Submission for Office of Management and Budget Review; Child Support Portal Registration (Office of Management and Budget #: 0970-0370), 97623-97624 [2024-28761]
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97623
Federal Register / Vol. 89, No. 236 / Monday, December 9, 2024 / Notices
Authority: 22 U.S.C. 7105.
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024–28819 Filed 12–6–24; 8:45 am]
BILLING CODE 4184–47–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for Office of Management
and Budget Review; Child Support
Portal Registration (Office of
Management and Budget #: 0970–0370)
Office of Child Support
Services, Administration for Children
and Families, U.S. Department of Health
and Human Services.
ACTION: Request for public comments.
AGENCY:
The Office of Child Support
Services (OCSS), Administration for
Children and Families (ACF), is
requesting the federal Office of
Management and Budget (OMB)
approve the ‘‘Child Support Portal
Registration,’’ with minor revisions, for
an additional three years. The OCSS
Child Support Portal (‘‘Portal’’) contains
applications to help state child support
agencies administer their programs.
Authorized Portal users must register
with OCSS to access Portal applications
and provide OCSS with certain Portal
SUMMARY:
application preferences. The current
OMB approval expires on February 28,
2025.
DATES: Comments due January 8, 2025.
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 infocollection@
acf.hhs.gov. Identify all emailed
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: OCSS maintains the
Portal, which contains various
applications through which authorized
users may view, update, upload, or
download information for child support
purposes. Authorized users must
register to access the Portal. The OCSS
Portal authenticates registrants and then
creates secure profiles for authorized
users for employers, insurers, and
financial institutions based on
information provided in the Employer
Services Profile and Insurance Match
Debt Inquiry Portal Agreement and
Profile forms. Information provided in
the electronic National Medical Support
Notice (e-NMSN), the electronic
Incoming Withholding Order (e-IWO),
and the Federally Assisted State
Transmitted (FAST) Levy Financial
Institution Profile forms gives OCSS the
necessary information to set up the
respective program user’s process and
capture preferences. State child support
agencies manage and authenticate
authorization for individual users via
the state proxy server; therefore, a Portal
Registration form is not required. State
users must, however, provide OCSS
with their respective Portal preferences.
The information OCSS collects for the
Portal registration and profiles remains
the same but they underwent minor
clarification revisions and edits to
update ‘‘Office of Child Support
Enforcement (OCSE)’’ to ‘‘Office of
Child Support Services (OCSS).’’ OCSS
revised the ‘‘Registration Screen’’
burden after the 60-day notice
published to correctly reflect the current
number of respondents and removed
‘‘agreement’’ from the Employer
Services Profile form. OCSS also
removed the e-NMSN Plan
Administrator form because there are no
respondents.
Respondents: Employers, Financial
Institutions, Insurers, and State Child
Support Agencies.
ANNUAL BURDEN ESTIMATES
Total annual
estimated
number of
respondents
Information collection instrument
ddrumheller on DSK120RN23PROD with NOTICES1
Portal Registration Screens .............................................................................
Employer Services Profile ................................................................................
e-NMSN: Employer Profile ...............................................................................
e-NMSN: State Profile .....................................................................................
e-IWO Employer/Payroll Provider Profile ........................................................
Insurance Match Debt Inquiry Agreement and Profile ....................................
FAST Levy Financial Institution Profile ............................................................
VerDate Sep<11>2014
16:08 Dec 06, 2024
Jkt 265001
PO 00000
Frm 00042
Fmt 4703
Sfmt 9990
Total annual
number of
responses per
respondent
16,268
20,040
20
4
117
6
2
E:\FR\FM\09DEN1.SGM
1
1
1
1
1
1
1
09DEN1
Average
burden hours
per response
0.15
0.08
0.22
0.22
0.08
0.08
0.08
Total annual
burden hours
2,440.20
1,603.20
4.40
0.88
9.36
0.48
0.16
97624
Federal Register / Vol. 89, No. 236 / Monday, December 9, 2024 / Notices
Estimated Total Annual Burden
Hours: 4,058.68.
Authority: 42 U.S.C. 653(m)(2) and 44
U.S.C. 3554.
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024–28761 Filed 12–6–24; 8:45 am]
BILLING CODE 4184–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–D–0481]
Standardized Format for Electronic
Submission of Marketing Application
Content for the Planning of
Bioresearch Monitoring Inspections for
Center for Drug Evaluation and
Research Submissions; Guidance for
Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or the Agency) is
announcing the availability of the
guidance for industry entitled
‘‘Standardized Format for Electronic
Submission of NDA and BLA Content
for the Planning of Bioresearch
Monitoring (BIMO) Inspections for
CDER Submissions.’’ This guidance
describes the electronic submission of
certain data and information in
standardized formats. This information
is used by the Center for Drug
Evaluation and Research (CDER) in the
planning of, and by FDA’s Office of
Inspections and Investigations (OII) in
the conduct of, BIMO inspections.
