DOT Rule 49 CFR Part 40 Appendix B

Appendix B to Part 40—Oral Fluid Collection Kit Contents

1. Oral Fluid Collection Device

a. A single device, which can be subdivided in the employee's presence into an “A” specimen and a “B” split specimen bottle sufficient for laboratory testing,...

DOT Rule 49 CFR Part 40 Section 40.311

Subpart O - Substance Abuse Professionals and the Return-to-Duty Process § 40.311 What are the requirements concerning SAP reports? (a) As the SAP conducting the required evaluations, you must send the written reports required by this section in writing directly to the DER and not...

DOT Rule 49 CFR Part 40 Section 40.331

Subpart P - Confidentiality and Release of Information§ 40.331 To what additional parties must employers and service agents release information? As an employer or service agent you must release information under the following circumstances: (a) If you receive a specific, written consent...

DOT Rule 49 CFR Part 40 Section 40.329

Subpart P - Confidentiality and Release of Information § 40.329 What information must laboratories, MROs, and other service agents release to employees? (a) As an MRO or service agent you must provide, within 10 business days of receiving a written request from an employee, copies...

DOT Rule 49 CFR Part 40 Section 40.111

Subpart F - Drug Testing Laboratories § 40.111 When and how must a laboratory disclose statistical summaries and other information it maintains?

(a) As a laboratory, you must transmit an aggregate statistical summary, by employer, of the data listed in Appendix D to this part to...

DOT Rule 49 CFR Part 40 Section 40.109

Subpart F - Drug Testing Laboratories§ 40.109 What documentation must the laboratory keep, and for how long? (a) As a laboratory, you must retain all records pertaining to each employee urine specimen for a minimum of two years. (b) As a laboratory, you must also keep for two years...

DOT Rule 49 CFR Part 40 Section 40.107

Subpart F - Drug Testing Laboratories§ 40.107 Who may inspect laboratories?

As a laboratory, you must permit an inspection, with or without prior notice, by ODAPC, a DOT agency, or a DOT-regulated employer that contracts with the laboratory for drug testing under the DOT drug testing program, or...

DOT Rule 49 CFR Part 40 Section 40.101

Subpart F - Drug Testing Laboratories§ 40.101 What relationship may a laboratory have with an MRO? (a) As a laboratory, you may not enter into any relationship with an MRO that creates a conflict of interest or the appearance of a conflict of interest with the MRO's responsibilities for the...

DOT Rule 49 CFR Part 40 Section 40.97

Subpart F - Drug Testing Laboratories § 40.97 What do laboratories report and how do they report it?

(a) As a laboratory, when reporting a result of any kind, you must report the specimen type.

(b) You must report the results for each primary specimen, which will fall into one of...

DOT Rule 49 CFR Part 40 Section 40.93

Subpart F - Drug Testing Laboratories § 40.93 What validity tests must laboratories conduct on primary oral fluid specimens?

As a laboratory, if you conduct validity testing under § 40.92, you must conduct it in accordance with the requirements of this section.

(a) You...

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