Proposed Data Collections Submitted for Public Comment and Recommendations, 15840-15842 [2018-07563]

Download as PDF 15840 Federal Register / Vol. 83, No. 71 / Thursday, April 12, 2018 / Notices and healthful working conditions for men and women (Occupational Safety and Health Act, 1970, Pub. L. 91–596 (Section 20[a][1])). The National Personal Protective Technology Laboratory focuses on improving personal protective equipment across many industries, including the fire services. NIOSH seeks to request a three-year Office of Management and Budget approval to gather data about Personal Protective Equipment (PPE) use conditions. Turnout gear is a type of PPE used by the 1.1 million U.S. fire fighters to shield the body from carcinogens, flames, heat, and chemical/biological agents. It serves as a barrier to external hazards while simultaneously allowing for the escape of metabolic heat to prevent elevated core body temperatures. To provide the necessary performance characteristics, turnout gear design is complex, consisting of three major layers that work as a composite—a thermal liner, a moisture barrier, and an outer shell. Consensus standards provide performance requirements and retirement criteria for turnout gear. The retirement criteria is based on visual inspections and a 10-year age cap with visual inspection being less effective for the moisture barrier and thermal liner layers. Recent data of turnout gear (2) surveying the fire fighters assigned to each set of sampled gear to obtain one-month of retrospective information about the use conditions to which it was likely exposed; and (3) a 6-month prospective data collection where the fire fighters assigned to each set of sampled gear provide information about their shiftspecific exposures. The survey will provide details about the use conditions (e.g., number and type of launderings, repair history, and exposure to fire-related calls) specific to the fire fighters who used the sampled turnout gear. The data produced by this study will be used to improve confidence that turnout gear will remain protective throughout its lifecycle. Samples of 300 individuals will be collected from three fire departments. The time required to complete a data collection instrument will be about 30 minutes for the paper retrospective study and 10 minutes for each electronic prospective survey to be completed at the end of each shift, which is estimated to be 60 shifts over a 6-month period. The following table provides an estimate of the annualized burden hours. The estimated total hours for this information collection is 3,150, over a three-year timeframe, with a maximum of 300 people. donated from fire departments demonstrates that turnout gear from 2 to 10 years old was unable to meet all performance requirements. Thus, under the current retirement criteria, turnout gear that may not be protective against all hazards is being used by fire fighters. Intuitively, the use conditions to which turnout gear would be exposed to when used by a large or medium metropolitan fire department would be very different from those of a smaller department. However, the absence of scientific data to link performance to use conditions (e.g., number and type of washings, number of fire-related calls) provides a barrier to transitioning to an alternative approach to retirement. This study will obtain a statistically meaningful sample of turnout gear from three fire departments. The use conditions for the sampled turnout gear will be determined, and the gear will be subjected to established performance requirements. For each set of gear, its performance will be directly linked to its use condition history. This combined lab and field data will help determine if there is a relationship between turnout and gear use conditions. As well as the ability for turnout, gear too effectively protect the user. The use conditions for each set of sampled gear will be determined by: (1) Reviewing fire department records, practices, and policies; ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Number of responses per respondent Average burden per response (in hours) Total burden (in hours) Type of respondents Form name Individual Fire Fighter .... Turnout Gear Safety Survey—Retrospective Exposures for past month. Turnout Gear Safety Survey—Prospective Exposures for six months. 100 1 30/60 50 100 60 10/60 1,000 .............................................................................. ........................ ........................ ........................ 1,050 Total ........................ 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. 2018–07562 Filed 4–11–18; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–18–0200; Docket No. CDC–2018– 0030] sradovich on DSK3GMQ082PROD with NOTICES BILLING CODE 4163–18–P Proposed Data Collections Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of SUMMARY: VerDate Sep<11>2014 19:20 Apr 11, 2018 Jkt 244001 PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled ‘‘Coal Workers’ Health Surveillance Program (CWHSP). The CWHSP is a congressionally-mandated medical examination program for monitoring the health of coal miners and was originally established under the Federal Coal Mine Health and Safety E:\FR\FM\12APN1.SGM 12APN1 Federal Register / Vol. 83, No. 71 / Thursday, April 12, 2018 / Notices Act of 1969 with all subsequent amendments (the Act). DATES: CDC must receive written comments on or before June 11, 2018. ADDRESSES: You may submit comments, identified by Docket No. CDC–2018– 0030 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Leroy A. Richardson, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS– D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov. Please note: Submit all Federal comments through the Federal eRulemaking portal (regulations.gov) or by U.S. mail to the address listed above. To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Leroy A. Richardson, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS–D74, Atlanta, Georgia 30329; phone: 404–639–7570; Email: omb@cdc.gov. