Proposed Data Collections Submitted for Public Comment and Recommendations, 47044-47045 [E7-16591]
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47044
Federal Register / Vol. 72, No. 162 / Wednesday, August 22, 2007 / Notices
Testing and Medical Records Review;
June 13, 2007.
Sal’s Auto Repair; April 4, 2007.
Topps Cleaners Site—Public Health
Implications and Interpretation of
Tetrachloroethylene (PCE) Exposure
in Indoor Air; April 4, 2007.
Dated: August 15, 2007.
Kenneth Rose,
Director, Office of Policy, Planning, and
Evaluation, National Center for
Environmental Health/Agency for Toxic
Substances and Disease Registry.
[FR Doc. E7–16548 Filed 8–21–07; 8:45 am]
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New Mexico
Grants Chlorinated Solvents Plume Site;
April 10, 2007.
New York
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Great Kills Park—Gateway National
Recreation Area; May 31, 2007.
Centers for Disease Control and
Prevention
Ohio
[60Day–07–0109]
Laugh and Learn Daycare; June 18,
2007.
Washington County Air Quality; June
18, 2007.
Proposed Data Collections Submitted
for Public Comment and
Recommendations
Oregon
North Morrow Perchlorate Area—
Exposure Investigation Report; April
18, 2007.
Pennsylvania
Crown Industries Site; June 12, 2007.
Langner Enterprises Site (Residential
Wells); June 14, 2007.
Tennessee
Hardeman County Landfill (a/k/a
Velsicol Chemical Corporation); April
16, 2007.
Pesticide Contamination in a Home;
April 19, 2007.
Utah
An Investigation of Cancer Incidence in
Census Tracts—1251.03, 1251.04,
1258.04, 1258.05, 1258.06, 1259.04,
1259.05, and 1259.06, 1978–2001;
June 15, 2007.
Washington
Evaluation of Selected Metals in
Geoduck Tissue from Tracts 09950
and 10400; April 18, 2007.
Progress Elementary School—
Evaluation of Soil Contamination;
June 21, 2007.
jlentini on PROD1PC65 with NOTICES
West Virginia
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 404–639–5960 or send
comments to Maryam I. Daneshvar, CDC
Assistant Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail 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 will 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.
Holder Chemical Corporation—
Exposure to Chemicals in
Groundwater; June 14, 2007.
Krouts Creek Site—Vapor Intrusion;
June 14, 2007.
Nitro School Dioxin Site—Dioxin in
Dust in Schools and Community
Center; April 18, 2007.
Respiratory Protective Devices—42
CFR part 84—Regulation—(0920–
0109)—Extension—National Institute
for Occupational Safety and Health
(NIOSH), of the Centers for Disease
Control and Prevention (CDC).
Wisconsin
Background and Brief Description
Primary School Campus of St. Katharine
Drexel School—Vapor Intrusion at a
School; June 20, 2007.
This data collection was formerly
named Respiratory Protective Devices
30 CFR part 11 but in 1995, the
VerDate Aug<31>2005
16:26 Aug 21, 2007
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Proposed Project
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Frm 00093
Fmt 4703
Sfmt 4703
respirator standard was moved to 42
CFR part 84. The regulatory authority
for the National Institute for
Occupational Safety and Health
(NIOSH) certification program for
respiratory protective devices is found
in the Mine Safety and Health
Amendments Act of 1977 (30 U.S.C.
577a, 651 et seq., and 657(g)) and the
Occupational Safety and Health Act of
1970 (30 U.S.C. 3, 5, 7, 811, 842(h),
844). These regulations have as their
basis the performance tests and criteria
for approval of respirators used by
millions of American construction
workers, miners, painters, asbestos
removal workers, fabric mill workers,
and fire fighters. In addition to
benefiting industrial workers, the testing
requirements also benefit health care
workers implementing the current CDC
Guidelines for Preventing the
Transmission of Tuberculosis.
Regulations of the Environmental
Protection Agency (EPA) and the
Nuclear Regulatory Commission (NRC)
also require the use of NIOSH-approved
respirators. Recent developments in this
program have provided approvals for
self-contained breathing apparatus
(SCBA), Air-Purifying respirators,
Powered Air-Purifying (PAPR) and AirPurifying Escape respirators for use by
fire fighters and other first responders to
potential terrorist attacks. These
regulations also establish methods for
respirator manufacturers to submit
respirators for testing under the
regulation and have them certified as
NIOSH-approved if they meet the
criteria given in the above regulation.
NIOSH, in accordance with 42 CFR 84:
(1) Issues certificates of approval for
respirators which have met specified
construction, performance, and
protection requirements; (2) establishes
procedures and requirements to be met
in filing applications for approval; (3)
specifies minimum requirements and
methods to be employed by NIOSH and
by applicants in conducting inspections,
examinations, and tests to determine
effectiveness of respirators; (4)
establishes a schedule of fees to be
charged applicants for testing and
certification, and (5) establishes
approval labeling requirements.
