Agency Forms Undergoing Paperwork Reduction Act Review, 12595-12596 [2012-4950]
Download as PDF
<![CDATA[
12595
Federal Register / Vol. 77, No. 41 / Thursday, March 1, 2012 / Notices
Amendments and Reauthorization Act
of 1986.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Michigan Shoreline Anglers ............................
Screening Questionnaire ................................
Telephone Questions for Scheduling Appointments.
Informed Consent ...........................................
Biomonitoring Questionnaire ..........................
Recruitment Calling Script .............................
Refusal Questions Form ................................
Individual Consent Form ................................
Contact Information Form ..............................
Study Participant Questionnaire ....................
Clinic Visit Form .............................................
Participation Record .......................................
Mail-in Eligibility Screening Survey ................
Online Eligibility Screening Survey ................
Telephone Script for Non-responders to
Screening.
Telephone Script for Eligible Responders to
Screening.
Informed Consent ...........................................
Interview Questionnaire .................................
Eligibility Screening Survey ............................
Informed Consent ...........................................
Interview Questionnaire .................................
Network Size Questions for Respondent
Driven Sampling.
American Indians from Minnesota ..................
New York State Licensed Anglers ..................
Immigrants from Burma and Descendants .....
Kimberly S. Lane,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2012–4947 Filed 2–29–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–12–0338]
mstockstill on DSK4VPTVN1PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
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 404–639–7570 or send
comments to Kimberly Lane, CDC
Reports Clearance Officer, 1600 Clifton
Road, MS D–74, Atlanta, GA 30333 or
send an email to omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
VerDate Mar<15>2010
17:25 Feb 29, 2012
Jkt 226001
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
Annual Submission of the Ingredients
Added to, and the Quantity of Nicotine
Contained in, Smokeless Tobacco
Manufactured, Imported, or Packaged in
the U.S. (OMB No. 0920–0338, exp. 9/
30/2012)—Extension—Office on
Smoking and Health, National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
The oral use of smokeless tobacco
(SLT) products represents a significant
health risk. Smokeless tobacco products
contain carcinogens which can cause
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
Number
responses per
respondent
Average
burden per
response
(in hours)
350
250
1
1
5/60
7/60
200
200
312
62
250
250
250
250
250
300
450
500
1
1
1
1
1
1
1
1
1
1
1
1
1/60
54/60
5/60
2/60
3/60
2/60
30/60
1/60
3/60
5/60
5/60
5/60
150
1
5/60
200
200
92
50
50
50
1
1
1
1
1
1
1/60
30/60
5/60
1/60
1
5/60
cancer and a number of non-cancerous
oral conditions, as well as leading to
nicotine addiction and dependence.
Furthermore, SLT use is not a safe
substitute for cigarette smoking.
Adolescents who use smokeless tobacco
are more likely to become cigarette
smokers.
The Centers for Disease Control and
Prevention (CDC), Office on Smoking
and Health (OSH), has primary
responsibility for the Department of
Health and Human Services (HHS)
smoking and health program. HHS’s
overall goal is to reduce death and
disability resulting from the use of
smokeless tobacco products and other
forms of tobacco through programs of
information, education and research.
The Comprehensive Smokeless
Tobacco Health Education Act of 1986
(CSTHEA, 15 U.S.C. 4401 et seq., Pub.
L. 99–252) requires each person who
manufactures, packages, or imports
smokeless tobacco products 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. CSTHEA
further requires submission of the
quantity of nicotine contained in each
smokeless tobacco product. Finally, the
legislation authorizes HHS to undertake
research, and to report to Congress (as
E:\FR\FM\01MRN1.SGM
01MRN1
12596
Federal Register / Vol. 77, No. 41 / Thursday, March 1, 2012 / Notices
deemed appropriate) discussing the
health effects of these ingredients.
HHS has delegated responsibility for
implementing the required information
collection to CDC’s Office on Smoking
and Health. Respondents are not
required to submit specific forms;
however, they are required to meet
reporting guidelines and to submit the
ingredient report by chemical name and
Chemical Abstract Service (CAS)
Registration Number, consistent with
accepted reporting practices for other
companies that are required to report
ingredients added to other consumer
products. Typically, respondents submit
respondent’s letterhead, by CD, threeinch floppy disk, or thumb drive.
Electronic mail submissions are not
accepted. Upon receipt and verification
of the annual nicotine and ingredient
report, OSH issues a Certificate of
Compliance to the respondent.
There are no changes to information
collection procedures or the estimated
burden per response. There is an
increase in total estimated burden due
to an increase in the estimated number
of respondents, from 11 to 13. There are
no costs to respondents other than their
time.
a summary report to CDC with the
ingredient information for multiple
products, or a statement that there are
no changes to their previously
submitted ingredient report.
Respondents may submit the required
information to CDC through a
designated representative. The
information collection is subject to strict
confidentiality provisions.
Ingredient reports for new SLT
products are due at the time of first
importation. Thereafter, ingredient
reports are due annually on March 31.
Information is submitted to OSH by
mailing a written report on the
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Smokeless Tobacco Manufacturers,
Packagers, and Importers.
SLT Nicotine and Ingredient and
Report.
13
1
1,713
22,269
Kimberly S. Lane,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2012–4950 Filed 2–29–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
mstockstill on DSK4VPTVN1PROD with NOTICES
Title: Objective Work Plan (OWP),
Objective Progress Report (OPR) and
Project Abstract.
OMB No.: 0980–0204.
