Proposed Data Collection Submitted for Public Comment and Recommendations, 96454-96456 [2016-31738]

Download as PDF srobinson on DSK5SPTVN1PROD with NOTICES 96454 Federal Register / Vol. 81, No. 251 / Friday, December 30, 2016 / Notices quality, utility, and clarity of the information collected; ways to minimize the burden of the collection of information on the respondents, including the use of automated collection techniques or other forms of information technology; and ways to further reduce the information collection burden on small business concerns with fewer than 25 employees. The FCC may not conduct or sponsor a collection of information unless it displays a currently valid Office of Management and Budget (OMB) control number. No person shall be subject to any penalty for failing to comply with a collection of information subject to the PRA that does not display a valid OMB control number. DATES: Written comments should be submitted on or before January 30, 2017. If you anticipate that you will be submitting comments, but find it difficult to do so within the period of time allowed by this notice, you should advise the contacts below as soon as possible. ADDRESSES: Direct all PRA comments to Kimberly R. Keravuori, OMB, via email Kimberly_R_Keravuori@omb.eop.gov; and to Nicole Ongele, FCC, via email PRA@fcc.gov and to Nicole.Ongele@fcc.gov. Include in the comments the OMB control number as shown in the SUPPLEMENTARY INFORMATION section below. FOR FURTHER INFORMATION CONTACT: For additional information or copies of the information collection, contact Nicole Ongele at (202) 418–2991. To view a copy of this information collection request (ICR) submitted to OMB: (1) Go to the Web page http://www.reginfo.gov/ public/do/PRAMain, (2) look for the section of the Web page called ‘‘Currently Under Review,’’ (3) click on the downward-pointing arrow in the ‘‘Select Agency’’ box below the ‘‘Currently Under Review’’ heading, (4) select ‘‘Federal Communications Commission’’ from the list of agencies presented in the ‘‘Select Agency’’ box, (5) click the ‘‘Submit’’ button to the right of the ‘‘Select Agency’’ box, (6) when the list of FCC ICRs currently under review appears, look for the OMB control number of this ICR and then click on the ICR Reference Number. A copy of the FCC submission to OMB will be displayed. SUPPLEMENTARY INFORMATION: OMB Control Number: 3060–XXXX. Title: Connect America Fund—High Cost Portal Filing. Form Number: N/A. Type of Review: New collection. Respondents: Business or other forprofit. VerDate Sep<11>2014 19:18 Dec 29, 2016 Jkt 241001 Number of Respondents and Responses: 1,526 unique respondents; 3,595 responses. Estimated Time per Response: 8 hours—30 hours. Frequency of Response: On occasion, quarterly reporting requirements, annual reporting requirements, one-time reporting requirement and recordkeeping requirement. Obligation to Respond: Required to obtain or retain benefits. Statutory authority for this information collection is contained in 47 U.S.C. 151–154, 155, 201–206, 214, 218–220, 251, 252, 254, 256, 303(r), 332, 403, 405, 410, and 1302. Total Annual Burden: 65,713 hours. Total Annual Cost: No Cost. Privacy Act Impact Assessment: No impact(s). Nature and Extent of Confidentiality: We note that USAC must preserve the confidentiality of certain data obtained from respondents; must not use the data except for purposes of administering the universal service programs or other purposes specified by the Commission; and must not disclose data in companyspecific form unless directed to do so by the Commission. Respondents may request materials or information submitted to the Commission or the Administrator believed confidential to be withheld from public inspection under 47 CFR 0.459 of the FCC’s rules. Needs and Uses: The Commission is requesting approval for this new information collection. In March 2016, the Commission adopted an order reforming its universal service support program in areas served by rate-ofreturn carriers. Connect America Fund et al., WC Docket Nos. 10–90 et al., Report and Order, Order and Order on Reconsideration, and Further Notice of Proposed Rulemaking, FCC 16–33 (Rateof-Return Order). Also, in May 2016, the Commission adopted rules to implement a competitive bidding process for Phase II of the Connect America Fund. Connect America Fund et al., WC Docket Nos. 10–90 et al., Report and Order and Further Notice of Proposed Rulemaking, FCC 16–64 (Phase II Auction Order). This information collection addresses the requirement that certain carriers with high cost reporting obligations must file information about their locations which meet their broadband deployment public interest obligations via an electronic portal (‘‘portal’’). The Rate-of-Return Order required that the Universal Service Administrative Company (USAC) establish the portal so that carriers could file their location data with the portal starting in 2017. The Rate-of-Return Order required all PO 00000 Frm 00022 Fmt 4703 Sfmt 4703 recipients of Phase II model-based support and rate-of-return carriers to submit geocoded location data and related certifications to the portal. Recipients of Phase II model-based