Emergency Clearance: Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB), 52478-52479 [2015-21476]
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Federal Register / Vol. 80, No. 168 / Monday, August 31, 2015 / Notices
achieved by Hospira, and advice and
training from knowledgeable employees
of the parties.
The purpose of this analysis is to
facilitate public comment on the
proposed Consent Agreement, and it is
not intended to constitute an official
interpretation of the proposed Order or
to modify its terms in any way.
By direction of the Commission.
Donald S. Clark,
Secretary.
[Docket No.: 108002015–1111–07]
Notice of Standard Terms and
Conditions for Council Grants
Gulf Coast Ecosystem
Restoration Council.
AGENCY:
Notice.
The Gulf Coast Ecosystem
Restoration Council (Council) has
established Financial Assistance
Standard Terms and Conditions (STCs)
that will apply to all grants awarded by
the Council.
SUMMARY:
The STCs are effective on August
31, 2015.
DATES:
FOR FURTHER INFORMATION CONTACT:
Kristin Smith, Council staff, telephone
number: 504–444–3558.
The
Council is authorized to award grants
pursuant to the Council-Selected
Restoration and Spill Impact
Components of the Resources and
Ecosystems Sustainability, Tourist
Opportunities, and Revived Economies
of the Gulf Coast States Act of 2012
(RESTORE Act), 33 U.S.C. 1321(t)(2)
and 1321(t)(3). The Council has
established STCs that will apply to and
be incorporated into all grants awarded
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be viewed and downloaded at
www.restorethegulf.gov/resources/foialibrary-council-documents.
SUPPLEMENTARY INFORMATION:
tkelley on DSK3SPTVN1PROD with NOTICES
Emergency Clearance: Public
Information Collection Requirements
Submitted to the Office of Management
and Budget (OMB)
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 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
We are, however, requesting an
emergency review of the information
collection referenced below. In
compliance with the requirement of
section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, we have
submitted to the Office of Management
and Budget (OMB) the following
requirements for emergency review.
This is necessary to ensure compliance
with an initiative of the Administration.
We are requesting an emergency review
under 5 CFR 1320.13(a)(2)(i) because
public harm is reasonably likely to
result if the normal clearance
procedures are followed. We are seeking
emergency approval for modifications to
the information collection request (ICR)
currently approved under Office of
Management and Budget (OMB) control
number 0938–1155. CMS seeks an
emergency revision to the ICR approved
under 0938–1155 to collect additional
information from health insurance
companies as part of the MLR and risk
corridors programs. This ICR is
necessary to validate data that issuers
have previously submitted to CMS in
SUMMARY:
GULF COAST ECOSYSTEM
RESTORATION COUNCIL
Will D. Spoon,
Program Analyst, Gulf Coast Ecosystem
Restoration Council.
[FR Doc. 2015–21417 Filed 8–28–15; 8:45 am]
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[Document Identifiers: CMS–10401]
Centers for Medicare &
Medicaid Services.
ACTION: Notice.
BILLING CODE 6750–01–P
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Centers for Medicare & Medicaid
Services
AGENCY:
[FR Doc. 2015–21513 Filed 8–28–15; 8:45 am]
ACTION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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more detail than CMS has previously
anticipated. While conducting program
integrity reviews of submitted data,
CMS has identified a number of
significant discrepancies in the 2014
benefit year submissions that issuers
made for MLR and risk corridors on July
31, 2015. CMS also identified a number
of common errors that may lead to
submissions that do not comply with
CMS regulations and guidance. In order
to resolve these potential discrepancies,
ensure all submissions comply with
applicable guidance, and operate the
MLR and risk corridors program
accurately and effectively, CMS needs
additional information to explain the
data found in issuers’ underlying MLR
and risk corridors submissions. Without
this additional information, CMS will be
unable to verify the accuracy of the
submission and validate the data
needed to operate the MLR or risk
corridors programs.
DATES: Comments must be received by
September 3, 2015.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: CMS–10401/OMB Control
Number 0938–1155, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
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’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
E:\FR\FM\31AUN1.SGM
31AUN1
Federal Register / Vol. 80, No. 168 / Monday, August 31, 2015 / Notices
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–10401 Standards Related to
Reinsurance, Risk Corridors, and Risk
Adjustment
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. In
compliance with the requirement of
section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, we have
submitted to the Office of Management
and Budget (OMB) the following
requirements for emergency review.