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. The OMB is particularly interested in comments that will help: 1. 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; 2. Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, sradovich on DSK3GMQ082PROD with NOTICES FOR FURTHER INFORMATION CONTACT: VerDate Sep<11>2014 19:20 Apr 11, 2018 Jkt 244001 including the validity of the methodology and assumptions used; 3. Enhance the quality, utility, and clarity of the information to be collected; and 4. 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 submissions of responses. 5. Assess information collection costs. Proposed Project Coal Workers’ Health Surveillance Program (CWHSP), OMB Number 0920– 0020, expires 06/30/2018—Extension— for National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC). Background and Brief Description NIOSH would like to extend the Coal Workers’ Health Surveillance Program (CWHSP) data collection project. This request incorporates all components of the CWHSP. Those components includes Coal Workers’ X-ray Surveillance Program (CWXSP), B Reader Program, Enhanced Coal Workers’ Health Surveillance Program (ECWHSP), Expanded Coal Workers’ Health Surveillance Program, and National Coal Workers’ Autopsy Study (NCWAS). The CWHSP is a congressionally mandated medical examination program for monitoring the health of coal miners and was originally established under the Federal Coal Mine Health and Safety Act of 1969 with all subsequent amendments (the Act). The Act provides the regulatory authority for the administration of the CWHSP. This Program, which operates in accordance with 42 CFR part 37, is useful in providing information for protecting the health of and also in documenting trends and patterns in the prevalence of coal workers’ pneumoconiosis (‘black lung’ disease) among miners employed in U.S. coal mines. The total estimated annualized burden hours of 20,281 is based on the following collection instruments: • Coal Mine Operator Plan (2.10) and Coal Contractor Plan (2.18)—Under 42 CFR part 37, every coal operator and coal contractor in the U.S. must submit a plan approximately every 4 years, providing information on how they plan to notify their miners of the opportunity to obtain the medical examination. Completion of this form with all requested information (including a PO 00000 Frm 00058 Fmt 4703 Sfmt 4703 15841 roster of current employees) takes approximately 30 minutes. • Radiographic Facility Certification Document (2.11)—X-ray facilities seeking NIOSH approval to provide miner radiographs under the CWHSP must complete an approval packet including this form that requires approximately 30 minutes for completion. • Miner Identification Document (2.9)—Miners who elect to participate in the CWHSP must fill out this document, which requires approximately 20 minutes. This document records demographic and occupational history, as well as information required under the regulations in relation to the examinations. • Chest Radiograph Classification Form (2.8)—NIOSH utilizes a radiographic classification system developed by the International Labour Office (ILO) in the determination of pneumoconiosis among coal miners. Physicians (B Readers) fill out this form regarding their interpretations of the radiographs (each image has at least two separate interpretations, and approximately 7% of the images require additional interpretations). Based on prior practice it takes the physician approximately three minutes per form. • Physician Application for Certification (2.12)—Physicians taking the B Reader examination are asked to complete this registration form, which provides demographic information as well as information regarding their medical practices. It typically takes the physician about 10 minutes to complete this form. • Guidelines for Spirometry in the ECWHSP Mobile (Internal use, no form number assigned)—Miners (both active and former) participating in the ECWHSP component of the Program are offered a spirometry test. This form is administered by a NIOSH employee (or contractor) in the ECWHSP Mobile Unit during the initial intake process and takes approximately five minutes to complete. This information is required to make sure that the spirometry test can be done safely and that the miner is physically capable of performing the spirometry maneuvers. • Spirometry Facility Certification Document (2.14)—This form is analogous to the Radiographic Facility Certification Document (2.11) and records the spirometry facility equipment/staffing information. Spirometry facilities seeking NIOSH approval to provide miner spirometry testing under the CWHSP must complete an approval packet, which includes this form. It is estimated that it will take approximately 30 minutes E:\FR\FM\12APN1.SGM 12APN1 15842 Federal Register / Vol. 83, No. 71 / Thursday, April 12, 2018 / Notices for this form to be completed at the facility. • Respiratory Assessment Form (2.13)—This form is designed to assess respiratory symptoms and certain medical conditions and risk factors. It is estimated that it will take approximately five minutes for this form to be administered to the miner by an employee at the facility. • Spirometry Results Notification