Information is collected from those who
apply for certification in order to
properly establish the scope and intent
of request. Contact information, type of
respirator, quality assurance plans and
procedures that are used in producing
the respirator, and draft labels, as
specified in the regulation, are the types
of data collected. Respirator
manufacturers (approximately 43), are
the respondents and upon completion of
E:\FR\FM\22AUN1.SGM
22AUN1
47045
Federal Register / Vol. 72, No. 162 / Wednesday, August 22, 2007 / Notices
the forms, their requests for approval are
evaluated. There is no cost to
respondents other than their time to
participate.
Estimated Annualized Burden Hours:
Section name
Data type
Number of respondents
Number of responses per
respondent
Average burden response
(in hours)
84.11 .................................................
84.33 .................................................
84.35 .................................................
84.41 .................................................
84.43 .................................................
84.257 ...............................................
84.1103 .............................................
Total ...........................................
Applications ......................................
Labeling ............................................
Modifications ....................................
Reporting ..........................................
Record Keeping ...............................
Labeling ............................................
Labeling ............................................
...........................................................
43
43
43
43
43
43
43
........................
8
8
8
8
8
8
8
........................
86
2
66
23
46
3
3
........................
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–16591 Filed 8–21–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
National Institute for Occupational
Safety and Health (NIOSH) Advisory
Board on Radiation and Worker Health
(ABRWH or Advisory Board)
jlentini on PROD1PC65 with NOTICES
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention announces the
following committee meeting:
Name: Advisory Board on Radiation and
Worker Health, National Institute for
Occupational Safety and Health.
Audio Conference Call Time and Date: 11
a.m.–4 p.m., EST, Tuesday, September 4,
2007.
Place: Audio Conference Call via FTS
Conferencing. The USA toll free dial in
number is 1–866–643–6504 with a pass code
of 9448550.
Status: Open to the public, but without a
public comment period.
Background: The Advisory Board was
established under the Energy Employees
Occupational Illness Compensation Program
Act of 2000 to advise the President on a
variety of policy and technical functions
required to implement and effectively
manage the new compensation program. Key
functions of the Advisory Board include
providing advice on the development of
probability of causation guidelines which
have been promulgated by the Department of
Health and Human Services (HHS) as a final
rule, advice on methods of dose
reconstruction which have also been
promulgated by HHS as a final rule, advice
on the scientific validity and quality of dose
estimation and reconstruction efforts being
performed for purposes of the compensation
VerDate Aug<31>2005
17:18 Aug 21, 2007
Jkt 211001
program, and advice on petitions to add
classes of workers to the Special Exposure
Cohort (SEC).
In December 2000, the President delegated
responsibility for funding, staffing, and
operating the Advisory Board to HHS, which
subsequently delegated this authority to the
CDC. NIOSH implements this responsibility
for CDC. The charter was issued on August
3, 2001, renewed at appropriate intervals,
most recently, August 3, 2007, and will
expire on August 3, 2009.
Purpose: This Advisory Board is charged
with (a) providing advice to the Secretary,
HHS, on the development of guidelines
under Executive Order 13179; (b) providing
advice to the Secretary, HHS, on the
scientific validity and quality of dose
reconstruction efforts performed for this
program; and (c) upon request by the
Secretary, HHS, advising the Secretary on
whether there is a class of employees at any
Department of Energy facility who were
exposed to radiation but for whom it is not
feasible to estimate their radiation dose, and
on whether there is reasonable likelihood
that such radiation doses may have
endangered the health of members of this
class.
Matters To Be Discussed: The agenda for
the conference call includes: Report of Board
Member Votes Recorded Since the Last Board
Meeting; Update on Rocky Flats Follow-Up
Actions; Update on SC&A Review of TBD
6000 and General Steel Industries Appendix;
Report on SC&A Contract Talks for FY08;
Discussions of Initial Steps for a Board
Contractor for FY09 and Beyond; Report on
Privacy Act ‘‘Clearance’’ Procedures; Update
on Letters to DOE and DOL on Chapman
Valve; Work Group Updates; Status of and
Plans for Future Board Activities; and Board
Working Time.
The agenda is subject to change as
priorities dictate.
Recommended changes to the agenda from
the Office of General Counsel resulted in the
Federal Register notice being published less
that fifteen days before the date of the
meeting.
Because there is not a public comment
period, written comments may be submitted.
Any written comments received will be
included in the official record of the meeting
PO 00000
Frm 00094
Fmt 4703
Sfmt 4703
Total burden
hours
29,584
688
22,704
7,912
15,824
1,032
1,032
78,776
and should be submitted to the contact
person below well in advance of the meeting.
