Proposed Data Collections Submitted for Public Comment and Recommendations, 44268-44269 [E8-17418]
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44268
Federal Register / Vol. 73, No. 147 / Wednesday, July 30, 2008 / Notices
FEDERAL TRADE COMMISSION
[Project No. P944509]
Reopening and Extension of Time for
Comments Concerning Proposal to
Rescind Guidance Concerning the
Current Cigarette Test Method
Federal Trade Commission.
Notice of extension of comment
AGENCY:
ACTION:
period.
SUMMARY: The Federal Trade
Commission \(‘‘FTC’’ or ‘‘Commission’’)
has extended the date by which
comments must be submitted
concerning its proposal to rescind
Commission guidance that it is
generally not a violation of the FTC Act
to make factual statements of the tar and
nicotine yields of cigarettes when
statements of such yields are supported
by testing conducted pursuant to the
Cambridge Filter Method. This
document informs prospective
commenters of this change and sets a
new date of September 12, 2008.
DATES: Comments must be submitted on
or before September 12, 2008.
ADDRESSES: Interested parties are
invited to submit comments. Comments
should refer to ‘‘Cigarette Test Method,
[P944509]’’ to facilitate the organization
of comments. A comment filed in paper
form should include this reference both
in the text and on the envelope, and
should be mailed or delivered, with two
complete copies, to the following
address: Federal Trade Commission,
Office of the Secretary, Room H–135
(Annex L), 600 Pennsylvania Avenue,
NW., Washington, DC 20580. Because
paper mail in the Washington area and
at the Commission is subject to delay,
please consider submitting your
comments in electronic form, as
described below. However, if the
comment contains any material for
which confidential treatment is
requested, it must be filed in paper
form, and the first page of the document
must be clearly labeled ‘‘Confidential.’’ 1
Comments filed in electronic form
should be submitted by following the
instructions on the web-based form at
https://secure.commentworks.com/ftcCigaretteTestMethod. To ensure that the
Commission considers an electronic
comment, you must file it on the web-
based form at the https://secure.
commentworks.com/ftc-CigaretteTest
Method weblink. If this Notice appears
at https://www.regulations.gov, you may
also file an electronic comment through
that Web site. The Commission will
consider all comments that
regulations.gov forwards to it.
The FTC Act and other laws the
Commission administers permit the
collection of public comments to
consider and use in this proceeding as
appropriate. All timely and responsive
public comments, whether filed in
paper or electronic form, will be
considered by the Commission, and will
be available to the public on the FTC
Web site, to the extent practicable, at
https://www.ftc.gov. As a matter of
discretion, the FTC makes every effort to
remove home contact information for
individuals from the public comments it
receives before placing those comments
on the FTC Web site. More information,
including routine uses permitted by the
Privacy Act, may be found in the FTC’s
privacy policy at https://www.ftc.gov/ftc/
privacy/htm.
FOR FURTHER INFORMATION CONTACT:
Requests for additional information
should be addressed to Rosemary Rosso,
Senior Attorney, Division of Advertising
Practices, Bureau of Consumer
Protection, Federal Trade Commission,
600 Pennsylvania Avenue, NW.,
Washington, DC 20580, (202) 326–2174.
SUPPLEMENTARY INFORMATION: On July
14, 2008, the Commission published in
the Federal Register a Request for
Comments on its proposal to rescind the
FTC’s guidance concerning the current
cigarette test method.2 That guidance,
announced in 1966, indicates that
factual statements of tar and nicotine
yields based on the Cambridge Filter
Method generally will not violate the
FTC Act.3 If the Commission withdraws
this guidance, advertisers should not
use terms such as ‘‘per FTC Method’’ or
other phrases that state or imply FTC
endorsement or approval of the
Cambridge Filter Method or other
machine-based test methods. The
Federal Register Notice (‘‘Notice’’)
sought public comment on its proposal
as well as comment on the effects the
proposal would likely have on smokers’
2 73
FR 40,350 (Jul. 14, 2008).
