Submission for OMB Review; Information Comparison With Insurance Data (OMB #0970-0342), 68885-68886 [2020-24141]
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68885
Federal Register / Vol. 85, No. 211 / Friday, October 30, 2020 / Notices
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
2. Call the Reports Clearance Office at
(410) 786–1326.
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–381 Identification of Extension
Units of Medicare Approved
Outpatient Physical Therapy/
Outpatient Speech Pathology (OPT/
OSP) Providers and Supporting
Regulations
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 Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Identification of
Extension Units of Medicare Approved
Outpatient Physical Therapy/Outpatient
Speech Pathology (OPT/OSP) Providers
and Supporting Regulations; Use: Form
CMS–381 was developed to ensure that
each OPT/OSP extension location at
which OPT/OSP providers furnish
services, must be reported by the
providers to the State Survey Agencies
(SAs). Form CMS–381 is completed
when: (1) New OPT/OSP providers
enter the Medicare program; (2) when
existing OPT/OPS providers delete or
add a service, or close or add an
extension location; or, (3) when existing
OPT/OSP providers are recertified by
the State Survey Agency every 6 years.
Form Number: CMS–381 (OMB control
number: 0938–0273); Frequency:
Occasionally; Affected Public: Private
Sector; Business or other for-profit and
not-for-profit institutions; Number of
Respondents: 2,083; Total Annual
Responses: 443; Total Annual Hours:
111. (For policy questions regarding this
collection contact Caroline Gallaher at
410–786–8705.)
Dated: October 27, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2020–24132 Filed 10–29–20; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Information Comparison With
Insurance Data (OMB #0970–0342)
Office of Child Support
Enforcement, Administration for
Children and Families, HHS.
ACTION: Request for Public Comment.
AGENCY:
The Administration for
Children and Families’ (ACF) Office of
Child Support Enforcement (OCSE) is
requesting a 3-year extension of the
currently approved Information
Comparison with Insurance Data (OMB
#0970–0342; Expires 1/31/2021).
DATES: Comments due within 30 days of
publication. OMB is required to make a
SUMMARY:
decision concerning 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.
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.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
Description: The Deficit Reduction
Act of 2005 amended Section 452 of the
Social Security Act to authorize the
Secretary, through the Federal Parent
Locator Service (FPLS), to conduct
comparisons of information concerning
individuals owing past-due child
support with information maintained by
insurers (or their agents) concerning
insurance claims, settlements, awards,
and payments. The two options to
participate in the Information
Comparison with Insurance Data
program are (1) insurers submit
information concerning claims,
settlements, awards, and payments to
the federal OCSE. OCSE compares it to
information pertaining to parents who
owe past-due support. (2) OCSE will
send a file containing information about
parents who owe past-due support to
the insurer, or their agent, to compare
with their claims, settlements, awards,
and payments. The insurer or their
agent sends any resulting insurance data
matches to OCSE. On a daily basis,
OCSE sends the results of the insurance
data match in an ‘‘Insurance Match
Response Record’’ to child support
agencies responsible for collecting pastdue support. The child support agencies
use the insurance data matches to
collect past-due support from the
insurance proceeds.
Respondents: Insurers or their agents,
including the U.S. Department of Labor
and state agencies administering
workers’ compensation programs, and
the Insurance Services Office.
jbell on DSKJLSW7X2PROD with NOTICES
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
annually
Instrument
Insurance Match File: Monthly, Reporting Electronically ................................
Insurance Match File: Weekly, Reporting Electronically .................................
VerDate Sep<11>2014
21:10 Oct 29, 2020
Jkt 253001
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
Total number
of annual
responses per
respondent
Average
annual burden
hours per
response
12
52
0.083
0.083
26
9
E:\FR\FM\30OCN1.SGM
30OCN1
Total/annual
burden hours
25.90
38.84
68886
Federal Register / Vol. 85, No. 211 / Friday, October 30, 2020 / Notices
ANNUAL BURDEN ESTIMATES—Continued
Total
number of
respondents
annually
Instrument
Insurance Match File: Daily, Reporting Electronically .....................................
Match File: Daily, Reporting Manually .............................................................
Estimated Total Annual Burden
Hours: 2,817.21.
Authority: 42 U.S.C. 652(a)(9), which
requires OCSE to operate the FPLS
established by 42 U.S.C. 653(a)(1) and 42
U.S.C. 652(m), which authorizes OCSE,
through the FPLS, to compare information
concerning individuals owing past-due
support with information maintained by
insurers (or their agents) concerning
insurance claims, settlements, awards, and
payments, and to furnish information
resulting from the data matches to the state
child support agencies responsible for
collecting child support from the individuals.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020–24141 Filed 10–29–20; 8:45 am]
BILLING CODE 4184–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2015–N–3326]
Reauthorization of the Biosimilar User
Fee Act; Public Meeting; Request for
Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice of public meeting;
request for comments.