Contact Person for More Information: Dr.
Lewis V. Wade, Executive Secretary, NIOSH,
CDC, 4676 Columbia Parkway, Cincinnati,
OH 45226, Telephone 513.533.6825, Fax
513.533.6826.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: August 16, 2007.
Michael Tropauer,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. E7–16557 Filed 8–21–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers For Medicare & Medicaid
Services
Privacy Act of 1974; Report of a
Modified System of Records
Department of Health and
Human Services (HHS), Center for
Medicare & Medicaid Services (CMS).
AGENCY:
Notice of a Modified System of
Records (SOR).
ACTION:
SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
we propose to modify an existing
system titled, ‘‘National Emphysema
Treatment Trial (NETT), System No. 09–
70–0531,’’ established at 65 Federal
Register 47995 (August 4, 2000). We
propose to modify existing routine use
number 1 that permits disclosure to
agency contractors and consultants to
include disclosure to CMS grantees who
perform a task for the agency. CMS
grantees, charged with completing
E:\FR\FM\22AUN1.SGM
22AUN1
Agencies
[Federal Register Volume 72, Number 162 (Wednesday, August 22, 2007)]
[Notices]
[Pages 47044-47045]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-16591]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-07-0109]
Proposed Data Collections Submitted for Public Comment and
Recommendations
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 404-639-5960 or
send comments to Maryam I. Daneshvar, CDC Assistant Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
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 will 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
Respiratory Protective Devices--42 CFR part 84--Regulation--(0920-
0109)--Extension--National Institute for Occupational Safety and Health
(NIOSH), of the Centers for Disease Control and Prevention (CDC).
Background and Brief Description
This data collection was formerly named Respiratory Protective
Devices 30 CFR part 11 but in 1995, the respirator standard was moved
to 42 CFR part 84. The regulatory authority for the National Institute
for Occupational Safety and Health (NIOSH) certification program for
respiratory protective devices is found in the Mine Safety and Health
Amendments Act of 1977 (30 U.S.C. 577a, 651 et seq., and 657(g)) and
the Occupational Safety and Health Act of 1970 (30 U.S.C. 3, 5, 7, 811,
842(h), 844). These regulations have as their basis the performance
tests and criteria for approval of respirators used by millions of
American construction workers, miners, painters, asbestos removal
workers, fabric mill workers, and fire fighters. In addition to
benefiting industrial workers, the testing requirements also benefit
health care workers implementing the current CDC Guidelines for
Preventing the Transmission of Tuberculosis. Regulations of the
Environmental Protection Agency (EPA) and the Nuclear Regulatory
Commission (NRC) also require the use of NIOSH-approved respirators.
Recent developments in this program have provided approvals for self-
contained breathing apparatus (SCBA), Air-Purifying respirators,
Powered Air-Purifying (PAPR) and Air-Purifying Escape respirators for
use by fire fighters and other first responders to potential terrorist
attacks. These regulations also establish methods for respirator
manufacturers to submit respirators for testing under the regulation
and have them certified as NIOSH-approved if they meet the criteria
given in the above regulation. NIOSH, in accordance with 42 CFR 84: (1)
Issues certificates of approval for respirators which have met
specified construction, performance, and protection requirements; (2)
establishes procedures and requirements to be met in filing
applications for approval; (3) specifies minimum requirements and
methods to be employed by NIOSH and by applicants in conducting
inspections, examinations, and tests to determine effectiveness of
respirators; (4) establishes a schedule of fees to be charged
applicants for testing and certification, and (5) establishes approval
labeling requirements. Information is collected from those who apply
for certification in order to properly establish the scope and intent
of request. Contact information, type of respirator, quality assurance
plans and procedures that are used in producing the respirator, and
draft labels, as specified in the regulation, are the types of data
collected. Respirator manufacturers (approximately 43), are the
respondents and upon completion of
[[Page 47045]]
the forms, their requests for approval are evaluated. There is no cost
to respondents other than their time to participate.
Estimated Annualized Burden Hours:
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Section name Data type Number of responses per response (in Total burden
respondents respondent hours) hours
----------------------------------------------------------------------------------------------------------------
84.11......................... Applications.... 43 8 86 29,584
84.33......................... Labeling........ 43 8 2 688
84.35......................... Modifications... 43 8 66 22,704
84.41......................... Reporting....... 43 8 23 7,912
84.43......................... Record Keeping.. 43 8 46 15,824
84.257........................ Labeling........ 43 8 3 1,032
84.1103....................... Labeling........ 43 8 3 1,032
Total..................... ................ .............. .............. .............. 78,776
----------------------------------------------------------------------------------------------------------------
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E7-16591 Filed 8-21-07; 8:45 am]
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