60d FRN - published

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Federal Register / Vol. 82, No. 80 / Thursday, April 27, 2017 / Notices

Bennington counties, Vermont, and
Franklin and Berkshire counties,
Massachusetts.
g. Filed Pursuant to: Federal Power
Act, 16 U.S.C. 791a–825r.
h. Applicant Contact: John Ragonese,
TransCanada Hydro Northeast Inc., 4
Park Street, Suite 402, Concord, NH
03301–6373, (603) 225–5528.
i. FERC Contact: Zeena Aljibury, (202)
502–6065, [email protected].
j. Deadline for filing comments,
motions to intervene, and protests: May
5, 2017.
The Commission strongly encourages
electronic filing. Please file motions to
intervene, protests, comments, or
recommendations using the
Commission’s eFiling system at http://
www.ferc.gov/docs-filing/efiling.asp.
Commenters can submit brief comments
up to 6,000 characters, without prior
registration, using the eComment system
at http://www.ferc.gov/docs-filing/
ecomment.asp. You must include your
name and contact information at the end
of your comments. For assistance,
please contact FERC Online Support at
[email protected], (866)
208–3676 (toll free), or (202) 502–8659
(TTY). In lieu of electronic filing, please
send a paper copy to: Secretary, Federal
Energy Regulatory Commission, 888
First Street NE., Washington, DC 20426.
The first page of any filing should
include docket number P–2323–216.
k. Description of Request:
TransCanada Hydro Northeast, Inc.
requests approval to amend license
Articles 401, 402, 403, and 406 as well
as the approved Vermont Flow
Monitoring and Reservoir Operations
Plan to adjust the target elevation of
Somerset Reservoir during the common
loon nesting period from 2,128.58 feet
mean sea level (msl) to 2,128.23 feet
msl, as requested by the Vermont
Agency of Natural Resources and the
Vermont Division of Fish and Wildlife
to protect observed loon nests. The
licensee also requests, with agency
support, to change the target elevation
period from May 1 to May 15 to align
with the end of the minimum flow
constraint at the Searsburg development
and avoid conflicting resource
requirements. Finally, the licensee
proposes, with agency support, to adjust
the start of operations data collection for
reporting to the resources agencies from
April 1 to April 15.
l. Locations of the Application: A
copy of the application is available for
inspection and reproduction at the
Commission’s Public Reference Room,
located at 888 First Street NE., Room
2A, Washington, DC 20426, or by calling
(202) 502–8371. This filing may also be
viewed on the Commission’s Web site at

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http://www.ferc.gov using the
‘‘eLibrary’’ link. Enter the docket
number excluding the last three digits
(P–2323) in the docket number field to
access the document. You may also
register online at http://www.ferc.gov/
docs-filing/esubscription.asp to be
notified via email of new filings and
issuances related to this or other
pending projects. For assistance, call 1–
866–208–3676 or email
[email protected], for TTY,
call (202) 502–8659. A copy is also
available for inspection and
reproduction at the address in item (h)
above. Agencies may obtain copies of
the application directly from the
applicant.
m. Individuals desiring to be included
on the Commission’s mailing list should
so indicate by writing to the Secretary
of the Commission.
n. Comments, Protests, or Motions to
Intervene: Anyone may submit
comments, a protest, or a motion to
intervene in accordance with the
requirements of Rules of Practice and
Procedure, 18 CFR 385.210, .211, .214,
respectively. In determining the
appropriate action to take, the
Commission will consider all protests or
other comments filed, but only those
who file a motion to intervene in
accordance with the Commission’s
Rules may become a party to the
proceeding. Any comments, protests, or
motions to intervene must be received
on or before the specified comment date
for the particular application.
o. Filing and Service of Documents:
Any filing must (1) bear in all capital
letters the title ‘‘COMMENTS’’,
‘‘PROTEST’’, or ‘‘MOTION TO
INTERVENE’’ as applicable; (2) set forth
in the heading the name of the applicant
and the project number of the
application to which the filing
responds; (3) furnish the name, address,
and telephone number of the person
commenting, protesting or intervening;
and (4) otherwise comply with the
requirements of 18 CFR 385.2001
through 385.2005. All comments,
motions to intervene, or protests must
set forth their evidentiary basis and
otherwise comply with the requirements
of 18 CFR 4.34(b). All comments,
motions to intervene, or protests should
relate to project works that are the
subject of the license amendment.
Agencies may obtain copies of the
application directly from the applicant.
A copy of any protest or motion to
intervene must be served upon each
representative of the applicant specified
in the particular application. If an
intervener files comments or documents
with the Commission relating to the
merits of an issue that may affect the

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responsibilities of a particular resource
agency, they must also serve a copy of
the document on that resource agency.
A copy of all other filings in reference
to this application must be accompanied
by proof of service on all persons listed
in the service list prepared by the
Commission in this proceeding, in
accordance with 18 CFR 4.34(b) and
385.2010.
Dated: April 20, 2017.
Kimberly D. Bose,
Secretary.
[FR Doc. 2017–08475 Filed 4–26–17; 8:45 am]
BILLING CODE 6717–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–17NW; Docket No. CDC–2017–
0011]

