Approved Tobacco Retailer Training Program; Request for Comments, 65129-65130 [E9-29288]
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65129
Federal Register / Vol. 74, No. 235 / Wednesday, December 9, 2009 / Notices
Assets and a trustee to divest any
divestiture assets that SCI fails to timely
divest. The Commission also may seek
civil penalties from SCI for noncompliance with the Consent
Agreement.
The proposed Consent Agreement
prohibits SCI from acquiring any
interest or assets engaged in the
provision of cemetery services in the
Las Vegas metropolitan area for ten (10)
years without providing prior written
notice to the Commission. In addition,
SCI is required to file periodic reports
of compliance with the proposed orders.
The purpose of this analysis is to
facilitate public comment on the
proposed Consent Agreement, and it is
not intended to constitute an official
interpretation of the proposed Consent
Agreement or to modify its terms in any
way.
By direction of the Commission.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Donald S. Clark,
Secretary.
[FR Doc. E9–29332 Filed 12–8–09; 9:02 am]
Proposed Project
National Coal Workers’ Autopsy
Study (NCWAS)—Extension—(0920–
0021 Exp. 1/31/2010) National Institute
for Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
BILLING CODE: 6750–01–S
Centers for Disease Control and
Prevention
[30Day–10–0021]
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 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.
Background and Brief Description
Under the Federal Coal Mine Health
and Safety Act of 1977, Public Law 91–
173 (amended the Federal Coal Mine
and Safety Act of 1969); the Public
Health Service has developed a
nationwide autopsy program (NCWAS)
for underground coal miners. The
Consent Release and History Form are
primarily used to obtain written
authorization from the next-of-kin to
perform an autopsy on the deceased
miner. Because a basic reason for the
post-mortem examination is research
(both epidemiological and clinical), a
minimum of essential information is
collected regarding the deceased miners,
including occupational history and
smoking history. The data collected will
be used by the staff at NIOSH for
research purposes in defining the
diagnostic criteria for coal workers’
pneumoconiosis (black lung) and
pathologic changes and will be
correlated with x-ray findings.
It is estimated that only 5 minutes is
required for the pathologist to put a
statement on the invoice affirming that
no other compensation is received for
the autopsy. From past experience, it is
estimated that 15 minutes is required for
the next-of-kin to complete the Consent
Release and History Form. Since an
autopsy report is routinely completed
by a pathologist, the only additional
burden is the specific request of abstract
of terminal illness and final diagnosis
relating to pneumoconiosis. Therefore,
only 5 minutes of additional burden is
estimated for the autopsy report.
There are no costs to respondents
other than their time. The total
estimated burden hours are 21.
ESTIMATED ANNUALIZED BURDEN
Form name
Pathologist ................................................
Pathologist ................................................
Next-of-Kin ................................................
Invoice ......................................................
NCWAS Checklist ....................................
Consent Release History .........................
Dated: December 3, 2009.
Maryam Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–29385 Filed 12–8–09; 8:45 am]
BILLING CODE 4163–18–P
WReier-Aviles on DSKGBLS3C1PROD with NOTICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0569]
Approved Tobacco Retailer Training
Program; Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
VerDate Nov<24>2008
15:02 Dec 08, 2009
Jkt 220001
ACTION:
Notice; request for comments.
SUMMARY: The Food and Drug
Administration (FDA) is establishing a
public docket to obtain information on
suggested elements for approved
tobacco retailer training programs. FDA
is establishing this docket in order to
provide an opportunity for interested
parties to provide information and share
views on elements that should be
included in an effective retailer training
program as provided for in the Family
Smoking Prevention and Tobacco
Control Act (the Tobacco Control Act).
DATES: Submit electronic or written
comments by January 8, 2010.
ADDRESSES: Submit electronic
comments to https://www.
PO 00000
Frm 00042
Fmt 4703
Number of
responses per
respondent
Number of
respondents
Type of respondents
Sfmt 4703
50
50
50
Average burden
per response (in
hours)
1
1
1
5/60
5/60
15/60
regulations.gov. Submit written
comments to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Anne Kirchner, Center for Tobacco
Products, Food and Drug
Administration, 9200 Corporate Blvd.,
Rockville, MD 20850–3229, 301–796–
4800, Anne.Kirchner@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Tobacco products are responsible for
more than 440,000 deaths each year.
