Proposed Information Collection; Comment Request; National Immunization Survey Evaluation Study, 58534-58535 [E8-23559]
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58534
Federal Register / Vol. 73, No. 195 / Tuesday, October 7, 2008 / Notices
mstockstill on PROD1PC66 with NOTICES
and April and May 2007, public
workshops were held in Fort Jones,
Happy Camp, Macdoel, and Yreka, CA
to gather information about which
routes the public uses. In March 2008,
public workshops were held in those
same locations as well as Orleans, CA,
to continue gathering information about
which routes the public uses and to
identify routes missed in the inventory
of unauthorized routes. Additionally,
maps of inventoried routes were
available on the Forest’s Web site and
Forest Service offices. The public used
these maps to provide input into the
process.
The comment period on the proposed
action will extend 30 days from the date
this Notice of Intent is published in the
Federal Register.
The draft environmental impact
statement is expected to be filed with
the Environmental Protection Agency
(EPA) and to be available for public
review by May 2009. EPA will publish
a notice of availability of the draft EIS
in the Federal Register. The comment
period on the draft EIS will extend 45days from the date the EPA notice
appears in the Federal Register. At that
time, copies of the draft EIS will be
distributed to interested and affected
agencies, organizations, and members of
the public for their review and
comment. It is very important that those
interested in the management of the
Klamath NF participate at that time.
The final EIS is scheduled to be
completed in July 2009. In the final EIS,
the Forest Service will respond to
comments received during the comment
period that are: within the scope of the
proposed action; specific to the
proposed action; have a direct
relationship with the proposed action;
and include supporting reasons for the
responsible official to consider.
Submission of comments to the draft
EIS is a prerequisite for eligibility to
appeal under the 36 CFR part 215
regulations.
Comment Requested
This Notice of Intent initiates the
scoping process which guides the
development of the environmental
impact statement.
Early Notice of Importance of Public
Participation in Subsequent
Environmental Review: A draft EIS will
be prepared for comment. The comment
period on the draft EIS will be 45 days
from the date the EPA publishes the
notice of availability in the Federal
Register.
At this early stage, it is important to
give reviewers notice of several court
rulings related to public participation in
the environmental review process. First,
VerDate Aug<31>2005
18:23 Oct 06, 2008
Jkt 217001
reviewers of draft EISs must structure
their participation in the environmental
review of the proposal so that it is
meaningful and alerts an agency to the
reviewer’s position and contentions.
Vermont Yankee Nuclear Power Corp. v.
NRDC, 435 U.S. 519, 553 (1978). Also,
environmental objections that could be
raised at the draft EIS stage but that are
not raised until after completion of the
final EIS may be waived or dismissed by
the courts. City of Angoon v. Hodel, 803
F.2d 1016, 1022 (9th Cir. 1986) and
Wisconsin Heritages, Inc. v. Harris, 490
F. Supp. 1334, 1338 (E.D. Wis. 1980).
Because of these court rulings, it is very
important that those interested in this
proposed action participate by the close
of the 45-day comment period so that
comments and objections are made
available to the Forest Service at a time
when it can meaningfully consider them
and respond to them in the final EIS.
To assist the Forest Service in
identifying and considering issues and
concerns on the proposed action,
comments on the draft EIS should be as
specific as possible. It is also helpful if
comments refer to specific pages or
chapters of the draft EIS. Comments
may also address the adequacy of the
draft EIS or the merits of the alternatives
formulated and discussed in the
statement. Reviewers may wish to refer
to the Council on Environmental
Quality Regulations for implementing
the procedural provisions of the
National Environmental Policy Act at 40
CFR 1503.3 in addressing these points.
Comments received, including the
names and addresses of those who
comment, will be considered part of the
public record on this proposal and will
be available for public inspection.
Authority: 40 CFR 1501.7 and 1508.22;
Forest Service Handbook 1909.15, Section
21.
Dated: September 30, 2008.
Patricia A. Grantham,
Forest Supervisor.
[FR Doc. E8–23683 Filed 10–6–08; 8:45 am]
BILLING CODE 3410–11–P
DEPARTMENT OF COMMERCE
Census Bureau
Proposed Information Collection;
Comment Request; National
Immunization Survey Evaluation Study
U.S. Census Bureau.
Notice.
AGENCY:
ACTION:
SUMMARY: The Department of
Commerce, as part of its continuing
effort to reduce paperwork and
respondent burden, invites the general
PO 00000
Frm 00006
Fmt 4703
Sfmt 4703
public and other Federal agencies to
take this opportunity to comment on
proposed and/or continuing information
collections, as required by the
Paperwork Reduction Act of 1995,
Public Law 104–13 (44 U.S.C.
3506(c)(2)(A)).
DATES: To ensure consideration, written
comments must be submitted on or
before December 8, 2008.
