Att 2a_ 0469_60-day FRN

Att 2a_ 0469_60-day FRN.pdf

National Program of Cancer Registries Cancer Surveillance System (NPCR CSS)

Att 2a_ 0469_60-day FRN

OMB: 0920-0469

Document [pdf]
Download: pdf | pdf
37038

Federal Register / Vol. 74, No. 142 / Monday, July 27, 2009 / Notices

child, information describing the type of
trafficking and circumstances
surrounding the situation, and the
strengths and needs of the child. The
form also asks the requestor to verify the
information contained in the form
because the information could be the
basis for a determination of an alien
child’s eligibility for federally funded
benefits. Finally, the form takes into
consideration the need to compile
information regarding a child’s
circumstances and experiences in a non-

directive, child-friendly way, and assists
the potential requestor in assessing
whether the child may have been
subjected to trafficking in persons.
The information provided through the
completion of a Request for Assistance
for Child Victims of Human Trafficking
form will enable HHS to make prompt
determinations regarding the eligibility
of an alien child for interim assistance,
inform HHS’ determination regarding
the child’s eligibility for assistance as a
victim of a severe form of trafficking in

persons, facilitate the required
consultation process, and enable HHS to
assess and address potential child
protection issues.
Respondents: Representatives of
governmental and nongovernmental
entities providing social, legal, or
protective services to non-U.S. citizen
(alien) individuals under the age of 18
(children) in the United States who may
have been subjected to severe forms of
trafficking in persons.

ANNUAL BURDEN ESTIMATES
Number of
respondents

Instrument
Request for Assistance for Child Victims of Human Trafficking .....................

Estimated Total Annual Burden
Hours: 50
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
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: 202–395–7245,
Attn: Desk Officer for the
Administration for Children and
Families.
Dated: July 22, 2009.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E9–17816 Filed 7–24–09; 8:45 am]

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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–09–0469]

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 Maryam I. Daneshvar, CDC
Acting Reports Clearance Officer, 1600
Clifton Road, MS D–74, Atlanta, GA
30333 or send an email 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)
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.

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Number of
responses per
respondent
1

Average
burden hours
per response
1

Total burden
hours
50

Proposed Project
National Program of Cancer Registries
Cancer Surveillance System—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Cancer is the second leading cause of
death in the United States, second only
to heart disease. In 2005, the most
recent year for which complete
information is available, more than
500,000 people died of cancer and more
than 1.34 million were diagnosed with
cancer. In addition to the personal
impact of cancer, the financial burden is
also substantial. The direct treatment
costs of cancer in 2008 have been
estimated at $93.2 billion, with
additional indirect costs of $134.9
billion in lost productivity due to illness
and premature death.
In 1992, Congress passed the Cancer
Registries Amendment Act which
established the National Program of
Cancer Registries (NPCR). The NPCR
provides support for central cancer
registries (CCR) that collect, manage and
analyze data about cancer cases. The
NPCR-funded CCRs, which are located
in states, the District of Columbia, and
U.S. territories, report information to
CDC annually through the National
Program of Cancer Registries Cancer
Surveillance System (NPCR CSS) (OMB
No. 0920–0469, exp. 1/31/2010). CDC
plans to request OMB approval to
continue collecting this information for
three years.
The NPCR CSS allows CDC to collect,
aggregate, evaluate and disseminate
cancer incidence data at the national
level. The NPCR CSS is the primary
source of information for United States

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Federal Register / Vol. 74, No. 142 / Monday, July 27, 2009 / Notices
Cancer Statistics (USCS), which CDC
has published annually since 2002. The
latest USCS report published in 2009
provided cancer statistics for 96% of the
United States population from all cancer
registries whose data met national data
standards. Prior to the publication of
USCS, cancer incidence data at the
national level were available for only
14% of the population of the United
States.
The NPCR CSS also allows CDC to
monitor cancer trends over time,
describe geographic variation in cancer
incidence throughout the country, and
provide incidence data on minority
populations and rare cancers. These
activities and analyses further support
CDC’s planning and evaluation efforts
for state and national cancer control and
prevention. In addition, datasets can be
made available for secondary analysis.

Puerto Rico, and the CCR that aggregates
information from 10 flag territories and
freely associated states in the Pacific
Islands. In the previous OMB approval
period, the territories, commonwealths,
or freely-associated states were counted
as individual respondents. In the next
OMB approval period, the 10 flag
territories, commonwealths, and freelyassociated states will be counted as one
respondent to more accurately reflect
funding, operations and actual response
burden. States that receive sole funding
from the National Cancer Institute are
not included as respondents. The
adjusted number of respondents will
result in a reduction in the total
estimated burden hours for the NPCR
CSS. The estimated burden per response
will not change.
There are no costs to respondents
except their time.

Each responding CCR is asked to
report a cumulative file containing
incidence data from the first diagnosis
year for which the cancer registry
collected data with the assistance of
NPCR funds (e.g., 1995) through 12
months past the close of the most recent
diagnosis year (e.g., 2007). Because
cancer incidence data are already
collected and aggregated at the state
level the additional burden of reporting
the information to CDC is small.
Information is transmitted to CDC
electronically once per year.
The Revision request will include
changes. First, data definitions will be
updated to reflect changes in national
standards for cancer diagnosis and
coding. In addition, the number of
respondents will decrease. Respondents
will be 45 stated-based CCRs, the CCR
of the District of Columbia, the CCR of

ESTIMATED ANNUALIZED BURDEN HOURS
Respondents

Number of
respondents

Number of
responses per
respondent

Average
burden
per response
(in hours)

Total burden
(in hours)

Central Cancer Registries in States, Territories, and the District of Columbia

48

1

2

96

Dated: July 17, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–17781 Filed 7–24–09; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health

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National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.

Emphasis Panel, Clinical Trial Planning
Grant.
Date: August 13, 2009.
Time: 12 p.m. to 2 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6700B
Rockledge Drive, Bethesda, MD 20817
(Telephone Conference Call).
Contact Person: Kenneth E. Santora, PhD,
Scientific Review Officer, Scientific Review
Program, Division of Extramural Activities,
NIH/NIAID/DHHS, 6700B Rockledge Drive,
MSC 7616, Bethesda, MD 20892–7616, 301–
496–2550, ks216i@nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.855, Allergy, Immunology,
and Transplantation Research; 93.856,
Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
Dated: July 21, 2009.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. E9–17833 Filed 7–24–09; 8:45 am]
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Name of Committee: National Institute of
Allergy and Infectious Diseases Special

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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Alcohol Abuse
and Alcoholism; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute on
Alcohol Abuse and Alcoholism Special
Emphasis Panel; NIAAA–NOT–OD–09–058
Competitive Revision Supplement.
Date: July 29–August 3, 2009.
Time: 9 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).

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File Typeapplication/pdf
File TitleDocument
SubjectExtracted Pages
AuthorU.S. Government Printing Office
File Modified2009-07-25
File Created2009-07-25

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