Proposed Data Collections Submitted for Public Comment and Recommendations, 47848-47850 [2012-19675]

Download as PDF 47848 Federal Register / Vol. 77, No. 155 / Friday, August 10, 2012 / Notices Background and Brief Description of the Proposed Project One of the objectives of CDC’s epidemic services is to provide for the prevention and control of epidemics, and protect the population from public health crises such as human-made or natural biological disasters and chemical emergencies. CDC meets this objective, in part, by training investigators, maintaining laboratory capabilities for identifying potential problems, collecting and analyzing data, and recommending appropriate actions to protect the public’s health. When state, local, or foreign health authorities request help in controlling an epidemic or solving other health problems, CDC dispatches skilled epidemiologists from the Epidemic Intelligence Service (EIS) to investigate and resolve the problem. Resolving public health problems rapidly ensures cost-effective health care and enhances health promotion and disease prevention. The purpose of the Emergency Epidemic Investigation surveillance is to collect data from the general public on the conditions surrounding and investigations. This mechanism allows CDC to respond rapidly to public health problems in need of urgent attention, thereby providing an important service to state and other public health agencies. Through Epi-Aids, EIS officers (and, sometimes, other CDC trainees) receive supervised training while actively participating in epidemiologic investigations. EIS is a two-year program of training and service in applied epidemiology through CDC, primarily for persons holding doctoral degrees. Shortly after completion of the EpiAid investigation, an Epi Trip Report is delivered to the state health agency official(s) who requested assistance. The state and local health officials, requestors of the Epi-Aid assistance can comment on both the timeliness and the practical utility of the recommendations from the investigation by completing the Epi-Aid Satisfaction Survey for Requesting Officials to assess the promptness of the investigation and the usefulness of the recommendations. There is no cost to the respondents other than their time. preceding the onset of a problem. The data is collected from 15,000 respondents in the general public for an annualized total of 3,750 burden hours (15,000 respondents × 15 minutes per survey). These data are collected in a timely fashion so that information can be used to develop prevention and control techniques, to interrupt disease transmission, and to help identify the cause of an outbreak. The Epi-Aid Satisfaction Survey for Requesting Officials is to assess the promptness of the investigation and the usefulness of recommendations; data are collected from 100 state and local health officials for an annualized total of 25 burden hours (100 respondents × 15 minutes per survey). This survey of state and local health officials was modified to better measure and address overall satisfaction, communication, response, and team composition and professionalism of the Epi-Aid team. The Epi-Aid mechanism is a means for Epidemic Intelligence Service (EIS) officers of CDC, along with other CDC staff, to provide technical support to state health agencies requesting assistance with epidemiologic field ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Number of responses per respondent Avg burden per response (in hours) Total burden (in hours) Respondents Form Name Requestors of Epi-Aids ..................... 100 1 15/60 25 General Public ................................... Epi-Aid Satisfaction Survey for Requesting Official. Emergency Epidemic Investigations 15,000 1 15/60 3,750 Total ........................................... .......................................................... ........................ ........................ ........................ 3,775 Kimberly Lane, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2012–19679 Filed 8–9–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention mstockstill on DSK4VPTVN1PROD with NOTICES [60-Day–12–0573] 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 VerDate Mar<15>2010 18:02 Aug 09, 2012 Jkt 226001 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 and send comments to Kimberly S. Lane, 1600 Clifton Road, MS–D74, 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 PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 technology. Written comments should be received within 60 days of this notice. Proposed Project National HIV Surveillance System (NHSS) (OMB No. 0920–0573, Expiration 01/31/2013)-RevisionNational Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description CDC is authorized under Sections 304 and 306 of the Public Health Service Act (42 U.S.C. 242b and 242k) to collect information on cases of human immunodeficiency virus (HIV) and indicators of HIV disease and HIV disease progression including AIDS. These national HIV surveillance data collected by CDC are the primary source of information used to monitor the extent and characteristics of the HIV burden in the U.S. E:\FR\FM\10AUN1.SGM 10AUN1 47849 Federal Register / Vol. 77, No. 155 / Friday, August 10, 2012 / Notices The purpose of HIV surveillance is to monitor trends in HIV and describe the characteristics of infected persons (e.g., demographics, modes of exposure to HIV, clinical and laboratory markers of HIV disease, manifestations of severe HIV disease, and deaths among persons with HIV). HIV surveillance data are widely used at all government levels to assess the impact of HIV infection on morbidity and mortality, to allocate medical care resources and services, and to guide prevention and disease control activities. As science, technology, and our understanding of HIV have evolved, the NHSS has been updated periodically to meet the nation’s needs for information. CDC, in collaboration with health