Proposed Information Collection Activity; State Plan Child Support Collection and Establishment of Paternity Title IV-D OCSE-100 and OCSE-21-U4, 66914-66915 [2019-26323]
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Federal Register / Vol. 84, No. 235 / Friday, December 6, 2019 / Notices
of Information Collection: Statement of
Deficiencies and Plan of Correction
Supporting Regulations; Use: Section
1864(a) of the Social Security Act
DATES: Comments on the collection(s) of requires that the Secretary use state
survey agencies to conduct surveys to
information must be received by the
determine whether health care facilities
OMB desk officer by January 6, 2020.
meet Medicare and Clinical Laboratory
ADDRESSES: When commenting on the
Improvement Amendments
proposed information collections,
participation requirements. The Form
please reference the document identifier
CMS–2567 is the means by which the
or OMB control number. To be assured
survey findings are documented. This
consideration, comments and
section of the law further requires that
recommendations must be received by
compliance findings resulting from
the OMB desk officer via one of the
these surveys be made available to the
following transmissions: OMB, Office of
public within 90 days of such surveys.
Information and Regulatory Affairs,
The Form CMS–2567 is the vehicle for
Attention: CMS Desk Officer, Fax
this disclosure. The form is also used by
Number: (202) 395–5806 OR Email:
health care facilities to document their
OIRA_submission@omb.eop.gov.
plan of correction and by CMS, the
To obtain copies of a supporting
states, facilities, purchasers, consumers,
statement and any related forms for the
advocacy groups, and the public as a
proposed collection(s) summarized in
source of information about quality of
this notice, you may make your request
care and facility compliance. The
using one of following:
regulations at 42 CFR 488.18 require
1. Access CMS’ website address at
website address at https://www.cms.gov/ that state survey agencies document all
deficiency findings on a statement of
Regulations-and-Guidance/Legislation/
deficiencies and plan of correction,
PaperworkReductionActof1995/PRAwhich is the CMS–2567. Sections
Listing.html.
488.26 and 488.28 further delineate how
2. Email your request, including your
compliance findings must be recorded
address, phone number, OMB number,
and that CMS prescribed forms must be
and CMS document identifier, to
used. Form Number: CMS–2567 (OMB
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at Control Number: 0938–0391);
Frequency: Yearly and occasionally;
(410) 786–1326.
Affected Public: Private Sector (Business
FOR FURTHER INFORMATION CONTACT:
or other for-profit and Not-for-profit
William Parham at (410) 786–4669.
institutions); Number of Respondents:
SUPPLEMENTARY INFORMATION: Under the
64,500; Total Annual Responses:
Paperwork Reduction Act of 1995 (PRA) 64,500; Total Annual Hours: 129,000.
(44 U.S.C. 3501–3520), federal agencies
(For policy questions regarding this
must obtain approval from the Office of
collection contact Caecilia Blondiaux at
Management and Budget (OMB) for each 410–786–2190.)
collection of information they conduct
Dated: December 3, 2019.
or sponsor. The term ‘‘collection of
William N. Parham, III,
information’’ is defined in 44 U.S.C.
Director, Paperwork Reduction Staff, Office
3502(3) and 5 CFR 1320.3(c) and
of Strategic Operations and Regulatory
includes agency requests or
requirements that members of the public Affairs.
submit reports, keep records, or provide [FR Doc. 2019–26364 Filed 12–5–19; 8:45 am]
BILLING CODE 4120–01–P
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
DEPARTMENT OF HEALTH AND
to publish a 30-day notice in the
HUMAN SERVICES
Federal Register concerning each
proposed collection of information,
Administration for Children and
including each proposed extension or
Families
reinstatement of an existing collection
of information, before submitting the
Proposed Information Collection
collection to OMB for approval. To
Activity; State Plan Child Support
comply with this requirement, CMS is
Collection and Establishment of
publishing this notice that summarizes
Paternity Title IV–D OCSE–100 and
the following proposed collection(s) of
OCSE–21–U4
information for public comment:
1. Type of Information Collection
AGENCY: Office of Child Support
Request: Reinstatement without change
Enforcement, Administration for
of a currently approved collection; Title Children and Families, HHS.
lotter on DSKBCFDHB2PROD with NOTICES
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
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ACTION:
Request for public comment.
The Office of Child Support
Enforcement (OCSE), Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services (HHS), is requesting a threeyear extension of the forms OCSE–21–
U4: Transmittal and Notice of Approval
of State Plan Material for: Title IV–D of
the Social Security Act and OCSE–100:
State Plan (OMB #0970–0017,
expiration 7/31/2020).
SUMMARY:
Comments due within 60 days of
publication. In compliance with the
requirements of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
the Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
DATES:
Copies of the proposed
collection of information can be
obtained and comments may be
forwarded by emailing infocollection@
acf.hhs.gov. Alternatively, copies can
also be obtained by writing to the
Administration for Children and
Families, Office of Planning, Research,
and Evaluation (OPRE), 330 C Street
SW, Washington, DC 20201, Attn: ACF
Reports Clearance Officer. All requests,
emailed or written, should be identified
by the title of the information collection.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
Description: OCSE has approved an IV–
D state plan for each state. Federal
regulations require states to amend their
state plans only when necessary to
reflect new or revised federal statutes,
regulations, or material changes in any
state laws, regulations, policies, or IV–
D agency procedures. The requirement
for submission of a state plan and plan
amendments for the Child Support
Enforcement Program is found in
sections 452, 454, and 466 of the Social
Security Act. OCSE made minor
revisions to the OCSE–21–U4 to remove
outdated language and add an option for
states to electronically request or renew
an exemption from the mandatory laws
and procedures in Section 466 of the
Social Security Act via the online state
plan system. These revisions do not
increase the burden of the OCSE–21–
U4.