The Centers for Disease Control and
Prevention (CDC) report an estimated 60
million adults smoke cigarettes in the
E:\FR\FM\09DEN1.SGM
09DEN1
WReier-Aviles on DSKGBLS3C1PROD with NOTICES
65130
Federal Register / Vol. 74, No. 235 / Wednesday, December 9, 2009 / Notices
United States, even though this behavior
will result in death or disability for half
of all regular users. Paralleling this
enormous health burden is the
economic burden of tobacco use, which
is estimated to total $193 billion
annually in medical expenditures and
lost productivity. Curbing the
significant adverse consequences of
tobacco use is one of the most important
public health goals of our time. One way
to do this is to prevent youth from
beginning to smoke. According to the
Substance Abuse and Mental Health
Services Administration’s (SAMHSA’s)
National Survey on Drug Use and
Health, 80 percent of adults who are
nicotine dependent report that they
started smoking cigarettes before the age
of 18.
On June 22, 2009, the President
signed the Tobacco Control Act into
law. The Tobacco Control Act grants
FDA important new authority to
regulate the manufacture, marketing,
and distribution of tobacco products to
protect the public health generally and
to reduce tobacco use by minors.
Section 102 of the Tobacco Control Act
requires FDA to issue, with certain
modifications, its 1996 final regulation
restricting the sale and distribution of
cigarettes and smokeless tobacco
products (August 28, 1996, 61 FR 44396
at 44615 to 44618). The rule contains
provisions designed to limit young
people’s access to tobacco products, as
well as restrictions on marketing to curb
the appeal of these products to minors.
Section 103(q)(2) of the Tobacco
Control Act includes two schedules for
assessing civil money penalties against
retailers for violations of restrictions on
the sale and distribution of tobacco
products, including restrictions on
access to, and the promotion and
advertising of, tobacco products. Under
each schedule, violators are subject to
increasing penalties for repeated
violations within prescribed time
periods. For the first three violations in
a 24-month period, retailers with
approved training programs are subject
to lower penalties than retailers without
such programs. Section 103(q)(2)(B) of
the Tobacco Control Act defines
‘‘approved training program’’ as ‘‘a
training program that complies with
standards developed by the [FDA] for
such programs.’’
We are requesting comments that will
inform the development of guidance on
approved training programs. A copy of
the Family Smoking Prevention and
Tobacco Control Act is available on the
agency’s Web site at https://www.
fda.gov/TobaccoProducts/Guidance
ComplianceRegulatoryInformation/
default.htm.
VerDate Nov<24>2008
15:02 Dec 08, 2009
Jkt 220001
II. Request for Comments and
Information
We are interested in comments on the
characteristics that comprise an
effective training program for clerks
selling tobacco products in a retail
establishment. Such programs would
effectively teach such clerks how to
request and verify the photo
identification of purchasers younger
than 27 years of age and how to refuse
the sale of cigarettes or smokeless
tobacco to purchasers younger than 18
years of age. We are particularly
interested in information about
elements of current tobacco retailer
training programs developed by trade
associations, corporations, States and
localities, as well as any studies on the
effectiveness of these training programs
in reducing retail sales of tobacco
products to youth.
We believe that effective retailer
training programs may include many of
the following components and we
welcome input on any of these specific
elements:
• Methods for teaching salesclerks
about:
» Federal, State, and local laws
prohibiting youth access to tobacco.
» The health and societal costs of
tobacco use as the basis for youth
access laws.
» Company policies on youth access
to tobacco.
» The definition of tobacco products
covered by youth access laws.
» Laws and company policies on
requiring identification, including
the age that triggers ID verification
and the acceptable forms of ID.
» The need to closely examine ID,
including an explanation that many
illegal sales are made to minors
who produce IDs showing that they
are under the legal age to purchase
tobacco products.
» Verification of an ID’s authenticity,
including the features of an ID that
must be checked, how to tell if an
ID might have been altered and
what an employee should do if an
ID appears to be altered.