This is necessary to ensure compliance
with an initiative of the Administration.
We are requesting an emergency review
under 5 CFR 1320.13(a)(2)(i) because
public harm is reasonably likely to
result if the normal clearance
procedures are followed.
tkelley on DSK3SPTVN1PROD with NOTICES
Information Collection
1. Type of Information Collection
Request: Revision of a currently
approved information collection; Title
of Information Collection: Standards
Related to Reinsurance, Risk Corridors,
and Risk Adjustment; Use: Under
Section 1342 of the Patient Protection
and Affordable Care Act and
implementing regulation at 45 CFR part
153, issuers of qualified health plans
(QHPs) must participate in a risk
corridors program. A QHP issuer will
pay risk corridors charges or be eligible
to receive risk corridors payments or
based on the ratio of the issuer’s
allowable costs to the target amount. A
final rule (Standards Related to
Reinsurance, Risk Corridors and Risk
Adjustment) implementing the risk
corridors program was published on
March 23, 2012 (77 FR 17220), which
added part 153 to title 45 of the Code
of Federal Regulations. Final rules
(2014, 2015, and 2016 Payment Notices)
outlining the risk corridors benefit and
payment parameters for the 2014, 2015,
and 2016 benefit years were published
on March 11, 2013 (78 FR 15410),
March 11, 2014 (79 FR 13744), and
February 27, 2015 (80 FR 10750),
VerDate Sep<11>2014
16:19 Aug 28, 2015
Jkt 235001
respectively. Additionally, on October
30, 2013, HHS published the Second
Final Program Integrity rule (78 FR
65076) to align the risk corridors
program with the requirements of the
single risk pool provision at 45 CFR
156.80. The risk corridors data
collection applies to QHP issuers the
individual and small group markets.
Each QHP issuer is required to submit
an annual report to CMS concerning the
issuer’s allowable costs, allowable
administrative costs, premium, and
proportion of market premium in QHPs.
Risk corridors premium information
that is specific to an issuer’s QHPs is
collected through a separate data
reporting form.
The risk corridors plan-level reporting
form, and instructions for completing
the form were published as part of the
information collection approved under
OMB control number 0938–1164. In
§§ 153.530 and 153.540 we set forth a
data validation process for risk corridors
data submissions. The information
collection burden associated with the
risk corridors data validation process is
accounted for in the ‘‘Supporting
Statement for Paperwork Reduction Act
Submissions: Standards Related to
Reinsurance, Risk Corridors, Risk
Adjustment, and Appeals’’ approved
under OMB control number 0938–1155.
Based on CMS’s identification of more
significant data discrepancies than
previously anticipated, we are
requesting an emergency revision to the
risk corridors data validation
information collection requirement. We
are requiring all companies with QHP
issuers to complete a checklist to attest
that their submission complied with
critical guidelines for risk corridors and
MLR data submission. For companies
with issuers whose reported claims or
premium amounts for risk corridors and
MLR differ from data collected for other
premium stabilization programs by a
greater magnitude than expected, CMS
is requiring that issuers quantify these
differences, and provide a written
explanation of the magnitude of the
discrepancy. We require these
descriptions to be approved by an
actuary. The MLR Risk Corridors
Submission Checklist and the Risk
Corridors Data Discrepancy Worksheet
will be submitted via web form at the
company level, such that a company
will submit one checklist and one
discrepancy worksheet that includes
information for all of its applicable
issuers. As a result of this new
requirement, we are updating our
annual burden hour estimates to reflect
the actual numbers of risk corridors
submissions received by QHP issuers
and the increased annual burden hours
PO 00000
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52479
associated with submitting additional
data validation information to CMS.
Form Number: CMS–10401 (OMB
control number: 0938–1155); Frequency:
Annual; Affected Public: Health
insurance companies that issued
qualified health plans; Number of
Respondents: 250; Total Annual
Responses: 250; Total Annual Hours:
2,040. (For policy questions regarding
this collection contact Jaya Ghildiyal at
301–492–5149).
