Proposed Data Collection Submitted for Public Comment and Recommendations, 19368-19370 [2017-08540]
Download as PDF
mstockstill on DSK30JT082PROD with NOTICES
19368
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, zeena.aljibury@ferc.gov.
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 https://
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 https://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
FERCOnlineSupport@ferc.gov, (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
VerDate Sep<11>2014
17:07 Apr 26, 2017
Jkt 241001
https://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 https://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
FERCOnlineSupport@ferc.gov, 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
PO 00000
Frm 00019
Fmt 4703
Sfmt 4703
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:
E:\FR\FM\27APN1.SGM
27APN1
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: 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
VerDate Sep<11>2014
17:07 Apr 26, 2017
Jkt 241001
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
PO 00000
Frm 00020
Fmt 4703
Sfmt 4703
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
E:\FR\FM\27APN1.SGM
27APN1
19370
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
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hrs.)
Total
burden
(in hrs.)
Type of respondents
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,
mstockstill on DSK30JT082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:07 Apr 26, 2017
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:
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
PO 00000
Frm 00021
Fmt 4703
Sfmt 4703
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
E:\FR\FM\27APN1.SGM
27APN1
Agencies
[Federal Register Volume 82, Number 80 (Thursday, April 27, 2017)]
[Notices]
[Pages 19368-19370]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-08540]
=======================================================================
-----------------------------------------------------------------------
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
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 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 Industry-
Tuned 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.
[[Page 19369]]
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: 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
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 public-private 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 on-line 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 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 de-identified form, unless
otherwise
[[Page 19370]]
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
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hrs.)
respondent hrs.)
----------------------------------------------------------------------------------------------------------------
Private Sector Organization Interview Plan.. 45 1 1 45
Senior Leader.
Private Sector Organization Survey Plan..... 100 1 15/60 25
Manager.
---------------------------------------------------------------
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