» The fact that salesclerks are not
required to make a tobacco sale if
there is any question that doing so
would violate the law.
• Specific age-verifying protocols
designed to ensure that the date of birth
is read, clearly understood, and
compared to a calendar or other age
verification device.
• Practical techniques for:
» Asking for ID.
» When and how to ask for a second
ID.
» Declining a sale when the customer
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
has no ID or when the ID shows the
customer to be underage.
» Declining a sale because of
concerns about whether the ID has
been altered.
» Declining purchase attempts by a
minor made with written parental
permission.
» Resisting customer pressure.
» Declining to sell tobacco to
underage persons who are friends,
acquaintances, and peer group
members and the techniques for
refusal.
• Methods for ensuring and
documenting that employees have the
knowledge required to comply with
youth access laws.
We also believe that effective
programs would include strategies for
initial training of new employees and
refresher training for existing
employees. We are interested in
learning about programs that address
both of these aspects, as well as
information related to the appropriate
length of time between initial and
refresher training, and the most
appropriate methods for training (e.g.,
in-person training, Web-based training,
self-study). The agency will consider
information submitted to the docket in
developing guidance on approved
training programs.
III. Comments
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) electronic or written
comments regarding this document.
Submit a single copy of electronic
comments or two paper copies of any
mailed comments, except that
individuals may submit one paper copy.
Comments are to be identified with the
docket number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday.
Dated: December 3, 2009.
David Horowitz,
Assistant Commissioner for Policy.
[FR Doc. E9–29288 Filed 12–8–09; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Board of Scientific Counselors,
National Center for Public Health
Informatics: Notice of Charter Renewal
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
E:\FR\FM\09DEN1.SGM
09DEN1
Agencies
[Federal Register Volume 74, Number 235 (Wednesday, December 9, 2009)]
[Notices]
[Pages 65129-65130]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-29288]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2009-N-0569]
Approved Tobacco Retailer Training Program; Request for Comments
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; request for comments.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is establishing a
public docket to obtain information on suggested elements for approved
tobacco retailer training programs. FDA is establishing this docket in
order to provide an opportunity for interested parties to provide
information and share views on elements that should be included in an
effective retailer training program as provided for in the Family
Smoking Prevention and Tobacco Control Act (the Tobacco Control Act).
DATES: Submit electronic or written comments by January 8, 2010.
ADDRESSES: Submit electronic comments to https://www.regulations.gov.
Submit written comments to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Anne Kirchner, Center for Tobacco
Products, Food and Drug Administration, 9200 Corporate Blvd.,
Rockville, MD 20850-3229, 301-796-4800, Anne.Kirchner@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Tobacco products are responsible for more than 440,000 deaths each
year. The Centers for Disease Control and Prevention (CDC) report an
estimated 60 million adults smoke cigarettes in the
[[Page 65130]]
United States, even though this behavior will result in death or
disability for half of all regular users. Paralleling this enormous
health burden is the economic burden of tobacco use, which is estimated
to total $193 billion annually in medical expenditures and lost
productivity. Curbing the significant adverse consequences of tobacco
use is one of the most important public health goals of our time. One
way to do this is to prevent youth from beginning to smoke. According
to the Substance Abuse and Mental Health Services Administration's
(SAMHSA's) National Survey on Drug Use and Health, 80 percent of adults
who are nicotine dependent report that they started smoking cigarettes
before the age of 18.
On June 22, 2009, the President signed the Tobacco Control Act into
law. The Tobacco Control Act grants FDA important new authority to
regulate the manufacture, marketing, and distribution of tobacco
products to protect the public health generally and to reduce tobacco
use by minors. Section 102 of the Tobacco Control Act requires FDA to
issue, with certain modifications, its 1996 final regulation
restricting the sale and distribution of cigarettes and smokeless
tobacco products (August 28, 1996, 61 FR 44396 at 44615 to 44618). The
rule contains provisions designed to limit young people's access to
tobacco products, as well as restrictions on marketing to curb the
appeal of these products to minors.
