Proposed Data Collections Submitted for Public Comment and Recommendations, 47044-47045 [E7-16591]

Download as PDF 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] BILLING CODE 4163–70–P 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 Jkt 211001 Proposed Project PO 00000 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]
BILLING CODE 4163-18-P
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