support had been required to file such information in their annual reports due by July 1. The Phase II Auction Order requires auction winners to build-out networks capable of meeting their public interest obligations and report, to an online portal, locations to which auction winners had deployed such networks. This collection also implements the Rate-of-Return Order by moving and revising the currently approved requirements under OMB Control Numbers 3060–1200 and 3060– 0986 to enable recipients of Phase II model-based support and rural broadband experiment funding to file their location information and associated reports and certifications in the portal instead of on the FCC Form 481 or as is currently required. Federal Communications Commission. Katura Howard, Federal Register Liaison Officer. Office of the Secretary. [FR Doc. 2016–31722 Filed 12–29–16; 8:45 am] BILLING CODE 6712–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency for Toxic Substances and Disease Registry [60Day–17–17IY; Docket No. ATSDR–2016– 0122] Proposed Data Collection Submitted for Public Comment and Recommendations Agency for Toxic Substances and Disease Registry (ATSDR), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Agency for Toxic Substances and Disease Registry (ATSDR), as part of its continuing efforts to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995. This notice invites comment on ‘‘Biomonitoring of Great Lakes Populations Program III.’’ The purpose of the proposed study is to evaluate body burden levels of priority contaminants in Great Lakes residents, SUMMARY: E:\FR\FM\30DEN1.SGM 30DEN1 srobinson on DSK5SPTVN1PROD with NOTICES Federal Register / Vol. 81, No. 251 / Friday, December 30, 2016 / Notices particularly those who are at high exposure risk, in the Milwaukee Bay Estuary Area of Concern (AOC) area that was not previously addressed in ATSDR’s previous biomonitoring programs around the Great Lakes. DATES: Written comments must be received on or before February 28, 2017. ADDRESSES: You may submit comments, identified by Docket No. ATSDR–2016– 0122 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. All relevant comments received will be posted without change to Regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to Regulations.gov. Please note: All public comment should be submitted 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 the 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 OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have VerDate Sep<11>2014 19:18 Dec 29, 2016 Jkt 241001 practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology; and (e) estimates of capital or start-up costs and costs of operation, maintenance, and purchase of services to provide information. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose or provide information to or for a Federal agency. This includes the time needed to review instructions; to develop, acquire, install and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and to be able to respond to a collection of information, to search data sources, to complete and review the collection of information; and to transmit or otherwise disclose the information. Proposed Project Biomonitoring of Great Lakes Populations Program III—New—Agency for Toxic Substances and Disease Registry (ATSDR). Background and Brief Description The Agency for Toxic Substances and Disease Registry (ATSDR) is requesting a three-year Paperwork Reduction Act (PRA) clearance for a new information collection request (ICR) titled ‘‘Biomonitoring of Great Lakes Populations Program III.’’ ATSDR awarded funds to the Wisconsin Department of Health Services (WIDHS) to conduct this information collection under cooperative agreement #NU61TS000269–01–00. The purpose of the current program is to evaluate body burden levels of legacy and emerging contaminants in susceptible Great Lakes populations in the Milwaukee Estuary Area of Concern (AOC) in Wisconsin, an area that has not been previously covered by other Great Lakes initiatives. The Great Lakes Basin has suffered decades of pollution and ecosystem damage. Many chemicals persist in Great Lakes waters and sediments, as well as in wildlife. These chemicals can build up in the aquatic food chain, and eating contaminated fish is a known route of human exposure. In 2009, the Great Lakes Restoration Initiative (GLRI) was enacted by Public PO 00000 Frm 00023 Fmt 4703 Sfmt 4703 96455 Law 111–88 to make restoration and protection of the Great Lakes a national priority. The GLRI is led by the U.S. Environmental Protection Agency (US EPA). Under a 2015 interagency agreement with the US EPA, ATSDR initiated the Biomonitoring of Great Lakes Populations Program III program. This project will provide additional public health information to supplement the previous cooperative agreement programs CDC–RFA–TS10– 1001 ‘‘Biomonitoring of Great Lakes Populations’’ (hereafter referred to as ‘‘Program I,’’ OMB Control Number 0923–0044) and CDC–RFA–TS13–1302 ‘‘Biomonitoring of Great Lakes Populations-II’’ (hereafter referred to as ‘‘Program II,’’ OMB Control Number 0923–0052) initiated in FY2010 and FY2013, respectively. WIDHS received funding