ADDRESSES: Direct all written comments
to Diana Hynek, Departmental
Paperwork Clearance Officer,
Department of Commerce, Room 6625,
14th and Constitution Avenue, NW.,
Washington, DC 20230 (or via the
Internet at dHynek@doc.gov).
FOR FURTHER INFORMATION CONTACT:
Requests for additional information or
copies of the information collection
instrument(s) and instructions should
be directed to Andrea L. Piani, Census
Bureau, Room HQ–6H035, Washington,
DC 20233–8400, (301) 763–5379.
SUPPLEMENTARY INFORMATION
I. Abstract
At the behest of the Centers for
Disease Control and Prevention (CDC),
U.S. Department of Health and Human
Services, the Census Bureau plans to
conduct an evaluation study of the
National Immunization Survey (NIS).
The purpose of this study is to explore
how collaborating with the Census
Bureau and using the American
Community Survey (ACS) as the
sampling frame for selecting eligible
households could result in
improvements to the current NIS. Use of
the ACS as a sampling frame, which
includes non-landline households and
identifies households with age-eligible
children, could overcome the current
NIS non-coverage issue and
substantially reduce data collection
costs.
The NIS is a continuing, nationwide
random-digit-dialing (RDD) telephone
survey of families with children ages 19
to 35 months, or teens ages 13–17 years
followed by a mailed survey to
children’s immunization providers.
Since the survey’s inception to the
present, private contractors have
conducted the NIS for the CDC.
National, state, and local level estimates
of vaccine-specific coverage, including
newly licensed vaccines, are produced
annually.
The NIS was established to provide an
on-going, consistent data set for
analyzing vaccination coverage among
young children in the United States and
disseminating this information to state
and local health departments and other
interested public health partners. Legal
authorization to conduct the survey is
E:\FR\FM\07OCN1.SGM
07OCN1
Federal Register / Vol. 73, No. 195 / Tuesday, October 7, 2008 / Notices
mstockstill on PROD1PC66 with NOTICES
granted by Title 13, United States Code,
Section 8 and by the Public Health
Service Act, Title 42, United States
Code, Sections 306 & 2102(a)(7).
In response to one of the goals of the
1993 Childhood Immunization
Initiative, to monitor childhood
immunization coverage and provide
important statistics about childhood
vaccinations and related health matters,
funding for the NIS was provided and
data collection began in April 1994.
Furthermore, the scope of the program
expanded to include assessing progress
towards the national vaccination goals
set forth by the Childhood
Immunization Initiative of 1996.
Currently, the NIS provides vaccination
coverage estimates annually for children
aged 19–35 months and teens aged 13–
17 years, by state and at least six city/
county areas. The information collected
is used to evaluate state and local
immunization programs, to develop
health care policies, and to assist in the
determination of funding allocations for
the Vaccines for Children (VFC)
program. Since 1994, the VFC program
has helped families of children who
may not otherwise have access to
vaccines by providing free vaccines to
doctors who serve them.
In recent years, the NIS has covered
a decreasing portion of the target
population, particularly children aged
19–35 months living in households with
cell phone, but not landline telephone
service. As part of the CDC’s continuing
effort to evaluate and refine the NIS, this
study is intended to explore how
partnering with the Census Bureau and
sampling from the ACS for households
with age-eligible children having
landline, cell phone only, and no
telephone service could result in
improvements to the survey especially
in terms of coverage, response, and cost.
II. Method of Collection
Data collection for the NIS Evaluation
Study will use a multi-mode approach.
First, computer-assisted telephone
interviewing (CATI) will be conducted
with households with age-eligible
children (19–35 months) to collect
information on the vaccinations
received for each age-eligible child, as
well as information on vaccination
providers. Second, in-person follow-up
interviews with non-responders,
including households with no telephone
service, will be conducted. Due to
constraints in time and resources, the
follow-up interviews for the evaluation
study will be conducted using paperand-pencil interviewing methods. If the
results from the evaluation study prove
beneficial, in-person follow-up
interviews for the national survey will
VerDate Aug<31>2005
18:23 Oct 06, 2008
Jkt 217001
be conducted using computer-assisted
personal interviewing (CAPI) methods
whereby field representatives collect the
data from respondents using laptop
computers. Third, vaccination providers
will be contacted through the use of a
paper mail-out/mail-back process.
Providers will submit information on
vaccinations administered and the dates
the vaccinations were administered for
each child 19 through 35 months. Only
providers of age-eligible children whose
parent or guardian participated in the
telephone or paper follow-up survey
and who gave consent to follow-up with
the provider will be contacted. The
provider information on the type of
vaccine, the number of vaccinations,
and the dates of vaccination will be
used to estimate vaccination coverage
levels; the information obtained from
the parent or guardian will be used to
evaluate the completeness of the
provider-reported information.