Description: Content changes are
being proposed for the OPR and OWP
ONLY. The information in the OPR is
collected on a quarterly basis to monitor
the performance of grantees and better
gauge grantee progress. The
standardized format allows ANA to
report results across all its program
areas and flag grantees that may need
additional training and/or technical
assistance to successfully implement
their projects. The following are
proposed changes within specific
sections of the OPR form:
Objective Work Plan Update Section:
ANA has added fields for 1st through
4th Quarter (Q1,Q2,Q3,Q4) to report the
results for activities within each Project
Objective. The grantee may continue to
add to this form each quarter (rather
than to a new form), reflecting
cumulative results throughout the
project period instead of a single
quarter.
Financial Section: ANA has added 2
questions to: (1) Provide details on any
income generated as a result of ANA
project activities; (2) Provide details on
any changes made to the budget during
the reporting period.
Native American Youth and Elder
Opportunities Section: ANA has added
a question to: (1) Request details on any
intergenerational activities between
grandparents and their grandchildren.
Finally, ANA has added a new section
(last section) to the form titled:
PROJECT SUSTAINABILITY, to: (1)
Request details on the grantee’s
intention to continue the project
benefits and/or services after ANA’s
funding period for the project has
ended.
End of Changes to the OPR
The OWP: The information collected
through the OWP is needed to properly
administer and monitor the
Administration for Native Americans
(ANA) programs. The OWP assists
applicants in describing their projects’
objectives and activities, and also assists
independent panel reviewers, ANA staff
and the ANA Commissioner during
review and funding decision process.
Changes Specific Sections of the OWP
Problem Statement: ANA added a
field for applicants to include the
problem statement they identified in
their grant application.
Position Performing the Activity: On
the previous OWP, ANA requested
applicants to identify the position
responsible for each activity. ANA has
changed this title to ‘‘position
performing the activity’’ and applicants
are asked to identify the lead person in
one column and other support persons
in the second column.
End of Changes to the OWP
Project Abstract: The Project Abstract
form is no longer managed by ANA.
Respondents: Tribal Government,
Native Non-profit Organizations, Tribal
Colleges & Universities.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
OWP ................................................................................................................
OPR .................................................................................................................
VerDate Mar<15>2010
17:25 Feb 29, 2012
Jkt 226001
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
500
275
E:\FR\FM\01MRN1.SGM
1
4
01MRN1
Average
burden hours
per response
3
1
Total burden
hours
1,500
1,100
]]>Agencies
[Federal Register Volume 77, Number 41 (Thursday, March 1, 2012)]
[Notices]
[Pages 12595-12596]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-4950]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60-Day-12-0338]
Agency Forms Undergoing Paperwork Reduction Act Review
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 404-639-7570 or
send comments to Kimberly Lane, CDC Reports Clearance Officer, 1600
Clifton Road, MS D-74, Atlanta, GA 30333 or send an email 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
Annual Submission of the Ingredients Added to, and the Quantity of
Nicotine Contained in, Smokeless Tobacco Manufactured, Imported, or
Packaged in the U.S. (OMB No. 0920-0338, exp. 9/30/2012)--Extension--
Office on Smoking and Health, National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The oral use of smokeless tobacco (SLT) products represents a
significant health risk. Smokeless tobacco products contain carcinogens
which can cause cancer and a number of non-cancerous oral conditions,
as well as leading to nicotine addiction and dependence. Furthermore,
SLT use is not a safe substitute for cigarette smoking. Adolescents who
use smokeless tobacco are more likely to become cigarette smokers.
The Centers for Disease Control and Prevention (CDC), Office on
Smoking and Health (OSH), has primary responsibility for the Department
of Health and Human Services (HHS) smoking and health program. HHS's
overall goal is to reduce death and disability resulting from the use
of smokeless tobacco products and other forms of tobacco through
programs of information, education and research.
The Comprehensive Smokeless Tobacco Health Education Act of 1986
(CSTHEA, 15 U.S.C. 4401 et seq., Pub. L. 99-252) requires each person
who manufactures, packages, or imports smokeless tobacco products 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. CSTHEA further requires submission of the quantity of
nicotine contained in each smokeless tobacco product. Finally, the
legislation authorizes HHS to undertake research, and to report to
Congress (as
[[Page 12596]]
deemed appropriate) discussing the health effects of these ingredients.
HHS has delegated responsibility for implementing the required
information collection to CDC's Office on Smoking and Health.
Respondents are not required to submit specific forms; however, they
are required to meet reporting guidelines and to submit the ingredient
report by chemical name and Chemical Abstract Service (CAS)
Registration Number, consistent with accepted reporting practices for
other companies that are required to report ingredients added to other
consumer products. Typically, respondents submit a summary report to
CDC with the ingredient information for multiple products, or a
statement that there are no changes to their previously submitted
ingredient report. Respondents may submit the required information to
CDC through a designated representative. The information collection is
subject to strict confidentiality provisions.
Ingredient reports for new SLT products are due at the time of
first importation. Thereafter, ingredient reports are due annually on
March 31. Information is submitted to OSH by mailing a written report
on the respondent's letterhead, by CD, three-inch floppy disk, or thumb
drive. Electronic mail submissions are not accepted. Upon receipt and
verification of the annual nicotine and ingredient report, OSH issues a
Certificate of Compliance to the respondent.
There are no changes to information collection procedures or the
estimated burden per response. There is an increase in total estimated
burden due to an increase in the estimated number of respondents, from
11 to 13. There are no costs to respondents other than their time.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Smokeless Tobacco Manufacturers, Packagers, and SLT Nicotine and Ingredient and 13 1 1,713 22,269
Importers. Report.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Kimberly S. Lane,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2012-4950 Filed 2-29-12; 8:45 am]
BILLING CODE 4163-18-P
