Agency Information Collection Activities: Submission for OMB Review; Comment Request, 20023-20024 [2012-8080]
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Federal Register / Vol. 77, No. 64 / Tuesday, April 3, 2012 / Notices
20023
substances must be submitted within 30
days of the publication of this notice.
Substances To Be Evaluated for Set 26
Toxicological Profiles
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
You may submit
nominations, identified by Docket No.
ATSDR–2012–0001, by any of the
following methods:
• Internet: Access the Federal
eRulemaking portal at https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Division of Toxicology and
Human Health Sciences (proposed),
1600 Clifton Rd. NE., MS F–62, Atlanta,
Georgia 30333.
Instructions: All submissions must
include the agency name and docket
number for this notice. All relevant
comments will be posted without
change. This means that no confidential
business information or other
confidential information should be
submitted in response to this notice.
Refer to the section Submission of
Nominations (below) for the specific
information required.
Each year, ATSDR develops a list of
substances to be considered for
toxicological profile development. The
Set 26 nomination process includes
consideration of all substances on the
ATSDR’s Substance Priority List (SPL)
as well as other substances nominated
by the public. The 275 substances on
the list will be considered for Set 26
Toxicological Profile development. This
list may be found at the following Web
site: www.atsdr.cdc.gov/SPL, and in the
docket at www.regulations.gov.
Submission of Nominations for the
evaluation of Set 26 Substances:
Today’s notice invites voluntary public
nominations for substances included on
the SPL and for substances not listed on
the SPL. All nominations should
include full name of the nominator,
affiliation, and email address. When
nominating a non-SPL substance, please
include the rationale for the
nomination. Please note, email
addresses will not be posted on
regulations.gov.
ATSDR will evaluate all data and
information associated with nominated
substances and will determine the final
list of substances to be chosen for
toxicological profile development.
Substances will be chosen according to
ATSDR’s specific guidelines for
selection. These guidelines can be found
in the Selection Criteria announced in
the Federal Register on May 7, 1993
(58FR27286–27287). A hard copy of the
Selection Criteria is available upon
request or may be accessed at: https://
www.atsdr.cdc.gov/toxprofiles/
guidance/criteria_for_selecting_tp_
support.pdf.
Please ensure that your comments are
submitted within the specified
nomination period. Nominations
received after the closing date will be
marked as late and may be considered
only if time and resources permit.
Centers for Medicare & Medicaid
Services
ADDRESSES:
For
further information, please contact CDR
Jessilynn Taylor, Division of Toxicology
and Human Health Sciences (proposed),
1600 Clifton Rd. NE., MS F–62, Atlanta,
Georgia 30333, Email:
tpcandidatecomments@cdc.gov; phone:
1–800–232–4636.
FOR FURTHER INFORMATION CONTACT:
The
Superfund Amendments and
Reauthorization Act of 1986 (SARA)
[42 U.S.C. 9601 et seq.] amended the
Comprehensive Environmental
Response, Compensation, and Liability
Act of 1980 (CERCLA or Superfund) [42
U.S.C. 9601 et seq.] by establishing
certain requirements for ATSDR and the
U.S. Environmental Protection Agency
(EPA) with regard to hazardous
substances most commonly found at
facilities on the CERCLA National
Priorities List (NPL). Among these
statutory requirements is a mandate for
the Administrator of ATSDR to prepare
toxicological profiles for each substance
included on the Priority List of
Hazardous Substances (also called the
Substance Priority List). This list
identifies 275 hazardous substances that
ATSDR (in cooperation with EPA) have
determined pose the most significant
potential threat to human health. The
availability of the revised list of the 275
priority substances was announced in
the Federal Register on November 3rd,
2011 (76 FR 68193). For prior versions
of the list of substances, see Federal
Register notices dated December 7, 2005
(70 FR 70284); and March 6, 2008
(73 FR 12178).
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SUPPLEMENTARY INFORMATION:
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Dated: March 28, 2012.
Ken Rose,
Director, Office of Policy, Planning and
Evaluation, National Center for
Environmental Health/Agency for Toxic
Substances and Disease Registry.
[FR Doc. 2012–7975 Filed 4–2–12; 8:45 am]
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[Document Identifier: CMS–10418]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
and Human Services, is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate 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 function;
(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.
