Agency Information Collection Activities: Submission for OMB Review; Comment Request, 71427-71428 [2019-27926]
Download as PDF
Federal Register / Vol. 84, No. 248 / Friday, December 27, 2019 / Notices
date for this item. With regard to the
memoranda items related to cross
jurisdictional activity and derivatives in
Schedule E, certain of these items will
be calculated in large part consistent
with current reporting requirements for
the FFIEC 009. Therefore, the revisions
to Schedules D and E will become
effective for existing FR Y–15
respondents as of the December 31,
2019, report date, as originally
proposed.
One commenter asked if the Board
would require FBOs to complete the
proposed memorandum items,
including the trading volume
memorandum items, with respect to
their combined U.S. operations (CUSO),
as certain FBOs will begin filing the FR
Y–15 based on their CUSO as of June 30,
2020, consistent with the Board’s recent
tailoring rule. The Board has finalized
the FR Y–15 revisions with the
following effective dates for FBOs that
will be required to file the FR Y–15
based on their CUSO:
• June 30, 2020, report date:
Revisions to Schedule E;
• December 31, 2020, report date:
Revisions to Schedules C and D.8
For the trading volume memorandum
items being added to Schedule C, given
that the FBO will begin filing the FR Y–
15 based on its CUSO as of June 30,
2020, an FBO would annualize its
CUSO trading activity until it were to
file four quarters of the FR Y–15.
jbell on DSKJLSW7X2PROD with NOTICES
Comments on GSIB Surcharge
Methodology
One commenter requested that prior
to incorporating the proposed
memoranda items into the GSIB
surcharge framework, the Board
undertake a holistic review and
recalibration of the framework
methodology subject to public
comment. This commenter also
requested that the Board adopt a
procedural mechanism to ensure that
the GSIB surcharge methodology is
periodically reassessed, such as once
every three or four years. These
comments are beyond the scope of the
proposal; however staff notes that any
incorporation of these memoranda items
into the GSIB surcharge framework
would be subject to the rulemaking
process and provide opportunity for
public feedback.
8 An FBO required to file the FR Y–15 for its
CUSO as of December 31, 2020 would look back to
collect two quarters of trading volume data (i.e.,
trading volume information for July 1st–December
31st) and annualize the additional two quarters in
Schedule C.
VerDate Sep<11>2014
18:44 Dec 26, 2019
Jkt 250001
Board of Governors of the Federal Reserve
System, December 19, 2019.
Michele Taylor Fennell,
Assistant Secretary of the Board.
[FR Doc. 2019–27849 Filed 12–26–19; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10701, CMS–
10191 and CMS–10142]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid 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 27, 2020.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 OR, Email:
OIRA_submission@omb.eop.gov.
DATES:
PO 00000
Frm 00080
Fmt 4703
Sfmt 4703
71427
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.
1. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
2. Call the Reports Clearance Office at
(410) 786–1326.
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: New collection (Request for a
new OMB control number); Title of
Information Collection: Medicare
Beneficiary Experiences with Care
Survey System; Use: The MBECS system
is designed to conduct 1–2 surveys per
year on priority groups of interest,
thereby allowing CMS OMH to respond
quickly to the data needs of
stakeholders with interests in these
underrepresented groups. Data collected
through the MBECS system will be used
to better understand—and thus serve the
needs of—Medicare beneficiaries in
minority populations. The core
questionnaire will collect information
on communication with medical
professionals, coordination of health
care, experiences getting needed health
care, experiences with personal doctors
and specialists, and key demographics.
Data will be compared to benchmarks
from the FFS CAHPS, MA CAHPS, and
E:\FR\FM\27DEN1.SGM
27DEN1
jbell on DSKJLSW7X2PROD with NOTICES
71428
Federal Register / Vol. 84, No. 248 / Friday, December 27, 2019 / Notices
NAM CAHPS surveys. The populationspecific questionnaire module will
collect information about issues most
relevant for particular minority groups;
population-specific modules will be
described in individual information
collection requests. These data will be
compared to benchmarks from the
relevant CAHPS source surveys when
available.
