60 Day FRN

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Federal Register / Vol. 80, No. 167 / Friday, August 28, 2015 / Notices
Comment: The application form
should be used by all federal agencies.
Response: The current draft
application for wireless antenna
installations is being processed as a
Common Form for use by all federal
agencies. Once the Federal Register
posting process is complete, the
application will be submitted to OMB
for approval. An application for right-ofway and easements, the SF299
‘‘Application for Transportations and
Utility Systems on Federal Land,’’ is
already in existence, and its use is
required for all federal agencies. The
SF–299 was developed by the
Departments of Agriculture, Interior,
and Transportation.
Comment: Moratoria on accepting
applications are prohibited.
Response: This comment speaks not
to the application, but rather to shared
policy and procedures to be developed
by the executive landholding agencies
acting in common in support of the
application process. This comment will
be taken into consideration; however,
no change will be made to the
application in response to this
comment.
Comment: Timely responses to
applications are mandatory.
Response: It is agreed that timely
responses are important; however, the
comment speaks not to the application,
but rather to shared policy and
procedures to be developed by the
executive landholding agencies acting
in common in support of the application
process. No change will be made to the
application in response to this
comment.
Comment: Applications should be
‘‘deemed approved’’ upon passage of
time.
Response: While timely approval is a
shared goal, federal agencies must
perform the due diligence required to
confirm that implementation of a
proposal is in the best interests of the
Government and the taxpayer.
Comment: Applications should be
presumed consistent with each agency’s
mission and property use.
Response: Given the different
missions and property uses existent
among the executive landholding
agencies, it is not clear how making
such a presumption is in the best
interest of the Government and the
taxpayer.
Comment: The application form
should not implicate a Joint Spectrum
Center review for commercial providers
of unlicensed wireless services.
Response: The decision to use
unlicensed wireless services is an
internal policy decision to be developed
in concert among the executive

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landholding agencies in support of the
application process. No change will be
made to the application in response to
this comment.
Comment: Applicants may opt in to
the rates, terms, and conditions of other
providers located at the federal
property.
Response: This comment speaks not
to the application, but rather to shared
policy and procedures to be developed
by the executive landholding agencies
acting in common in support of the
application process. No change will be
made to the application in response to
this comment.
Comment: The ‘‘Notice of Competitive
Procedures’’ should be posted to
FedBizOps.gov upon receipt of an
application.
Response: This comment speaks not
to the application, but rather to shared
policy and procedures to be developed
by the executive landholding agencies
acting in common in support of the
application process. No change will be
made to the application in response to
this comment.
Comment: Application forms should
be utilized to initiate amendments to
existing installations and the applicable
lease, easement, or right-of-way.
Response: This comment speaks not
to the application, but rather to shared
policy and procedures to be developed
by the executive landholding agencies
acting in common in support of the
application process. No change will be
made to the application in response to
this comment.
Comment: Executive agencies may
utilize easements or leases with 25-year
terms for wireless siting requests.
Response: This comment speaks not
to the application, but rather to shared
policy and procedures to be developed
by the executive landholding agencies
acting in common in support of the
application process. No change will be
made to the application in response to
this comment.
C. Annual Reporting Burden
Respondents: 20.
Responses per Respondent: 1.
Total Response Hours: 20.
Hours per Response: 1.
Total Burden Hours: 20.
D. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary and whether it
will have practical utility; whether our
estimate of the public burden of this
collection of information is accurate and
based on valid assumptions and
methodology; ways to enhance the
quality, utility and clarity of the

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52287

information to be collected; and ways in
which we can minimize the burden of
the collection of information on those
who are to respond through the use of
appropriate technological collection
techniques or other forms of information
technology.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Second Floor,
Washington, DC 20405, telephone 202–
501–4755. Please cite OMB Control No.
3090–00XX, Wireless
Telecommunications Company
Application, in all correspondence.
Dated: August 21, 2015.
David A. Shive,
Chief Information Officer.
[FR Doc. 2015–21249 Filed 8–27–15; 8:45 am]
BILLING CODE 6820–14–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–15–0960: Docket No. CDC–2015–
0073]

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 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 Epidemiologic Study of
Health Effects Associated With Low
Pressure Events in Drinking Water
Distribution Systems.
DATES: Written comments must be
received on or before October 27, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0073 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
SUMMARY:

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Lhorne on DSK5TPTVN1PROD with NOTICES

52288

Federal Register / Vol. 80, No. 167 / Friday, August 28, 2015 / Notices

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: [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 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

