Submission for Office of Management and Budget Review; Federal Case Registry (Office of Management and Budget #0970-0421), 71575-71576 [2023-22809]
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Federal Register / Vol. 88, No. 199 / Tuesday, October 17, 2023 / Notices
emergent situations. The final rule also
provided new information regarding the
processes and procedures for
amendments and extensions for
approved waiver plans. Form Number:
CMS–10383 (OMB Control Number
0938–1389; Frequency: Occasionally;
Affected Public: State Governments;
Number of Respondents: 19; Total
Annual Responses: 399; Total Annual
Hours: 5,549. (For policy questions
regarding this collection contact Lina
Rashid at 301–492–4193.)
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Patient
Protection and Affordable Care Act;
Exchange Functions: Eligibility for
Exemptions; Use: The data collection
and reporting requirements in ‘‘Patient
Protection and Affordable Care Act;
Exchange Functions: Eligibility for
Exemptions; Miscellaneous Minimum
Essential Coverage Provisions’’ (78 FR
39494 (July 1, 2013)), address federal
requirements that states must meet with
regard to the Exchange minimum
function of performing eligibility
determinations and issuing certificates
of exemption from the shared
responsibility payment. In the final
regulation, CMS addresses standards
related to eligibility, including the
verification and eligibility
determination process, eligibility
redeterminations, options for states to
rely on HHS to make eligibility
determinations for certificates of
exemption, and reporting. CMS
developed four appendices of
application materials to illustrate the
process applicants use to apply for
exemptions from the shared
responsibility payment. This
information collection requests seeks
approval for the requirements associated
with the collection of information
associated with these four appendices.
Form Number: CMS–10466 (OMB
Control Number 0938–1190; Frequency:
Annually; Affected Public: Individuals
and Households—State, Local, or Tribal
Governments; Number of Respondents:
849; Total Annual Responses: 849; Total
Annual Hours: 1,962. (For policy
questions regarding this collection
contact John Kenna at 301–492–4452.)
Dated: October 12, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–22897 Filed 10–16–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for Office of Management
and Budget Review; Federal Case
Registry (Office of Management and
Budget #0970–0421)
Office of Child Support
Enforcement, Administration for
Children and Families, United States
Department of Health and Human
Services.
ACTION: Request for public comments.
AGENCY:
The Office of Child Support
Enforcement (OCSE), Administration for
Children and Families (ACF), is
requesting from the Office of
Management and Budget (OMB) to
extend approval of the Federal Case
Registry (FCR) for an additional three
years. The current approval expires
November 30, 2023. OCSE is proposing
minor changes to punctuation,
formatting, grammar, clarity, and
spacing to enable easier completion of
the form.
DATES: Comments due within 30 days of
publication. OMB must make a decision
about the collection of information
between 30 and 60 days after
publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
SUMMARY:
Written 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. You can also obtain
copies of the proposed collection of
information by emailing infocollection@
acf.hhs.gov. Identify all emailed
requests by the title of the information
collection.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
Description: The FCR is a national
database of information pertaining to
child support cases processed by state
child support agencies, referred to as
‘‘IV–D’’ cases, and non-IV–D support
orders privately established or modified
by courts or tribunals on or after
October 1, 1998. FCR information is
comprised of child support orders and
case information from each State Case
Registry (SCR). The FCR automatically
compares new SCR submissions to
existing FCR information and to wage
and employment information in the
National Directory of New Hires. The
Federal Parent Locator Service notifies
state agencies if a IV–D case participant
in the state matches a participant in a
IV–D or non-IV–D case in another state
and supplies any matched wage and
employment information. Matches
enable state agencies to locate parties
that live in different states to establish,
modify, or enforce child support
obligations; to establish paternity; to
enforce state law regarding parental
kidnapping; and to establish or enforce
child custody or visitation
determinations.
The FCR instrument, Appendix G:
Input Record Layout, contains minor
changes in punctuation, formatting,
grammar, clarity, and spacing to enable
easier completion of the form.
Respondents: State child support
enforcement agencies.
lotter on DSK11XQN23PROD with NOTICES1
ANNUAL BURDEN ESTIMATES
Instrument
Total
number of
respondents
Annual
number of
responses per
respondent
Average
burden hours
per response
Annual
burden hours
Appendix G: Input Transactions Layout ..........................................................
54
406
0.033
730
Estimated Total Annual Burden
Hours: 730.
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Authority: 42 U.S.C. 653(h); 42 U.S.C.
654a(e); 42 U.S.C. 654a(f)(1).
