Proposed Data Collection Submitted for Public Comment and Recommendations, 66707-66708 [2022-24048]
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66707
Federal Register / Vol. 87, No. 213 / Friday, November 4, 2022 / Notices
health interventions will help state and
local health departments determine the
appropriate level of follow up needed
based on the traveler’s level of risk and
rapidly identify any travelers with
symptoms that may need to be
prioritized for more targeted public
health measures, such as quarantine,
due to a higher risk of exposure to
Ebola. State and local health
departments will 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 Ebola and determine
if additional targeted public health
measures are necessary. 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.
CDC anticipates certain time and cost
burdens to respondents and record
keepers due to the requirements and
requests OMB approval for an estimated
4,550 annual burden hours. There are
no costs to respondents other than their
time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Information collection tool
Traveler ..........
Risk Assessment and Post-Arrival Monitoring Outcome
REDCap Reporting.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–24047 Filed 11–3–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Delegation of Authority Under Section
564A(e) of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 360bbb–3a(e))
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services.
ACTION: Notice.
AGENCY:
CDC has redelegated the
authority under the Federal Food, Drug,
and Cosmetic (FD&C) Act to create and
issue amended emergency use
instructions (EUI) to inform healthcare
providers or individuals to whom an
eligible product, as defined under the
FD&C Act, is to be administered,
concerning the product’s approved,
licensed, or cleared conditions of use
that deviate from approved labeling,
standard clinical practice, and/or
standard medical modality (e.g.,
individual prescription within the
patient-clinician relationship). This
notice announces the redelegation of the
above-mentioned authority, without the
authority to redelegate, from the
Director, CDC, to the Director, National
Center for Immunizations and
Respiratory Diseases (NCIRD).
DATES: This delegation was approved by
the Director, CDC, and is effective
October 28, 2022.
SUMMARY:
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Number of
respondents
Respondent
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18:12 Nov 03, 2022
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350
Only the
Director, CDC, can issue original EUIs.
The Director, NCIRD, may only issue
amendments that are substantially
within the scope of the original EUI and
only for countermeasures within the
scope of the NCIRD Director’s official
responsibilities. This authority shall be
exercised under section 564A(e) of the
FD&C Act (21 U.S.C. 360bbb–3a(e)), and
any related HHS policies. This
delegation became effective on October
28, 2022. The Director, CDC, affirms and
ratifies any actions taken that involve
the exercise of the authority delegated
herein prior to the effective date of this
delegation.
SUPPLEMENTARY INFORMATION:
Sherri A. Berger,
Chief of Staff, Centers for Disease Control
and Prevention.
[FR Doc. 2022–24044 Filed 11–3–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–23–1301; Docket No. CDC–2022–
0126]
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
SUMMARY:
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
52
Average
burden
per response
(in minutes)
15/60
Total burden
hours
4,550
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 Templates for
Extramural Data Management Plans.
The aim of this collection is to provide
contract and cooperative agreement
applicants and awardees with templates
for the creation of data management
plans (DMPs).
DATES: CDC must receive written
comments on or before January 3, 2023.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0126 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.
E:\FR\FM\04NON1.SGM
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66708
Federal Register / Vol. 87, No. 213 / Friday, November 4, 2022 / Notices
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
SUPPLEMENTARY INFORMATION:
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.
DMPs will be submitted to CDC by grant
and cooperative agreement awardees for
assessment to verify that they are
concordant with CDC’s data sharing
policy. CDC contractors collecting
public health data are also required to
create and submit DMPs. This
information collection request was
developed by CDC’s National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP) to create
standardized templates for DMPs so that
they will be easier to create, easier to
review, better able to ensure compliance
with CDC’s requirements, and able to
increase the likelihood of first draft
approval by project officers. The project
was initially approved from June 2019
through June 2023. CDC will request an
Extension for approval for another three
years. Minor updates will be made to
the templates for this extension period
to better serve awardee and CDC needs.
CDC requests OMB approval for an
estimated 1,240 annual burden hours.
There are no costs to respondents other
than their time to participate.
Proposed Project
Templates for Extramural Data
Management Plans (OMB Control No.
0920–1301, Exp. 6/30/2023)—
Extension—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Data management plans (DMPs) are
required of entities using CDC funds to
collect or generate public health data.
ESTIMATED ANNUALIZED BURDEN HOURS
Total burden
(in hours)
Form name
Applicants and Award Recipients .....
DMP Template .................................
1240
1
60/60
1240
Total ...........................................
...........................................................
........................
........................
........................
1240
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–24048 Filed 11–3–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–282]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
khammond on DSKJM1Z7X2PROD with NOTICES
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Type of respondents
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
SUMMARY:
VerDate Sep<11>2014
18:12 Nov 03, 2022
Jkt 259001
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
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.
Comments must be received by
January 3, 2023.
DATES:
PO 00000
Frm 00070
Fmt 4703
Sfmt 4703
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.
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: ll, 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
ADDRESSES:
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]]>Agencies
[Federal Register Volume 87, Number 213 (Friday, November 4, 2022)]
[Notices]
[Pages 66707-66708]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-24048]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-23-1301; Docket No. CDC-2022-0126]
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 continuing information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed information collection project
titled Templates for Extramural Data Management Plans. The aim of this
collection is to provide contract and cooperative agreement applicants
and awardees with templates for the creation of data management plans
(DMPs).
DATES: CDC must receive written comments on or before January 3, 2023.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2022-
0126 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].
[[Page 66708]]
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
Templates for Extramural Data Management Plans (OMB Control No.
0920-1301, Exp. 6/30/2023)--Extension--National Center for Chronic
Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Data management plans (DMPs) are required of entities using CDC
funds to collect or generate public health data. DMPs will be submitted
to CDC by grant and cooperative agreement awardees for assessment to
verify that they are concordant with CDC's data sharing policy. CDC
contractors collecting public health data are also required to create
and submit DMPs. This information collection request was developed by
CDC's National Center for Chronic Disease Prevention and Health
Promotion (NCCDPHP) to create standardized templates for DMPs so that
they will be easier to create, easier to review, better able to ensure
compliance with CDC's requirements, and able to increase the likelihood
of first draft approval by project officers. The project was initially
approved from June 2019 through June 2023. CDC will request an
Extension for approval for another three years. Minor updates will be
made to the templates for this extension period to better serve awardee
and CDC needs.
CDC requests OMB approval for an estimated 1,240 annual burden
hours. There are no costs to respondents other than their time to
participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
Applicants and Award DMP Template.... 1240 1 60/60 1240
Recipients.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1240
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-24048 Filed 11-3-22; 8:45 am]
BILLING CODE 4163-18-P
