Agency Forms Undergoing Paperwork Reduction Act Review, 6519-6520 [2015-02274]

Agencies

• Centers for Disease Control and Prevention
• DEPARTMENT OF HEALTH AND HUMAN SERVICES

[Federal Register Volume 80, Number 24 (Thursday, February 5, 2015)]
[Notices]
[Pages 6519-6520]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-02274]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-15-0530]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) has submitted 
the following information collection request to the Office of 
Management and Budget (OMB) for review and approval in accordance with 
the Paperwork Reduction Act of 1995. The notice for the proposed 
information collection is published to obtain comments from the public 
and affected agencies.
    Written comments and suggestions from the public and affected 
agencies concerning the proposed collection of information are 
encouraged. Your comments should address any of the following: (a) 
Evaluate whether the proposed collection of information is necessary 
for the proper performance of the functions of the agency, including 
whether the information will have practical utility; (b) Evaluate the 
accuracy of the agencies estimate of the burden of the proposed 
collection of information, including the validity of the methodology 
and assumptions used; (c) Enhance the quality, utility, and clarity of 
the information to be collected; (d) Minimize the burden of the 
collection of information on those who are to respond, including 
through the use of appropriate automated, electronic, mechanical, or 
other technological collection techniques or other forms of information 
technology, e.g., permitting electronic submission of responses; and 
(e) Assess information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or 
suggestions regarding the items contained in this notice should be 
directed to the Attention: CDC Desk Officer, Office of Management and 
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written 
comments should be received within 30 days of this notice.

Proposed Project

    EEOICPA Dose Reconstruction Interviews and Forms, OMB No. 0920-0530 
(Expiration, 02/28/2015)--Extension--The National Institute for 
Occupational Safety and Health (NIOSH), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    On October 30, 2000, the Energy Employees Occupational Illness 
Compensation Program Act of 2000 (42 U.S.C. 7384-7385) was enacted. 
This Act established a federal compensation program for employees of 
the Department of Energy (DOE) and certain of its contractors, 
subcontractors and vendors, who have suffered cancers and other 
designated illnesses as a result of exposures sustained in the 
production and testing of nuclear weapons.
    Executive Order 13179, issued on December 7, 2000, delegated 
authorities assigned to ``the President'' under the Act to the 
Departments of Labor, Health and Human Services, Energy and Justice. 
The Department of Health and Human Services (DHHS) was delegated the 
responsibility of establishing methods for estimating radiation doses 
received by eligible claimants with cancer applying for compensation. 
NIOSH is applying the following methods to estimate the radiation doses 
of individuals applying for compensation.
    In performance of its dose reconstruction responsibilities, under 
the Act, NIOSH is providing voluntary interview opportunities to 
claimants (or their survivors) individually and providing them with the 
opportunity to assist NIOSH in documenting the work history of the 
employee by characterizing the actual work tasks performed. In 
addition, NIOSH and the claimant may identify incidents that may have 
resulted in undocumented radiation exposures, characterizing 
radiological protection and monitoring practices, and identify co-
workers and other witnesses as may be necessary to confirm undocumented 
information. In this process, NIOSH uses a computer assisted telephone 
interview (CATI) system, which allows interviews to be conducted more 
efficiently and quickly as opposed to a paper-based interview 
instrument. Both interviews are voluntary and failure to participate in 
either or both interviews will not have a negative effect on the claim, 
although voluntary participation may assist the claimant by adding 
important information that may not be otherwise available. NIOSH is 
requesting a three-year approval for these data collection activities.

[[Page 6520]]

    NIOSH uses the data collected in this process to complete an 
individual dose reconstruction that accounts, as fully as possible, for 
the radiation dose incurred by the employee in the line of duty for DOE 
nuclear weapons production programs. After dose reconstruction, NIOSH 
also performs a brief, voluntary final interview with the claimant to 
explain the results and to allow the claimant to confirm or question 
the records NIOSH has compiled. This will also be the final opportunity 
for the claimant to supplement the dose reconstruction record. 
Approximately 3,600 claimants will be interviewed with an average 
burden of one hour per response.
    At the conclusion of the dose reconstruction process, the claimant 
submits a form to confirm that the claimant has no further information 
to provide to NIOSH about the claim at this time. The form notifies the 
claimant that signing the form allows NIOSH to forward a dose 
reconstruction report to DOL and to the claimant, and closes the record 
on data used for the dose reconstruction. Signing this form does not 
indicate that the claimant agrees with the outcome of the dose 
reconstruction. The dose reconstruction results will be supplied to the 
claimant and to the DOL, the agency that will utilize them as one part 
of its determination of whether the claimant is eligible for 
compensation under the Act. It is estimated that 3,600 claimants will 
complete the conclusion form which takes approximately five minutes per 
response.
    The total estimated burden hours are 3,900. There is no cost to 
respondents other than their time.

                                        Estimated Annualized Burden Hours
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                                                                                     Number of    Average burden
          Type of respondent                    Form name            Number of     responses per   per response
                                                                    respondents     respondent      (in hours)
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Claimant..............................  Initial interview.......           3,600               1               1
Claimant..............................  Conclusion form OCAS-1..           3,600               1            5/60
                                                                 -----------------------------------------------
    Total
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Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific 
Integrity, Office of the Associate Director for Science, Office of the 
Director, Centers for Disease Control and Prevention.
[FR Doc. 2015-02274 Filed 2-4-15; 8:45 am]
BILLING CODE 4163-18-P