Proposed Data Collection Submitted for Public Comment and Recommendations, 59431-59433 [2022-21220]

Download as PDF 59431 Federal Register / Vol. 87, No. 189 / Friday, September 30, 2022 / Notices members and professionals familiar with the population and focus groups to interpret standardized quantitative findings and inform grantee-developed recommendations for state/local public health partners. The data from qualitative interviews will be used to interpret standardized quantitative findings and inform recipient-developed recommendations for state and local public health authorities. No other federal agency collects this type of information in the populations at high risk in these selected geographic areas using mixed methods of quantitative and qualitative interviews. CDC estimates that during quantitative interviewing, 1338 individuals will complete the quantitative base eligibility screener, 1204 will complete the quantitative population eligibility screener, and 338 will be either not interested or ineligible, yielding a total of 1000 eligible respondents over a 12-month period. For qualitative data collection approximately 96 individuals will complete the eligibility screener, 16 of the respondents will be either not interested in completing a qualitative interview, or will be ineligible, yielding a total of 80 eligible respondents over a 12-month period. The total estimated annualized burden requested is 497 hours. Participation of is voluntary, and there are no costs to respondents other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Type of respondents Form name Persons Screened .......................................... Persons Screened .......................................... Eligible Participants ......................................... Eligible Participants ......................................... Persons Screened .......................................... Eligible Participant .......................................... Quantitative Base Eligibility Screener ............ Quantitative Population Eligibility Screener ... Quantitative Core Survey ............................... Quantitative Population-specific Questions ... Qualitative Eligibility Screener ....................... Qualitative interviews ..................................... Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2022–21215 Filed 9–29–22; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES [60Day–22–1030; Docket No. CDC–2022– 0117] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other federal agencies the opportunity to comment on a continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled Developmental Studies to improve the National Health Care Surveys. The goal of the project is to cover new survey research that will evaluate and improve upon survey jspears on DSK121TN23PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:52 Sep 29, 2022 Jkt 256001 design and operations, as well as examine the feasibility and address challenges that may arise with future expansions of the National Health Care Surveys. DATES: CDC must receive written comments on or before November 29, 2022. You may submit comments, identified by Docket No. CDC–2022– 0117 by either of the following methods: • Federal eRulemaking Portal: www.regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H21–8, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to www.regulations.gov. Please note: Submit all comments through the Federal eRulemaking portal (www.regulations.gov) or by U.S. mail to the address listed above. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H21–8, Atlanta, Georgia 30329; Telephone: 404–639–7570; Email: omb@ cdc.gov. ADDRESSES: Centers for Disease Control and Prevention Number of respondents PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 1338 1204 1000 1000 96 80 Number of responses per respondent 1 1 1 1 1 1 Average burden per response (in hours) 1/60 5/60 10/60 5/60 1/60 90/60 Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. The OMB is particularly interested in comments that will help: 1. Evaluate 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; 2. Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; 3. Enhance the quality, utility, and clarity of the information to be collected; 4. Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other SUPPLEMENTARY INFORMATION: E:\FR\FM\30SEN1.SGM 30SEN1 59432 Federal Register / Vol. 87, No. 189 / Friday, September 30, 2022 / Notices technological collection techniques or other forms of information technology, e.g., permitting electronic submissions of responses; and 5. Assess information collection costs. jspears on DSK121TN23PROD with NOTICES Proposed Project Developmental Studies to improve the National Health Care Surveys (OMB Control No. 0920–1030, Exp. 06/30/ 2023—Extension—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 the Secretary of Health and Human Services (DHHS), acting through the Division of Health Care Statistics (DHCS) within NCHS, shall collect statistics on the extent and nature of illness and disability of the population of the United States. The DHCS conducts the National Health Care Surveys, a family of nationally representative surveys of encounters and health care providers in inpatient, outpatient, ambulatory, and post-acute and