Proposed Data Collections Submitted for Public Comment and Recommendations, 40297-40298 [E7-14282]
Download as PDF
40297
Federal Register / Vol. 72, No. 141 / Tuesday, July 24, 2007 / Notices
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
Ingredients Added to, and the
Quantity of Nicotine Contained in,
Smokeless Tobacco Manufactured,
Imported, or Packaged in the U.S.—
Reinstatement with Change—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Comprehensive Smokeless
Tobacco Health Education Act of 1986
(15 U.S.C. 4401 et seq., Pub. L. 99–252)
requires each person who manufactures,
packages, or imports smokeless tobacco
(SLT) to provide the Secretary of Health
and Human Services (HHS) with a list
of ingredients added to tobacco in the
manufacture of smokeless tobacco
products. This legislation also
authorizes HHS to undertake research,
and submit an annual report to Congress
(as deemed appropriate) discussing the
health effects of the ingredients in
smokeless tobacco products. HHS has
delegated responsibility for the
implementation of this Act to CDC’s
Office on Smoking and Health (OSH).
The oral use of SLT represents a
significant health risk which can cause
cancer and a number of non-cancerous
oral conditions, and can lead to nicotine
addiction and dependence.
Furthermore, SLT use is not a safe
substitute for cigarette smoking.
Estimated burden for testing and
reporting of un-ionized nicotine, total
moisture, and pH for smokeless tobacco
is one response per year, averaging
1,713 hours to prepare, at a cost of
$1,139 per respondent, for 11
companies. The total hourly burden
would be 18,843 hours, with a total cost
of $12,529. The only cost to respondents
is their time to complete the survey.
ESTIMATED ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
Number of
responses per
respondent
Average
burden per response (in
hrs.)
Total burden
(in hours)
Smokeless Tobacco Products Manufacturers .................................................
11
1
1713
18,843
Dated: July 18, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–14273 Filed 7–23–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–07–07BJ]
mstockstill on PROD1PC66 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 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, 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
VerDate Aug<31>2005
17:50 Jul 23, 2007
Jkt 211001
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.
Proposed Project
Economic Analysis of the National
Program of Cancer Registries—NEW—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The National Program of Cancer
Registries (NPCR) is a nationwide,
comprehensive federally sponsored
public health program. Established by
Congress through the Cancer Registries
Amendment Act in 1992, and
administered by the Centers for Disease
Control and Prevention (CDC), the
NPCR collects data on the occurrence of
cancer; the type, extent, and location of
the cancer; and the type of initial
treatment. Since the establishment of
NPCR there has been no published
systematic analysis of the true economic
costs incurred by the program. As the
program matures and gains national
PO 00000
Frm 00028
Fmt 4703
Sfmt 4703
attention, and in light of the recent
increases in total program funding as
well as wide variations in the cost per
case collected, there is now a greater
need for an economic evaluation of the
program.
The purpose of this task is to assess
the costs, effectiveness, and costeffectiveness of NPCR in collecting high
quality data on cancer incidence, and to
develop tools for making resource
allocation decisions that will meet
program priorities. Performing an
assessment of the resources expended
on NPCR in relation to the value created
will provide critical information for
improving program efficiency within
the various components of the NPCR
and potentially identifying economies of
scale.
This task will involve collection and
analysis of cost and effectiveness data
from all 45 state registries, funded by
NPCR, for three years. A pilot
questionnaire was developed and
piloted tested with 7 registries and
information learn during the pilot
testing was incorporated to develop a
comprehensive cost collection tool. RTI
International, the contractor hired by
CDC will build a web based data
collection tool to collect annual cost
data from the 45 state registries. All data
will be submitted electronically by
grantees to reduce the respondent
burden and errors. The contractor will
also develop a user’s manual to assist
the grantees with completing their data
submission.
E:\FR\FM\24JYN1.SGM
24JYN1
40298
Federal Register / Vol. 72, No. 141 / Tuesday, July 24, 2007 / Notices
Since certain program level data are
already collected as part of NPCR
Annual Program Evaluation Instrument
(OMB i#0920–0706), the additional
burden on grantees will be modest.
for their time to complete the
questionnaire. All respondents will be
using the same cost assessment tool.
The only cost to the respondent is their
time.
Once the infrastructure is established to
capture the cost data from the NPCR
programs, the response burden is
expected to be reduced even further.
There are no costs to respondents except
ESTIMATED ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
Number of
responses per
respondent
Average
burden per response
(in hours)
Total burden
(in hours)
State Health Officials—NPCR funded registries .............................................
45
3
22
2,970
........................
........................
........................
2,970
Total ..........................................................................................................
Dated: July 18, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–14282 Filed 7–23–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Proposed Project
Centers for Disease Control and
Prevention
[60Day–07–07BK]
mstockstill on PROD1PC66 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 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, 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)
ways to enhance the quality, utility, and
VerDate Aug<31>2005
19:13 Jul 23, 2007
Jkt 211001
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.