Collection of these data from people
who have been identified through CMS
administrative data and administrative
flags as part of specific minority
populations will also serve as a critical
validation step of this method for
identifying difficult-to-study
populations, thus making it easier to
study beneficiaries in these groups in
the future. Form Number: CMS–10701
(OMB control number: 0938–NEW);
Frequency: Yearly; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 10,000; Total
Annual Responses: 10,000; Total
Annual Hours: 3,333. (For policy
questions regarding this collection
contact Luis Perez at 410–786–8557.)
2. Type of Information Collection
Request: Revision with change of a
currently approved collection; Title of
Information Collection: Medicare Parts
C and D Program Audit Protocols and
Data Requests; Use: Under the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 and
implementing regulations at 42 CFR
parts 422 and 423, Medicare Part D plan
sponsors and Medicare Advantage
organizations are required to comply
with all Medicare Parts C and D
program requirements. CMS’ annual
audit plan ensures that we evaluate
sponsoring organizations’ compliance
with these requirements. CMS program
audits focus on high-risk areas that have
the greatest potential for beneficiary
harm. As such, CMS has developed
several audit protocols that are included
within the program area data request
documents and that are posted to the
CMS website each year for use by
sponsoring organizations to prepare for
their audit. As part of a robust audit
process, CMS also requires sponsoring
organizations who have been audited
and found to have deficiencies to
undergo a validation audit to ensure
correction. The validation audit utilizes
the same audit protocols, but only tests
the elements where deficiencies were
found, as opposed to re-administering
the entire audit.
Currently CMS utilizes the following
5 protocols to audit sponsoring
organization performance: Part D
Formulary and Benefit Administration
(FA); Part D Coverage Determinations,
Appeals, and Grievances (CDAG); Part C
VerDate Sep<11>2014
18:44 Dec 26, 2019
Jkt 250001
Organization Determinations, Appeals,
and Grievances (ODAG); Special Needs
Model of Care (SNP–MOC) (only
administered on organizations who
operate SNPs); and, Compliance
Program Effectiveness (CPE). The data
collected is detailed in each of these
protocols and the exact fields are
located in the record layouts, at the end
of each protocol. In addition, this
collection request includes a pre-audit
issue summary, three CPE
questionnaires, one CPE organizational
structure presentation template, one FA
impact analysis template, two CDAG
impact analysis templates, four ODAG
impact analysis templates, three SNP–
MOC impact analysis templates, and a
SNP–MOC questionnaire.
The information gathered during this
audit will be used by the Medicare Parts
C and D Oversight and Enforcement
Group (MOEG) within the Center for
Medicare (CM) and CMS Regional
Offices to assess sponsoring
organizations’ compliance with
Medicare program requirements. If
outliers or other data anomalies are
detected, Regional Offices will work in
collaboration with MOEG and other
divisions within CMS for follow-up and
resolution. Additionally, MA and Part D
organizations will receive the audit
results and will be required to
implement corrective action to correct
any identified deficiencies. Form
Number: CMS–10191 (OMB control
number: 0938–1000); Frequency: Yearly;
Affected Public: State, Local, or Tribal
Governments; Number of Respondents:
201; Total Annual Responses: 207; Total
Annual Hours: 39,456. (For policy
questions regarding this collection
contact Brenda Hudson at 443–743–
9299.)
3. Type of Information Collection
Request: Revision with change of a
currently approved collection; Title of
Information Collection: Bid Pricing Tool
(BPT) for Medicare Advantage (MA)
Plans and Prescription Drug Plans
(PDP); Use: Under the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA), and
implementing regulations at 42 CFR,
Medicare Advantage organizations
(MAOs) and Prescription Drug Plans
(PDPs) are required to submit an
actuarial pricing ‘‘bid’’ for each plan
offered to Medicare beneficiaries for
approval by the Centers for Medicare &
Medicaid Services (CMS).
Medicare Advantage organizations
(MAO) and Prescription Drug Plans
(PDP) are required to submit an
actuarial pricing ‘‘bid’’ for each plan
offered to Medicare beneficiaries for
approval by CMS. The MAOs and PDPs
use the Bid Pricing Tool (BPT) software
PO 00000
Frm 00081
Fmt 4703
Sfmt 4703
to develop their actuarial pricing bid.