some time, the Commission has been
concerned that the machine-measured yields
determined by the Cambridge Filter Method may be
misleading to individual consumers who rely on
the yields as indicators of the amount of tar,
nicotine, and carbon monoxide they actually will
get from smoking a particular cigarette. In fact, the
current yields tend to be relatively poor indicators
of tar, nicotine, and carbon monoxide exposure, and
do not provide a good basis for comparison among
cigarettes.
mstockstill on PROD1PC66 with NOTICES
3 For
1 Commission Rule 4.2(d), 16 CFR 4.2(d). The
comment must be accompanied by an explicit
request for confidential treatment, including the
factual and legal basis for the request, and must
identify the specific portions of the comment to be
withheld from the public record. The request will
be granted or denied by the Commission’s General
Counsel, consistent with applicable law and the
public interest. See Commission Rule 4.9(c), 16 CFR
4.9(c).
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23:06 Jul 29, 2008
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purchases of cigarettes and/or their
smoking behavior. Pursuant to this
Federal Register Notice, the current
comment period is scheduled to end on
August 13, 2008.
Philip Morris USA has requested that
the Commission extend the comment
period for an additional 60 days, or
through October 14, 2008. According to
Philip Morris, the extension will allow
it and other interested parties to prepare
more considered and comprehensive
comments.
The Commission appreciates the need
to provide adequate opportunity for
commenters to submit timely
comments. The Commission likewise
recognizes the need to obtain comments
from parties directly affected by the
proposal. The Commission believes that
an additional 30 days is sufficient to
allow commenters to provide
considered and comprehensive
comments. Accordingly, the
Commission has decided to extend the
deadline for comments until September
12, 2008.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. E8–17421 Filed 7–29–08; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–08–08BJ]
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 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
E:\FR\FM\30JYN1.SGM
30JYN1
44269
Federal Register / Vol. 73, No. 147 / Wednesday, July 30, 2008 / Notices
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
A Study of Primary and Secondary
Prevention Behaviors Practiced Among
Five-Year Survivors of Colorectal
Cancer—New—Division of Cancer
Prevention and Control (DCPC),
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Colorectal cancer (CRC) is the third
most prevalent cancer and the second
leading cause of cancer death in both
men and women in the United States. In
2004, there were an estimated 145,083
new cases of colorectal cancer
diagnosed and 53,580 deaths. However,
the five-year relative survival rates of
patients diagnosed with CRC have been
steadily increasing since 1975 and there
are now over 1 million CRC survivors in
the U.S.
Despite improved survival rates, CRC
survivors are at an elevated risk for
cancer recurrence, second primary
cancers, and other health problems after
being treated for cancer. Research
evidence suggests that these elevated
risks can be mitigated by healthy
lifestyle practices such as exercise and
smoking cessation, and by undergoing
regular medical follow-up and cancer
screenings. A number of medical
organizations, therefore, recommend
that CRC survivors follow public health
and clinical guidelines for prevention
behaviors, medical follow-up, and
cancer screenings.
A thorough understanding of how
individuals make decisions about health
care and cancer prevention following
cancer diagnosis is imperative for
developing public health policies,
programs, and interventions to promote
health and increased quality of life after
cancer, but little is known about the
factors that motivate or hinder the
adoption of cancer prevention and
screening behaviors among cancer
survivors. Therefore, the goal of the
current study is to identify the key
factors associated with practicing (or not
practicing) recommended prevention
behaviors.
The proposed study will employ a
survey of 5-year CRC survivors to collect
information about knowledge, attitudes,
psychosocial factors, health status and
behaviors, and utilization of health care
services including screening services.
Respondents will be individuals who
have previously received a diagnosis of
CRC, and will be identified through
California Cancer Registry records.
Permission to contact these individuals
about participation in the study will be
obtained from their physicians. Each
physician associated with one or more
CRC patients will be responsible for
reviewing a customized list of names to
identify patients who should not be
contacted. Following receipt of
physician permission, individuals who
are eligible for the study will receive a
pre-notification letter to inform them
about the study and to give them an
option to decline participation.