departments in the 50 states, the District of Columbia, and U.S. dependent areas, conduct national surveillance for cases of HIV infection. National surveillance includes tracking critical data across the spectrum of HIV disease from HIV diagnosis, to AIDS, the end-stage disease caused by infection with HIV, and death. In addition, this national system provides essential data to estimate HIV incidence and monitor patterns in viral resistance and HIV–1 subtypes, as well as provide information on perinatal exposures in the U.S. The CDC surveillance case definition has been modified periodically to accurately monitor disease in adults, adolescents and children and reflect use of new testing technologies and changes in HIV treatment. Information is then updated in the case report forms and reporting software as needed. In 2008, the surveillance case definitions for adults and children for HIV and AIDS were revised. Since that time, the enhanced HIV/AIDS reporting system (eHARS) was fully deployed (2010) and forms have been updated to reflect those changes (2011). In 2012, CDC convened an expert consultation to consider revisions of various aspects of the case definition including criteria for reporting a potential case, criteria for a reporting a confirmed case, and case classification (disease staging system). Recommendations for revisions in the may be received from laboratories, vital statistics offices, or additional providers. CDC estimates approximately 1,469 updates to case reports will be processed by each of the 59 health departments annually. Additionally, 5,876 updates of laboratory test data will be processed, primarily through electronic laboratory reporting, by each of the 59 health departments annually. Health departments will de-identify compiled case report information and forward to CDC on a monthly basis for inclusion in the national HIV surveillance database. Evaluations are also conducted by health departments on a subset of case reports (e.g. including re-abstraction/validation activities and routine interstate deduplication). CDC estimates approximately 127 evaluations of case reports will be processed by each of the jurisdictions annually. Supplemental surveillance data are collected in a subset of areas to provide additional information necessary to estimate HIV incidence, to better describe the extent of HIV viral resistance and quantify HIV subtypes among persons infected with HIV and to monitor and evaluate perinatal HIV prevention efforts. Health departments funded for these supplemental data collections obtain this information from laboratories, health care providers, and medical records. CDC estimates that 2,729 reports containing HIV Incidence Surveillance (HIS) data elements will be processed on average by each of the 25 health departments funded to collect incidence data annually. Additionally, an estimated 718 reports containing additional data elements on HIV nucleotide sequences from genotype test results will be processed on average by each of the 53 health departments reporting MHS data annually. An estimated 114 reports containing perinatal exposure data elements will be processed on average, annually, by each of the 35 health departments reporting data collected as part of PHER. There are no costs to respondents except their time. case definition were adopted in a position statement by the Council of State and Territorial Epidemiologists in June 2012 and the final case definition revision is planned for 2012. The revisions requested include modifications to currently collected data elements and forms to align with anticipated changes in the case definitions for HIV surveillance to be published in 2012 and continuation of HIV surveillance activities funded under the new funding opportunity announcement CDC–RFA–PS13–1302 National HIV Surveillance System (NHSS). These include minor modifications of testing categories to accommodate new testing algorithms and modifications to staging criteria and non-substantial editorial changes aimed at improving the format and usability of the forms such as improved wording of terms and changes in the format of some response options. In addition, the number of data elements from the former enhanced perinatal surveillance (EPS) was reduced and the form modified for continuation in 2013 as Perinatal HIV Exposure Reporting (PHER). Surveillance data collection on variant and atypical strains (formerly variant, atypical and resistant HIV surveillance (VARHS)) will be continued as Molecular HIV Surveillance (MHS) with a reduced number of data elements previously approved under VARHS. CDC provides funding for 59 jurisdictions to conduct adult and pediatric HIV case surveillance. Health department staffs compile information from laboratories, physicians, hospitals, clinics and other health care providers in order to complete the HIV and pediatric case reports. CDC estimates that approximately 1,260 adult HIV case reports and 6 pediatric case reports are processed by each health department annually. These data are recorded on standard case report forms, processed by either paper or electronic format and entered into eHARS. Updates to case reports are also entered into eHARS by health departments, as additional information ESTIMATE OF ANNUALIZED BURDEN TABLE mstockstill on DSK4VPTVN1PROD with NOTICES Type of respondent Health Health Health Health Health Health Health Departments Departments Departments Departments Departments Departments Departments VerDate Mar<15>2010 .......................... .......................... .......................... .......................... .......................... .......................... .......................... 