for the current program. WIDHS will recruit and enroll two subpopulations of adults in the Milwaukee Bay Estuary Area of Concern (AOC) who are known to eat fish from the Milwaukee River Basin and Lake Michigan. This study will not include pregnant women. The target populations are: (1) Licensed anglers living in proximity to the Milwaukee Estuary AOC and (2) Burmese refugees who are known to eat a substantial amount of fish from this area. WIDHS study staff will work closely with local refugee and citizen support organizations on participant recruitment. The aims of the information collection in this surveillance project are: 1. Assess levels of contaminants (metals, polychlorinated biphenyls, chlorinated pesticides, perfluorinated compounds, and polyaromatic hydrocarbons) in blood and urine of residents who consume fish from contaminated areas that had not been studied in previous Programs I and II; 2. Use the project findings to inform public health officials and offer guidance on public health actions to reduce exposure to Great Lakes contaminants. This applied public health program aims to measure contaminants in biological samples (blood, urine and hair) from people who may be at high risk of chemical exposure in the Great Lakes area. These measurements will provide a baseline for current and future restoration activities. The results will be compared to available national estimates, such as those reported by the National Health and Nutrition Examination Survey (NHANES). Respondents will be screened for eligibility and consent will be obtained. Participants who consent will respond to a questionnaire and participate in E:\FR\FM\30DEN1.SGM 30DEN1 96456 Federal Register / Vol. 81, No. 251 / Friday, December 30, 2016 / Notices Respondents will also be interviewed. They will be asked about demographic and lifestyle factors, hobbies, health conditions that may affect fish consumption and fishing habits, and types of jobs which can contribute to chemical exposure. Some dietary questions will be asked with a focus on consumption of Great Lakes fish. clinic visits for body measurements and biological specimen collection (blood, urine, and hair). Their blood will be tested for polychlorinated biphenyls, metals, perfluorinated compounds, persistent pesticides, and lipids. Urine will be tested for polycyclic aromatic hydrocarbons and creatinine. The hair samples (optional) will be saved for a later analysis. Participation in the study is voluntary and there is no cost to respondents other than their time. The estimated annualized burden for the program averaged over the three-year study period is 231 hours among 166 respondents. There is no cost to respondents other than their time spent in the study. 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 Licensed Anglers ........... Eligibility Screening Survey (paper) .................... Eligibility Screening Survey (online) .................... Study Questionnaire (paper) ............................... Study Questionnaire (online) ............................... Clinic Visit Checklist and Body Measurements ... Follow-up Survey ................................................. Eligibility Screening Survey ................................. Contact Information Form .................................... Study Questionnaire ............................................ Clinic Visit Checklist and Body Measurements ... Network Size Questions ...................................... Follow-up Survey ................................................. 156 28 58 87 133 133 42 33 33 33 33 33 1 1 1 1 1 1 1 1 1 1 1 1 5/60 5/60 30/60 30/60 35/60 5/60 5/60 5/60 40/60 35/60 5/60 5/60 13 2 29 44 78 11 4 3 22 19 3 3 .............................................................................. ........................ ........................ ........................ 231 Burmese Refugees ........ 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. 2016–31738 Filed 12–29–16; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–17–0576; Docket No. CDC–2016– 0125] Proposed Data Collection 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 its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction srobinson on DSK5SPTVN1PROD with NOTICES SUMMARY: VerDate Sep<11>2014 19:18 Dec 29, 2016 Jkt 241001 Act of 1995. This notice invites comment on a proposed revision of the CDC information collection project entitled ‘‘Possession, Use, and Transfer of Select Agents and Toxins.’’ DATES: Written comments must be received on or before February 28, 2017. ADDRESSES: You may submit comments, identified by Docket No. CDC–2016– 0125 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. All relevant comments received will be posted without change to Regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to Regulations.gov. Please note: All public comments should be submitted 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 PO 00000 Frm 00024 Fmt 4703 Sfmt 4703 instruments, contact the 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 OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. Comments are invited on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be E:\FR\FM\30DEN1.SGM 30DEN1

