Submission for OMB Review; Comment Request, 11250-11251 [2011-4418]
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11250
Federal Register / Vol. 76, No. 40 / Tuesday, March 1, 2011 / Notices
Review Final Determination will be
posted as part of the rate review
consumer disclosure information on an
HHS Web site.
Final Justification for an Unreasonable
Rate Increase
The proposed rule states that if a
health insurance issuer implements a
rate increase determined by HHS or a
State to be unreasonable, the health
insurance issuer must provide a Final
Justification for an Unreasonable Rate
Increase. In the Final Justification,
issuers would have to provide a short
statement about why they are electing to
implement an unreasonable rate
increase. This statement would be
entered into a data entry text box in the
Rate Review Data Collection System and
would not need to be more than a
paragraph or two in length. There is no
form or instructions associated with this
statement apart from the requirements
provided in the proposed regulation.
The Final Justification Statement will
be posted on an HHS Web site in the
same location as the Preliminary
Justification and Rate Review Final
Determination. Additionally, health
insurance issuers implementing rate
increases that were determined to be
unreasonable, must post all of this
information—the Preliminary
Justification, the Rate Review Final
Determination, and the Final
Justification Statement on their Web
sites for a period of 3 years.
Form Number: CMS–10379; (OMB
Control No. 0938–NEW) Frequency:
Annually; Affected Public: Private
Sector; Number of Respondents: 1,543
Number of Responses: 1,546; Total
Annual Hours: 8,418. (For policy
questions regarding this collection,
contact Sally McCarty at (301) 492–4489
or RateReview@hhs.gov. 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
at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or e-
mail your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office at 410–786–
1326.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by May 2, 2011:
1. Electronically. You may submit
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) 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: Document Identifier/OMB
Control Number, Room C4–26–05, 7500
Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: February 23, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–4552 Filed 2–25–11; 11:15 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Child Care and Development
Fund Tribal Plan Preprint—ACF–118–
A.
OMB No.: 0970–0198.
Description: The Child Care and
Development Fund (CCDF) Plan (the
Plan) for Tribes (Indian Tribes, Tribal
consortia and Tribal organizations) is
required from each CCDF Lead agency
in accordance with Section 658E of the
Child Care and Development Block
Grant Act of 1990, as amended (Pub. L.
101–508, Pub. L. 104–193, and 42 U.S.C.
9858). The implementing regulations for
the statutorily required Plan are set forth
at 45 CFR 98.10 through 98.18. The
Plan, submitted on the ACF 118–A, is
required biennially, and remains in
effect for two years. The Plan provides
ACF and the public with a description
of, and assurance about, the Tribal child
care program. The ACF 118–A is
currently approved through September
30, 2011, making it available to Tribes
needing to submit Plan Amendments
through the end of the FY 2011 Plan
Period. However, on July 1, 2011, Tribes
will be required to submit their FY
2012–2013 Plans for approval by
September 30, 2011. Consistent with the
statute and regulations, ACF requests
revision of the ACF 118–A with minor
corrections and modifications.
The Office of Child Care(OCC) has
given thoughtful consideration to the
comments received from the 1st Public
Notice. OCC has revised the document
to reflect some of the changes made to
minimize the burden of the collection of
information on respondents. The
revised document contains revisions to
improve the accuracy and clarity of
questions in order to improve the
quality of information that is collected.
This second Public Comment Period
provides an opportunity for the public
to submit comments to the Office of
Management and Budget (OMB).
Copies of the proposed collection may
be obtained by writing to the
Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the title of the information
collection. E-mail address:
infocollection@acf.hhs.gov.
Respondents:
ANNUAL BURDEN ESTIMATES
Number of
respondents
Number of
responses per
respondent
Average burden
hours per
response
Total burden
hours
CCDF Tribal Plan ............................................................................
jlentini on DSKJ8SOYB1PROD with NOTICES
Instrument
257
0.5
120
15,420
Estimated Total Annual Burden
Hours: 15,420.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
VerDate Mar<15>2010
18:42 Feb 28, 2011
Jkt 223001
Children and Families, Office of
Administration, Office of Information
Services, 370 L’Enfant Promenade, SW.,
Washington, DC 20447, Attn: ACF
Reports Clearance Officer. All requests
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
should be identified by the title of the
information collection. E-mail address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
E:\FR\FM\01MRN1.SGM
01MRN1
Federal Register / Vol. 76, No. 40 / Tuesday, March 1, 2011 / Notices
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7285,
E-mail:
OIRA_SUBMISSION@OMB.EOP.GOV,
Attn: Desk Officer for the
Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011–4418 Filed 2–28–11; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0099]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Followup Study for
Infant Feeding Practices Study II
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. 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 and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
a study entitled ‘‘Followup Study for
Infant Feeding Practices Study II.’’
DATES: Submit either electronic or
written comments on the collection of
information by May 2, 2011.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Office of Information
jlentini on DSKJ8SOYB1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
18:42 Feb 28, 2011
Jkt 223001
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3793.
SUPPLEMENTARY INFORMATION: 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.