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 a new information
collection project titled ‘‘A Novel
Framework for Structuring IndustryTuned Public-Private Partnerships and
Economic Incentives for U.S. Health
Emergency Preparedness and
Response’’. This data collection will
conduct interviews with industry
leaders and survey private sector
organization managers to systematically
evaluate and explore the partnership
preferences of private sector
organizations, specifically when they
are interacting or considering an
interaction with government agencies.
DATES: Written comments must be
received on or before June 26, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0011 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
SUMMARY:

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mstockstill on DSK30JT082PROD with NOTICES

Federal Register / Vol. 82, No. 80 / Thursday, April 27, 2017 / Notices
• 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 Leroy A.
Richardson, of 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

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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
A Novel Framework for Structuring
Industry-Tuned Public-Private
Partnerships and Economic Incentives
for U.S. Health Emergency Preparedness
and Response—New—Office of Public
Health Preparedness and Response,
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Despite the important role of publicprivate partnerships in supporting the
U.S.’s public health preparedness and
response mission, many partnership
efforts are not successful due to poorly
aligned incentives or lack of awareness
of external market factors. There is little
research or information on private
sector incentive structures and
partnership opportunities and barriers
specific to public health preparedness
and response. This study will evaluate
the effectiveness of public-private
partnership incentives from the
perspective of private sector industries
within the public health preparedness
and response space.
CDC proposes to collect information
from the private industry leaders in the
public health preparedness and
response space to accomplish this goal.
Study activities will include (1)
identifying public-private partnership
incentives and target industries for
public health preparedness and
response; (2) conducting interviews
with industry leaders in person or via
telephone to identify related public
health emergency preparedness
activities and partnership opportunities
and barriers; and (3) surveying private
sector organization managers using online technology (Qualtrics) on key issues
and attractiveness of partnership
opportunities and incentives; and
develop a framework to identify
partnership target organizations,
opportunities, and incentives to

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19369

promote public health emergency
preparedness capabilities.
The information collection request is
composed of two parts: (1) Interviews
and (2) an on-line general survey
distributed. The targeted interviews will
seek respondents in the following eight
sectors: Pharmaceutical/life sciences (n
= 8), health IT/mobile (n = 8), retailers/
distributors (n = 6), academia/research
organization (n = 6), hospital/healthcare
provider (n = 5), health insurance (n =
4), logistics/transportation (n = 4), and
charitable organization/foundation (n =
4). The interview questions and the
information collected will vary
significantly across the different sectors.
The survey portion of the information
collection will be a larger survey that
will be sent to 200 individuals to reach
a total sample population of 100
(assuming a 50% response rate). The
interviews and survey will only be
administered one time to each
individual respondent. CDC plans to
conduct interviews and surveys within
six months after OMB approval.
Members of the research team will
conduct the interviews. Surveys will be
conducted using the secure online
software Qualtrics, and respondents will
receive an email with a unique link that
will direct them to the Qualtrics survey
platform. All data will then be
transferred to CDC’s preferred Secure
File Transfer Protocol (SFTP) client,
where it will be stored and later
accessed securely by members of the
research team. After this transfer, all
copies of the data that reside outside of
the SFTP will be destroyed. Only the
research team will have access to the
interview transcripts and survey
responses that will link responses to
personally identifiable information. Any
printed or hand-written documents
containing PII will be stored securely in
locked file cabinets when not in use,
and will be destroyed once the
information has been scanned or
otherwise transferred into electronic
files (which will also be transferred to
the SFTP client). Access to the SFTP
will require the user to enter a host
address, username, password and port
number, all of which will only be
provided to the research team.
CDC will make the collected data
available only to research team members
for analysis and will maintain the data
for the duration of the study.
Identifiable information may be filed by
the name of respondent on the SFTP,
but it will not be removed from the
SFTP in that format. Any information
removed from the SFTP client to be
shared with outside parties will be
presented in aggregated and deidentified form, unless otherwise

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Federal Register / Vol. 82, No. 80 / Thursday, April 27, 2017 / Notices

compelled by law. CDC will retain and
destroy all records in accordance with
the applicable CDC Records Control
Schedule.

OPHPR is requesting an approval
period of one year to collect this
information. There are no cost burdens
to respondents or record keepers for this

data collection. The total time burden to
respondents is 70 hours. See a summary
of the annualized burden hours in the
below table.

ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hrs.)

Total
burden
(in hrs.)

Form name

Private Sector Organization Senior Leader ..........
Private Sector Organization Manager ..................

Interview Plan ...............
Survey Plan ..................

45
100

1
1

1
15/60

45
25

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

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

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

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

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

70

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. 2017–08540 Filed 4–26–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-17–17ABU; Docket No. CDC–2017–
0037]

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 a proposed data collection
project titled ‘‘Emergency Zika Package:
Zika Reproductive Health Call-Back
Survey ZRHCS), 2017.’’
DATES: Written comments must be
received on or before June 26, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0037 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,
SUMMARY:

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Number of
responses per
respondent

Number of
respondents

Type of respondents

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Jkt 241001

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 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 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

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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
Zika Reproductive Health Call-Back
Survey (ZRHCS), 2017—New—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In May 2015, the World Health
Organization reported the first local
mosquito born transmission of Zika
virus in the Western Hemisphere, with
autochthonous cases identified in
Brazil. In response to the Zika virus
outbreak, and evidence that Zika virus
infection during pregnancy is a cause

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