Agency Forms Undergoing Paperwork Reduction Act Review, 1617-1618 [2011-335]
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1617
Federal Register / Vol. 76, No. 7 / Tuesday, January 11, 2011 / Notices
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.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, e-mail your request,
including your address, phone number,
OMB number, and OS document
identifier, to
Sherette.funncoleman@hhs.gov, or call
the Reports Clearance Office on (202)
690–6162. Written comments and
recommendations for the proposed
information collections must be directed
to the OS Paperwork Clearance Officer
at the above e-mail address within 60
days.
Proposed Project: Comparative
Effectiveness Research Inventory—OMB
No. 0990–New-Assistant Secretary for
Planning and Evaluation (ASPE).
inventory will be directed first to submit
such records to one of these main
primary source databases, as
appropriate. This method will not only
help to augment these existing
databases, it will enable efficient and
effective capture of CER information for
the CER Inventory via CER search
filters, etc., that have been developed for
those respective source databases. If
candidate CER records under
consideration are not suitable for
submission to one of these main
databases, an alternative method that
allows for direct submissions to the CER
inventory will be made available to
content users. Examples include reports
and published articles or projects and
programs that focus on areas of CER
outside of primary research (e.g.,
training and education). The pilot
inventory tool will provide a web form
that may be used by content owners to
submit CER records, subject to
validation. This process for direct
submission will draw from the
experience with content owner
submissions for such established
databases as HSRProj and
ClinicalTrials.gov.
Abstract: The Office of the Assistance
Secretary for Planning and Evaluation
(ASPE) is requesting approval by OMB
for the collection of information
submitted by content users directly to a
web-based inventory of comparative
effectiveness research (CER). The CER
Inventory will categorize and catalogue
Federal and non-Federal CER outputs
and activities across four main domains:
Research, human & scientific capital
(e.g., training/education, methods
development), data infrastructure, and
dissemination & translation. The CER
inventory will serve as a valuable tool
for researchers, providers, patients,
policymakers, and other users.
The CER inventory will draw upon
primary data sources, including
PubMed, HSRProj, ClinicalTrials.gov,
and NIH RePORTER. Working with
these four major sources and using the
Federal Coordinating Council for CER’s
definition of CER and strategic
framework, selection criteria and tools
to select and extract the appropriate
subsets of these datasets for inclusion in
the CER inventory will be identified. In
addition, content owners wishing to
submit CER records to the CER
ESTIMATED ANNUALIZED BURDEN TABLE
Form
Type of
respondent
CER Inventory Direct Submission Form
for Reports or Other Publications.
Researchers/
Research
Assistants.
Researchers/
Research
Assistants.
CER Inventory Direct Submission Form
for Projects.
Total ...................................................
.......................
Seleda M. Perryman,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. 2011–310 Filed 1–10–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
mstockstill on DSKH9S0YB1PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
17:33 Jan 10, 2011
Jkt 223001
Number of
responses per
respondent
Total
responses
Total burden
hours
1
400
25/60
167
100
1
100
28/60
47
........................
........................
........................
........................
214
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
List of Ingredients Added to Tobacco
in the Manufacture of Cigarette Products
(OMB# 0920–0210 Exp. 04/30/2011)—
Extension—Office on Smoking and
Health, National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention, (CDC).
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Average
burden hours
per response
400
Proposed Project
[30 Day-11–0210]
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Number of
respondents
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Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), Office on Smoking
and Health (OSH) has the primary
responsibility for the Department of
Health and Human Services (HHS)
smoking and health program. HHS’s
overall goal is to reduce death and
disability resulting from cigarette
smoking and other forms of tobacco use
through programs of information,
education and research.
Since 1986, as required by the
Comprehensive Smoking Education Act
of 1984 (CSEA, 15 U.S.C. 1336 or Pub.
L. 98–474), CDC has collected
information about the ingredients used
in cigarette products. Respondents are
commercial cigarette manufacturers,
packagers, or importers (or their
representatives), who are required by
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Federal Register / Vol. 76, No. 7 / Tuesday, January 11, 2011 / Notices
the CSEA to submit ingredient reports to
HHS on an annual basis.
Respondents are not required to
submit specific forms; however, they are
required to submit a list of all
ingredients used in their products. CDC
requires the ingredient report to be
submitted by chemical name and
Chemical Abstract Service (CAS)
Registration Number, consistent with
accepted reporting practices for other
companies currently required to report
ingredients added to other consumer
products. Typically, respondents submit
a summary report to CDC with the
ingredient information for multiple
products, or a statement that there are
no changes to their previously
submitted ingredient report.
Ingredient reports for new products
are due at the time of first importation.
Thereafter, ingredient reports are due
annually on March 31. Information is
submitted to OSH by mailing a written
report on the respondent’s letterhead, by
CD, three-inch floppy disk, or thumb
drive. Electronic mail submissions are
not accepted.
Upon receipt and verification of the
annual ingredient report, OSH issues a
Certificate of Compliance to the
respondent. OSH also uses the
information to report to the Congress (as
deemed appropriate) discussing the
health effects of these ingredients.
In this Extension request, there are no
changes to the estimated number of
respondents, the estimated burden per
response, or the information collection
methods. There are no costs to
respondents other than their time. The
total estimated annualized burden hours
are 930.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Number of
respondents
Number of
responses per
respondent
Estimated
burden hours
Cigarette Manufacturers, Packagers, and Importers ..................................................................