18:02 Aug 09, 2012 Number of respondents Form name Adult HIV Case Report .................... Pediatric HIV Case Report ............... Case Report Evaluations ................. Case Report Updates ...................... Laboratory Updates .......................... HIV Incidence Surveillance (HIS) .... Molecular HIV Surveillance (MHS) .. Jkt 226001 PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 Number of responses per respondent 59 59 59 59 59 25 53 E:\FR\FM\10AUN1.SGM 1,260 6 127 1,469 5,876 2,729 967 10AUN1 Avg. burden per response (in hours) 20/60 20/60 20/60 2/60 1/60 10/60 5/60 Total annual burden (in hours) 24,780 118 2,498 2,889 5,778 11,371 4,271 47850 Federal Register / Vol. 77, No. 155 / Friday, August 10, 2012 / Notices ESTIMATE OF ANNUALIZED BURDEN TABLE—Continued Number of responses per respondent Number of respondents Avg. burden per response (in hours) Total annual burden (in hours) Type of respondent Form name Health Departments .......................... Perinatal HIV Exposure Reporting (PHER). 35 114 30/60 1,995 Total ........................................... ........................................................... ........................ ........................ ........................ 53,700 Kimberly Lane, Deputy Director, Office of Scientific Integrity, Centers for Disease Control and Prevention. [FR Doc. 2012–19675 Filed 8–9–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Board of Scientific Counselors, National Institute for Occupational Safety and Health (BSC, NIOSH) mstockstill on DSK4VPTVN1PROD 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 (CDC) announces the following meeting of the aforementioned committee: Time and Date: 8:30 a.m.–3:15 p.m., September 18, 2012 Place: Patriots Plaza I, 395 E Street SW., Room 9200, Washington, DC 20201. Status: Open to the public, limited only by the space available. The meeting room accommodates approximately 50 people. If you wish to attend in person, please contact NIOSH at (202) 245–0625 or (202) 245–0626 for information on building access. Teleconference is available toll-free; please dial (877) 328–2816, Participant Pass Code 6558291. Purpose: The Secretary, the Assistant Secretary for Health, and by delegation the Director, Centers for Disease Control and Prevention, are authorized under Sections 301 and 308 of the Public Health Service Act to conduct directly or by grants or contracts, research, experiments, and demonstrations relating to occupational safety and health and to mine health. The Board of Scientific Counselors shall provide guidance to the Director, National Institute for Occupational Safety and Health on research and prevention programs. Specifically, the Board shall provide guidance on the Institute’s research activities related to developing and evaluating hypotheses, systematically documenting findings and disseminating results. The Board shall evaluate the degree to which the activities of the National Institute for Occupational Safety and Health: (1) Conform to appropriate scientific standards, (2) address current, relevant needs, and (3) produce intended results. Matters To Be Discussed: NIOSH Director Update; Implementation of the National Academies Program Recommendations for VerDate Mar<15>2010 18:02 Aug 09, 2012 Jkt 226001 Hearing Loss Prevention, Personal Protective Technologies, and Health Hazard Evaluations; Construction Safety and Health, Respiratory Disease Studies, and Traumatic Injury Prevention. Agenda items are subject to change as priorities dictate. Contact Person for More Information: Roger Rosa, Ph.D., Designated Federal Officer, BSC, NIOSH, CDC, 395 E Street SW., Suite 9200, Patriots Plaza Building, Washington, DC 20201, telephone (202) 245– 0655, fax (202) 245–0664. 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 the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry. Dated: July 27, 2012. Catherine Ramadei, Acting Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. 2012–19248 Filed 8–9–12; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier CMS–10203] Agency Information Collection Activities: Submission for OMB Review; Comment Request Centers for Medicare & Medicaid Services, HHS. In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid Services (CMS), Department of Health and Human Services, is publishing the following summary of proposed collections for public comment. Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the Agency’s function; AGENCY: PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. 1. Type of Information Collection Request: Revision of a currently approved collection; Title of Information Collection: Medicare Health Outcomes Survey (HOS); Use: CMS has a responsibility to its Medicare beneficiaries to require that care provided by managed care organizations under contract to CMS is of high quality. One way of ensuring high quality care in Medicare Managed Care Organizations (MCOs), or more commonly referred to as Medicare Advantage Organizations (MAOs), is through the development of standardized, uniform performance measures to enable CMS to gather the data needed to evaluate the care provided to Medicare beneficiaries. The goal of the Medicare Health Outcome Survey (HOS) program is to gather valid, reliable, clinically meaningful health status data in Medicare managed care for use in quality improvement activities, plan accountability, public reporting, and improving health. All managed care plans with Medicare Advantage (MA) contracts must participate. CMS, in collaboration with the National Committee for Quality Assurance (NCQA), launched the Medicare HOS as part of the Effectiveness of Care component of the former Health Plan Employer Data and Information Set, now known as the Healthcare Effectiveness Data and Information Set (HEDIS®). The HOS measure was developed under the guidance of a technical expert panel comprised of individuals with specific expertise in the health care industry and outcomes measurement. The measure includes the most recent advances in summarizing physical and mental health outcomes results and appropriate risk adjustment techniques. In addition to health outcomes measures, the HOS is used to collect the Management of Urinary Incontinence in E:\FR\FM\10AUN1.SGM 10AUN1