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71576
Federal Register / Vol. 88, No. 199 / Tuesday, October 17, 2023 / Notices
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2023–22809 Filed 10–16–23; 8:45 am]
BILLING CODE 4184–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2020–D–2016]
Policy for Testing of Alcohol (Ethanol)
and Isopropyl Alcohol for Methanol;
Guidance for Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a final
guidance for industry entitled ‘‘Policy
for Testing of Alcohol (Ethanol) and
Isopropyl Alcohol for Methanol.’’ This
guidance is intended to alert
pharmaceutical manufacturers and
pharmacists in State-licensed
pharmacies or Federal facilities who
engage in drug compounding to the
potential public health hazard of
alcohol (ethyl alcohol or ethanol) or
isopropyl alcohol contaminated with or
substituted with methanol. During the
Coronavirus Disease 2019 (COVID–19)
public health emergency (PHE), FDA
became aware of reports of fatal
methanol poisoning of consumers who
ingested alcohol-based hand sanitizer
products that were manufactured with
methanol or methanol-contaminated
ethanol. FDA is concerned that other
drug products containing ethanol or
isopropyl alcohol (pharmaceutical
alcohol), which are widely used active
ingredients in a variety of drug
products, could be similarly vulnerable
to methanol contamination. This
guidance replaces the guidance for
industry entitled ‘‘Policy for Testing
Alcohol (Ethanol) and Isopropyl
Alcohol for Methanol, Including During
the Public Health Emergency (COVID–
19)’’ published in January 2021.
DATES: The announcement of the
guidance is published in the Federal
Register on October 17, 2023.
ADDRESSES: You may submit either
electronic or written comments on
Agency guidances at any time as
follows:
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
VerDate Sep<11>2014
17:02 Oct 16, 2023
Jkt 262001
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2020–D–2016 for ‘‘Policy for Testing of
Alcohol (Ethanol) and Isopropyl
Alcohol for Methanol.’’ Received
comments will be placed in the docket
and, except for those submitted as
‘‘Confidential Submissions,’’ publicly
viewable at https://www.regulations.gov
or at the Dockets Management Staff
between 9 a.m. and 4 p.m., Monday
through Friday, 240–402–7500.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
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redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852, 240–402–7500.
You may submit comments on any
guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single
copies of the guidance to the Division of
Drug Information, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10001 New
Hampshire Ave., Hillandale Building,
4th Floor, Silver Spring, MD 20993–
0002; or to the Office of
Communication, Outreach and
Development, Center for Biologics
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 71, Rm. 3128,
Silver Spring, MD 20993–0002; or to
Policy and Regulations Staff, HFV–6,
Center for Veterinary Medicine, Food
and Drug Administration, 7500 Standish
Place, Rockville, MD 20855. Send one
self-addressed adhesive label to assist
that office in processing your requests.
See the SUPPLEMENTARY INFORMATION
section for electronic access to the
guidance document.
FOR FURTHER INFORMATION CONTACT:
Francis Godwin, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 4342,
Silver Spring, MD 20993–0002, 301–
796–5362; or Anne Taylor, Center for
Biologics Evaluation and Research,
Food and Drug Administration, 10903
New Hampshire Ave., Bldg. 71, Rm.
7301, Silver Spring, MD 20993–0002,
E:\FR\FM\17OCN1.SGM
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]]>Agencies
[Federal Register Volume 88, Number 199 (Tuesday, October 17, 2023)]
[Notices]
[Pages 71575-71576]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-22809]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for Office of Management and Budget Review; Federal
Case Registry (Office of Management and Budget #0970-0421)
AGENCY: Office of Child Support Enforcement, Administration for
Children and Families, United States Department of Health and Human
Services.
ACTION: Request for public comments.
-----------------------------------------------------------------------
SUMMARY: The Office of Child Support Enforcement (OCSE), Administration
for Children and Families (ACF), is requesting from the Office of
Management and Budget (OMB) to extend approval of the Federal Case
Registry (FCR) for an additional three years. The current approval
expires November 30, 2023. OCSE is proposing minor changes to
punctuation, formatting, grammar, clarity, and spacing to enable easier
completion of the form.
DATES: Comments due within 30 days of publication. OMB must make a
decision about the collection of information between 30 and 60 days
after publication of this document in the Federal Register. Therefore,
a comment is best assured of having its full effect if OMB receives it
within 30 days of publication.
ADDRESSES: Written 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. You can
also obtain copies of the proposed collection of information by
emailing [email protected]. Identify all emailed requests by
the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: The FCR is a national database of information
pertaining to child support cases processed by state child support
agencies, referred to as ``IV-D'' cases, and non-IV-D support orders
privately established or modified by courts or tribunals on or after
October 1, 1998. FCR information is comprised of child support orders
and case information from each State Case Registry (SCR). The FCR
automatically compares new SCR submissions to existing FCR information
and to wage and employment information in the National Directory of New
Hires. The Federal Parent Locator Service notifies state agencies if a
IV-D case participant in the state matches a participant in a IV-D or
non-IV-D case in another state and supplies any matched wage and
employment information. Matches enable state agencies to locate parties
that live in different states to establish, modify, or enforce child
support obligations; to establish paternity; to enforce state law
regarding parental kidnapping; and to establish or enforce child
custody or visitation determinations.
The FCR instrument, Appendix G: Input Record Layout, contains minor
changes in punctuation, formatting, grammar, clarity, and spacing to
enable easier completion of the form.
Respondents: State child support enforcement agencies.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Annual number Average burden
Instrument Total number of of responses hours per Annual burden
respondents per respondent response hours
----------------------------------------------------------------------------------------------------------------
Appendix G: Input Transactions Layout....... 54 406 0.033 730
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 730.
Authority: 42 U.S.C. 653(h); 42 U.S.C. 654a(e); 42 U.S.C.
654a(f)(1).
[[Page 71576]]
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2023-22809 Filed 10-16-23; 8:45 am]
BILLING CODE 4184-41-P
