In accordance with 5 CFR 1320, the information collection request is approved for three years. OMB requests that when the agency submits the package for renewal that it conduct consultations with up to 9 outside entities and incorporate those findings into the ICR package.
Inventory as of this Action
Requested
Previously Approved
11/30/2017
36 Months From Approved
11/30/2014
411,291
0
521,919
623,943
0
667,081
67,214
0
86,398
The NRC regulations in 10 CFR Part 26 prescribe requirements to establish, implement, and maintain FFD programs at affected licensees and other entities. The objectives of these requirements are to provide reasonable assurance that persons subject to the rule are trustworthy, reliable, and not under the influence of any substance, legal or illegal, or mentally or physically impaired from any cause, which in any way could adversely affect their ability to safely and competently perform their duties. These requirements also provide reasonable assurance that the effects of fatigue and degraded alertness on individual's abilities to safely and competently perform their duties are managed commensurate with maintaining public health and safety. The information collections required by Part 26 are necessary to properly manage FFD programs and to enable effective and efficient regulatory oversight of affected licensees other entities. These licensees and other entities must perform certain tasks, maintain records, and submit reports to comply with Part 26 drug and alcohol provisions and fatigue management requirements. These records and reports are necessary to enable regulatory inspection and evaluation of a licensee's or entity's compliance with NRC regulations, its FFD performance, and of any significant FFD-related event to help maintain public health and safety, promote the common defense and security, and protect the environment.
The total burden for Part 26 changed from 667,080.6 hours to 623,943.1 hours, a decrease of 43,137.5 hours. Changes to the total burden are based on the following 11 reasons: (1) Separating Drug and Alcohol Programs from Fatigue Management Programs, (2) Additional Reactor Construction Sites – Subpart K Drug and Alcohol Programs, (3) Reassessment of Corporate-based FFD Programs for Multiple Facilities, (4) Decrease in the number of Operating Commercial Nuclear Power Reactors (5) Reduction in the number of Fatigue Management Programs, (6) Two newly identified Third-Party Burdens, (7) Burden Consolidation, (8) Inclusion of burdens for a Mixed-Oxide (MOX) Fuel Fabrication Facility, (9) An increase of two HHS-certified Laboratories, (10) A decrease in the number of Licensee Testing Facilities (LTFs) from 31 to 7, and (11) Voluntary Use of NRC's FFD Program Performance Electronic Reporting Forms.
This clearance also includes three electronic reporting forms (i.e., e-forms) that have been developed by the NRC, with input from the industry, to improve reporting efficiency:
• NRC Form 890, "Single Positive Test Form;"
• NRC Form 891, "Annual Reporting Form for Drug and Alcohol Tests;" and
• NRC Form 892, "Annual Fatigue Reporting Form."
This renewal represents the first submission of these forms to OMB. The e-forms facilitate consistency and accuracy through the use of a fill-in-the-blank format and drop-down menus. The forms provide a voluntary alternative means of reporting information required under 26.717 for drug and alcohol tests and 26.203(e) for fatigue and work hour controls. Licensees may still report this information in any format they choose; however, the forms provide a more efficient and standardized way or reporting should licensees choose to use them. The time to complete the forms is based on the estimates established for the associated requirements in the previous clearance package (2011-2014 clearance period).
$845,104
No
No
No
No
No
Uncollected
Paul Harris 301 415-1169 paul.harris@nrc.gov
No
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.