‘‘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 provide a 60-day notice in the
Federal Register concerning each
proposed collection of information
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Followup Study for Infant Feeding
Practices Study II (OMB Control
Number 0910–NEW)
I. Background
FDA is planning to conduct a survey
of the mothers who participated in the
Infant Feeding Practices Study II (IFPS
II) (Ref. 1). The IFPS II sample was
drawn from a commercial consumer
opinion panel, and so participants are
expected to be easier to re-contact than
would be the case for a random sample
of the population. Some participants
will still be panel members. The
purpose of the study is to enhance
FDA’s understanding of the associations
between infant feeding practices and
diet quality, food allergy, overweight
and obesity, and other health and
development outcomes in young
children.
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11251
The study results will be used to help
the Agency to understand the possible
role of infant feeding practices in the
development and progression of food
allergy and childhood overweight and
obesity, in addition to resistance to
infection and other health and
development outcomes. The results of
the study will not be used to develop
population estimates.
The data will be collected by a mailed
questionnaire from most respondents
and by telephone from those who do not
respond to the mailed questionnaire.
The study will focus on the following
types of information: The child’s
consumption of various food groups; the
child’s other consumption practices
(such as how often the child eats dinner
with a parent and how often the child
eats from fast food restaurants); the
mother’s control over the child’s eating
patterns; the child’s physical activity
and time spent watching a screen (TV or
computer); the child’s sleep patterns;
extent of the child’s cognitive
stimulation at home; the child’s height,
weight, and waist circumference; the
child’s visits to a dentist and number of
cavities; number of the child’s recent
physician visits; number of various
types of infections the child had in the
past year; whether the child has various
health conditions including digestive
problems, eczema, food allergy,
respiratory allergy, attention deficit
disorder, developmental delay, anxiety
problems, depression, or asthma; the
child’s social development; the child’s
family medical history; the mother’s
height and weight, physical activity,
depression, pregnancies subsequent to
the sample child and whether
subsequent children were breastfed, and
employment conditions; the mother or
child’s participation in certain
government programs; and the child’s
potential exposure to certain
environmental contaminants including
cigarette smoke and pesticides. A
demographic questionnaire will also be
mailed to respondents for whom current
information is not available through the
consumer opinion panel. Participation
in the study is voluntary.
To refine the questionnaire used in
the study, a pretest will be conducted
with 100 participants, 91 by mailed
questionnaire and 9 by telephone
interview. We estimate that it will take
a respondent 20 minutes (0.33 hours) to
complete the survey and 5 minutes (0.08
hours) to complete debriefing questions
for the pretest, for a total of 25 minutes
(0.42 hours) per respondent and a total
of 38 hours for the mailed and 4 hours
for the interview pretest. The sample for
the pretest will be panel members who
are mothers of children 5 to 7 years old
E:\FR\FM\01MRN1.SGM
01MRN1
]]>Agencies
[Federal Register Volume 76, Number 40 (Tuesday, March 1, 2011)]
[Notices]
[Pages 11250-11251]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-4418]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Child Care and Development Fund Tribal Plan Preprint--ACF-
118-A.
OMB No.: 0970-0198.
Description: The Child Care and Development Fund (CCDF) Plan (the
Plan) for Tribes (Indian Tribes, Tribal consortia and Tribal
organizations) is required from each CCDF Lead agency in accordance
with Section 658E of the Child Care and Development Block Grant Act of
1990, as amended (Pub. L. 101-508, Pub. L. 104-193, and 42 U.S.C.
9858). The implementing regulations for the statutorily required Plan
are set forth at 45 CFR 98.10 through 98.18. The Plan, submitted on the
ACF 118-A, is required biennially, and remains in effect for two years.
The Plan provides ACF and the public with a description of, and
assurance about, the Tribal child care program. The ACF 118-A is
currently approved through September 30, 2011, making it available to
Tribes needing to submit Plan Amendments through the end of the FY 2011
Plan Period. However, on July 1, 2011, Tribes will be required to
submit their FY 2012-2013 Plans for approval by September 30, 2011.
Consistent with the statute and regulations, ACF requests revision of
the ACF 118-A with minor corrections and modifications.
The Office of Child Care(OCC) has given thoughtful consideration to
the comments received from the 1st Public Notice. OCC has revised the
document to reflect some of the changes made to minimize the burden of
the collection of information on respondents. The revised document
contains revisions to improve the accuracy and clarity of questions in
order to improve the quality of information that is collected. This
second Public Comment Period provides an opportunity for the public to
submit comments to the Office of Management and Budget (OMB).
Copies of the proposed collection may be obtained by writing to the
Administration for Children and Families, Office of Administration,
Office of Information Services, 370 L'Enfant Promenade, SW.,
Washington, DC 20447, Attn: ACF Reports Clearance Officer. All requests
should be identified by the title of the information collection. E-mail
address: infocollection@acf.hhs.gov.
Respondents:
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
CCDF Tribal Plan.................... 257 0.5 120 15,420
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 15,420.
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of Administration, Office of Information Services, 370 L'Enfant
Promenade, SW., Washington, DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be identified by the title of the
information collection. E-mail address: infocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
[[Page 11251]]
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect if OMB receives it within 30 days of
publication. Written comments and recommendations for the proposed
information collection should be sent directly to the following: Office
of Management and Budget, Paperwork Reduction Project, Fax: 202-395-
7285, E-mail: OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the
Administration for Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011-4418 Filed 2-28-11; 8:45 am]
BILLING CODE 4184-01-P
