Agency Recordkeeping/Reporting Requirements Under Emergency Review by the Office of Management and Budget (OMB), 78662-78663 [2011-32349]
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78662
Federal Register / Vol. 76, No. 243 / Monday, December 19, 2011 / Notices
Mailstop F–59, 1600 Clifton Road NE.,
Atlanta, Georgia 30333, email:
viequesreport@cdc.gov.
SUPPLEMENTARY INFORMATION: This
report’s principal focus is to review
updated environmental data on Vieques
air, water, soil, seafood, and locally
grown foods. In addition, this report
evaluates human biomonitoring and
health outcome data. ATSDR is
providing a public comment period for
this draft report as a means to best serve
public health and the residents of
Vieques, Puerto Rico. The Draft Vieques
Report is available in English and
Spanish at www.regulations.gov in the
docket identified by Docket ID No.
CDC–2011–0014 and
www.atsdr.cdc.gov/sites/vieques/.
Dated: December 13, 2011.
Thomas Sinks,
Deputy Director, National Center for
Environmental Health/Agency for Toxic
Substances and Disease Registry.
[FR Doc. 2011–32371 Filed 12–16–11; 8:45 am]
BILLING CODE 4163–70–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects:
Title: Plan for Foster Care and
Adoption Assistance—Title IV–E.
OMB No.: 0980–0141.
Description: A title IV–E plan is
required by section 471, part IV–E of the
Social Security Act (the Act) for each
public child welfare agency requesting
Federal funding for foster care, adoption
assistance and guardianship assistance
under the Act. Section 479B of the Act
provides for an Indian tribe, tribal
organization or tribal consortium (Tribe)
to operate a title IV–E program in the
same manner as a State with minimal
exceptions. The Tribe must have an
approved title IV–E Plan. The title
IV–E plan provides assurances the
programs will be administered in
conformity with the specific
requirements stipulated in title IV–E.
The plan must include all applicable
State or Tribal statutory, regulatory, or
policy references and citations for each
requirement as well as supporting
documentation. A title IV–E agency may
use the pre-print format prepared by the
Children’s Bureau of the Administration
for Children and Families or a different
format, on the condition that the format
used includes all of the title IV–E plan
requirements of the law.
Respondents: Title IV–E agencies
administering or supervising the
administration of the title IV–E
programs.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Title IV–E Plan .................................................................................................
emcdonald on DSK5VPTVN1PROD with NOTICES
Instrument
17
1
16
272
Estimated Total Annual Burden
Hours: 272.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade, SW., Washington, DC
20447, Attn: ACF Reports Clearance
Officer. Email address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
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)
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ways to minimize the burden
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.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011–32410 Filed 12–16–11; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Agency Recordkeeping/Reporting
Requirements Under Emergency
Review by the Office of Management
and Budget (OMB)
Title: State Court Improvement
Program.
OMB No.: New Collection.
Description: The Court Improvement
Program (CIP) is composed of three
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Fmt 4703
Sfmt 4703
grants, the basic, data, and training
grants, governed by two separate
Program Instructions (PIs). The training
and data grants are governed by the
‘‘new grant’’ PI and the basic grant is
governed by the ‘‘basic grant’’ PI.
Current PIs require separate
applications and program assessment
reports for each grant. Every State
applies for at least two of the grants
annually and most States apply for all
three. As many of the application
requirements are the same for all three
grants, this results in duplicative work
and high degrees of repetition for State
courts applying for more than one CIP
grant.
The purpose of this Program
Instruction is to streamline and simplify
the application and reporting processes
by consolidating the PIs into one single
PI and requiring one single,
consolidated application (App) package
and program assessment report (PAR)
per State court annually. These
revisions will satisfy statutory
programmatic requirements and reduce
both the number of required responses
and associated total burden hours for
State courts.
This new PI also describes
programmatic and fiscal provisions and
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78663
Federal Register / Vol. 76, No. 243 / Monday, December 19, 2011 / Notices
reporting requirements for the grants,
specifies the application submittal and
approval procedures for the grants for
fiscal years 2012 through 2015, and
identifies technical resources for use by
State courts during the course of the
grants. The agency uses the information
received to ensure compliance with the
statute and provide training and
technical assistance to the grantees.
Respondents: Highest State Courts of
Appeal.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Application .......................................................................................................
Program Assessment Report ...........................................................................
Estimated Total Annual Burden
Hours: 9256.
Additional Information: ACF is
requesting that OMB grant a 180 day
approval for this information collection
under procedures for emergency
processing by December 20, 2011. A
copy of this information collection, with
applicable supporting documentation,
may be obtained by calling the
Administration for Children and
Families, Reports Clearance Officer,
Robert Sargis at (202) 690–7275.
Comments and questions about the
information collection described above
should be directed to the Office of
Information and Regulatory Affairs,
Attn: OMB Desk Officer for ACF, Office
of Management and Budget, Paperwork
Reduction Project, 725 17th Street NW.,
Washington, DC 20503; FAX: (202) 395–
7285; email:
oira_submission@omb.eop.gov.
52
52
Robert Sargis,
Reports Clearance Officer.
Fax written comments on the
collection of information by January 18,
2012.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
(202) 395–7285, or emailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–New and
title, Examination of Online Direct-toConsumer Prescription Drug Promotion.
