60-day Federal Register Notice

58091

Federal Register / Vol. 87, No. 184 / Friday, September 23, 2022 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name

Organizations that provide prevention, education, testing, and healthcare services relating to HIV/AIDS, viral hepatitis, STD, and
TB.

NPIN Online Questionnaire ............................

Jeffery M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2022–20600 Filed 9–22–22; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–22–0729; Docket No. CDC–2022–
0114]

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 the opportunity to comment on
a continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Customer
Surveys Generic Clearance for the
National Center for Health Statistics.
The goal of this project is to conduct
voluntary customer surveys to assess
strengths in agency products and
services, and to evaluate how well it
addresses the emerging needs of its data
users.
DATES: CDC must receive written
comments on or before November 22,
2022.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0114 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
SUMMARY:

lotter on DSK11XQN23PROD with NOTICES1

Number of
respondents

Type of respondents

VerDate Sep<11>2014

17:04 Sep 22, 2022

Jkt 256001

Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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 Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;

PO 00000

Frm 00038

Fmt 4703

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1,605

Number of
responses per
respondent
1

Average
burden per
response
(in hours)
6/60

3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Customer Surveys Generic Clearance
for the National Center for Health
Statistics (OMB Control No.0920–0729,
Exp. 08/31/2023)—Extension—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the U.S. Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on ‘‘the extent and nature of
illness and disability of the population
of the United States.’’ This is an
Extension request for a Generic approval
from OMB to conduct customer surveys
over the next three years at an overall
burden rate of 2,250 hours annually.
As part of a comprehensive program,
the National Center for Health Statistics
(NCHS) plans to continue to assess its
customers’ satisfaction with the content,
quality and relevance of the information
it produces. NCHS will conduct
voluntary customer surveys to assess
strengths in agency products and
services and to evaluate how well it
addresses the emerging needs of its data
users. Results of these surveys will be
used in future planning initiatives.
The data will be collected using a
combination of methodologies
appropriate to each survey. These may
include: evaluation forms, mail surveys,
focus groups, automated and electronic
technology (e.g., email, Web-based
surveys), and telephone surveys.
Systematic surveys of several groups
will be folded into the program. Among

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58092

Federal Register / Vol. 87, No. 184 / Friday, September 23, 2022 / Notices

these are federal customers and policy
makers, state and local officials who
rely on NCHS data, the broader
educational, research, and public health
community, and other data users.
Respondents may include data users
who register for and/or attend NCHS
sponsored conferences; persons who
access the NCHS website and the
detailed data available through it;
consultants; and others. Respondent
data items may include (in broad

categories) information regarding
respondent’s gender, age, occupation,
affiliation, location, etc., to be used to
characterize responses only. Other
questions will attempt to obtain
information that will characterize the
respondents’ familiarity with and use of
NCHS data, their assessment of data
content and usefulness, general
satisfaction with available services and
products, and suggestions for

improvement of surveys, services and
products.
In order to capture anticipated
feedback opportunities, this extension
request allows for both respondents and
time per response for a total estimated
annual burden total of 2,250 hours.
There is no cost to respondents other
than their time to participate in the
survey. The resulting information will
be for NCHS internal use.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Questionnaire for conference registrants/attendees.
Focus groups ....................................
Web-based Surveys ..........................
Other Customer Surveys ..................
Total ...........................................

Public/private researchers,
ants, and others.
Public/private researchers,
ants, and others.
Public/private researchers,
ants, and others.
Public/private researchers,
ants, and others.

1

15/60

250

Consult-

500

1

1

500

Consult-

4,000

1

15/60

1,000

Consult-

2,000

1

15/60

500

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

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

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

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

2,250

BILLING CODE 4163–18–P

products for HIV prevention among
potential users and providers.
DATES: CDC must receive written
comments on or before November 22,
2022.
You may submit comments,
identified by Docket No. CDC–2022–
0113 by either of the following methods:
• Federal eRulemaking Portal:
www.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 H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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 Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7118; Email: omb@
cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
ADDRESSES:

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–22IX; Docket No. CDC–2022–
0113]

Proposed Data Collections 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, invites the general public and
other federal agencies to take this
opportunity to comment on proposed
information collections, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Study of PrEPline reported PrEPadherent patients with HIV acquisition.
The purpose of this project is to
understand preferences for long-acting
pre-exposure prophylaxis (LA-PrEP)

SUMMARY:

lotter on DSK11XQN23PROD with NOTICES1

Total burden
(in hrs.)

1,000

[FR Doc. 2022–20603 Filed 9–22–22; 8:45 am]

17:04 Sep 22, 2022

Avg. burden
per response
(in hrs.)

Consult-

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.

VerDate Sep<11>2014

Number of
responses per
respondent

Number of
respondents

Form name

Jkt 256001

PO 00000

Frm 00039

Fmt 4703

Sfmt 4703

(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.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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

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23SEN1