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Federal Register / Vol. 86, No. 28 / Friday, February 12, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Number of
responses per
respondent

Avg. burden
per
response
(in hrs.)

Total
burden
(in hr.)

Type of respondents

Form name

Adult/Adolescent Facility Users ........
Parents/Guardians of Youth/Child
Facility Users.
Youth/Child Facility Users .................

Eligibility Screening Script ................
Adult and Adolescent Questionnaire
Exposure Measurement Form .........
Eligibility Screening Script ................
Youth and Child Questionnaire ........
Exposure Measurement Form .........

110
100
100
110
100
100

1
1
1
1
1
1

5/60
30/60
20/60
5/60
30/60
20/60

9
50
33
9
50
33

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

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

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

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

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

184

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–02949 Filed 2–11–21; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Board of Scientific Counselors,
National Center for Injury Prevention
and Control; Correction
Notice is hereby given of a change in
the meeting of the Board of Scientific
Counselors, National Center for Injury
Prevention and Control; February 16,
2021, 10:00 a.m. to 4:15 p.m., EST
which was published in the Federal
Register on January 8, 2021, Volume 86,
Number 5, page 1502.
The dates and addresses should read
as follows:
DATES: The meeting will be held on
February 16, 2021, from 10:00 a.m.–4:30
p.m., EST.
ADDRESSES: Zoom Virtual Meeting. If
you would like to attend the virtual
meeting, please pre-register by accessing
the link at https://
dceproductions.zoom.us/webinar/
register/WN_AQ70-aWpTqKvPX9Ftap_
UA. Instructions to access the Zoom
virtual meeting will be provided in the
link following your registration.
Meeting Information: There will be a
public comment period at the end of the
meeting; from 3:45 p.m.–4:15 p.m. The
public is encouraged to register to
provide public comment using the
registration form available at the link
provided: https://
www.surveymonkey.com/r/cbyh878.
Individuals registered to provide
public comment will be called upon
first to speak based on the order of
registration, followed by others from the
public. All public comments will be
limited to two (2) minutes per speaker.

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Written comments may also be
submitted for the meeting record and
must be received on or before February
23, 2021; [email protected].
FOR FURTHER INFORMATION CONTACT:
Gwendolyn H. Cattledge, Ph.D.,
M.S.E.H., Deputy Associate Director for
Science, NCIPC, CDC, 4770 Buford
Highway NE, Mailstop S–106–9,
Atlanta, Georgia 30341, Telephone:
(770) 488–1430, Email: ncipcbsc@
cdc.gov.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2021–02849 Filed 2–11–21; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–21–1071]

Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Generic
Clearance for the Collection of
Qualitative Feedback on Agency Service
Delivery to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted

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for Public Comment and
Recommendations’’ notice on October
21, 2020 to obtain comments from the
public and affected agencies. CDC did
not receive comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the

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9343

Federal Register / Vol. 86, No. 28 / Friday, February 12, 2021 / Notices
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Generic Clearance for the Collection
of Qualitative Feedback on Agency
Service Delivery (OMB Control No.
0920–1071, Exp. 2/28/2021)—
Extension—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
CDC/NCEZID is seeking a three-year
extension of OMB control No. 0920–
1071 to continue collecting routine
customer feedback on agency service
delivery. Executive Order 12862 directs
Federal agencies to provide service to
the public that matches or exceeds the
best service available in the private
sector. In order to work continuously to

ensure that our programs are effective
and meet our customers’ needs, the
National Center for Emerging and
Zoonotic Infectious Diseases, Centers for
Disease Control and Prevention (CDC)
(hereafter the ‘‘Agency’’) seeks to obtain
OMB approval of a generic clearance to
collect qualitative feedback on our
service delivery. By qualitative feedback
we mean information that provides
useful insights on perceptions and
opinions, but are not statistical surveys
that yield quantitative results that can
be generalized to the population of
study.
This collection of information is
necessary to enable the Agency to garner
customer and stakeholder feedback in
an efficient, timely manner, in
accordance with our commitment to
improving service delivery. The
information collected from our
customers and stakeholders will help
ensure that users have an effective,
efficient, and satisfying experience with
the Agency’s programs. This feedback

will provide insights into customer or
stakeholder perceptions, experiences
and expectations, provide an early
warning of issues with service, or focus
attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
Since getting approval in February
2018, NCEZID has utilized 0920–1071
ten separate times. The total number of
responses was 15,585. The total number
of burden hours was 2,525. Authorizing
legislation for this collection comes
from Section 301 of the Public Health
Service Act (42 U.S.C. 241). The
estimated annual burden hours
requested for this Extension are 3,850.
There is no cost to respondents other
than the time to participate.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondents

Form name

General public .................................................

Online surveys ...............................................
Focus groups .................................................
In-person surveys ...........................................
Usability testing ..............................................
Customer comment cards ..............................

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–02948 Filed 2–11–21; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–21–21CT; Docket No. CDC–2021–
0006]

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

SUMMARY:

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government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
request for emergency clearance of the
information collection titled
Requirement for Negative Pre-Departure
Covid–19 Test Result or Documentation
of Recovery from Covid–19 for all
Airline or other Aircraft Passengers
arriving into the United States from any
foreign country. This collection
accompanies a CDC Order of the same
name and is designed to prohibit the
introduction into the United States of
any airline passenger departing from the
any foreign country unless the
passenger:
(1) Has a negative pre-departure test
result for COVID–19 (Qualifying Test),
or (2) has written or electronic
documentation of recovery from
COVID–19 in the form of a positive viral
test result and a letter from a licensed
health care provider or public health

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1500
800
1000
1500
1000

Number of
responses per
respondent
1
1
1
1
1

Average
burden per
response
(in hours)
30/60
2
30/60
30/60
15/60

official stating that the passenger has
been cleared for travel.
DATES: CDC must receive written
comments on or before April 13, 2021.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2021–
0006 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and

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