60 Day FRN

24004

Federal Register / Vol. 89, No. 67 / Friday, April 5, 2024 / Notices

of Multiple Forms of Violence.’’ Agenda
items are subject to change as priorities
dictate.
The Director, Office of Strategic
Business Initiatives, 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, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.

Please note: Submit all comments through
the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to the
address listed above.

[FR Doc. 2024–07300 Filed 4–4–24; 8:45 am]
BILLING CODE 4163–18–P

FOR FURTHER INFORMATION CONTACT:

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24EE; Docket No. CDC–2024–
0023]

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 proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled DFWED
National Hypothesis Generation and
Investigation Module. The proposed
data collection will define a core set of
standardized data elements and forms
used for outbreak investigations and
surveillance activities for a variety of
enteric illnesses.

khammond on DSKJM1Z7X2PROD with NOTICES

SUMMARY:

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16:44 Apr 04, 2024

Jkt 262001

CDC must receive written
comments on or before June 4, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0023 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.
DATES:

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

PO 00000

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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
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses; and
5. Assess information collection costs.
Proposed Project
DFWED National Hypothesis
Generation and Investigation Module—
New—National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Division of Foodborne,
Waterborne, and Environmental
Diseases (DFWED) at the Centers for
Disease Control and Prevention (CDC)
aims to protect public health through
the prevention and control of disease,
disability, and death caused by
foodborne, enteric, waterborne, and
environmentally transmitted infections.
To overcome challenges presented by
the changing landscape of enteric
diseases, the need for comprehensive
hypothesis generating questionnaires
focused on a range of settings, activities,
and potential modes of transmission are
essential to guide prevention and
control activities. The submitted forms
standardize hypothesis generating
instruments used during enteric disease
outbreak investigations and
surveillance. This includes foodborne,
waterborne, and zoonotic disease
surveillance and outbreak
investigations. In addition, enhanced
surveillance for antibiotic resistant
isolates is also included in this package.
CDC requests OMB approval for an
estimated 5,852 annual burden hours.
There is no cost to respondents other
than their time to participate.

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24005

Federal Register / Vol. 89, No. 67 / Friday, April 5, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Cluster and outbreak case patients ..............

National Hypothesis Generating Questionnaire.
Foodborne Focus Questionnaire.
Animal Contact Focus Questionnaire.
Shigella Hypothesis Generating Questionnaire.
NARMS SIRI Questionnaire
Module 1.

Cluster and outbreak case patients ..............
Cluster and outbreak case patients ..............
Shigellosis case patients ..............................
Nontyphoidal Salmonella, STEC, Vibrio, or
Campylobacter case patients whose bacterial isolates have concerning antimicrobial resistance.
Nontyphoidal Salmonella (except Newport
strain), STEC, or Vibrio case patients
whose bacterial isolates have concerning
antimicrobial resistance.
Multidrug-resistant Salmonella Newport
case patients.
Campylobacter case patients whose bacterial isolates have concerning antimicrobial resistance.
Salmonella Typhi or Paratyphi case patients
whose bacterial isolates have concerning
antimicrobial resistance.
Total .......................................................

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2024–07287 Filed 4–4–24; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[60Day–24–0556; Docket No. CDC–2024–
0025]

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

SUMMARY:

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16:44 Apr 04, 2024

Jkt 262001

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
hours

4,000

1

45/60

3,000

4,000

1

20/60

1,333

450

1

30 min

225

1500

1

45/60

1,125

305

1

15/60

77

NARMS SIRI Questionnaire
Module 2.

130

1

10/60

22

NARMS SIRI Questionnaire
Module 3.
NARMS SIRI Questionnaire
Module 4.

125

1

15/60

32

50

1

25/60

21

NARMS SIRI Questionnaire
Module 5.

50

1

20/60

17

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

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

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

5,852

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

collection project titled Assisted
Reproductive Technology (ART)
Program Reporting System. This study
is designed to collect information on
ART cycles to publish information on
pregnancy success rates as required
under Section 2(a) of the Federal Clinic
Success Rate and Certification Act
(FCSRCA).
CDC must receive written
comments on or before June 4, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0025 by either of the following methods:
b Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
b 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.
DATES:

Centers for Disease Control and
Prevention

khammond on DSKJM1Z7X2PROD with NOTICES

Number of
respondents

Type of respondents

Please note: Submit all comments through
the Federal eRulemaking portal
(www.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

FOR FURTHER INFORMATION CONTACT:

PO 00000

Frm 00045

Fmt 4703

Sfmt 4703

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.
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;

SUPPLEMENTARY INFORMATION:

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05APN1