Control of Alcohol and Drug Use in Railroad Operations: Addition of Post-Accident Toxicological Testing for Non-Controlled Substances

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
May 30, 2019, FR Notice (30-Day).pdf	Supplementary Document	Uploaded 2019-05-30	Repair queued
February 22, 2019, FR Notice (60-Day; Saf.App.Stds.).pdf	Supplementary Document	Uploaded 2019-05-30	Available
PATT 2130-0598E.doc	Supporting Statement A	Uploaded 2019-05-30	Available
49 CFR 219.211.doc	Supplementary Document	Uploaded 2012-05-17	Available
21 U.S.C. 801.doc	Supplementary Document	Uploaded 2012-05-17	Available
49 CFR 1.49 (4-10).doc	Supplementary Document	Uploaded 2012-05-17	Available
49 U.S.C. 20103.doc	Supplementary Document	Uploaded 2012-05-17	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
202333	Control of Alcohol and Drug Use: Addition of Post-Accident Toxicological Testing for Non-Controlled Substances		Modified

ICR Details

OMB Control No: 2130-0598	ICR Reference No: 201905-2130-003
Status: Historical Inactive	Previous ICR Reference No: 201603-2130-005
Agency/Subagency: DOT/FRA	Agency Tracking No:
Title: Control of Alcohol and Drug Use in Railroad Operations: Addition of Post-Accident Toxicological Testing for Non-Controlled Substances
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Withdrawn and continue	Conclusion Date: 09/10/2019
	Date Received in OIRA: 06/12/2019
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	06/30/2019	36 Months From Approved	09/30/2019
Responses	32	0	32
Time Burden (Hours)	5	0	5
Cost Burden (Dollars)	0	0	0

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Abstract: The Federal Railroad Administration and railroads use the information to determine the extent of alcohol and drug abuse on railroad property as well as to curtail widespread alcohol and drug use. FRA has added non-controlled substances to its standard post-accident testing panel because FRA research indicates that use of prescription and over-the-counter drugs, most of which are non-controlled substances, is prevalent among railroad employees. FRA is using the additional information collected for research and accident investigation purposes. The addition of non-controlled substances to the post-accident testing panel helps inform FRA about a broader range of potentially impairing prescription and OTC drugs that may be currently contributing to the cause or severity of train accidents/incidents. Research generated by these data will help inform future agency policy decisions regarding these non-controlled substances.

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Authorizing Statute(s): US Code: 49 USC 20103 Name of Law: Federal Railroad Safety Act of 1970
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 5807	02/22/2019
30-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 25114	05/30/2019
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

table that charts list of burden

IC Title	Form No.	Form Name
Control of Alcohol and Drug Use: Addition of Post-Accident Toxicological Testing for Non-Controlled Substances

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Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement: This is a request for an extension with change of the last approved submission. FRA is requesting a total burden of three (3) hours, and 18 responses. Adjustments shown in the provided table in answer to question number 15 of the attached Supporting Justification decreased the burden by two (2) hours and by 14 responses. There are no program changes at this time. The current OMB inventory for this information collection shows a total burden of five (5) hours and 32 responses, while the present submission exhibits a total burden of three (3) hours and 18 responses. Hence, there is a burden decrease of two (2) hours and 14 responses. There are no additional costs to respondents other than the burden hours specified in the answer to question number 12 of this document. So, there is no change in cost to respondents.

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Annual Cost to Federal Government: $21,952

Does this IC contain surveys, censuses, or employ statistical methods? No

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     No

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 06/12/2019

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