We are requesting OMB review and
approval of this collection by September
4, 2015, with a 180-day approval period.
Written comments and
recommendations will be considered
from the public if received by the date
and address noted above.
Dated: August 26, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2015–21476 Filed 8–27–15; 4:15 pm]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
Notice is hereby given that
the Office of Research Integrity (ORI)
has taken final action in the following
case:
Peter Littlefield, University of
California, San Francisco: Based on an
assessment conducted by the University
of California, San Francisco (UCSF), the
Respondent’s admission, and analysis
conducted by ORI, ORI and UCSF found
that Mr. Peter Littlefield, Graduate
Student on a leave of absence from the
Tetrad Graduate Program, UCSF,
engaged in research misconduct in
research supported by National Institute
of General Medical Sciences (NIGMS),
National Institutes of Health (NIH),
training grant T32 GM007810 and grant
R01 GM109176.
ORI found that the Respondent
engaged in research misconduct by
falsifying and/or fabricating data in the
following two (2) publications:
• Science Signaling 7:ra114, 2014
(hereafter referred to as ‘‘Paper 1’’)
• Chemistry & Biology 21:453–458,
2014 (hereafter referred to as ‘‘Paper
2’’)
ORI found that Respondent
knowingly falsified and/or fabricated
data and related text by altering the
SUMMARY:
E:\FR\FM\31AUN1.SGM
31AUN1
Agencies
[Federal Register Volume 80, Number 168 (Monday, August 31, 2015)]
[Notices]
[Pages 52478-52479]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-21476]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10401]
Emergency Clearance: Public Information Collection Requirements
Submitted to the Office of Management and Budget (OMB)
AGENCY: Centers for Medicare & Medicaid Services.
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 (the PRA), federal agencies are required to publish notice
in the Federal Register concerning each proposed collection of
information. Interested persons are invited to send comments regarding
our burden estimates or any other aspect of this collection of
information, including any of the following subjects: (1) The necessity
and utility of the proposed information collection for the proper
performance of the agency's functions; (2) the accuracy of the
estimated burden; (3) ways to enhance the quality, utility, and clarity
of the information to be collected; and (4) the use of automated
collection techniques or other forms of information technology to
minimize the information collection burden.
We are, however, requesting an emergency review of the information
collection referenced below. In compliance with the requirement of
section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, we have
submitted to the Office of Management and Budget (OMB) the following
requirements for emergency review. This is necessary to ensure
compliance with an initiative of the Administration. We are requesting
an emergency review under 5 CFR 1320.13(a)(2)(i) because public harm is
reasonably likely to result if the normal clearance procedures are
followed. We are seeking emergency approval for modifications to the
information collection request (ICR) currently approved under Office of
Management and Budget (OMB) control number 0938-1155. CMS seeks an
emergency revision to the ICR approved under 0938-1155 to collect
additional information from health insurance companies as part of the
MLR and risk corridors programs. This ICR is necessary to validate data
that issuers have previously submitted to CMS in more detail than CMS
has previously anticipated. While conducting program integrity reviews
of submitted data, CMS has identified a number of significant
discrepancies in the 2014 benefit year submissions that issuers made
for MLR and risk corridors on July 31, 2015. CMS also identified a
number of common errors that may lead to submissions that do not comply
with CMS regulations and guidance. In order to resolve these potential
discrepancies, ensure all submissions comply with applicable guidance,
and operate the MLR and risk corridors program accurately and
effectively, CMS needs additional information to explain the data found
in issuers' underlying MLR and risk corridors submissions. Without this
additional information, CMS will be unable to verify the accuracy of
the submission and validate the data needed to operate the MLR or risk
corridors programs.
DATES: Comments must be received by September 3, 2015.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number. To be assured consideration, comments and
recommendations must be submitted in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) that are accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: CMS-10401/OMB Control
Number 0938-1155, Room C4-26-05, 7500 Security Boulevard, Baltimore,
Maryland 21244-1850.
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' Web site address at https://www.cms.hhs.gov/PaperworkReductionActof1995.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: Reports Clearance Office at (410) 786-
1326.