long-term care settings. This information collection request (ICR) is for the Extension of a Generic clearance to conduct developmental studies to improve this family of surveys. This three-year clearance period will include studies to evaluate and improve upon existing survey design and operations, as well as to examine the feasibility of, and address challenges that may arise with, future expansions of the National Health Care Surveys. Specifically, this request covers developmental research with the following aims: (1) to explore ways to refine and improve upon existing survey designs and procedures; and (2) to explore and evaluate proposed survey designs and alternative approaches to data collection. The goal of these research studies is to further enhance DHCS existing and future data collection protocols to increase research capacity and improve health care data quality for the purpose of monitoring public health and well-being at the national, state, and local levels, thereby informing health policy decisionmaking process. The information collected through this Generic ICR will not be used to make generalizable statements about the population of interest or to inform public policy; however, methodological findings may be reported. VerDate Sep<11>2014 18:52 Sep 29, 2022 Jkt 256001 This Generic ICR would include studies conducted in person, via the telephone or web surveys, and by postal or electronic mail. Methods covered would include qualitative (e.g., usability testing, focus groups, ethnographic studies, and respondent debriefing questionnaires) and/or quantitative (e.g., pilot tests, pre-tests and split sample experiments) research methodologies. Examples of studies to improve existing survey designs and procedures may include evaluation of incentive approaches to improve recruitment and increase participation rates; testing of new survey items to obtain additional data on providers, patients, residents, and their encounters while minimizing misinterpretation and human error in data collection; testing data collection in panel surveys; triangulating and validating survey responses from multiple data sources; assessment of the feasibility of data retrieval; and development of protocols that will locate, identify, and collect accurate survey data in the least labor-intensive and burdensome manner at the sampled practice site. To explore and evaluate proposed survey designs and alternative approaches to collecting data, especially with the nationwide adoption of electronic health records, studies may expand the evaluation of data extraction of electronic health records and submission via continuity of care documentation to small/mid-size/large medical providers and hospital networks, managed care health plans, retail health clinics, and other inpatient, outpatient, ambulatory, and long-term care settings that are currently either inscope or out-of-scope of the National Health Care Surveys. Research on feasibility, data quality and respondent burden also may be carried out in the context of developing new surveys of health care providers and establishments that are currently out-ofscope of the National Health Care Surveys. Specific motivations for conducting developmental studies include: (1) Within the National Ambulatory Medical Care Survey (NAMCS), new clinical groups may be expanded to include dentists, psychologists, podiatrists, chiropractors, optometrists), mid-level providers, and allied-health professionals (e.g., certified nursing aides, medical assistants, radiology technicians, laboratory technicians, pharmacists, dieticians/nutritionists). PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 Current sampling frames such as those from the American Medical Association may be obtained and studied, as well as frames that are not currently in use by NAMCS, such as state and organizational listings of other licensed providers; (2) Within the National Study of Post-Acute and Long-Term Care Providers, additional new frames may be sought, developed, and evaluated and data items from home care agencies, long-term care hospitals, and facilities exclusively serving individuals with intellectual/developmental disability may be tested. Similarly, data may be obtained from lists compiled by states and other organizations. Data about the facilities as well as residents and their visits will be investigated; (3) In the inpatient and outpatient care settings, the National Hospital Care Survey (NHCS) may investigate the addition of facility and patient information especially as it relates to insurance and electronic medical records. The National Health Care Surveys collect critical, accurate data that are used to produce reliable national estimates—and in recent years, statelevel estimates—of clinical services and of the providers who delivered those services in inpatient, outpatient, ambulatory, and long-term care settings. The data from these surveys are used by providers, policy makers and researchers to address important topics of interest, including the quality and disparities of care among populations, epidemiology of medical conditions, diffusion of technologies, effects of policies and practice guidelines, and changes in health care over time. Research studies need to be conducted to improve existing and proposed survey