III. Data
OMB Control Number: None.
Form Number: None.
Type of Review: Regular submission.
Affected Public: Individuals/
households; business or other for-profit
organizations (Health Care Providers).
Estimated Number of Respondents:
1,200 children in 1,185 households;
1,510 providers.
Estimated Time Per Response: 28
minutes, 2 seconds (household
component); 25 minutes, 2 seconds
(provider verification component).
Estimated Total Annual Burden
Hours: 564 hours (household
component), 634 hours (provider
verification component).
Estimated Total Annual Cost: $0.
Respondent’s Obligation: Voluntary.
Legal Authority: All information
collected about individuals or
households is confidential by law Title
13, United States Code, Section 9. Legal
authorization to conduct the survey is
granted by Title 13, United States Code,
Section 8 and by the Public Health
Service Act, Title 42, United States
Code, Sections 306 & 2102(a)(7).
IV. Request for Comments
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
(including hours and cost) 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
PO 00000
Frm 00007
Fmt 4703
Sfmt 4703
58535
on respondents, including through the
use of automated collection techniques
or other forms of information
technology.
Comments submitted in response to
this notice will be summarized and/or
included in the request for OMB
approval of this information collection;
they also will become a matter of public
record.
Dated: October 1, 2008.
Gwellnar Banks,
Management Analyst, Office of the Chief
Information Officer.
[FR Doc. E8–23559 Filed 10–6–08; 8:45 am]
BILLING CODE 3510–07–P
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[Docket 51–2008]
Foreign-Trade Zone 82—Mobile, AL;
Application for Subzone;
ThyssenKrupp Steel and Stainless
USA, LLC, (Stainless and Carbon Steel
Products), Calvert, AL
An application has been submitted to
the Foreign-Trade Zones Board (the
Board) by the City of Mobile, grantee of
FTZ 82, requesting special-purpose
subzone status for the stainless and
carbon steel products manufacturing
facility of ThyssenKrupp Steel and
Stainless USA, LLC (ThyssenKrupp),
located in Calvert, Alabama. The
application was submitted pursuant to
the provisions of the Foreign-Trade
Zones Act, as amended (19 U.S.C. 81a–
81u), and the regulations of the Board
(15 CFR part 400). It was formally filed
on October 1, 2008.
The ThyssenKrupp facility (2,500
employees, 3,515 acres/square feet, 4.5
million metric ton capacity for carbon
steel products and 1 million metric ton
capacity for stainless steel products) is
located at 1 ThyssenKrupp Drive, near
the city of Calvert, Washington and
Mobile Counties, Alabama. The facility
will be used for the manufacturing,
processing and distribution of carbon
and stainless steel products.
Components and materials sourced from
abroad (representing 44% of the value of
finished stainless steel products and
45% of the value of the finished carbon
steel products) include: Ferrochromium,
unwrought molybdenum, ferrosilicon,
articles of titanium, ferrosilicon
manganese, unwrought titanium, ferroniobium, ferro-boron, wire and rods of
agglom, unwrought aluminum and zinc
(duty rate ranges from duty-free to
15%).
FTZ procedures would exempt
ThyssenKrupp from customs duty
E:\FR\FM\07OCN1.SGM
07OCN1
Agencies
[Federal Register Volume 73, Number 195 (Tuesday, October 7, 2008)]
[Notices]
[Pages 58534-58535]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-23559]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
Census Bureau
Proposed Information Collection; Comment Request; National
Immunization Survey Evaluation Study
AGENCY: U.S. Census Bureau.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Department of Commerce, as part of its continuing effort
to reduce paperwork and respondent burden, invites the general public
and other Federal agencies to take this opportunity to comment on
proposed and/or continuing information collections, as required by the
Paperwork Reduction Act of 1995, Public Law 104-13 (44 U.S.C.
3506(c)(2)(A)).
DATES: To ensure consideration, written comments must be submitted on
or before December 8, 2008.
ADDRESSES: Direct all written comments to Diana Hynek, Departmental
Paperwork Clearance Officer, Department of Commerce, Room 6625, 14th
and Constitution Avenue, NW., Washington, DC 20230 (or via the Internet
at dHynek@doc.gov).
FOR FURTHER INFORMATION CONTACT: Requests for additional information or
copies of the information collection instrument(s) and instructions
should be directed to Andrea L. Piani, Census Bureau, Room HQ-6H035,
Washington, DC 20233-8400, (301) 763-5379.
SUPPLEMENTARY INFORMATION
I. Abstract
At the behest of the Centers for Disease Control and Prevention
(CDC), U.S. Department of Health and Human Services, the Census Bureau
plans to conduct an evaluation study of the National Immunization
Survey (NIS). The purpose of this study is to explore how collaborating
with the Census Bureau and using the American Community Survey (ACS) as
the sampling frame for selecting eligible households could result in
improvements to the current NIS. Use of the ACS as a sampling frame,
which includes non-landline households and identifies households with
age-eligible children, could overcome the current NIS non-coverage
issue and substantially reduce data collection costs.