DATES: The announcement of the
guidance is published in the Federal
Register on December 9, 2024.
ADDRESSES: You may submit either
electronic or written comments on
Agency guidances at any time as
follows:
SUMMARY:
ddrumheller on DSK120RN23PROD with NOTICES1
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
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,
VerDate Sep<11>2014
16:08 Dec 06, 2024
Jkt 265001
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–
2018–D–0481 for ‘‘Standardized Format
for Electronic Submission of NDA and
BLA Content for the Planning of
Bioresearch Monitoring (BIMO)
Inspections for CDER Submissions.’’
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
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
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
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
‘‘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 this 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. 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:
Emily Gebbia, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Silver Spring, MD
20993–0002, 240–402–0980.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a guidance for industry entitled
‘‘Standardized Format for Electronic
Submission of NDA and BLA Content
for the Planning of Bioresearch
Monitoring Inspections (BIMO) for
CDER Submissions.’’ This guidance
describes the electronic submission of
certain data and information in
standardized formats. CDER uses the
data and information described in the
guidance to plan BIMO inspections. The
guidance addresses major (i.e., pivotal)
studies used to support safety and
efficacy claims in new drug applications
(NDAs), biologic license applications
(BLAs) regulated by CDER, as well as
supplements containing new clinical
study reports.
E:\FR\FM\09DEN1.SGM
09DEN1
]]>Agencies
[Federal Register Volume 89, Number 236 (Monday, December 9, 2024)]
[Notices]
[Pages 97623-97624]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-28761]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for Office of Management and Budget Review; Child
Support Portal Registration (Office of Management and Budget #: 0970-
0370)
AGENCY: Office of Child Support Services, Administration for Children
and Families, U.S. Department of Health and Human Services.
ACTION: Request for public comments.
-----------------------------------------------------------------------
SUMMARY: The Office of Child Support Services (OCSS), Administration
for Children and Families (ACF), is requesting the federal Office of
Management and Budget (OMB) approve the ``Child Support Portal
Registration,'' with minor revisions, for an additional three years.
The OCSS Child Support Portal (``Portal'') contains applications to
help state child support agencies administer their programs. Authorized
Portal users must register with OCSS to access Portal applications and
provide OCSS with certain Portal application preferences. The current
OMB approval expires on February 28, 2025.
DATES: Comments due January 8, 2025. 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: OCSS maintains the Portal, which contains various
applications through which authorized users may view, update, upload,
or download information for child support purposes. Authorized users
must register to access the Portal. The OCSS Portal authenticates
registrants and then creates secure profiles for authorized users for
employers, insurers, and financial institutions based on information
provided in the Employer Services Profile and Insurance Match Debt
Inquiry Portal Agreement and Profile forms. Information provided in the
electronic National Medical Support Notice (e-NMSN), the electronic
Incoming Withholding Order (e-IWO), and the Federally Assisted State
Transmitted (FAST) Levy Financial Institution Profile forms gives OCSS
the necessary information to set up the respective program user's
process and capture preferences. State child support agencies manage
and authenticate authorization for individual users via the state proxy
server; therefore, a Portal Registration form is not required. State
users must, however, provide OCSS with their respective Portal
preferences. The information OCSS collects for the Portal registration
and profiles remains the same but they underwent minor clarification
revisions and edits to update ``Office of Child Support Enforcement
(OCSE)'' to ``Office of Child Support Services (OCSS).'' OCSS revised
the ``Registration Screen'' burden after the 60-day notice published to
correctly reflect the current number of respondents and removed
``agreement'' from the Employer Services Profile form. OCSS also
removed the e-NMSN Plan Administrator form because there are no
respondents.
Respondents: Employers, Financial Institutions, Insurers, and State
Child Support Agencies.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total annual Total annual
estimated number of Average burden Total annual
Information collection instrument number of responses per hours per burden hours
respondents respondent response
----------------------------------------------------------------------------------------------------------------
Portal Registration Screens..................... 16,268 1 0.15 2,440.20
Employer Services Profile....................... 20,040 1 0.08 1,603.20
e-NMSN: Employer Profile........................ 20 1 0.22 4.40
e-NMSN: State Profile........................... 4 1 0.22 0.88
e-IWO Employer/Payroll Provider Profile......... 117 1 0.08 9.36
Insurance Match Debt Inquiry Agreement and 6 1 0.08 0.48
Profile........................................
FAST Levy Financial Institution Profile......... 2 1 0.08 0.16
----------------------------------------------------------------------------------------------------------------
[[Page 97624]]
Estimated Total Annual Burden Hours: 4,058.68.
Authority: 42 U.S.C. 653(m)(2) and 44 U.S.C. 3554.
Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024-28761 Filed 12-6-24; 8:45 am]
BILLING CODE 4184-41-P
