Proposed Data Collections Submitted for Public Comment and Recommendations, 62834-62835 [2010-25694]

Download as PDF 62834 Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Notices ESTIMATE OF ANNUALIZED BURDEN HOURS—Continued Number of respondents Form number and name Respondents 57.137: Patient Safety Component—Annual Facility Survey for LTCF. 57.138: Laboratory-identified MDRO or CDI Event for LTCF. 57.139: MDRO and CDI Prevention Process Measures Monthly Monitoring for LTCF. 57.140: Urinary Tract Infection (UTI) for LTCF .... Registered Nurse (Infection Preventionist). Registered Nurse (Infection Preventionist). Registered Nurse (Infection Preventionist). Registered Nurse (Infection Preventionist). Occupational Health RN/Specialist. Occupational Health RN/Specialist. Occupational Health RN/Specialist. Occupational Health RN/Specialist. Occupational Health RN/Specialist. Laboratory Technician .. Occupational Health RN/Specialist. Occupational Health RN/Specialist. Occupational Health RN/Specialist. Occupational Health RN/Specialist. Occupational Health RN/Specialist. Medical/Clinical Laboratory Technologist. Medical/Clinical Laboratory Technologist. Medical/Clinical Laboratory Technologist. Medical/Clinical Laboratory Technologist. Medical/Clinical Laboratory Technologist. 57.202: Healthcare Worker Survey ...................... 57.203: Healthcare Personnel Safety Monthly Reporting Plan. 57.204: Healthcare Worker Demographic Data ... 57.205: Exposure to Blood/Body Fluids ............... 57.206: Healthcare Worker Prophylaxis/Treatment. 57.207: Follow-Up Laboratory Testing ................. 57.208: Healthcare Worker Vaccination History .. 57.210: Healthcare Worker Prophylaxis/Treatment—Influenza. 57.211: Pre-season Survey on Influenza Vaccination Programs for Healthcare Personnel. 57.212: Post-season Survey on Influenza Vaccination Programs for Healthcare Personnel. 57.213: Healthcare Personnel Influenza Vaccination Monthly Summary. 57.300: Hemovigilance Module Annual Survey ... 57.301: Hemovigilance Module Monthly Reporting Plan. 57.303: Hemovigilance Module Monthly Reporting Denominators. 57.304: Hemovigilance Adverse Reaction ........... 57.305: Hemovigilance Incident ........................... Total Est Annual Burden Hours .................... Dated: October 5, 2010. Carol E. Walker, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–25695 Filed 10–12–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention mstockstill on DSKH9S0YB1PROD with NOTICES [60Day–11–0729] 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 VerDate Mar<15>2010 17:22 Oct 12, 2010 Jkt 223001 ....................................... Frm 00080 Fmt 4703 Burden per response (in hours) Total annual burden (in hours) 250 1 25/60 104 250 8 30/60 1,000 250 3 7/60 88 250 9 30/60 1,125 600 100 10/60 10,000 600 9 10/60 900 600 200 20/60 40,000 600 50 1 30,000 600 10 15/60 1,500 600 600 100 300 15/60 10/60 15,000 30,000 600 50 10/60 5,000 600 1 10/60 100 600 1 10/60 100 6,000 6 2 72,000 500 1 2 1,000 500 12 2/60 200 500 12 30/60 3,000 500 120 10/60 10,000 500 72 10/60 6,000 ........................ ........................ ........................ 3,914,125 Centers for Disease Control and Prevention (CDC) will publish periodic summaries of proposed projects. To request more information on the proposed project or to obtain a copy of data collection plans and instruments, call 404–639–5960 or send comments to Carol E. Walker, Acting Reports Clearance Officer, 1600 Clifton Road, MS D–74, 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 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 PO 00000 Responses per respondent Sfmt 4703 on respondents, including 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 Customer Surveys Generic Clearance for the National Center for Health Statistics (0920–0729 exp. 6/30/2009)— Reinstatement—National Center for Health Statistics (NCHS), Centers for Disease Control and Prevention (CDC). Background and Brief Description Section 306 of the Public Health Service (PHS) Act (42 U.S.C. 242k), as amended, authorizes that the Secretary of Health and Human Services (DHHS), acting through NCHS, shall collect statistics on ‘‘the extent and nature of illness and disability of the population of the United States.’’ This is a reinstatement request for a generic E:\FR\FM\13OCN1.SGM 13OCN1 62835 Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Notices approval from OMB to conduct customer surveys over the next three years. As part of a comprehensive program, the National Center for Health Statistics (NCHS) plans to continue to assess its customers’ satisfaction with the content, quality and relevance of the information it produces. NCHS will conduct voluntary customer surveys to assess strengths in agency products and services and to evaluate how well it addresses the emerging needs of its data users. Results of these surveys will be used in future planning initiatives. The data will be collected using a combination of methodologies appropriate to each survey. These may include: Evaluation forms, mail surveys, focus groups, automated and electronic technology (e.g., e-mail, Web-based surveys), and telephone surveys. Systematic surveys of several groups will be folded into the program. Among these are Federal customers and policy makers, state and local officials who rely on NCHS data, the broader educational, research, and public health community, and other data users. Respondents may include data users who register for and/or attend NCHS sponsored conferences; persons who access the NCHS Web site and the detailed data available through it; consultants; and others. Respondent data items may include (in broad categories) information regarding respondent’s gender, age, occupation, affiliation, location, etc., to be used to characterize responses only. Other questions will attempt to obtain information that will characterize the respondents’ familiarity with and use of NCHS data, their assessment of data content and usefulness, general satisfaction with available services and products, and suggestions for improvement of surveys, services and products. The resulting information will be for NCHS internal use. There is no cost to respondents other than their time to participate in the survey. ESTIMATED ANNUALIZED BURDEN TABLE Type of survey Questionnaire for conference registrants/attendees. Focus groups ..................................... Web-based ........................................ Other customer surveys .................... Total ........................................... Public/private researchers, ants, and others. Public/private researchers, ants, and others. Public/private researchers, ants, and others. Public/private researchers, ants, and others. Total burden hours 1 10/60 500 Consult- 240 1 1 240 Consult- 3,600 1 10/60 600 Consult- 1,200 1 15/60 300 .......................................................... 8,040 ........................ ........................ 1,640 BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–11–0776] Proposed Data Collections Submitted for Public Comment and Recommendations mstockstill on DSKH9S0YB1PROD with NOTICES Average burden/response (in hours) 3,000 [FR Doc. 2010–25694 Filed 10–12–10; 8:45 am] 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 project or to obtain a copy of the data collection plans and instruments, call 404–639–5960 or send comments to Carol E. Walker, CDC Acting Reports Clearance Officer, 1600 17:22 Oct 12, 2010 Number of responses/ respondent Consult- Dated: October 6, 2010. Carol E. Walker, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. VerDate Mar<15>2010 Number of respondents Respondents Jkt 223001 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 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 Economic Analysis of the National Breast and Cervical Cancer Early Detection Program—Revision—Division of Cancer Prevention and Control, National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). PO 00000 Frm 00081 Fmt 4703 Sfmt 4703 Background and Brief Description CDC administers the National Breast and Cervical Cancer Early Detection Program (NBCCEDP), the largest organized cancer screening program in the United States. The NBCCEDP provides critical breast and cervical cancer screening services to uninsured and underserved low-income women in all 50 States, the District of Columbia, five U.S. territories, and 12 American Indian/Alaska Native organizations. The program provides breast and cervical cancer screening for eligible women who participate in the program as well as diagnostic procedures for women who have abnormal findings. During the past decade, the NBCCEDP has provided over 9.2 million breast and cervical cancer screening and diagnostic exams to over 3.7 million low-income women. Those who are diagnosed with cancer through the program are eligible for Medicaid coverage through the Breast and Cervical Cancer Prevention and Treatment Act passed by Congress in 2000. In 2008, CDC received OMB approval to collect one year of activity-based economic cost data from NBCCEDP grantees. In 2009, CDC received OMB approval to collect two additional cycles of cost data for fiscal year 2009 (FY09) E:\FR\FM\13OCN1.SGM 13OCN1

