Proposed Data Collection Submitted for Public Comment and Recommendations, 84152-84154 [2024-24305]
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84152
Federal Register / Vol. 89, No. 203 / Monday, October 21, 2024 / Notices
Practice held by the DOP TA Center, a
subset of attendees will be invited to
participate in Focus Groups. Ultimately,
the evaluation data will inform
subsequent rounds of TA and allow TA
providers to make necessary
adjustments to the overall TA strategy
for continuous quality improvement.
This will ensure recipients have the
support necessary to implement
strategies that will improve opioid
surveillance and prevention policies
and practices within their communities.
CDC requests OMB approval for an
estimated 388 annual burden hours for
this collection. There are no costs to
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hours)
Form name
OD2A (OD2A in States and OD2A: LOCAL)
Recipients.
TA Feedback Form Individual ........................
618
2
5/60
TA Feedback Form Universal ........................
Annual Technical Assistance Survey .............
Implementation Feedback Survey .................
Email invitation for Annual Survey .................
Focus Groups Email invitation .......................
Focus Group Session Script ..........................
617
162
18
900
600
100
2
1
1
1
1
1
5/60
10/60
15/60
2/60
2/60
1
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2024–24302 Filed 10–18–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–25AF; Docket No. CDC–2024–
0079]
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 2024 Marburg
Traveler Monitoring Assessment. This
information collection is intended to
determine the number of travelers
coming to the United States from
Rwanda, where a Marburg outbreak is
occurring, that are enrolled by
jurisdictions into monitoring, if
recommended, and the proportion of
travelers that completed monitoring.
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Number of
respondents
Type of respondents
VerDate Sep<11>2014
16:27 Oct 18, 2024
Jkt 265001
CDC must receive written
comments on or before December 20,
2024.
DATES:
You may submit comments,
identified by Docket No. CDC–2024–
0079 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: 404–639–7570; 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
ADDRESSES:
PO 00000
Frm 00044
Fmt 4703
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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;
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
2024 Marburg Traveler Monitoring
Assessment—New—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), National Center for
E:\FR\FM\21OCN1.SGM
21OCN1
84153
Federal Register / Vol. 89, No. 203 / Monday, October 21, 2024 / Notices
Emerging and Zoonotic Infectious
Diseases (NCEZID), Division of Global
Migration Health (DGMH) requests an
Emergency approval for a New
information collection. Section 361 of
the Public Health Service (PHS) Act (42
U.S.C. 264) authorizes the Secretary of
Health and Human Services to make
and enforce regulations necessary to
prevent the introduction, transmission
or spread of communicable diseases
from foreign countries into the United
States. Under its delegated authority,
DGMH works to fulfill this
responsibility through a variety of
activities, including the operation of
Quarantine Stations at ports of entry
and administration of foreign quarantine
regulations; 42 Code of Federal
Regulation part 71, specifically 42 CFR
71.20 Public health prevention
measures to detect communicable
disease. This information collection
concerns CDC’s statutory and regulatory
authority related to conducting public
health screening of travelers upon
arrival to the United States and
assessing individual travelers for public
health risk following a report of illness
from a conveyance.
The purpose of this information
collection is to inform CDC and
interagency decision makers on state/
local health department activities
related to travelers coming from areas
affected by an Marburg outbreak
originating in Rwanda. This information
will be used to: (1) gather feedback from
state and local health department
partners on CDC’s interim guidance and
post-arrival management of travelers; (2)
assess the quality of contact information
provided to states by determining the
proportion of travelers that state and
local health departments were able to
contact for recommended assessment
and monitoring; and (3) inform the
development of future guidance and
recommendations for post-arrival
traveler management during Marburg
outbreaks abroad.
CDC collects international travelers’
contact information under authorities in
the Interim Final Rule: Control of
Communicable Diseases: Foreign
Quarantine and CDC’s Order
Requirement for Airlines and Operators
to Collect and Transmit Designated
Information for Passengers and Crew
Arriving Into the United States;
Requirement for Passengers to Provide
Designated Information. Traveler
contact information is sent to CDC
though an existing data-sharing
infrastructure in place between the
United States Department of Homeland
Security (DHS) and HHS/CDC and
approved for in OMB Control Number
0920–1354. Contact information for
travelers who have been to an area
affected by the outbreak during the 21
days prior to arrival will be confirmed
at the port of entry. CDC will share
contact information for these travelers
with state and local health departments
so that they can do possible public
health follow up, including public
health assessment of exposure risk and
monitoring for Marburg symptoms, and
education to travelers. These public
health interventions will help state and
local health departments determine the
appropriate level of follow needed
based on the traveler’s level of risk and
rapidly identify any travelers with
symptoms that could which travelers
may need to be prioritized for more
targeted public health measures, such as
quarantine, due to a higher risk of
exposure to Marburg.