Agencies

[Federal Register Volume 77, Number 155 (Friday, August 10, 2012)]
[Notices]
[Pages 47848-47850]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-19675]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60-Day-12-0573]


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 404-639-7570 
and send comments to Kimberly S. Lane, 1600 Clifton Road, MS-D74, 
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

    National HIV Surveillance System (NHSS) (OMB No. 0920-0573, 
Expiration 01/31/2013)-Revision- National Center for HIV/AIDS, Viral 
Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease 
Control and Prevention (CDC).

Background and Brief Description

    CDC is authorized under Sections 304 and 306 of the Public Health 
Service Act (42 U.S.C. 242b and 242k) to collect information on cases 
of human immunodeficiency virus (HIV) and indicators of HIV disease and 
HIV disease progression including AIDS. These national HIV surveillance 
data collected by CDC are the primary source of information used to 
monitor the extent and characteristics of the HIV burden in the U.S.

[[Page 47849]]

    The purpose of HIV surveillance is to monitor trends in HIV and 
describe the characteristics of infected persons (e.g., demographics, 
modes of exposure to HIV, clinical and laboratory markers of HIV 
disease, manifestations of severe HIV disease, and deaths among persons 
with HIV). HIV surveillance data are widely used at all government 
levels to assess the impact of HIV infection on morbidity and 
mortality, to allocate medical care resources and services, and to 
guide prevention and disease control activities.
    As science, technology, and our understanding of HIV have evolved, 
the NHSS has been updated periodically to meet the nation's needs for 
information. CDC, in collaboration with health departments in the 50 
states, the District of Columbia, and U.S. dependent areas, conduct 
national surveillance for cases of HIV infection. National surveillance 
includes tracking critical data across the spectrum of HIV disease from 
HIV diagnosis, to AIDS, the end-stage disease caused by infection with 
HIV, and death. In addition, this national system provides essential 
data to estimate HIV incidence and monitor patterns in viral resistance 
and HIV-1 subtypes, as well as provide information on perinatal 
exposures in the U.S.
    The CDC surveillance case definition has been modified periodically 
to accurately monitor disease in adults, adolescents and children and 
reflect use of new testing technologies and changes in HIV treatment. 
Information is then updated in the case report forms and reporting 
software as needed. In 2008, the surveillance case definitions for 
adults and children for HIV and AIDS were revised. Since that time, the 
enhanced HIV/AIDS reporting system (eHARS) was fully deployed (2010) 
and forms have been updated to reflect those changes (2011). In 2012, 
CDC convened an expert consultation to consider revisions of various 
aspects of the case definition including criteria for reporting a 
potential case, criteria for a reporting a confirmed case, and case 
classification (disease staging system). Recommendations for revisions 
in the case definition were adopted in a position statement by the 
Council of State and Territorial Epidemiologists in June 2012 and the 
final case definition revision is planned for 2012.
    The revisions requested include modifications to currently 
collected data elements and forms to align with anticipated changes in 
the case definitions for HIV surveillance to be published in 2012 and 
continuation of HIV surveillance activities funded under the new 
funding opportunity announcement CDC-RFA-PS13-1302 National HIV 
Surveillance System (NHSS). These include minor modifications of 
testing categories to accommodate new testing algorithms and 
modifications to staging criteria and non-substantial editorial changes 
aimed at improving the format and usability of the forms such as 
improved wording of terms and changes in the format of some response 
options. In addition, the number of data elements from the former 
enhanced perinatal surveillance (EPS) was reduced and the form modified 
for continuation in 2013 as Perinatal HIV Exposure Reporting (PHER). 
Surveillance data collection on variant and atypical strains (formerly 
variant, atypical and resistant HIV surveillance (VARHS)) will be 
continued as Molecular HIV Surveillance (MHS) with a reduced number of 
data elements previously approved under VARHS.
    CDC provides funding for 59 jurisdictions to conduct adult and 
pediatric HIV case surveillance. Health department staffs compile 
information from laboratories, physicians, hospitals, clinics and other 
health care providers in order to complete the HIV and pediatric case 