Agencies

[Federal Register Volume 75, Number 197 (Wednesday, October 13, 2010)]
[Notices]
[Pages 62834-62835]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-25694]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-11-0729]


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 project or to obtain a copy 
of data collection plans and instruments, call 404-639-5960 or send 
comments to Carol E. Walker, Acting Reports Clearance Officer, 1600 
Clifton Road, MS D-74, 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 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 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

    Customer Surveys Generic Clearance for the National Center for 
Health Statistics (0920-0729 exp. 6/30/2009)--Reinstatement--National 
Center for Health Statistics (NCHS), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    Section 306 of the Public Health Service (PHS) Act (42 U.S.C. 
242k), as amended, authorizes that the Secretary of Health and Human 
Services (DHHS), acting through NCHS, shall collect statistics on ``the 
extent and nature of illness and disability of the population of the 
United States.'' This is a reinstatement request for a generic

[[Page 62835]]

approval from OMB to conduct customer surveys over the next three 
years.
    As part of a comprehensive program, the National Center for Health 
Statistics (NCHS) plans to continue to assess its customers' 
satisfaction with the content, quality and relevance of the information 
it produces. NCHS will conduct voluntary customer surveys to assess 
strengths in agency products and services and to evaluate how well it 
addresses the emerging needs of its data users. Results of these 
surveys will be used in future planning initiatives.
    The data will be collected using a combination of methodologies 
appropriate to each survey. These may include: Evaluation forms, mail 
surveys, focus groups, automated and electronic technology (e.g., e-
mail, Web-based surveys), and telephone surveys. Systematic surveys of 
several groups will be folded into the program. Among these are Federal 
customers and policy makers, state and local officials who rely on NCHS 
data, the broader educational, research, and public health community, 
and other data users. Respondents may include data users who register 
for and/or attend NCHS sponsored conferences; persons who access the 
NCHS Web site and the detailed data available through it; consultants; 
and others. Respondent data items may include (in broad categories) 
information regarding respondent's gender, age, occupation, 
affiliation, location, etc., to be used to characterize responses only. 
Other questions will attempt to obtain information that will 
characterize the respondents' familiarity with and use of NCHS data, 
their assessment of data content and usefulness, general satisfaction 
with available services and products, and suggestions for improvement 
of surveys, services and products.
    The resulting information will be for NCHS internal use. There is 
no cost to respondents other than their time to participate in the 
survey.

                                                            Estimated Annualized Burden Table
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                                                             Number of    Average burden/
               Type of survey                                 Respondents                    Number of      responses/     response (in    Total burden
                                                                                            respondents     respondent        hours)           hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Questionnaire for conference registrants/     Public/private researchers, Consultants,             3,000               1           10/60             500
 attendees.                                    and others.
Focus groups................................  Public/private researchers, Consultants,               240               1               1             240
                                               and others.
Web-based...................................  Public/private researchers, Consultants,             3,600               1           10/60             600
                                               and others.
Other customer surveys......................  Public/private researchers, Consultants,             1,200               1           15/60             300
                                               and others.
                                                                                         ---------------------------------------------------------------
    Total...................................  ..........................................           8,040  ..............  ..............           1,640
--------------------------------------------------------------------------------------------------------------------------------------------------------


    Dated: October 6, 2010.
Carol E. Walker,
Acting Reports Clearance Officer, Centers for Disease Control and 
Prevention.
[FR Doc. 2010-25694 Filed 10-12-10; 8:45 am]
BILLING CODE 4163-18-P
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