Approved Tobacco Retailer Training Program; Request for Comments, 65129-65130 [E9-29288]

Download as PDF 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]


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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
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