Also include the FDA docket number
found in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Juanmanuel Vilela, Office of
Information Management, Food and
Drug Administration, 1350 Piccard Dr.,
PI50–400B, Rockville, MD 20850, (301)
796–7651,
juanmanuel.vilela@fda.hhs.gov..
[FR Doc. 2011–32349 Filed 12–16–11; 8:45 am]
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Examination of Online Direct-toConsumer Prescription Drug
Promotion—(OMB Control Number
0910—New)
Food and Drug Administration
[Docket No. FDA–2011–N–0230]
I. Background
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Examination of
Online Direct-to-Consumer
Prescription Drug Promotion
AGENCY:
Food and Drug Administration,
emcdonald on DSK5VPTVN1PROD with NOTICES
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
SUMMARY:
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19:31 Dec 16, 2011
Jkt 226001
DATES:
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
BILLING CODE 4184–01–P
Pharmaceutical products are launched
and marketed in a number of new
modalities and venues that did not exist
a short time ago. Increasingly,
prescription products are promoted to
consumers online in such formats as
banners, Web sites, and videos. The
interactive nature of the Internet allows
for features not possible with traditional
media (i.e., print, radio, and television),
such as scrolling information, popup
windows, linking to additional
information, and embedded videos.
FDA regulations require that
prescription drug advertisements
include a ‘‘fair balance’’ of information
about the benefits and risks of
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Number of
responses per
respondent
1
1
Average
burden hours
per response
92
86
Total burden
hours
4784
4472
advertised products, both in terms of the
content and presentation of the
information (21 CFR 202.1(e)(5)(ii)). All
prescription drug promotion that makes
claims about a product must, therefore,
also include risk information in a
‘‘balanced’’ manner. Currently, there are
a number of questions surrounding how
to achieve ‘‘fair balance’’ in online
direct-to-consumer (DTC) promotion.
A few studies have examined how
well online DTC Web sites
communicate benefit and risk
information. Although content analyses
demonstrate that most Web sites include
information on side effects and
contraindications (Ref. 1), risk
information is often presented less
prominently and in fewer locations on
the Web site (Refs. 2, 3, and 4). Content
analyses also suggest that risk
information on DTC prescription drug
Web sites is often incomplete (Ref. 5)
and written at very high literacy levels
(Ref. 6).
One study examined how users
interact with prescription drug Web
sites (Ref. 7). This study found that the
placement of risk and benefit
information on a Web site is an
important factor in whether it achieves
‘‘fair balance.’’ Specifically,
participants’ ability to find and
accurately recall risk information was
enhanced when risk and benefit
information were presented separately
and when risk information was
presented on a higher order page (i.e.,
on a second-level page clearly linked
from the homepage, or on the
homepage).
This project is designed to test
different ways of presenting
prescription drug risk and benefit
information on branded drug Web sites.
This research is relevant to current
policy questions and debate and will
complement qualitative research we
plan to conduct on issues surrounding
social media. The series of studies
described in this document will provide
data that, along with other input and
considerations, will inform the
development of future guidance.
E:\FR\FM\19DEN1.SGM
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]]>Agencies
[Federal Register Volume 76, Number 243 (Monday, December 19, 2011)]
[Notices]
[Pages 78662-78663]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-32349]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Agency Recordkeeping/Reporting Requirements Under Emergency
Review by the Office of Management and Budget (OMB)
Title: State Court Improvement Program.
OMB No.: New Collection.
Description: The Court Improvement Program (CIP) is composed of
three grants, the basic, data, and training grants, governed by two
separate Program Instructions (PIs). The training and data grants are
governed by the ``new grant'' PI and the basic grant is governed by the
``basic grant'' PI. Current PIs require separate applications and
program assessment reports for each grant. Every State applies for at
least two of the grants annually and most States apply for all three.
As many of the application requirements are the same for all three
grants, this results in duplicative work and high degrees of repetition
for State courts applying for more than one CIP grant.
The purpose of this Program Instruction is to streamline and
simplify the application and reporting processes by consolidating the
PIs into one single PI and requiring one single, consolidated
application (App) package and program assessment report (PAR) per State
court annually. These revisions will satisfy statutory programmatic
requirements and reduce both the number of required responses and
associated total burden hours for State courts.
This new PI also describes programmatic and fiscal provisions and
[[Page 78663]]
reporting requirements for the grants, specifies the application
submittal and approval procedures for the grants for fiscal years 2012
through 2015, and identifies technical resources for use by State
courts during the course of the grants. The agency uses the information
received to ensure compliance with the statute and provide training and
technical assistance to the grantees.
Respondents: Highest State Courts of Appeal.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average
Instrument Number of responses per burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
Application..................................... 52 1 92 4784
Program Assessment Report....................... 52 1 86 4472
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 9256.
Additional Information: ACF is requesting that OMB grant a 180 day
approval for this information collection under procedures for emergency
processing by December 20, 2011. A copy of this information collection,
with applicable supporting documentation, may be obtained by calling
the Administration for Children and Families, Reports Clearance
Officer, Robert Sargis at (202) 690-7275.
Comments and questions about the information collection described
above should be directed to the Office of Information and Regulatory
Affairs, Attn: OMB Desk Officer for ACF, Office of Management and
Budget, Paperwork Reduction Project, 725 17th Street NW., Washington,
DC 20503; FAX: (202) 395-7285; email: oira_submission@omb.eop.gov.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011-32349 Filed 12-16-11; 8:45 am]
BILLING CODE 4184-01-P