1. Title of Information Collection:
Annual MLR and Rebate Calculation
Report; Type of Collection: New
collection; Use: Under Section 2718 of
the Affordable Care Act and
implementing regulation at 45 CFR Part
158 (75 FR 74865, December 1, 2010) as
modified by technical corrections on
December 30, 2010 (75 FR 82277), a
health insurance issuer (issuer) offering
group or individual health insurance
coverage must submit a report to the
Secretary concerning the amount the
issuer spends each year on claims,
quality improvement expenses, nonclaims costs, Federal and State taxes
and licensing and regulatory fees, and
the amount of earned premium. An
issuer must provide an annual rebate to
enrollees if the amount it spends on
certain costs compared to its premium
revenue (excluding Federal and State
taxes and licensing and regulatory fees)
does not meet a certain ratio, referred to
as the medical loss ratio (MLR). An
interim final rule (IFR) implementing
the MLR was published on December 1,
2010 (75 FR 74865) and modified by
technical corrections on December 30,
2010 (75 FR 82277), which added Part
158 to Title 45 of the Code of Federal
Regulations. The IFR is effective January
AGENCY:
E:\FR\FM\03APN1.SGM
03APN1
20024
Federal Register / Vol. 77, No. 64 / Tuesday, April 3, 2012 / Notices
1, 2011. A final rule regarding selected
provisions of the IFR was published on
December 7, 2011 (76 FR 76574, CMS–
9998–FC) and an interim final rule
regarding an issue not included in
issuers’ reporting obligations
(disbursement of rebates by non-federal
governmental plans) was also published
December 7, 2011 (76 FR 76596, CMS–
9998–IFC2). Both rules published on
December 7, 2011 are effective January
1, 2012. Each issuer is required to
submit annually MLR data, including
information about any rebates it must
provide, on a form prescribed by CMS,
for each State in which the issuer
conducts business. Each issuer is also
required to provide a rebate notice to
each enrollee that is due a rebate
payment for any given MLR reporting
year. Additionally, each issuer is
required to maintain for a period of
seven years all documents, records and
other evidence that support the data
included in each issuer’s annual report
to the Secretary.
The original 60-day comment period
began on December 16, 2011 and
pertained to the MLR Annual Reporting
Form, and closed on February 14, 2012.
On February 16, we published an
amended PRA package with Notices to
Consumers and reopened the public
comment period until March 2, 2012 to
accommodate comments on the
amendments to the PRA package. We
received a total of 15 public comments
regarding the Annual Reporting Form
and 11 public comments regarding the
Notices to Consumers and Instructions
for these notices. Most public comments
addressed multiple issues. We have
taken into consideration all the
proposed suggestions and have made
changes to the Annual Reporting Form
and Instructions, as well as to the
Notices to Consumers and Instructions.
In addition, CMS is adjusting the
estimated burden that correlates with
the Rebate Notices and the MLR
Information Notices.
Form Number: CMS–10418 (OCN:
0938–New); Frequency: Annual
submission for each respondent;
Affected Public: Private Sector: Business
or other for-profits and not-for-profit
institutions; Number of Respondents:
527; Number of Responses: 5,530; Total
Annual Hours: 352,563. (For policy
questions regarding this collection,
contact Carol Jimenez at (301) 492–
4457. For all other issues, call (410)
786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS Web site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or email
your request, including your address,
phone number, OMB number, and CMS
document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received by the OMB desk officer at
the address below, no later than 5 p.m.
on May 3, 2012.
OMB, Office of Information and
Regulatory Affairs, Attention: CMS
Desk Officer, Fax Number: (202) 395–
6974, Email:
OIRA_submission@omb.eop.gov.
Dated: March 30, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–8080 Filed 4–2–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
OMB No.: New Collection.
Description: The Study of
Coordination of Tribal TANF and Child
Welfare Services is sponsored by the
Office of Planning, Research and
Evaluation (OPRE), Administration for
Children and Families of the U.S.
Department of Health and Human
Services. The study examines the
approaches and strategies utilized by
tribes and tribal organizations that were
awarded the grants for Coordination of
Tribal TANF and Child Welfare Services
to Tribal Families at Risk of Child
Abuse or Neglect.
The descriptive study of these
programs that serve tribal communities
will document the way in which the
tribal grantees are creating and adapting
culturally relevant and appropriate
approaches, systems, and programs to
increase coordination and enhance
service delivery to address child abuse
and neglect. The study will also
document challenges faced and lessons
learned to inform the field of practice as
well as policymakers and funders at
various levels.
The proposed information collection
activities consist of semi-structured
interviews, conducted at each of the 14
tribal communities, and a grantee
feedback survey on the usefulness of
periodically held cross-grantee learning
events.
Respondents: Program director(s),
tribal TANF and child welfare staff and
supervisors, program partners, and
tribal leaders or elders. The information
collection does not include direct
interaction with individuals or families
that receive the services.
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Study of Coordination of Tribal
TANF and Child Welfare Services.