Respondents who are recruited to the
study will complete a self-administered
survey that will be delivered and
returned by mail. Non-response will be
followed by an invitation to complete
the survey via telephone interview. We
estimate that 1,950 physicians will be
contacted and that we will receive
completed surveys from 1,000 CRC
survivors.
Findings from this study will help
guide future policies, programs, and
interventions developed to enhance and
improve the long-term health and well
being of cancer survivors.
There are no costs to respondents
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses
per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Type of respondents
Form name
Physicians .........................................
CRC Survivors ..................................
List of Potential Study Participants ..
Survey of Health Behaviors .............
1,950
1,000
1
1
13/60
40/60
423
667
Total ...........................................
...........................................................
........................
........................
........................
1,090
Dated: July 23, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–17418 Filed 7–29–08; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
[60Day–08–05CS]
Centers for Disease Control and
Prevention
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
VerDate Aug<31>2005
23:06 Jul 29, 2008
Jkt 214001
PO 00000
Frm 00059
Fmt 4703
Sfmt 4703
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–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
E:\FR\FM\30JYN1.SGM
30JYN1
]]>Agencies
[Federal Register Volume 73, Number 147 (Wednesday, July 30, 2008)]
[Notices]
[Pages 44268-44269]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-17418]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-08-08BJ]
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 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
[[Page 44269]]
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
A Study of Primary and Secondary Prevention Behaviors Practiced
Among Five-Year Survivors of Colorectal Cancer--New--Division of Cancer
Prevention and Control (DCPC), National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Colorectal cancer (CRC) is the third most prevalent cancer and the
second leading cause of cancer death in both men and women in the
United States. In 2004, there were an estimated 145,083 new cases of
colorectal cancer diagnosed and 53,580 deaths. However, the five-year
relative survival rates of patients diagnosed with CRC have been
steadily increasing since 1975 and there are now over 1 million CRC
survivors in the U.S.
Despite improved survival rates, CRC survivors are at an elevated
risk for cancer recurrence, second primary cancers, and other health
problems after being treated for cancer. Research evidence suggests
that these elevated risks can be mitigated by healthy lifestyle
practices such as exercise and smoking cessation, and by undergoing
regular medical follow-up and cancer screenings. A number of medical
organizations, therefore, recommend that CRC survivors follow public
health and clinical guidelines for prevention behaviors, medical
follow-up, and cancer screenings.
A thorough understanding of how individuals make decisions about
health care and cancer prevention following cancer diagnosis is
imperative for developing public health policies, programs, and
interventions to promote health and increased quality of life after
cancer, but little is known about the factors that motivate or hinder
the adoption of cancer prevention and screening behaviors among cancer
survivors. Therefore, the goal of the current study is to identify the
key factors associated with practicing (or not practicing) recommended
prevention behaviors.
The proposed study will employ a survey of 5-year CRC survivors to
collect information about knowledge, attitudes, psychosocial factors,
health status and behaviors, and utilization of health care services
including screening services. Respondents will be individuals who have
previously received a diagnosis of CRC, and will be identified through
California Cancer Registry records. Permission to contact these
individuals about participation in the study will be obtained from
their physicians. Each physician associated with one or more CRC
patients will be responsible for reviewing a customized list of names
to identify patients who should not be contacted. Following receipt of
physician permission, individuals who are eligible for the study will
receive a pre-notification letter to inform them about the study and to
give them an option to decline participation. Respondents who are
recruited to the study will complete a self-administered survey that
will be delivered and returned by mail. Non-response will be followed
by an invitation to complete the survey via telephone interview. We
estimate that 1,950 physicians will be contacted and that we will
receive completed surveys from 1,000 CRC survivors.
Findings from this study will help guide future policies, programs,
and interventions developed to enhance and improve the long-term health
and well being of cancer survivors.
There are no costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
Physicians.................... List of 1,950 1 13/60 423
Potential Study
Participants.
CRC Survivors................. Survey of Health 1,000 1 40/60 667
Behaviors.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1,090
----------------------------------------------------------------------------------------------------------------
Dated: July 23, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-17418 Filed 7-29-08; 8:45 am]
BILLING CODE 4163-18-P