Transgender HIV Behavioral Survey
(THBS)—New—National Center for HIV,
Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The purpose of this data collection is
to pilot a survey that will be used to
monitor behaviors related to Human
Immunodeficiency Virus (HIV) infection
among transgender persons who are
assigned a male sex at birth. The goal of
the survey will be to obtain data from
samples of transgender persons to (a)
describe the prevalence in risk
behaviors; (b) describe the prevalence of
HIV testing and HIV infection; (c)
describe the prevalence of the use of
HIV prevention services; (d) identify
met and unmet needs for HIV
prevention services in order to inform
health departments, community based
organizations, community planning
groups and other stakeholders. The
objectives of the pilot will be to assess
the content of the questionnaire as well
as the efficiency and feasibility of the
methods for sampling and recruiting
transgender persons. This project
addresses the goals of CDC’s HIV
Prevention Strategic Plan, specifically
the goal of strengthening the national
capacity to monitor the HIV epidemic to
PO 00000
Frm 00029
Fmt 4703
Sfmt 4703
better direct and evaluate prevention
efforts.
Data will be collected through inperson and computer-assisted self
interviews conducted in 4 Metropolitan
Statistical Areas (MSA) throughout the
United States. The MSA chosen will be
among those currently participating in
the National HIV Behavioral
Surveillance system (see Federal
Registry dated January 19, 2007: Vol. 72,
No. 12, pages 2529–2530). A brief inperson screening interview will be used
to determine eligibility for participation
in the full survey. Data for the full
survey will be collected using
computer-assisted self interviews.
Besides determining the content of the
final survey instrument and the
sampling methods, the data from the
full survey will provide estimates of
behavior related to the risk of HIV and
other sexually transmitted diseases,
prior testing for HIV, and use of HIV
prevention services. No other federal
agency systematically collects this type
of information from transgender persons
at risk for HIV infection. This data will
have substantial impact on prevention
program development and monitoring at
the local, state, and national levels.
CDC will request a 2-year clearance
for this information collection. CDC
estimates that, in each year, THBS will
involve eligibility screening of a total of
240 persons and will collect survey
information from 200 eligible
respondents. Thus, over the two year
period 480 persons are estimated to
complete the screener and 400 eligible
respondents to complete the survey.
Participation of respondents is
voluntary and there is no cost to the
respondents other than their time.
E:\FR\FM\24JYN1.SGM
24JYN1
Agencies
[Federal Register Volume 72, Number 141 (Tuesday, July 24, 2007)]
[Notices]
[Pages 40297-40298]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-14282]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-07-07BJ]
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
and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance
Officer, 1600 Clifton Road, MS-D74, 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) 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.
Proposed Project
Economic Analysis of the National Program of Cancer Registries--
NEW--National Center for Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The National Program of Cancer Registries (NPCR) is a nationwide,
comprehensive federally sponsored public health program. Established by
Congress through the Cancer Registries Amendment Act in 1992, and
administered by the Centers for Disease Control and Prevention (CDC),
the NPCR collects data on the occurrence of cancer; the type, extent,
and location of the cancer; and the type of initial treatment. Since
the establishment of NPCR there has been no published systematic
analysis of the true economic costs incurred by the program. As the
program matures and gains national attention, and in light of the
recent increases in total program funding as well as wide variations in
the cost per case collected, there is now a greater need for an
economic evaluation of the program.
The purpose of this task is to assess the costs, effectiveness, and
cost-effectiveness of NPCR in collecting high quality data on cancer
incidence, and to develop tools for making resource allocation
decisions that will meet program priorities. Performing an assessment
of the resources expended on NPCR in relation to the value created will
provide critical information for improving program efficiency within
the various components of the NPCR and potentially identifying
economies of scale.
This task will involve collection and analysis of cost and
effectiveness data from all 45 state registries, funded by NPCR, for
three years. A pilot questionnaire was developed and piloted tested
with 7 registries and information learn during the pilot testing was
incorporated to develop a comprehensive cost collection tool. RTI
International, the contractor hired by CDC will build a web based data
collection tool to collect annual cost data from the 45 state
registries. All data will be submitted electronically by grantees to
reduce the respondent burden and errors. The contractor will also
develop a user's manual to assist the grantees with completing their
data submission.
[[Page 40298]]
Since certain program level data are already collected as part of
NPCR Annual Program Evaluation Instrument (OMB i0920-0706),
the additional burden on grantees will be modest. Once the
infrastructure is established to capture the cost data from the NPCR
programs, the response burden is expected to be reduced even further.
There are no costs to respondents except for their time to complete the
questionnaire. All respondents will be using the same cost assessment
tool. The only cost to the respondent is their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondents Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
State Health Officials--NPCR funded 45 3 22 2,970
registries.................................
-------------------------------------------------------------------
Total................................... ............... ............... ............... 2,970
----------------------------------------------------------------------------------------------------------------
Dated: July 18, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E7-14282 Filed 7-23-07; 8:45 am]
BILLING CODE 4163-18-P