Agencies

[Federal Register Volume 81, Number 251 (Friday, December 30, 2016)]
[Notices]
[Pages 96454-96456]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-31738]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Agency for Toxic Substances and Disease Registry

[60Day-17-17IY; Docket No. ATSDR-2016-0122]


Proposed Data Collection Submitted for Public Comment and 
Recommendations

AGENCY: Agency for Toxic Substances and Disease Registry (ATSDR), 
Department of Health and Human Services (HHS).

ACTION: Notice with comment period.

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

SUMMARY: The Agency for Toxic Substances and Disease Registry (ATSDR), 
as part of its continuing efforts to reduce public burden and maximize 
the utility of government information, invites the general public and 
other Federal agencies to take this opportunity to comment on proposed 
and/or continuing information collections, as required by the Paperwork 
Reduction Act of 1995. This notice invites comment on ``Biomonitoring 
of Great Lakes Populations Program III.'' The purpose of the proposed 
study is to evaluate body burden levels of priority contaminants in 
Great Lakes residents,

[[Page 96455]]

particularly those who are at high exposure risk, in the Milwaukee Bay 
Estuary Area of Concern (AOC) area that was not previously addressed in 
ATSDR's previous biomonitoring programs around the Great Lakes.

DATES: Written comments must be received on or before February 28, 
2017.

ADDRESSES: You may submit comments, identified by Docket No. ATSDR-
2016-0122 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. All relevant comments received will be posted 
without change to Regulations.gov, including any personal information 
provided. For access to the docket to read background documents or 
comments received, go to Regulations.gov.
    Please note: All public comment should be submitted 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 the 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 OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    Comments are invited on: (a) Whether the proposed collection of 
information is necessary for the proper performance of the functions of 
the agency, including whether the information shall have practical 
utility; (b) the accuracy of the agency's estimate of the burden of the 
proposed collection of information; (c) ways to enhance the quality, 
utility, and clarity of the information to be collected; (d) ways to 
minimize the burden of the collection of information on respondents, 
including through the use of automated collection techniques or other 
forms of information technology; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services 
to provide information. Burden means the total time, effort, or 
financial resources expended by persons to generate, maintain, retain, 
disclose or provide information to or for a Federal agency. This 
includes the time needed to review instructions; to develop, acquire, 
install and utilize technology and systems for the purpose of 
collecting, validating and verifying information, processing and 
maintaining information, and disclosing and providing information; to 
train personnel and to be able to respond to a collection of 
information, to search data sources, to complete and review the 
collection of information; and to transmit or otherwise disclose the 
information.

Proposed Project

    Biomonitoring of Great Lakes Populations Program III--New--Agency 
for Toxic Substances and Disease Registry (ATSDR).