Form (2.15)—This form is used to: Collect information that will allow NIOSH to identify the miner in order to provide notification of the spirometry test results; assure that the test can be done safely; record certain factors that can affect test results; provide documentation that the required components of the spirometry examination have been transmitted to NIOSH for processing; and conduct quality assurance audits and autopsy. Since an autopsy report is routinely completed by a pathologist, the only additional burden is the specific request for a clinical abstract of terminal illness and final diagnosis relating to pneumoconiosis. Therefore, only 5 minutes of additional burden is estimated for the pathologist’s report. • Consent, Release and History Form (2.6)—This form documents written authorization from the next-of-kin to perform an autopsy on the deceased miner. A minimum of essential information is collected regarding the deceased miner including an occupational history and a smoking history. From experience, it is estimated that 15 minutes is required for the nextof-kin to complete this form. There are no costs to respondents other than their time. interpretation of results. It is estimated that it will take the facility approximately 20 minutes to complete this form. • Pathologist Invoice—Under the NCWAS, the invoice submitted by the pathologist must contain a statement that the pathologist is not receiving any other compensation for the autopsy. Each participating pathologist may use their individual invoice as long as this statement is added. It is estimated that only 5 minutes is required for the pathologist to add this statement to the standard invoice that they routinely use. • Pathologist Report—Under the NCWAS, the pathologist must submit information found at autopsy, slides, blocks of tissue, and a final diagnosis indicating presence or absence of pneumoconiosis. The format of the autopsy reports is variable depending on the pathologist conducting the ESTIMATED ANNUALIZED BURDEN HOURS Number of responses per respondent Number of respondents Average burden per response (in hours) Total burden (in hours) Type of respondents Form name Coal Mine Operator .......................... Coal Mine Contractor ........................ X-ray Facility Supervisor ................... Coal Miner ......................................... Coal Miner ......................................... B Reader Physician .......................... Physicians taking the B Reader Examination. Spirometry Facility Supervisor .......... Spirometry Facility Employee ........... Spirometry Technician ...................... Coal Miner ......................................... Pathologist ........................................ Pathologist ........................................ 2.10 .................................................. 2.18 .................................................. 2.11 .................................................. 2.9 .................................................... No form ............................................ 2.8 .................................................... 2.12 .................................................. 388 575 40 14,560 14,560 10 100 1 1 1 1 1 3014 1 30/60 30/60 30/60 20/60 15/60 3/60 10/60 194 288 20 4,854 3,640 1,507 17 100 14,560 14,560 14,560 1 1 1 1 1 1 1 l 30/60 5/60 20/60 15/60 5/60 5/60 50 1,214 4,854 3,640 1 1 Next-of-kin for deceased miner ........ 2.14 .................................................. 2.13 .................................................. 2.15 .................................................. No form ............................................ Invoice—No standard form .............. Pathology Report—No standard form. 2.6 .................................................... 1 1 15/60 1 Total ........................................... ........................................................... ........................ ........................ ........................ 20,281 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. 2018–07563 Filed 4–11–18; 8:45 am] BILLING CODE 4163–18–P sradovich on DSK3GMQ082PROD with NOTICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Intergovernmental Reference Guide (IRG). VerDate Sep<11>2014 19:20 Apr 11, 2018 Jkt 244001 OMB No.: 0970–0209. Description: The Intergovernmental Reference Guide (IRG) is a centralized and automated repository of state and tribal profiles, which contains highlevel descriptions of each state and the tribal child support enforcement (CSE) program. These profiles provide state and tribal CSE agencies, and foreign countries with an effective and efficient method for updating and accessing information needed to process intergovernmental child support cases. The IRG information collection activities are authorized by: (1) 42 U.S.C. 652(a)(7), which requires the federal Office of Child Support Enforcement (OCSE) to provide technical assistance to state child PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 support enforcement agencies to help them establish effective systems for collecting child and spousal support; (2) 42 U.S.C. 666(f), which requires states to enact the Uniform Interstate Family Support Act; (3) 45CFR 301.1, which defines an intergovernmental case to include cases between states and tribes; (4) 45 CFR309.120, which requires a tribal child support program to include intergovernmental procedures in its tribal IV–D plan; and (5) 45 CFR 303.7, which requires state child support agencies to provide services in intergovernmental cases. Respondents: All state and tribal CSE agencies. E:\FR\FM\12APN1.SGM 12APN1

