Agency Information Collection Activities: Submission for OMB Review; Comment Request, 78109-78110 [2022-27739]
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Federal Register / Vol. 87, No. 244 / Wednesday, December 21, 2022 / Notices
FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–855I and CMS–
855O]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
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
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(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
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate 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.
SUMMARY:
Comments on the collection(s) of
information must be received by the
OMB desk officer by January 20, 2023.
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.
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
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
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DATES:
VerDate Sep<11>2014
19:56 Dec 20, 2022
Jkt 259001
William Parham at (410) 786–4669.
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. 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 (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-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 that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare
Registration Application; Use: Various
sections of the Social Security Act (Act),
the United States Code (U.S.C.), Internal
Revenue Service Code (Code) and the
Code of Federal Regulations (CFR)
require providers and suppliers to
furnish information concerning the
amounts due and the identification of
individuals or entities that furnish
medical services to beneficiaries before
allowing payment. The principal
function of the CMS–855O is to gather
information from a physician or other
eligible professional to help CMS
determine whether he or she meets
certain qualifications to enroll in the
Medicare program for the sole purpose
of ordering or certifying certain
Medicare items or services. The CMS–
855O allows a physician or other
eligible professional to enroll in
Medicare without approval for billing
privileges.
The collection and verification of this
information protects our beneficiaries
from illegitimate providers/suppliers.
These procedures also protect the
Medicare Trust Funds against fraud.
The CMS–855O gathers information that
allow Medicare contractors to ensure
that the physician or eligible
professional is not sanctioned from the
Medicare and/or Medicaid program(s),
or debarred, or excluded from any other
Federal agency or program.
Furthermore, the data collected also
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Frm 00068
Fmt 4703
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78109
ensures that the applicant has the
necessary credentials to order and
certify health care services. This is the
sole instrument implemented for this
purpose.
Form Number: CMS- 855O (OMB
control number 0938–1135); Frequency:
Occasionally; Affected Public: Private
Sector (Business or other for-profits),
State, Local, or Tribal Governments;
Number of Respondents: 6,190; Number
of Responses: 6,190; Total Annual
Hours: 3,095. (For policy questions
regarding this collection contact Frank
Whelan at 410–786–1302).
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare
Enrollment Application for Physician
and Non-Physician Practitioners; Use:
The Social Security Act (Act) requires
providers and suppliers to furnish
information concerning the amounts
due and the identification of individuals
or entities that furnish medical services
to beneficiaries before allowing
payment. The primary function of the
CMS–855I Medicare enrollment
application for physicians and nonphysician practitioners is to gather
information from an individual provider
or supplier that tells us who he/she is,
whether he/she meets certain
qualifications to be a Medicare health
care provider or supplier, where he/she
practices or renders services, and other
information necessary to establish
correct claims payments.
The collection and verification of this
information is the first line defense to
defend and protect our beneficiaries
from illegitimate physicians, nonphysician practitioners, and other
eligible professionals and to protect the
Medicare Trust Fund against fraud. It
gathers information that allow Medicare
contractors to ensure only legitimate
physicians, non-physician practitioners,
and other eligible professionals enroll in
the Medicare program, and are not
sanctioned from the Medicare and/or
Medicaid program(s), or debarred, or
excluded from any other Federal agency
or program. This is the sole instrument
implemented for this purpose. Form
Number: CMS–855I (OMB control
number 0938–1355); Frequency:
Occasionally; Affected Public: State,
Local, or Tribal Governments, Private
Sector (not-for-profit institutions);
Number of Respondents: 472,617;
Number of Responses: 472,617; Total
Annual Hours: 961,651. (For policy
questions regarding this collection
contact Frank Whelan at 410–786–
1302).
E:\FR\FM\21DEN1.SGM
21DEN1
78110
Federal Register / Vol. 87, No. 244 / Wednesday, December 21, 2022 / Notices
Dated: December 16, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2022–27739 Filed 12–20–22; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Child Care and Development
Fund (CCDF) Consumer Education
Website and Reports of Serious
Injuries and Death
Office of Child Care,
Administration for Children and
Families, Department of Health and
Human Services.
ACTION: Request for Public Comments.
AGENCY:
The Office of Child Care
(OCC), Administration for Children and
SUMMARY:
Families (ACF), U.S. Department of
Health and Human Services (HHS), is
requesting a 3-year extension of the
CCDF Consumer Education website and
Reports of Serious Incidents and Death
(Office of Management and Budget
(OMB) #: 0970–0473, expiration date:
April 30, 2023). There are no changes
requested to the reporting requirements.
DATES: Comments due within 60 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act of 1995, ACF is soliciting
public comment on the specific aspects
of the information collection described
above.
ADDRESSES: You can obtain copies of the
proposed collection of information and
submit comments by emailing
infocollection@acf.hhs.gov. Identify all
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: The existing Consumer
Education website reporting
requirement will not be modified and
requires states and territories to include
information about state or territory
policies (related to licensing,
monitoring, and background checks)
and provider-specific information,
including results of monitoring and
inspection reports and, if available,
information about quality. The existing
Reporting of Serious Injuries and Death
reporting requirement will not be
modified. CCDF Lead Agencies must
establish procedures that require child
care providers that care for children
receiving CCDF subsidies to report to a
designated state, territorial, or tribal
entity any serious injuries or deaths of
children occurring in child care. There
are no standard federal forms associated
with these reporting requirements.
Respondents: The Consumer
Education website information
collection requirement applies to the 50
states, the District of Columbia, and 5
territories that receive CCDF grants.
Reporting of Serious Injuries and Death
is a requirement for child care
providers.
ANNUAL BURDEN ESTIMATES
Total number
of respondents
Instrument
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Consumer Education Website .............................................