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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
Epidemiologic Study of Health Effects
Associated With Low Pressure Events in
Drinking Water Distribution Systems
(OMB Control Number 0920–0960,
Expiration 3/31/2016)—Extension—
National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In the United States (U.S.), drinking
water distribution systems are designed
to deliver safe, pressurized drinking
water to our homes, hospitals, schools
and businesses. However, the water
distribution infrastructure is 50–100
years old in much of the U.S. and an
estimated 240,000 water main breaks
occur each year. Failures in the
distribution system such as water main
breaks, cross-connections, back-flow,
and pressure fluctuations can result in
potential intrusion of microbes and
other contaminants that can cause
health effects, including acute
gastrointestinal and respiratory illness.
Approximately 200 million cases of
acute gastrointestinal illness occur in
the U.S. each year, but we lack reliable
data to assess how many of these cases
are associated with drinking water.
Further, data are even more limited on
the human health risks associated with
exposure to drinking water during and
after the occurrence of low pressure
events (such as water main breaks) in
drinking water distribution systems. A
study conducted in Norway from 2003–
2004 found that people exposed to low
pressure events in the water distribution
system had a higher risk for
gastrointestinal illness. A similar study
is needed in the United States.
The purpose of this data collection is
to conduct an epidemiologic study in

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the U.S. to assess whether individuals
exposed to low pressure events in the
water distribution system are at an
increased risk for acute gastrointestinal
or respiratory illness. This study would
be, to our knowledge, the first U.S.
study to systematically examine the
association between low pressure events
and acute gastrointestinal and
respiratory illnesses. Study findings will
inform the Environmental Protection
Agency (EPA), CDC, and other drinking
water stakeholders of the potential
health risks associated with low
pressure events in drinking water
distribution systems and whether
additional measures (e.g., new
standards, additional research, or policy
development) are needed to reduce the
risk for health effects associated with
low pressure events in the drinking
water distribution system.
We will conduct a cohort study
among households that receive water
from six water utilities across the U.S.
The water systems will be
geographically diverse and will include
both chlorinated and chloraminated
systems. These water utilities will
provide information about low pressure
events that occur during the study
period using a standardized form
(approximately 11 events per utility).
Utilities will provide address listings of
households in areas exposed to the low
pressure event and comparable
households in an unexposed area to
CDC staff, who will randomly select
participants and send them an
introductory letter and questionnaire.
Consenting household respondents will
be asked about symptoms and duration
of any recent gastrointestinal or
respiratory illness, tap water
consumption, and other exposures
including international travel, daycare
attendance or employment, animal
contacts, and recreational water
exposures. Study participants may
choose between two methods of survey
response: A mail-in paper survey and a
web-based survey.
Participation in this study will be
voluntary. No financial compensation
will be provided to study participants.
The study duration is anticipated to last
30 months. An estimated 6,750
individuals will be contacted and we
anticipate 4,050 utility customers (18
years of age or older) will consent to
participate in this study. The total
estimated annualized hours associated
with this study is expected to be 548.
There are no costs to respondents
other than their time.

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52289

Federal Register / Vol. 80, No. 167 / Friday, August 28, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hrs.)

Total burden
(in hrs.)

Form name

Households ................................
Households ................................
Utility employees ........................
Utility employees ........................
Utility employees ........................

1,215
810
6
6
6

1
1
5
3
2

12/60
12/60
3
130/60
30/60

243
162
90
39
6

Utility employees ........................

Paper-based questionnaire .....................
Web-based questionnaire .......................
Household listing .....................................
Water sample collection (grab samples)
Water sample collection (ultrafiltration
samples).
Low pressure event form ........................

6

5

15/60

8

Total ....................................

.................................................................

........................

........................

........................

548

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. 2015–21346 Filed 8–27–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–0307; Docket No. CDC–2015–
0072]

Proposed Data Collections Submitted
for Public Comment and
Recommendations
The Centers for Disease Control
and Prevention (CDC).
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
Act of 1995. This notice invites
comment on the proposed extension of
the information collection entitled The
Gonococcal Isolate Surveillance Project
(GISP), which is the only source in the
United States of national, regional, and
site-specific gonococcal antibiotic
resistance information that provides
information to support informed and
scientifically-based treatment
recommendations.
To request more information on the
below proposed project or to obtain a
copy of the information collection plan
and instruments, call 404–639–7570 or
send comments to Leroy A. Richardson,
1600 Clifton Road, MS–D74, Atlanta,

SUMMARY:

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Number of
responses per
respondent

Number of
respondents

Type of respondents

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GA 30333 or send an email to omb@
cdc.gov.
DATES: Written comments must be
received on or before October 27, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0072 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.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.

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: [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
FOR FURTHER INFORMATION CONTACT:

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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
The Gonococcal Isolate Surveillance
Project (GISP), (OMB No.0920–0307
exp. 08/31/2016)—Extension—National
Center for HIV/AIDS, Viral Hepatitis,
STD, and TB Prevention (NCHHSTP),

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