ACTION:
The Food and Drug
Administration (FDA or Agency) is
hosting a virtual public meeting on the
reauthorization of the Biosimilar User
Fee Act (BsUFA) for fiscal years (FYs)
2023 through 2027. BsUFA authorizes
FDA to collect user fees to support the
process for the review of biosimilar
biological products. The current
legislative authority for BsUFA expires
in September 2022. At that time, new
legislation will be required for FDA to
continue collecting user fees in future
fiscal years. FDA begins the BsUFA
reauthorization process by publishing a
notice in the Federal Register
requesting public input and holding a
public meeting where the public may
present its views on the reauthorization.
FDA invites public comment as the
Agency begins the process to
reauthorize the program for FYs 2023
through 2027. These comments will be
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
21:10 Oct 29, 2020
Jkt 253001
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,
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
Frm 00054
Fmt 4703
Sfmt 4703
Average
annual burden
hours per
response
251
251
0.083
0.1
2
108
published and available on FDA’s
website.
DATES: The public meeting will be held
on November 19, 2020, from 9 a.m. to
12:30 p.m., and will be held by webcast
only. Registration to attend the meeting
and other information can be found at
https://bsufaiiipublicmeeting.eventbrite.com. Submit
either electronic or written comments
on this public meeting by December 19,
2020. See the SUPPLEMENTARY
INFORMATION section for registration date
and information.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before December 19,
2020. The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of December 19, 2020.
Comments received by mail/hand
delivery/courier (for written/paper
submissions) will be considered timely
if they are postmarked or the delivery
service acceptance receipt is on or
before that date.
PO 00000
Total number
of annual
responses per
respondent
Total/annual
burden hours
41.67
2,710.80
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,
240–402–7500.
• 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–
2015–N–3326 for ‘‘Reauthorization of
the Biosimilar User Fee Act; Public
Meeting; Request for Comments.’’
Received comments, those filed in a
timely manner (see ADDRESSES), 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.
• 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
available, you can provide this
information on the cover sheet and not
E:\FR\FM\30OCN1.SGM
30OCN1
Agencies
[Federal Register Volume 85, Number 211 (Friday, October 30, 2020)]
[Notices]
[Pages 68885-68886]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-24141]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Information Comparison With Insurance
Data (OMB #0970-0342)
AGENCY: Office of Child Support Enforcement, Administration for
Children and Families, HHS.
ACTION: Request for Public Comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families' (ACF) Office of
Child Support Enforcement (OCSE) is requesting a 3-year extension of
the currently approved Information Comparison with Insurance Data (OMB
#0970-0342; Expires 1/31/2021).
DATES: Comments due within 30 days of publication. OMB is required to
make a decision concerning 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.
SUPPLEMENTARY INFORMATION:
Description: The Deficit Reduction Act of 2005 amended Section 452
of the Social Security Act to authorize the Secretary, through the
Federal Parent Locator Service (FPLS), to conduct comparisons of
information concerning individuals owing past-due child support with
information maintained by insurers (or their agents) concerning
insurance claims, settlements, awards, and payments. The two options to
participate in the Information Comparison with Insurance Data program
are (1) insurers submit information concerning claims, settlements,
awards, and payments to the federal OCSE. OCSE compares it to
information pertaining to parents who owe past-due support. (2) OCSE
will send a file containing information about parents who owe past-due
support to the insurer, or their agent, to compare with their claims,
settlements, awards, and payments. The insurer or their agent sends any
resulting insurance data matches to OCSE. On a daily basis, OCSE sends
the results of the insurance data match in an ``Insurance Match
Response Record'' to child support agencies responsible for collecting
past-due support. The child support agencies use the insurance data
matches to collect past-due support from the insurance proceeds.
Respondents: Insurers or their agents, including the U.S.
Department of Labor and state agencies administering workers'
compensation programs, and the Insurance Services Office.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total number Total number Average
of of annual annual burden Total/annual
Instrument respondents responses per hours per burden hours
annually respondent response
----------------------------------------------------------------------------------------------------------------
Insurance Match File: Monthly, Reporting 26 12 0.083 25.90
Electronically.................................
Insurance Match File: Weekly, Reporting 9 52 0.083 38.84
Electronically.................................
[[Page 68886]]
Insurance Match File: Daily, Reporting 2 251 0.083 41.67
Electronically.................................
Match File: Daily, Reporting Manually........... 108 251 0.1 2,710.80
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 2,817.21.
Authority: 42 U.S.C. 652(a)(9), which requires OCSE to operate
the FPLS established by 42 U.S.C. 653(a)(1) and 42 U.S.C. 652(m),
which authorizes OCSE, through the FPLS, to compare information
concerning individuals owing past-due support with information
maintained by insurers (or their agents) concerning insurance
claims, settlements, awards, and payments, and to furnish
information resulting from the data matches to the state child
support agencies responsible for collecting child support from the
individuals.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020-24141 Filed 10-29-20; 8:45 am]
BILLING CODE 4184-41-P