Agencies

[Federal Register Volume 83, Number 71 (Thursday, April 12, 2018)]
[Notices]
[Pages 15840-15842]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-07563]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-18-0200; Docket No. CDC-2018-0030]


Proposed Data Collections Submitted for Public Comment and 
Recommendations

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

-----------------------------------------------------------------------

SUMMARY: The Centers for Disease Control and Prevention (CDC), as part 
of its continuing effort to reduce public burden and maximize the 
utility of government information, invites the general public and other 
Federal agencies the opportunity to comment on a proposed and/or 
continuing information collection, as required by the Paperwork 
Reduction Act of 1995. This notice invites comment on a proposed 
information collection project titled ``Coal Workers' Health 
Surveillance Program (CWHSP). The CWHSP is a congressionally-mandated 
medical examination program for monitoring the health of coal miners 
and was originally established under the Federal Coal Mine Health and 
Safety

[[Page 15841]]

Act of 1969 with all subsequent amendments (the Act).

DATES: CDC must receive written comments on or before June 11, 2018.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2018-
0030 by any of the following methods:
     Federal eRulemaking Portal: Regulations.gov. Follow the 
instructions for submitting comments.
     Mail: Leroy A. Richardson, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS-D74, Atlanta, Georgia 30329.
    Instructions: All submissions received must include the agency name 
and Docket Number. CDC will post, without change, all relevant comments 
to Regulations.gov.

     Please note: Submit all Federal comments through the Federal 
eRulemaking portal (regulations.gov) or by U.S. mail to the address 
listed above.


FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the information collection plan 
and instruments, contact Leroy A. Richardson, Information Collection 
Review Office, Centers for Disease Control and Prevention, 1600 Clifton 
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: 
[email protected].

SUPPLEMENTARY INFORMATION: 
    Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-
3520), Federal agencies must obtain approval from the Office of 
Management and Budget (OMB) for each collection of information they 
conduct or sponsor. In addition, the PRA also requires Federal agencies 
to provide a 60-day notice in the Federal Register concerning each 
proposed collection of information, including each new proposed 
collection, each proposed extension of existing collection of 
information, and each reinstatement of previously approved information 
collection before submitting the collection to the OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    The OMB is particularly interested in comments that will help:
    1. 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;
    2. Evaluate the accuracy of the agency's estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    3. Enhance the quality, utility, and clarity of the information to 
be collected; and
    4. 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 
submissions of responses.
    5. Assess information collection costs.

Proposed Project

    Coal Workers' Health Surveillance Program (CWHSP), OMB Number 0920-
0020, expires 06/30/2018--Extension--for National Institute for 
Occupational Safety and Health (NIOSH), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    NIOSH would like to extend the Coal Workers' Health Surveillance 
Program (CWHSP) data collection project. This request incorporates all 
components of the CWHSP. Those components includes Coal Workers' X-ray 
Surveillance Program (CWXSP), B Reader Program, Enhanced Coal Workers' 
Health Surveillance Program (ECWHSP), Expanded Coal Workers' Health 
Surveillance Program, and National Coal Workers' Autopsy Study (NCWAS).
    The CWHSP is a congressionally mandated medical examination program 
for monitoring the health of coal miners and was originally established 
under the Federal Coal Mine Health and Safety Act of 1969 with all 
subsequent amendments (the Act). The Act provides the regulatory 
authority for the administration of the CWHSP. This Program, which 
operates in accordance with 42 CFR part 37, is useful in providing 
information for protecting the health of and also in documenting trends 
and patterns in the prevalence of coal workers' pneumoconiosis (`black 
lung' disease) among miners employed in U.S. coal mines. The total 
estimated annualized burden hours of 20,281 is based on the following 
collection instruments:
     Coal Mine Operator Plan (2.10) and Coal Contractor Plan 
(2.18)--Under 42 CFR part 37, every coal operator and coal contractor 
in the U.S. must submit a plan approximately every 4 years, providing 
information on how they plan to notify their miners of the opportunity 
to obtain the medical examination. Completion of this form with all 
requested information (including a roster of current employees) takes 
approximately 30 minutes.
     Radiographic Facility Certification Document (2.11)--X-ray 
facilities seeking NIOSH approval to provide miner radiographs under 
the CWHSP must complete an approval packet including this form that 
requires approximately 30 minutes for completion.
     Miner Identification Document (2.9)--Miners who elect to 
participate in the CWHSP must fill out this document, which requires 
approximately 20 minutes. This document records demographic and 
occupational history, as well as information required under the 
regulations in relation to the examinations.
     Chest Radiograph Classification Form (2.8)--NIOSH utilizes 
a radiographic classification system developed by the International 
Labour Office (ILO) in the determination of pneumoconiosis among coal 
miners. Physicians (B Readers) fill out this form regarding their 
interpretations of the radiographs (each image has at least two 
separate interpretations, and approximately 7% of the images require 
additional interpretations). Based on prior practice it takes the 
physician approximately three minutes per form.
     Physician Application for Certification (2.12)--Physicians 
taking the B Reader examination are asked to complete this registration 
form, which provides demographic information as well as information 
regarding their medical practices. It typically takes the physician 
about 10 minutes to complete this form.
     Guidelines for Spirometry in the ECWHSP Mobile (Internal 
use, no form number assigned)--Miners (both active and former) 
participating in the ECWHSP component of the Program are offered a 
spirometry test. This form is administered by a NIOSH employee (or 
contractor) in the ECWHSP Mobile Unit during the initial intake process 
and takes approximately five minutes to complete. This information is 
required to make sure that the spirometry test can be done safely and 
that the miner is physically capable of performing the spirometry 
maneuvers.
     Spirometry Facility Certification Document (2.14)--This 
form is analogous to the Radiographic Facility Certification Document 
(2.11) and records the spirometry facility equipment/staffing 
information. Spirometry facilities seeking NIOSH approval to provide 
miner spirometry testing under the CWHSP must complete an approval 
packet, which includes this form. It is estimated that it will take 
approximately 30 minutes