The competitive bidding process
defined by the ‘‘The Medicare
Prescription Drug, Improvement, and
Modernization Act’’ (MMA) applies to
both the MA and Part D programs. It is
an annual process that encompasses the
release of the MA rate book in April, the
bid’s that plans submit to CMS in June,
and the release of the Part D and RPPO
benchmarks, which typically occurs in
August. Form Number: CMS–10142
(OMB control number: 0938–0944);
Frequency: Yearly; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 555; Total
Annual Responses: 4995; Total Annual
Hours: 149,850. (For policy questions
regarding this collection contact Rachel
Shevland at 410–786–3026.)
Dated: December 20, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2019–27926 Filed 12–26–19; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[CFDA Numbers: 93.581, 93.587, 93.612]
Notice for Public Comment on
Administration for Native Americans’
Program Policies and Procedures
Administration for Native
Americans (ANA), Administration for
Children and Families (ACF),
Department of Health and Human
Services (HHS).
ACTION: Notice for public comment.
AGENCY:
Pursuant to Section 814 of the
Native American Programs Act of 1974
(NAPA), as amended, the ANA is
required to provide members of the
public an opportunity to comment on
proposed changes in interpretive rules
and general statements of policy and to
give notice of the proposed changes no
less than 30 days before such changes
become effective. In accordance with
notice requirements of NAPA, ANA
herein describes proposed interpretive
rules and general statements of policy
that relate to ANA’s funding
opportunities in Fiscal Year (FY) 2020.
Changes to FY 2020 Funding
Opportunity Announcements (FOAs)
will be based on the following
previously published programs:
Environmental Regulatory Enhancement
(ERE), HHS–2018–ACF–ANA–NR–1344;
Native American Language Preservation
SUMMARY:
E:\FR\FM\27DEN1.SGM
27DEN1
Agencies
[Federal Register Volume 84, Number 248 (Friday, December 27, 2019)]
[Notices]
[Pages 71427-71428]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-27926]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-10701, CMS-10191 and CMS-10142]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid 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 27, 2020.
ADDRESSES: When commenting on the proposed information collections,
please reference the document identifier or OMB control number. To be
assured consideration, comments and recommendations must be received by
the OMB desk officer via one of the following transmissions: OMB,
Office of Information and Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395-5806 OR, Email:
[email protected].
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/PRA-Listing.html.
1. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to [email protected].
2. Call the Reports Clearance Office at (410) 786-1326.
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: New collection (Request
for a new OMB control number); Title of Information Collection:
Medicare Beneficiary Experiences with Care Survey System; Use: The
MBECS system is designed to conduct 1-2 surveys per year on priority
groups of interest, thereby allowing CMS OMH to respond quickly to the
data needs of stakeholders with interests in these underrepresented
groups. Data collected through the MBECS system will be used to better
understand--and thus serve the needs of--Medicare beneficiaries in
minority populations. The core questionnaire will collect information
on communication with medical professionals, coordination of health
care, experiences getting needed health care, experiences with personal
doctors and specialists, and key demographics. Data will be compared to
benchmarks from the FFS CAHPS, MA CAHPS, and
[[Page 71428]]
NAM CAHPS surveys. The population-specific questionnaire module will
collect information about issues most relevant for particular minority
groups; population-specific modules will be described in individual
information collection requests. These data will be compared to
benchmarks from the relevant CAHPS source surveys when available.
Collection of these data from people who have been identified
through CMS administrative data and administrative flags as part of
specific minority populations will also serve as a critical validation
step of this method for identifying difficult-to-study populations,
thus making it easier to study beneficiaries in these groups in the
future. Form Number: CMS-10701 (OMB control number: 0938-NEW);
Frequency: Yearly; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 10,000; Total Annual Responses:
10,000; Total Annual Hours: 3,333. (For policy questions regarding this
collection contact Luis Perez at 410-786-8557.)