CDC is currently sharing contact
information and public health
assessment of exposure risk to Marburg
for travelers with state and local health
departments through existing datasharing infrastructure. State and local
health departments utilize the contact
information provided by CDC to
prioritize and identify the level of
follow up needed based on the level of
risk of exposure to Marburg and
determine additional if additional
targeted public health measures are
necessary. State/local health department
partners are contacting travelers in order
to determine if they are symptomatic
and require additional screening for
possible Marburg infection. The purpose
of this evaluation will be to gather
feedback from state and local health
departments regarding traveler
monitoring activities and determine the
usability of contact information and
public health risk assessment
information shared by CDC. A one-time
survey at the end of the response will
collect information related to resources
needed by health department for this
response.
CDC requests OMB approval for an
estimated 630 annual burden hours.
There is no cost to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
State/Local Health Department.
State/Local Health Department.
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Total ...............................
VerDate Sep<11>2014
16:27 Oct 18, 2024
Number of
respondents
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total
burden
(in hours)
CDC—Marburg Virus Disease Healthcare Worker Monitoring 2024.
MVD Final Survey_10.08.2024 ............................
70
104
5/60
607
70
1
20/60
23
..............................................................................
......................
..........................
....................
630
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E:\FR\FM\21OCN1.SGM
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84154
Federal Register / Vol. 89, No. 203 / Monday, October 21, 2024 / Notices
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. 2024–24305 Filed 10–18–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10171]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
December 20, 2024.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
16:27 Oct 18, 2024
Jkt 265001
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number: lll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, please access the CMS PRA
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10171 Part D Coordination of
Benefits Data
Under the 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.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collections
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Part D
Coordination of Benefits Data; Use:
Sections 1860D–23 and 1860D–24 of the
Act require the Secretary to establish
requirements for prescription drug plans
to promote effective coordination
between Part D plans and SPAPs and
other payers. These Part D Coordination
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Frm 00046
Fmt 4703
Sfmt 4703
of Benefits (COB) requirements have
been codified into the Code of Federal
Regulations at 42 CFR 423.464. In
particular, CMS’ requirements relate to
the following elements: (1) enrollment
file sharing; (2) claims processing and
payment; (3) claims reconciliation
reports; (4) application of the
protections against high out-of-pocket
expenditures by tracking TrOOP
expenditures; and (5) other processes
that the Secretary determines.
This information collection request
assists CMS, pharmacists, Part D plans,
and other payers coordinate
prescription drug benefits at the pointof-sale and track beneficiary True outof-pocket (TrOOP) expenditures using
the Part D Transaction Facilitator
(PDTF). Form Number: CMS–10171
(OMB control number: 0938–0978);
Frequency: Yearly; Affected Public:
State, Local, or Tribal Government;
Number of Respondents: 67,043; Total
Annual Responses: 935,730,342; Total
Annual Hours: 1,011,740. (For policy
questions regarding this collection
contact Chad Buskirk at 410–786–1630
or chad.buskirk@cms.hhs.gov.)
William N. Parham, III,
Director, Division of Information Collections
and Regulatory Impacts, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2024–24266 Filed 10–18–24; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10114 and CMS–
10147]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
SUMMARY:
E:\FR\FM\21OCN1.SGM
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]]>Agencies
[Federal Register Volume 89, Number 203 (Monday, October 21, 2024)]
[Notices]
[Pages 84152-84154]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-24305]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-25-25AF; Docket No. CDC-2024-0079]
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 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 2024 Marburg Traveler Monitoring Assessment. This information
collection is intended to determine the number of travelers coming to
the United States from Rwanda, where a Marburg outbreak is occurring,
that are enrolled by jurisdictions into monitoring, if recommended, and
the proportion of travelers that completed monitoring.