[[Page 15842]]

for this form to be completed at the facility.
     Respiratory Assessment Form (2.13)--This form is designed 
to assess respiratory symptoms and certain medical conditions and risk 
factors. It is estimated that it will take approximately five minutes 
for this form to be administered to the miner by an employee at the 
facility.
     Spirometry Results Notification Form (2.15)--This form is 
used to: Collect information that will allow NIOSH to identify the 
miner in order to provide notification of the spirometry test results; 
assure that the test can be done safely; record certain factors that 
can affect test results; provide documentation that the required 
components of the spirometry examination have been transmitted to NIOSH 
for processing; and conduct quality assurance audits and interpretation 
of results. It is estimated that it will take the facility 
approximately 20 minutes to complete this form.
     Pathologist Invoice--Under the NCWAS, the invoice 
submitted by the pathologist must contain a statement that the 
pathologist is not receiving any other compensation for the autopsy. 
Each participating pathologist may use their individual invoice as long 
as this statement is added. It is estimated that only 5 minutes is 
required for the pathologist to add this statement to the standard 
invoice that they routinely use.
     Pathologist Report--Under the NCWAS, the pathologist must 
submit information found at autopsy, slides, blocks of tissue, and a 
final diagnosis indicating presence or absence of pneumoconiosis. The 
format of the autopsy reports is variable depending on the pathologist 
conducting the autopsy. Since an autopsy report is routinely completed 
by a pathologist, the only additional burden is the specific request 
for a clinical abstract of terminal illness and final diagnosis 
relating to pneumoconiosis. Therefore, only 5 minutes of additional 
burden is estimated for the pathologist's report.
     Consent, Release and History Form (2.6)--This form 
documents written authorization from the next-of-kin to perform an 
autopsy on the deceased miner. A minimum of essential information is 
collected regarding the deceased miner including an occupational 
history and a smoking history. From experience, it is estimated that 15 
minutes is required for the next-of-kin to complete this form.
    There are no costs to respondents other than their time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondents           Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)      (in hours)
----------------------------------------------------------------------------------------------------------------
Coal Mine Operator............  2.10............             388               1           30/60             194
Coal Mine Contractor..........  2.18............             575               1           30/60             288
X-ray Facility Supervisor.....  2.11............              40               1           30/60              20
Coal Miner....................  2.9.............          14,560               1           20/60           4,854
Coal Miner....................  No form.........          14,560               1           15/60           3,640
B Reader Physician............  2.8.............              10            3014            3/60           1,507
Physicians taking the B Reader  2.12............             100               1           10/60              17
 Examination.
Spirometry Facility Supervisor  2.14............             100               1           30/60              50
Spirometry Facility Employee..  2.13............          14,560               1            5/60           1,214
Spirometry Technician.........  2.15............          14,560               1           20/60           4,854
Coal Miner....................  No form.........          14,560               1           15/60           3,640
Pathologist...................  Invoice--No                    1               1            5/60               1
                                 standard form.
Pathologist...................  Pathology                      1               l            5/60               1
                                 Report--No
                                 standard form.
Next-of-kin for deceased miner  2.6.............               1               1           15/60               1
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............          20,281
----------------------------------------------------------------------------------------------------------------


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. 2018-07563 Filed 4-11-18; 8:45 am]
 BILLING CODE 4163-18-P


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