design and procedures of the National Health Care Surveys, as well as to evaluate alternative data collection approaches particularly due to the expansion of electronic health record use, and to develop new sample frames of currently out-of-scope providers and settings of care. Average burdens are designed to cover 15–40 min interviews as well as 90-minute focus groups, longer on-site visits, and situations where organizations may be preparing electronic data files. CDC requests OMB approval for an estimated 3,000 annual burden hours. There is no cost to respondents other than their time to participate. E:\FR\FM\30SEN1.SGM 30SEN1 59433 Federal Register / Vol. 87, No. 189 / Friday, September 30, 2022 / Notices ESTIMATED ANNUALIZED BURDEN HOURS Average burden per response (in hours) Total burden hours Form name Health Care Providers and Business entities. 2,582 1 1 2,582 Health Care Providers, State/local government agencies, and business entities. Interviews, surveys, focus groups, experiments (in person, phone, internet, postal/electronic mail). Interviews, surveys, focus groups, experiments (in person, phone, internet, postal/electronic mail). 167 1 2.5 418 Total ........................................... ........................................................... ........................ ........................ ........................ 3,000 Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2022–21220 Filed 9–29–22; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–22–22ES] Agency Forms Undergoing Paperwork Reduction Act Review jspears on DSK121TN23PROD with NOTICES Number of responses per respondent Number of respondents Type of respondents In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) has submitted the information collection request titled ‘‘Assessing Respirator Perceptions, Experiences, and Maintenance’’ to the Office of Management and Budget (OMB) for review and approval. CDC previously published a ‘‘Proposed Data Collection Submitted for Public Comment and Recommendations’’ notice on May 6, 2022, to obtain comments from the public and affected agencies. CDC did not receive comments related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments. CDC will accept all comments for this proposed information collection project. The Office of Management and Budget is particularly interested in comments that: (a) Evaluate 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) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; VerDate Sep<11>2014 18:52 Sep 29, 2022 Jkt 256001 (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including, through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639–7570. Comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/ do/PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 395–5806. Provide written comments within 30 days of notice publication. Proposed Project Assessing Respirator Perceptions, Experiences, and Maintenance—New— National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC). Background and Brief Description The Centers for Disease Control and Prevention (CDC), National Institute for Occupational Safety and Health (NIOSH), is requesting approval of a new Generic information collection for a period of three years under the project titled ‘‘Assessing Respirator Perceptions, Experiences, and Maintenance.’’ PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 The National Personal Protective Technology Laboratory (NPPTL) is a division of NIOSH which operates within the CDC. NPPTL was established in 2001, at the request of Congress, with the mission of preventing disease, injury, and death for the millions of working men and women relying on personal protective technology (PPT). As the nation’s respirator approver for all workplaces (42 CFR part 84), the development of NPPTL filled a need for improved personal protective equipment (PPE) and focused research into PPT. To this end, NPPTL conducts respiratory protection research to examine exposures to inhalation hazards, dermal hazards, and any other hazardous environmental threats within an occupational setting. Federal regulations exist regarding the use of respirators in the workplace. The Occupational Safety and Health Administration (OSHA) requires employers whose hazard management includes the use of respirators to have a respiratory protection program (RPP), which has specified components. Thus, the information collected from human subjects about their use of respirators is generally consistent across NPPTL studies with only the use conditions changing (e.g., respirator type or management implementation practices related to cleaning/decontamination, fit testing, and training). NPPTL requests a Generic information collection package for information collected from individual workers and managers related to the perceptions, maintenance, and evaluation of respirator use on the job. Different types of data collection including surveys, focus groups, interviews, and physiological monitoring will be used to: (1) assess workers’ health and safety knowledge, attitudes, skills, and other personal attributes as they relate to their respiratory protection use and maintenance; (2) identify and overcome barriers that workers face while using respiratory protection to prevent E:\FR\FM\30SEN1.SGM 30SEN1