SUPPLEMENTARY INFORMATION:
[[Page 52479]]
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-10401 Standards Related to Reinsurance, Risk Corridors, and Risk
Adjustment
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. In compliance with the requirement of section
3506(c)(2)(A) of the Paperwork Reduction Act of 1995, we have submitted
to the Office of Management and Budget (OMB) the following requirements
for emergency review. This is necessary to ensure compliance with an
initiative of the Administration. We are requesting an emergency review
under 5 CFR 1320.13(a)(2)(i) because public harm is reasonably likely
to result if the normal clearance procedures are followed.
Information Collection
1. Type of Information Collection Request: Revision of a currently
approved information collection; Title of Information Collection:
Standards Related to Reinsurance, Risk Corridors, and Risk Adjustment;
Use: Under Section 1342 of the Patient Protection and Affordable Care
Act and implementing regulation at 45 CFR part 153, issuers of
qualified health plans (QHPs) must participate in a risk corridors
program. A QHP issuer will pay risk corridors charges or be eligible to
receive risk corridors payments or based on the ratio of the issuer's
allowable costs to the target amount. A final rule (Standards Related
to Reinsurance, Risk Corridors and Risk Adjustment) implementing the
risk corridors program was published on March 23, 2012 (77 FR 17220),
which added part 153 to title 45 of the Code of Federal Regulations.
Final rules (2014, 2015, and 2016 Payment Notices) outlining the risk
corridors benefit and payment parameters for the 2014, 2015, and 2016
benefit years were published on March 11, 2013 (78 FR 15410), March 11,
2014 (79 FR 13744), and February 27, 2015 (80 FR 10750), respectively.
Additionally, on October 30, 2013, HHS published the Second Final
Program Integrity rule (78 FR 65076) to align the risk corridors
program with the requirements of the single risk pool provision at 45
CFR 156.80. The risk corridors data collection applies to QHP issuers
the individual and small group markets. Each QHP issuer is required to
submit an annual report to CMS concerning the issuer's allowable costs,
allowable administrative costs, premium, and proportion of market
premium in QHPs. Risk corridors premium information that is specific to
an issuer's QHPs is collected through a separate data reporting form.
The risk corridors plan-level reporting form, and instructions for
completing the form were published as part of the information
collection approved under OMB control number 0938-1164. In Sec. Sec.
153.530 and 153.540 we set forth a data validation process for risk
corridors data submissions. The information collection burden
associated with the risk corridors data validation process is accounted
for in the ``Supporting Statement for Paperwork Reduction Act
Submissions: Standards Related to Reinsurance, Risk Corridors, Risk
Adjustment, and Appeals'' approved under OMB control number 0938-1155.
Based on CMS's identification of more significant data
discrepancies than previously anticipated, we are requesting an
emergency revision to the risk corridors data validation information
collection requirement. We are requiring all companies with QHP issuers
to complete a checklist to attest that their submission complied with
critical guidelines for risk corridors and MLR data submission. For
companies with issuers whose reported claims or premium amounts for
risk corridors and MLR differ from data collected for other premium
stabilization programs by a greater magnitude than expected, CMS is
requiring that issuers quantify these differences, and provide a
written explanation of the magnitude of the discrepancy. We require
these descriptions to be approved by an actuary. The MLR Risk Corridors
Submission Checklist and the Risk Corridors Data Discrepancy Worksheet
will be submitted via web form at the company level, such that a
company will submit one checklist and one discrepancy worksheet that
includes information for all of its applicable issuers. As a result of
this new requirement, we are updating our annual burden hour estimates
to reflect the actual numbers of risk corridors submissions received by
QHP issuers and the increased annual burden hours associated with
submitting additional data validation information to CMS. Form Number:
CMS-10401 (OMB control number: 0938-1155); Frequency: Annual; Affected
Public: Health insurance companies that issued qualified health plans;
Number of Respondents: 250; Total Annual Responses: 250; Total Annual
Hours: 2,040. (For policy questions regarding this collection contact
Jaya Ghildiyal at 301-492-5149).
We are requesting OMB review and approval of this collection by
September 4, 2015, with a 180-day approval period. Written comments and
recommendations will be considered from the public if received by the
date and address noted above.
Dated: August 26, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2015-21476 Filed 8-27-15; 4:15 pm]
BILLING CODE 4120-01-P