The NIS is a continuing, nationwide random-digit-dialing (RDD)
telephone survey of families with children ages 19 to 35 months, or
teens ages 13-17 years followed by a mailed survey to children's
immunization providers. Since the survey's inception to the present,
private contractors have conducted the NIS for the CDC. National,
state, and local level estimates of vaccine-specific coverage,
including newly licensed vaccines, are produced annually.
The NIS was established to provide an on-going, consistent data set
for analyzing vaccination coverage among young children in the United
States and disseminating this information to state and local health
departments and other interested public health partners. Legal
authorization to conduct the survey is
[[Page 58535]]
granted by Title 13, United States Code, Section 8 and by the Public
Health Service Act, Title 42, United States Code, Sections 306 &
2102(a)(7).
In response to one of the goals of the 1993 Childhood Immunization
Initiative, to monitor childhood immunization coverage and provide
important statistics about childhood vaccinations and related health
matters, funding for the NIS was provided and data collection began in
April 1994. Furthermore, the scope of the program expanded to include
assessing progress towards the national vaccination goals set forth by
the Childhood Immunization Initiative of 1996. Currently, the NIS
provides vaccination coverage estimates annually for children aged 19-
35 months and teens aged 13-17 years, by state and at least six city/
county areas. The information collected is used to evaluate state and
local immunization programs, to develop health care policies, and to
assist in the determination of funding allocations for the Vaccines for
Children (VFC) program. Since 1994, the VFC program has helped families
of children who may not otherwise have access to vaccines by providing
free vaccines to doctors who serve them.
In recent years, the NIS has covered a decreasing portion of the
target population, particularly children aged 19-35 months living in
households with cell phone, but not landline telephone service. As part
of the CDC's continuing effort to evaluate and refine the NIS, this
study is intended to explore how partnering with the Census Bureau and
sampling from the ACS for households with age-eligible children having
landline, cell phone only, and no telephone service could result in
improvements to the survey especially in terms of coverage, response,
and cost.
II. Method of Collection
Data collection for the NIS Evaluation Study will use a multi-mode
approach. First, computer-assisted telephone interviewing (CATI) will
be conducted with households with age-eligible children (19-35 months)
to collect information on the vaccinations received for each age-
eligible child, as well as information on vaccination providers.
Second, in-person follow-up interviews with non-responders, including
households with no telephone service, will be conducted. Due to
constraints in time and resources, the follow-up interviews for the
evaluation study will be conducted using paper-and-pencil interviewing
methods. If the results from the evaluation study prove beneficial, in-
person follow-up interviews for the national survey will be conducted
using computer-assisted personal interviewing (CAPI) methods whereby
field representatives collect the data from respondents using laptop
computers. Third, vaccination providers will be contacted through the
use of a paper mail-out/mail-back process. Providers will submit
information on vaccinations administered and the dates the vaccinations
were administered for each child 19 through 35 months. Only providers
of age-eligible children whose parent or guardian participated in the
telephone or paper follow-up survey and who gave consent to follow-up
with the provider will be contacted. The provider information on the
type of vaccine, the number of vaccinations, and the dates of
vaccination will be used to estimate vaccination coverage levels; the
information obtained from the parent or guardian will be used to
evaluate the completeness of the provider-reported information.
III. Data
OMB Control Number: None.
Form Number: None.
Type of Review: Regular submission.
Affected Public: Individuals/households; business or other for-
profit organizations (Health Care Providers).
Estimated Number of Respondents: 1,200 children in 1,185
households; 1,510 providers.
Estimated Time Per Response: 28 minutes, 2 seconds (household
component); 25 minutes, 2 seconds (provider verification component).
Estimated Total Annual Burden Hours: 564 hours (household
component), 634 hours (provider verification component).
Estimated Total Annual Cost: $0.
Respondent's Obligation: Voluntary.
Legal Authority: All information collected about individuals or
households is confidential by law Title 13, United States Code, Section
9. Legal authorization to conduct the survey is granted by Title 13,
United States Code, Section 8 and by the Public Health Service Act,
Title 42, United States Code, Sections 306 & 2102(a)(7).
IV. Request for Comments
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
(including hours and cost) 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.
Comments submitted in response to this notice will be summarized
and/or included in the request for OMB approval of this information
collection; they also will become a matter of public record.
Dated: October 1, 2008.
Gwellnar Banks,
Management Analyst, Office of the Chief Information Officer.
[FR Doc. E8-23559 Filed 10-6-08; 8:45 am]
BILLING CODE 3510-07-P