Reporting of Serious Injuries and Death .............................
Estimated Total Annual Burden
Hours: 26,800.
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: Pub. L. 113–186; 42 U.S.C.
9858 et seq.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2022–27665 Filed 12–20–22; 8:45 am]
BILLING CODE 4184–43–P
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Total number
of responses
per
respondent
56
10,000
1
1
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–P–1189]
Canned Tuna Deviating From Identity
Standard; Amendment of Temporary
Marketing Permit
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or we) is
amending StarKist Co.’s temporary
permit to market test canned tuna. The
temporary permit is amended to add
one additional manufacturing location.
This amendment will allow the
applicant to continue to test market and
collect data on consumer acceptance of
the test product.
FOR FURTHER INFORMATION CONTACT:
Marjan Morravej, Center for Food Safety
and Applied Nutrition (HFS–820), Food
and Drug Administration, 5001 Campus
Dr., College Park, MD 20740, 240–402–
2371.
SUMMARY:
PO 00000
Frm 00069
Fmt 4703
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Average
burden hours
per response
300
1
Total burden
hours
Annual burden
hours
50,400
30,000
16,800
10,000
In the
Federal Register of June 20, 2014 (79 FR
35362), we issued a notice announcing
that we had issued a temporary permit
to StarKist Co., 225 North Shore Dr.,
Pittsburgh, PA 15212, to market test
products identified as canned tuna
products. The permit allowed for the
test product to be manufactured at
Galapesca S.A., Km. 12.5 Via A Duale,
Guayaquil, Ecuador, and StarKist Samoa
Co., 368 Atu’u Rd., Pago Pago, American
Samoa 96799. We issued the permit to
facilitate market testing of products that
deviate from the requirements of the
standard of identity for canned tuna in
21 CFR 161.190, which was issued
under section 401 of the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. 341).
In the Federal Register of March 7,
2016 (81 FR 11813), we issued a notice
announcing that we were extending the
temporary market permit issued to
StarKist Co., among other parties. The
extension allows the applicants to
continue to measure consumer
acceptance of the products and assess
the commercial feasibility of the
products, in support of a petition to
SUPPLEMENTARY INFORMATION:
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21DEN1
Agencies
[Federal Register Volume 87, Number 244 (Wednesday, December 21, 2022)]
[Notices]
[Pages 78109-78110]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-27739]
[[Page 78109]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-855I and CMS-855O]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (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 a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the burden estimate 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.
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by January 20, 2023.
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.
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 website by copying and pasting the following web address
into your web browser: https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
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. 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 (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-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 that
summarizes the following proposed collection(s) of information for
public comment:
1. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicare
Registration Application; Use: Various sections of the Social Security
Act (Act), the United States Code (U.S.C.), Internal Revenue Service
Code (Code) and the Code of Federal Regulations (CFR) require providers
and suppliers to furnish information concerning the amounts due and the
identification of individuals or entities that furnish medical services
to beneficiaries before allowing payment. The principal function of the
CMS-855O is to gather information from a physician or other eligible
professional to help CMS determine whether he or she meets certain
qualifications to enroll in the Medicare program for the sole purpose
of ordering or certifying certain Medicare items or services. The CMS-
855O allows a physician or other eligible professional to enroll in
Medicare without approval for billing privileges.
The collection and verification of this information protects our
beneficiaries from illegitimate providers/suppliers. These procedures
also protect the Medicare Trust Funds against fraud. The CMS-855O
gathers information that allow Medicare contractors to ensure that the
physician or eligible professional is not sanctioned from the Medicare
and/or Medicaid program(s), or debarred, or excluded from any other
Federal agency or program. Furthermore, the data collected also ensures
that the applicant has the necessary credentials to order and certify
health care services. This is the sole instrument implemented for this
purpose.
Form Number: CMS- 855O (OMB control number 0938-1135); Frequency:
Occasionally; Affected Public: Private Sector (Business or other for-
profits), State, Local, or Tribal Governments; Number of Respondents:
6,190; Number of Responses: 6,190; Total Annual Hours: 3,095. (For
policy questions regarding this collection contact Frank Whelan at 410-
786-1302).
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicare
Enrollment Application for Physician and Non-Physician Practitioners;
Use: The Social Security Act (Act) requires providers and suppliers to
furnish information concerning the amounts due and the identification
of individuals or entities that furnish medical services to
beneficiaries before allowing payment. The primary function of the CMS-
855I Medicare enrollment application for physicians and non-physician
practitioners is to gather information from an individual provider or
supplier that tells us who he/she is, whether he/she meets certain
qualifications to be a Medicare health care provider or supplier, where
he/she practices or renders services, and other information necessary
to establish correct claims payments.
The collection and verification of this information is the first
line defense to defend and protect our beneficiaries from illegitimate
physicians, non-physician practitioners, and other eligible
professionals and to protect the Medicare Trust Fund against fraud. It
gathers information that allow Medicare contractors to ensure only
legitimate physicians, non-physician practitioners, and other eligible
professionals enroll in the Medicare program, and are not sanctioned
from the Medicare and/or Medicaid program(s), or debarred, or excluded
from any other Federal agency or program. This is the sole instrument
implemented for this purpose. Form Number: CMS-855I (OMB control number
0938-1355); Frequency: Occasionally; Affected Public: State, Local, or
Tribal Governments, Private Sector (not-for-profit institutions);
Number of Respondents: 472,617; Number of Responses: 472,617; Total
Annual Hours: 961,651. (For policy questions regarding this collection
contact Frank Whelan at 410-786-1302).
[[Page 78110]]
Dated: December 16, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2022-27739 Filed 12-20-22; 8:45 am]
BILLING CODE 4120-01-P