143
1
6.5
Dated: January 5, 2011.
Carol E. Walker,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2011–335 Filed 1–10–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Proposed Project
Centers for Disease Control and
Prevention
[60 Day-11–0672]
mstockstill on DSKH9S0YB1PROD with NOTICES
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 or send
comments to Carol E. Walker, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS D–74, Atlanta, GA
30333 or send an e-mail to
omb@cdc.gov.
Comments are invited 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)
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17:33 Jan 10, 2011
Jkt 223001
ways to enhance the quality, utility, and
clarity of the 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. Written comments should
be received within 60 days of this
notice.
Indicators of the Performance of
Local, State, Territorial, and Tribal
Education Agencies in HIV Prevention,
Coordinated School Health Program,
and Asthma Management Activities for
Adolescent and School Health Programs
(OMB No. 0920–0672, exp. 6/30/2011)—
Revision—Division of Adolescent and
School Health, National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Division of Adolescent and
School Health (DASH), CDC, supports
HIV prevention activities, coordinated
school health program (CSHP) activities,
and asthma management activities
conducted by local education agencies
(LEA), state education agencies (SEA),
territorial education agencies (TEA), and
tribal governments (TG). DASH
currently collects information about
these activities under OMB control
number 0920–0672 (exp. 6/30/2011).
Because there is currently no other
standardized annual reporting process
for DASH-funded HIV prevention
activities, CSHP activities, and asthma
management activities, DASH seeks
OMB approval to continue the
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information collection for three years
(FY2010—FY2012 data). The previously
approved questionnaires will be used to
collect FY2010 data. Minor changes to
the questionnaires will be implemented
for the FY2011 and FY2012 data
collections.
Information collection consists of four
Web-based questionnaires that
correspond to specific funding sources
within DASH. Two questionnaires
pertain to HIV-prevention program
activities among LEAs and SEAs/TEAs/
TGs, the third questionnaire pertains to
CSHP activities among SEAs, and the
fourth questionnaire pertains to asthma
management activities among LEAs.
There are no changes to the estimated
burden per response for any of the
questionnaires.
The two HIV questionnaires include
questions about planning and improving
projects; development and distribution
of materials, professional development
and individualized technical assistance
on school policies; development and
distribution of materials, professional
development and individualized
technical assistance on education
curricula and instruction; collaboration
with external partners; reducing
disparities among populations of youth
at disproportionate risk; and
information about additional program
activities.
The CSHP/PANT questionnaire also
asks the questions above, but focuses on
physical activity, healthy eating, and
tobacco-use prevention activities. It
includes additional questions about
joint activities of the State Education
Agency and State Health Agency (SHA);
activities of the CSHP state-wide
coalition; and development and
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Agencies
[Federal Register Volume 76, Number 7 (Tuesday, January 11, 2011)]
[Notices]
[Pages 1617-1618]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-335]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30 Day-11-0210]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
List of Ingredients Added to Tobacco in the Manufacture of
Cigarette Products (OMB 0920-0210 Exp. 04/30/2011)--
Extension--Office on Smoking and Health, National Center for Chronic
Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease
Control and Prevention, (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC), Office on
Smoking and Health (OSH) has the primary responsibility for the
Department of Health and Human Services (HHS) smoking and health
program. HHS's overall goal is to reduce death and disability resulting
from cigarette smoking and other forms of tobacco use through programs
of information, education and research.
Since 1986, as required by the Comprehensive Smoking Education Act
of 1984 (CSEA, 15 U.S.C. 1336 or Pub. L. 98-474), CDC has collected
information about the ingredients used in cigarette products.
Respondents are commercial cigarette manufacturers, packagers, or
importers (or their representatives), who are required by
[[Page 1618]]
the CSEA to submit ingredient reports to HHS on an annual basis.
Respondents are not required to submit specific forms; however,
they are required to submit a list of all ingredients used in their
products. CDC requires the ingredient report to be submitted by
chemical name and Chemical Abstract Service (CAS) Registration Number,
consistent with accepted reporting practices for other companies
currently required to report ingredients added to other consumer
products. Typically, respondents submit a summary report to CDC with
the ingredient information for multiple products, or a statement that
there are no changes to their previously submitted ingredient report.
Ingredient reports for new products are due at the time of first
importation. Thereafter, ingredient reports are due annually on March
31. Information is submitted to OSH by mailing a written report on the
respondent's letterhead, by CD, three-inch floppy disk, or thumb drive.
Electronic mail submissions are not accepted.
Upon receipt and verification of the annual ingredient report, OSH
issues a Certificate of Compliance to the respondent. OSH also uses the
information to report to the Congress (as deemed appropriate)
discussing the health effects of these ingredients.
In this Extension request, there are no changes to the estimated
number of respondents, the estimated burden per response, or the
information collection methods. There are no costs to respondents other
than their time. The total estimated annualized burden hours are 930.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Type of respondents Number of responses per Estimated
respondents respondent burden hours
----------------------------------------------------------------------------------------------------------------
Cigarette Manufacturers, Packagers, and Importers............ 143 1 6.5
----------------------------------------------------------------------------------------------------------------
Dated: January 5, 2011.
Carol E. Walker,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2011-335 Filed 1-10-11; 8:45 am]
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