Agency Forms Undergoing Paperwork Reduction Act Review, 65129 [E9-29385]
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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
]]>Agencies
[Federal Register Volume 74, Number 235 (Wednesday, December 9, 2009)]
[Notices]
[Page 65129]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-29385]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
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 e-mail
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.
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).
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
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response (in
respondents respondent hours)
----------------------------------------------------------------------------------------------------------------
Pathologist........................ Invoice.............. 50 1 5/60
Pathologist........................ NCWAS Checklist...... 50 1 5/60
Next-of-Kin........................ Consent Release 50 1 15/60
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
