Report It?

    49 CFR Part 40 - §40.97 What Do Laboratories Report And How Do They Report It?

  25. 49 CFR Part 40 - 40.96 What Criteria Do Laboratories Use To Establish That a Specimen Is Invalid?

    49 CFR Part 40 - 40.96 What Criteria Do Laboratories Use To Establish That a Specimen Is Invalid?