2. Type of Information Collection Request: Revision with change of
a currently approved collection; Title of Information Collection:
Medicare Parts C and D Program Audit Protocols and Data Requests; Use:
Under the Medicare Prescription Drug, Improvement, and Modernization
Act of 2003 and implementing regulations at 42 CFR parts 422 and 423,
Medicare Part D plan sponsors and Medicare Advantage organizations are
required to comply with all Medicare Parts C and D program
requirements. CMS' annual audit plan ensures that we evaluate
sponsoring organizations' compliance with these requirements. CMS
program audits focus on high-risk areas that have the greatest
potential for beneficiary harm. As such, CMS has developed several
audit protocols that are included within the program area data request
documents and that are posted to the CMS website each year for use by
sponsoring organizations to prepare for their audit. As part of a
robust audit process, CMS also requires sponsoring organizations who
have been audited and found to have deficiencies to undergo a
validation audit to ensure correction. The validation audit utilizes
the same audit protocols, but only tests the elements where
deficiencies were found, as opposed to re-administering the entire
audit.
Currently CMS utilizes the following 5 protocols to audit
sponsoring organization performance: Part D Formulary and Benefit
Administration (FA); Part D Coverage Determinations, Appeals, and
Grievances (CDAG); Part C Organization Determinations, Appeals, and
Grievances (ODAG); Special Needs Model of Care (SNP-MOC) (only
administered on organizations who operate SNPs); and, Compliance
Program Effectiveness (CPE). The data collected is detailed in each of
these protocols and the exact fields are located in the record layouts,
at the end of each protocol. In addition, this collection request
includes a pre-audit issue summary, three CPE questionnaires, one CPE
organizational structure presentation template, one FA impact analysis
template, two CDAG impact analysis templates, four ODAG impact analysis
templates, three SNP-MOC impact analysis templates, and a SNP-MOC
questionnaire.
The information gathered during this audit will be used by the
Medicare Parts C and D Oversight and Enforcement Group (MOEG) within
the Center for Medicare (CM) and CMS Regional Offices to assess
sponsoring organizations' compliance with Medicare program
requirements. If outliers or other data anomalies are detected,
Regional Offices will work in collaboration with MOEG and other
divisions within CMS for follow-up and resolution. Additionally, MA and
Part D organizations will receive the audit results and will be
required to implement corrective action to correct any identified
deficiencies. Form Number: CMS-10191 (OMB control number: 0938-1000);
Frequency: Yearly; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 201; Total Annual Responses: 207;
Total Annual Hours: 39,456. (For policy questions regarding this
collection contact Brenda Hudson at 443-743-9299.)
3. Type of Information Collection Request: Revision with change of
a currently approved collection; Title of Information Collection: Bid
Pricing Tool (BPT) for Medicare Advantage (MA) Plans and Prescription
Drug Plans (PDP); Use: Under the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA), and implementing
regulations at 42 CFR, Medicare Advantage organizations (MAOs) and
Prescription Drug Plans (PDPs) are required to submit an actuarial
pricing ``bid'' for each plan offered to Medicare beneficiaries for
approval by the Centers for Medicare & Medicaid Services (CMS).
Medicare Advantage organizations (MAO) and Prescription Drug Plans
(PDP) are required to submit an actuarial pricing ``bid'' for each plan
offered to Medicare beneficiaries for approval by CMS. The MAOs and
PDPs use the Bid Pricing Tool (BPT) software to develop their actuarial
pricing bid. The competitive bidding process defined by the ``The
Medicare Prescription Drug, Improvement, and Modernization Act'' (MMA)
applies to both the MA and Part D programs. It is an annual process
that encompasses the release of the MA rate book in April, the bid's
that plans submit to CMS in June, and the release of the Part D and
RPPO benchmarks, which typically occurs in August. Form Number: CMS-
10142 (OMB control number: 0938-0944); Frequency: Yearly; Affected
Public: State, Local, or Tribal Governments; Number of Respondents:
555; Total Annual Responses: 4995; Total Annual Hours: 149,850. (For
policy questions regarding this collection contact Rachel Shevland at
410-786-3026.)
Dated: December 20, 2019.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2019-27926 Filed 12-26-19; 8:45 am]
BILLING CODE 4120-01-P