Section 103(q)(2) of the Tobacco Control Act includes two schedules
for assessing civil money penalties against retailers for violations of
restrictions on the sale and distribution of tobacco products,
including restrictions on access to, and the promotion and advertising
of, tobacco products. Under each schedule, violators are subject to
increasing penalties for repeated violations within prescribed time
periods. For the first three violations in a 24-month period, retailers
with approved training programs are subject to lower penalties than
retailers without such programs. Section 103(q)(2)(B) of the Tobacco
Control Act defines ``approved training program'' as ``a training
program that complies with standards developed by the [FDA] for such
programs.''
We are requesting comments that will inform the development of
guidance on approved training programs. A copy of the Family Smoking
Prevention and Tobacco Control Act is available on the agency's Web
site at https://www.fda.gov/TobaccoProducts/GuidanceComplianceRegulatoryInformation/default.htm.
II. Request for Comments and Information
We are interested in comments on the characteristics that comprise
an effective training program for clerks selling tobacco products in a
retail establishment. Such programs would effectively teach such clerks
how to request and verify the photo identification of purchasers
younger than 27 years of age and how to refuse the sale of cigarettes
or smokeless tobacco to purchasers younger than 18 years of age. We are
particularly interested in information about elements of current
tobacco retailer training programs developed by trade associations,
corporations, States and localities, as well as any studies on the
effectiveness of these training programs in reducing retail sales of
tobacco products to youth.
We believe that effective retailer training programs may include
many of the following components and we welcome input on any of these
specific elements:
Methods for teaching salesclerks about:
[ctrcir] Federal, State, and local laws prohibiting youth access to
tobacco.
[ctrcir] The health and societal costs of tobacco use as the basis
for youth access laws.
[ctrcir] Company policies on youth access to tobacco.
[ctrcir] The definition of tobacco products covered by youth access
laws.
[ctrcir] Laws and company policies on requiring identification,
including the age that triggers ID verification and the acceptable
forms of ID.
[ctrcir] The need to closely examine ID, including an explanation
that many illegal sales are made to minors who produce IDs showing that
they are under the legal age to purchase tobacco products.
[ctrcir] Verification of an ID's authenticity, including the
features of an ID that must be checked, how to tell if an ID might have
been altered and what an employee should do if an ID appears to be
altered.
[ctrcir] The fact that salesclerks are not required to make a
tobacco sale if there is any question that doing so would violate the
law.
Specific age-verifying protocols designed to ensure that
the date of birth is read, clearly understood, and compared to a
calendar or other age verification device.
Practical techniques for:
[ctrcir] Asking for ID.
[ctrcir] When and how to ask for a second ID.
[ctrcir] Declining a sale when the customer has no ID or when the
ID shows the customer to be underage.
[ctrcir] Declining a sale because of concerns about whether the ID
has been altered.
[ctrcir] Declining purchase attempts by a minor made with written
parental permission.
[ctrcir] Resisting customer pressure.
[ctrcir] Declining to sell tobacco to underage persons who are
friends, acquaintances, and peer group members and the techniques for
refusal.
Methods for ensuring and documenting that employees have
the knowledge required to comply with youth access laws.
We also believe that effective programs would include strategies
for initial training of new employees and refresher training for
existing employees. We are interested in learning about programs that
address both of these aspects, as well as information related to the
appropriate length of time between initial and refresher training, and
the most appropriate methods for training (e.g., in-person training,
Web-based training, self-study). The agency will consider information
submitted to the docket in developing guidance on approved training
programs.
III. Comments
Interested persons may submit to the Division of Dockets Management
(see ADDRESSES) electronic or written comments regarding this document.
Submit a single copy of electronic comments or two paper copies of any
mailed comments, except that individuals may submit one paper copy.
Comments are to be identified with the docket number found in brackets
in the heading of this document. Received comments may be seen in the
Division of Dockets Management between 9 a.m. and 4 p.m., Monday
through Friday.
Dated: December 3, 2009.
David Horowitz,
Assistant Commissioner for Policy.
[FR Doc. E9-29288 Filed 12-8-09; 8:45 am]
BILLING CODE 4160-01-S