Respondents: State IV–D Agencies.
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Federal Register / Vol. 84, No. 235 / Friday, December 6, 2019 / Notices
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
Instrument
State Plan (OCSE–100) ..................................................................................
State Plan Transmittal (OCSE–21–U4) ...........................................................
Estimated Total Annual Burden
Hours: 486.
Comments: The Department
specifically requests comments on: (a)
Whether the proposed collection of
information is necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) the quality, utility,
and clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Consideration will be given
to comments and suggestions submitted
within 60 days of this publication.
Authority: Sections 452, 454, and 466 of
the Social Security Act
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019–26323 Filed 12–5–19; 8:45 am]
BILLING CODE 4184–41–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2019–N–5552]
Joint Meeting of the Anesthetic and
Analgesic Drug Products Advisory
Committee and the Drug Safety and
Risk Management Advisory
Committee; Notice of Meeting;
Establishment of a Public Docket;
Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice; establishment of a
public docket; request for comments.
ACTION:
The Food and Drug
Administration (FDA) announces a
forthcoming public advisory committee
meeting of the Anesthetic and Analgesic
Drug Products Advisory Committee and
the Drug Safety and Risk Management
Advisory Committee. The general
function of the committees is to provide
advice and recommendations to FDA on
regulatory issues. The meeting will be
lotter on DSKBCFDHB2PROD with NOTICES
SUMMARY:
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open to the public. FDA is establishing
a docket for public comment on this
document.
DATES: The meeting will be held on
January 14, 2020, from 8 a.m. to 5:30
p.m.
ADDRESSES: FDA White Oak Campus,
10903 New Hampshire Ave., Bldg. 31
Conference Center, the Great Room (Rm.
1503), Silver Spring, MD 20993–0002.
Answers to commonly asked questions
including information regarding special
accommodations due to a disability,
visitor parking, and transportation may
be accessed at: https://www.fda.gov/
AdvisoryCommittees/
AboutAdvisoryCommittees/
ucm408555.htm.
FDA is establishing a docket for
public comment on this meeting. The
docket number is FDA–2019–N–5552.
The docket will close on January 13,
2020. Submit either electronic or
written comments on this public
meeting by January 13, 2020. Please
note that late, untimely filed comments
will not be considered. Electronic
comments must be submitted on or
before January 13, 2020. The https://
www.regulations.gov electronic filing
system will accept comments until
11:59 p.m. Eastern Time at the end of
January 13, 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.
Comments received on or before
December 30, 2019, will be provided to
the committees. Comments received
after that date will be taken into
consideration by FDA. In the event that
the meeting is cancelled, FDA will
continue to evaluate any relevant
applications or information, and
consider any comments submitted to the
docket, as appropriate.
You may submit comments as
follows:
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,
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Total
number of
responses per
respondent
12
12
Average
burden
hours per
response
.5
.25
Total
burden hours
324
162
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–
2019–N–5552 for ‘‘Joint Meeting of the
Anesthetic and Analgesic Drug Products
Advisory Committee and the Drug
Safety and Risk Management Advisory
Committee; Notice of Meeting;
Establishment of a Public Docket;
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.
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]]>Agencies
[Federal Register Volume 84, Number 235 (Friday, December 6, 2019)]
[Notices]
[Pages 66914-66915]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-26323]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; State Plan Child
Support Collection and Establishment of Paternity Title IV-D OCSE-100
and OCSE-21-U4
AGENCY: Office of Child Support Enforcement, Administration for
Children and Families, HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Office of Child Support Enforcement (OCSE), Administration
for Children and Families (ACF), U.S. Department of Health and Human
Services (HHS), is requesting a three-year extension of the forms OCSE-
21-U4: Transmittal and Notice of Approval of State Plan Material for:
Title IV-D of the Social Security Act and OCSE-100: State Plan (OMB
#0970-0017, expiration 7/31/2020).
DATES: Comments due within 60 days of publication. In compliance with
the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction
Act of 1995, the Administration for Children and Families is soliciting
public comment on the specific aspects of the information collection
described above.
ADDRESSES: Copies of the proposed collection of information can be
obtained and comments may be forwarded by emailing
[email protected]. Alternatively, copies can also be obtained
by writing to the Administration for Children and Families, Office of
Planning, Research, and Evaluation (OPRE), 330 C Street SW, Washington,
DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or
written, should be identified by the title of the information
collection.
SUPPLEMENTARY INFORMATION: Description: OCSE has approved an IV-D state
plan for each state. Federal regulations require states to amend their
state plans only when necessary to reflect new or revised federal
statutes, regulations, or material changes in any state laws,
regulations, policies, or IV-D agency procedures. The requirement for
submission of a state plan and plan amendments for the Child Support
Enforcement Program is found in sections 452, 454, and 466 of the
Social Security Act. OCSE made minor revisions to the OCSE-21-U4 to
remove outdated language and add an option for states to electronically
request or renew an exemption from the mandatory laws and procedures in
Section 466 of the Social Security Act via the online state plan
system. These revisions do not increase the burden of the OCSE-21-U4.
Respondents: State IV-D Agencies.
[[Page 66915]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total number
Total number of responses Average Total burden
Instrument of per burden hours hours
respondents respondent per response
----------------------------------------------------------------------------------------------------------------
State Plan (OCSE-100)........................... 54 12 .5 324
State Plan Transmittal (OCSE-21-U4)............. 54 12 .25 162
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 486.
Comments: The Department specifically requests comments on: (a)
Whether the proposed collection of information is necessary for the
proper performance of the functions of the agency, including whether
the information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Authority: Sections 452, 454, and 466 of the Social Security Act
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019-26323 Filed 12-5-19; 8:45 am]
BILLING CODE 4184-41-P