reports. CDC estimates that approximately 1,260 adult HIV case reports 
and 6 pediatric case reports are processed by each health department 
annually.
    These data are recorded on standard case report forms, processed by 
either paper or electronic format and entered into eHARS. Updates to 
case reports are also entered into eHARS by health departments, as 
additional information may be received from laboratories, vital 
statistics offices, or additional providers. CDC estimates 
approximately 1,469 updates to case reports will be processed by each 
of the 59 health departments annually. Additionally, 5,876 updates of 
laboratory test data will be processed, primarily through electronic 
laboratory reporting, by each of the 59 health departments annually. 
Health departments will de-identify compiled case report information 
and forward to CDC on a monthly basis for inclusion in the national HIV 
surveillance database. Evaluations are also conducted by health 
departments on a subset of case reports (e.g. including re-abstraction/
validation activities and routine interstate de-duplication). CDC 
estimates approximately 127 evaluations of case reports will be 
processed by each of the jurisdictions annually.
    Supplemental surveillance data are collected in a subset of areas 
to provide additional information necessary to estimate HIV incidence, 
to better describe the extent of HIV viral resistance and quantify HIV 
subtypes among persons infected with HIV and to monitor and evaluate 
perinatal HIV prevention efforts. Health departments funded for these 
supplemental data collections obtain this information from 
laboratories, health care providers, and medical records. CDC estimates 
that 2,729 reports containing HIV Incidence Surveillance (HIS) data 
elements will be processed on average by each of the 25 health 
departments funded to collect incidence data annually. Additionally, an 
estimated 718 reports containing additional data elements on HIV 
nucleotide sequences from genotype test results will be processed on 
average by each of the 53 health departments reporting MHS data 
annually. An estimated 114 reports containing perinatal exposure data 
elements will be processed on average, annually, by each of the 35 
health departments reporting data collected as part of PHER.
    There are no costs to respondents except their time.

                                       Estimate of Annualized Burden Table
----------------------------------------------------------------------------------------------------------------
                                                                     Number of      Avg. burden    Total annual
      Type of respondent            Form name        Number of     responses per   per response     burden  (in
                                                    respondents     respondent      (in hours)        hours)
----------------------------------------------------------------------------------------------------------------
Health Departments............  Adult HIV Case                59           1,260           20/60          24,780
                                 Report.
Health Departments............  Pediatric HIV                 59               6           20/60             118
                                 Case Report.
Health Departments............  Case Report                   59             127           20/60           2,498
                                 Evaluations.
Health Departments............  Case Report                   59           1,469            2/60           2,889
                                 Updates.
Health Departments............  Laboratory                    59           5,876            1/60           5,778
                                 Updates.
Health Departments............  HIV Incidence                 25           2,729           10/60          11,371
                                 Surveillance
                                 (HIS).
Health Departments............  Molecular HIV                 53             967            5/60           4,271
                                 Surveillance
                                 (MHS).

[[Page 47850]]

 
Health Departments............  Perinatal HIV                 35             114           30/60           1,995
                                 Exposure
                                 Reporting
                                 (PHER).
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............          53,700
----------------------------------------------------------------------------------------------------------------


Kimberly Lane,
Deputy Director, Office of Scientific Integrity, Centers for Disease 
Control and Prevention.
[FR Doc. 2012-19675 Filed 8-9-12; 8:45 am]
BILLING CODE 4163-18-P
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