DATES: CDC must receive written comments on or before December 20,
2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0079 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: 404-639-7570;
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 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;
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
2024 Marburg Traveler Monitoring Assessment--New--National Center
for Emerging and Zoonotic Infectious Diseases (NCEZID), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC), National
Center for
[[Page 84153]]
Emerging and Zoonotic Infectious Diseases (NCEZID), Division of Global
Migration Health (DGMH) requests an Emergency approval for a New
information collection. Section 361 of the Public Health Service (PHS)
Act (42 U.S.C. 264) authorizes the Secretary of Health and Human
Services to make and enforce regulations necessary to prevent the
introduction, transmission or spread of communicable diseases from
foreign countries into the United States. Under its delegated
authority, DGMH works to fulfill this responsibility through a variety
of activities, including the operation of Quarantine Stations at ports
of entry and administration of foreign quarantine regulations; 42 Code
of Federal Regulation part 71, specifically 42 CFR 71.20 Public health
prevention measures to detect communicable disease. This information
collection concerns CDC's statutory and regulatory authority related to
conducting public health screening of travelers upon arrival to the
United States and assessing individual travelers for public health risk
following a report of illness from a conveyance.
The purpose of this information collection is to inform CDC and
interagency decision makers on state/local health department activities
related to travelers coming from areas affected by an Marburg outbreak
originating in Rwanda. This information will be used to: (1) gather
feedback from state and local health department partners on CDC's
interim guidance and post-arrival management of travelers; (2) assess
the quality of contact information provided to states by determining
the proportion of travelers that state and local health departments
were able to contact for recommended assessment and monitoring; and (3)
inform the development of future guidance and recommendations for post-
arrival traveler management during Marburg outbreaks abroad.
CDC collects international travelers' contact information under
authorities in the Interim Final Rule: Control of Communicable
Diseases: Foreign Quarantine and CDC's Order Requirement for Airlines
and Operators to Collect and Transmit Designated Information for
Passengers and Crew Arriving Into the United States; Requirement for
Passengers to Provide Designated Information. Traveler contact
information is sent to CDC though an existing data-sharing
infrastructure in place between the United States Department of
Homeland Security (DHS) and HHS/CDC and approved for in OMB Control
Number 0920-1354. Contact information for travelers who have been to an
area affected by the outbreak during the 21 days prior to arrival will
be confirmed at the port of entry. CDC will share contact information
for these travelers with state and local health departments so that
they can do possible public health follow up, including public health
assessment of exposure risk and monitoring for Marburg symptoms, and
education to travelers. These public health interventions will help
state and local health departments determine the appropriate level of
follow needed based on the traveler's level of risk and rapidly
identify any travelers with symptoms that could which travelers may
need to be prioritized for more targeted public health measures, such
as quarantine, due to a higher risk of exposure to Marburg.
CDC is currently sharing contact information and public health
assessment of exposure risk to Marburg for travelers with state and
local health departments through existing data-sharing infrastructure.
State and local health departments utilize the contact information
provided by CDC to prioritize and identify the level of follow up
needed based on the level of risk of exposure to Marburg and determine
additional if additional targeted public health measures are necessary.
State/local health department partners are contacting travelers in
order to determine if they are symptomatic and require additional
screening for possible Marburg infection. The purpose of this
evaluation will be to gather feedback from state and local health
departments regarding traveler monitoring activities and determine the
usability of contact information and public health risk assessment
information shared by CDC. A one-time survey at the end of the response
will collect information related to resources needed by health
department for this response.
CDC requests OMB approval for an estimated 630 annual burden hours.
There is no cost to respondents other than their time to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total
Type of respondents Form name respondents responses per response burden (in
respondent (in hours) hours)
----------------------------------------------------------------------------------------------------------------
State/Local Health Department.... CDC--Marburg Virus 70 104 5/60 607
Disease Healthcare
Worker Monitoring
2024.
State/Local Health Department.... MVD Final 70 1 20/60 23
Survey_10.08.2024.
--------------------------------------------------------
Total........................ .................... ............ ............... ........... 630
----------------------------------------------------------------------------------------------------------------
[[Page 84154]]
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. 2024-24305 Filed 10-18-24; 8:45 am]
BILLING CODE 4163-18-P