ANNUAL BURDEN ESTIMATES
Annual
number of
respondents
mstockstill on DSK4VPTVN1PROD with NOTICES
Instrument
Interview Protocol for Program Staff .............................................................
Interview Protocol for TANF and CW Staff ...................................................
Interview Protocol for Tribal or Community Partners ....................................
Interview Protocol for Tribal Leaders or Elders .............................................
Feedback Form for Community of Learning Events .....................................
Estimated Total Annual Burden
Hours: 153.
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Average burden
hours per
response
3
3
3
3
5
1.5
1
.75
1
.15
9
19
9
9
10
In compliance with the requirements
of Section 3506(c)(2)(A) of the
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Number of
responses per
respondent
Total annual
burden hours
Paperwork Reduction Act of 1995, the
Administration for Children and
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8
Agencies
[Federal Register Volume 77, Number 64 (Tuesday, April 3, 2012)]
[Notices]
[Pages 20023-20024]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-8080]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10418]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS), Department of Health and Human Services, is publishing
the following summary of proposed collections for public comment.
Interested persons are invited to send comments regarding this burden
estimate 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 function; (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.
1. Title of Information Collection: Annual MLR and Rebate
Calculation Report; Type of Collection: New collection; Use: Under
Section 2718 of the Affordable Care Act and implementing regulation at
45 CFR Part 158 (75 FR 74865, December 1, 2010) as modified by
technical corrections on December 30, 2010 (75 FR 82277), a health
insurance issuer (issuer) offering group or individual health insurance
coverage must submit a report to the Secretary concerning the amount
the issuer spends each year on claims, quality improvement expenses,
non-claims costs, Federal and State taxes and licensing and regulatory
fees, and the amount of earned premium. An issuer must provide an
annual rebate to enrollees if the amount it spends on certain costs
compared to its premium revenue (excluding Federal and State taxes and
licensing and regulatory fees) does not meet a certain ratio, referred
to as the medical loss ratio (MLR). An interim final rule (IFR)
implementing the MLR was published on December 1, 2010 (75 FR 74865)
and modified by technical corrections on December 30, 2010 (75 FR
82277), which added Part 158 to Title 45 of the Code of Federal
Regulations. The IFR is effective January
[[Page 20024]]
1, 2011. A final rule regarding selected provisions of the IFR was
published on December 7, 2011 (76 FR 76574, CMS-9998-FC) and an interim
final rule regarding an issue not included in issuers' reporting
obligations (disbursement of rebates by non-federal governmental plans)
was also published December 7, 2011 (76 FR 76596, CMS-9998-IFC2). Both
rules published on December 7, 2011 are effective January 1, 2012. Each
issuer is required to submit annually MLR data, including information
about any rebates it must provide, on a form prescribed by CMS, for
each State in which the issuer conducts business. Each issuer is also
required to provide a rebate notice to each enrollee that is due a
rebate payment for any given MLR reporting year. Additionally, each
issuer is required to maintain for a period of seven years all
documents, records and other evidence that support the data included in
each issuer's annual report to the Secretary.
The original 60-day comment period began on December 16, 2011 and
pertained to the MLR Annual Reporting Form, and closed on February 14,
2012. On February 16, we published an amended PRA package with Notices
to Consumers and reopened the public comment period until March 2, 2012
to accommodate comments on the amendments to the PRA package. We
received a total of 15 public comments regarding the Annual Reporting
Form and 11 public comments regarding the Notices to Consumers and
Instructions for these notices. Most public comments addressed multiple
issues. We have taken into consideration all the proposed suggestions
and have made changes to the Annual Reporting Form and Instructions, as
well as to the Notices to Consumers and Instructions. In addition, CMS
is adjusting the estimated burden that correlates with the Rebate
Notices and the MLR Information Notices.
Form Number: CMS-10418 (OCN: 0938-New); Frequency: Annual
submission for each respondent; Affected Public: Private Sector:
Business or other for-profits and not-for-profit institutions; Number
of Respondents: 527; Number of Responses: 5,530; Total Annual Hours:
352,563. (For policy questions regarding this collection, contact Carol
Jimenez at (301) 492-4457. For all other issues, call (410) 786-1326.)
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS Web
site address at https://www.cms.hhs.gov/PaperworkReductionActof1995, or
email your request, including your address, phone number, OMB number,
and CMS document identifier, to Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786-1326.
To be assured consideration, comments and recommendations for the
proposed information collections must be received by the OMB desk
officer at the address below, no later than 5 p.m. on May 3, 2012.
OMB, Office of Information and Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395-6974, Email: OIRA_submission@omb.eop.gov.
Dated: March 30, 2012.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2012-8080 Filed 4-2-12; 8:45 am]
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