FRA uses the information obtained through its accident/incident regulations to maintain a current and historical databased so that it can monitor the safety and operational practices of the nation's railroads; to identify and promptly ameliorate hazardous conditions associated with rail transportation; and to assure compliance with Federal railroad safety laws.
US Code:
49 USC 20901
Name of Law: (Formerly Part of Accident Reports Act)
FRA F 6180.98, FRA F 6180.56, FRA F 6180.107, FRA F 6180.55a, FRA F 6180.150, FRA F6180.55, FRA F 6180.54, FRA F 6180.78, FRA F 6180.97, FRA F 6180.57, FRA F 6180.81
The newly revised Code of Federal Regulations (49 CFR 219.201(a)), effective June 12, 2017, requires post-accident toxicological testing of railroad employees when one or more of five specific requirements are met for certain human-factor categories of highway-rail grade crossing accidents and incidents. In this submission, FRA is revising the instructions for Form FRA F 6180.57 to enable FRA to capture information concerning post-accident toxicological testing for certain human factor, highway-rail grade crossing accidents and incidents in the narrative block of this form. This the program change. FRA is not revising the Form 57 itself at this time. Since the average burden time for Form FRA F 6180.57 has extra time built in for the narrative block in order to add all essential information, it remains unchanged at two hours per form. Thus, the previously total burden of 46,577 hours and 109,440 responses remains unchanged.
There are no adjustments at this time.
******Although neither the total burden hours nor the total burden responses have changed, FRA has provided a separate IC for each of the 11 forms that are part of the main submission (thus totaling 12 ICs). The Summary of Burden above reflects the calculations for all 12 ICs and shows FRA is requesting no change from the last approved submission.
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:
(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;
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.