Background and Brief Description

    The Agency for Toxic Substances and Disease Registry (ATSDR) is 
requesting a three-year Paperwork Reduction Act (PRA) clearance for a 
new information collection request (ICR) titled ``Biomonitoring of 
Great Lakes Populations Program III.'' ATSDR awarded funds to the 
Wisconsin Department of Health Services (WIDHS) to conduct this 
information collection under cooperative agreement #NU61TS000269-01-00. 
The purpose of the current program is to evaluate body burden levels of 
legacy and emerging contaminants in susceptible Great Lakes populations 
in the Milwaukee Estuary Area of Concern (AOC) in Wisconsin, an area 
that has not been previously covered by other Great Lakes initiatives.
    The Great Lakes Basin has suffered decades of pollution and 
ecosystem damage. Many chemicals persist in Great Lakes waters and 
sediments, as well as in wildlife. These chemicals can build up in the 
aquatic food chain, and eating contaminated fish is a known route of 
human exposure.
    In 2009, the Great Lakes Restoration Initiative (GLRI) was enacted 
by Public Law 111-88 to make restoration and protection of the Great 
Lakes a national priority. The GLRI is led by the U.S. Environmental 
Protection Agency (US EPA). Under a 2015 interagency agreement with the 
US EPA, ATSDR initiated the Biomonitoring of Great Lakes Populations 
Program III program. This project will provide additional public health 
information to supplement the previous cooperative agreement programs 
CDC-RFA-TS10-1001 ``Biomonitoring of Great Lakes Populations'' 
(hereafter referred to as ``Program I,'' OMB Control Number 0923-0044) 
and CDC-RFA-TS13-1302 ``Biomonitoring of Great Lakes Populations-II'' 
(hereafter referred to as ``Program II,'' OMB Control Number 0923-0052) 
initiated in FY2010 and FY2013, respectively.
    WIDHS received funding for the current program. WIDHS will recruit 
and enroll two subpopulations of adults in the Milwaukee Bay Estuary 
Area of Concern (AOC) who are known to eat fish from the Milwaukee 
River Basin and Lake Michigan. This study will not include pregnant 
women.
    The target populations are: (1) Licensed anglers living in 
proximity to the Milwaukee Estuary AOC and (2) Burmese refugees who are 
known to eat a substantial amount of fish from this area. WIDHS study 
staff will work closely with local refugee and citizen support 
organizations on participant recruitment.
    The aims of the information collection in this surveillance project 
are:
    1. Assess levels of contaminants (metals, polychlorinated 
biphenyls, chlorinated pesticides, perfluorinated compounds, and 
polyaromatic hydrocarbons) in blood and urine of residents who consume 
fish from contaminated areas that had not been studied in previous 
Programs I and II;
    2. Use the project findings to inform public health officials and 
offer guidance on public health actions to reduce exposure to Great 
Lakes contaminants.
    This applied public health program aims to measure contaminants in 
biological samples (blood, urine and hair) from people who may be at 
high risk of chemical exposure in the Great Lakes area. These 
measurements will provide a baseline for current and future restoration 
activities. The results will be compared to available national 
estimates, such as those reported by the National Health and Nutrition 
Examination Survey (NHANES).
    Respondents will be screened for eligibility and consent will be 
obtained. Participants who consent will respond to a questionnaire and 
participate in

[[Page 96456]]

clinic visits for body measurements and biological specimen collection 
(blood, urine, and hair). Their blood will be tested for 
polychlorinated biphenyls, metals, perfluorinated compounds, persistent 
pesticides, and lipids. Urine will be tested for polycyclic aromatic 
hydrocarbons and creatinine. The hair samples (optional) will be saved 
for a later analysis.
    Respondents will also be interviewed. They will be asked about 
demographic and lifestyle factors, hobbies, health conditions that may 
affect fish consumption and fishing habits, and types of jobs which can 
contribute to chemical exposure. Some dietary questions will be asked 
with a focus on consumption of Great Lakes fish.
    Participation in the study is voluntary and there is no cost to 
respondents other than their time. The estimated annualized burden for 
the program averaged over the three-year study period is 231 hours 
among 166 respondents. There is no cost to respondents other than their 
time spent in the study.

                                                            Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                                                              Average
                                                                                             Number of       Number of      burden per     Total burden
              Type of respondents                               Form name                   respondents    responses per   response  (in    (in hours)
                                                                                                            respondent        hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Licensed Anglers...............................  Eligibility Screening Survey (paper)...             156               1            5/60              13
                                                 Eligibility Screening Survey (online)..              28               1            5/60               2
                                                 Study Questionnaire (paper)............              58               1           30/60              29
                                                 Study Questionnaire (online)...........              87               1           30/60              44
                                                 Clinic Visit Checklist and Body                     133               1           35/60              78
                                                  Measurements.
                                                 Follow-up Survey.......................             133               1            5/60              11
Burmese Refugees...............................  Eligibility Screening Survey...........              42               1            5/60               4
                                                 Contact Information Form...............              33               1            5/60               3
                                                 Study Questionnaire....................              33               1           40/60              22
                                                 Clinic Visit Checklist and Body                      33               1           35/60              19
                                                  Measurements.
                                                 Network Size Questions.................              33               1            5/60               3
                                                 Follow-up Survey.......................              33               1            5/60               3
                                                                                         ---------------------------------------------------------------
    Total......................................  .......................................  ..............  ..............  ..............             231
--------------------------------------------------------------------------------------------------------------------------------------------------------


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. 2016-31738 Filed 12-29-16; 8:45 am]
BILLING CODE 4163-18-P