Agencies

[Federal Register Volume 87, Number 189 (Friday, September 30, 2022)]
[Notices]
[Pages 59431-59433]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-21220]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-22-1030; Docket No. CDC-2022-0117]


Proposed Data Collection Submitted for Public Comment and 
Recommendations

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

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

SUMMARY: The Centers for Disease Control and Prevention (CDC), as part 
of its continuing effort to reduce public burden and maximize the 
utility of government information, invites the general public and other 
federal agencies the opportunity to comment on a continuing information 
collection, as required by the Paperwork Reduction Act of 1995. This 
notice invites comment on a proposed information collection project 
titled Developmental Studies to improve the National Health Care 
Surveys. The goal of the project is to cover new survey research that 
will evaluate and improve upon survey design and operations, as well as 
examine the feasibility and address challenges that may arise with 
future expansions of the National Health Care Surveys.

DATES: CDC must receive written comments on or before November 29, 
2022.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2022-
0117 by either of the following methods:
     Federal eRulemaking Portal: www.regulations.gov. Follow 
the instructions for submitting comments.
     Mail: Jeffrey M. Zirger, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS H21-8, Atlanta, Georgia 30329.
    Instructions: All submissions received must include the agency name 
and Docket Number. CDC will post, without change, all relevant comments 
to www.regulations.gov.
    Please note: Submit all comments through the Federal eRulemaking 
portal (www.regulations.gov) or by U.S. mail to the address listed 
above.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the information collection plan 
and instruments, contact Jeffrey M. Zirger, Information Collection 
Review Office, Centers for Disease Control and Prevention, 1600 Clifton 
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7570; 
Email: [email protected].

SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from 
the Office of Management and Budget (OMB) for each collection of 
information they conduct or sponsor. In addition, the PRA also requires 
federal agencies to provide a 60-day notice in the Federal Register 
concerning each proposed collection of information, including each new 
proposed collection, each proposed extension of existing collection of 
information, and each reinstatement of previously approved information 
collection before submitting the collection to the OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    The OMB is particularly interested in comments that will help:
    1. Evaluate 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;
    2. Evaluate the accuracy of the agency's estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    3. Enhance the quality, utility, and clarity of the information to 
be collected;
    4. Minimize the burden of the collection of information on those 
who are to respond, including through the use of appropriate automated, 
electronic, mechanical, or other

[[Page 59432]]

technological collection techniques or other forms of information 
technology, e.g., permitting electronic submissions of responses; and
    5. Assess information collection costs.

Proposed Project

    Developmental Studies to improve the National Health Care Surveys 
(OMB Control No. 0920-1030, Exp. 06/30/2023--Extension--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 the Secretary of Health and Human 
Services (DHHS), acting through the Division of Health Care Statistics 
(DHCS) within NCHS, shall collect statistics on the extent and nature 
of illness and disability of the population of the United States.
    The DHCS conducts the National Health Care Surveys, a family of 
nationally representative surveys of encounters and health care 
providers in inpatient, outpatient, ambulatory, and post-acute and 
long-term care settings. This information collection request (ICR) is 
for the Extension of a Generic clearance to conduct developmental 
studies to improve this family of surveys. This three-year clearance 
period will include studies to evaluate and improve upon existing 
survey design and operations, as well as to examine the feasibility of, 
and address challenges that may arise with, future expansions of the 
National Health Care Surveys.
    Specifically, this request covers developmental research with the 
following aims: (1) to explore ways to refine and improve upon existing 
survey designs and procedures; and (2) to explore and evaluate proposed 
survey designs and alternative approaches to data collection. The goal 
of these research studies is to further enhance DHCS existing and 
future data collection protocols to increase research capacity and 
improve health care data quality for the purpose of monitoring public 
health and well-being at the national, state, and local levels, thereby 
informing health policy decision-making process. The information 
collected through this Generic ICR will not be used to make 
generalizable statements about the population of interest or to inform 
public policy; however, methodological findings may be reported.
    This Generic ICR would include studies conducted in person, via the 
telephone or web surveys, and by postal or electronic mail. Methods 
covered would include qualitative (e.g., usability testing, focus 
groups, ethnographic studies, and respondent debriefing questionnaires) 
and/or quantitative (e.g., pilot tests, pre-tests and split sample 
experiments) research methodologies. Examples of studies to improve 
existing survey designs and procedures may include evaluation of 
incentive approaches to improve recruitment and increase participation 
rates; testing of new survey items to obtain additional data on 
providers, patients, residents, and their encounters while minimizing 
misinterpretation and human error in data collection; testing data 
collection in panel surveys; triangulating and validating survey 
responses from multiple data sources; assessment of the feasibility of 
data retrieval; and development of protocols that will locate, 
identify, and collect accurate survey data in the least labor-intensive 
and burdensome manner at the sampled practice site.
    To explore and evaluate proposed survey designs and alternative 
approaches to collecting data, especially with the nationwide adoption 
of electronic health records, studies may expand the evaluation of data 
extraction of electronic health records and submission via continuity 
of care documentation to small/mid-size/large medical providers and 
hospital networks, managed care health plans, retail health clinics, 
and other inpatient, outpatient, ambulatory, and long-term care 
settings that are currently either in-scope or out-of-scope of the 
National Health Care Surveys. Research on feasibility, data quality and 
respondent burden also may be carried out in the context of developing 
new surveys of health care providers and establishments that are 
currently out-of-scope of the National Health Care Surveys.
    Specific motivations for conducting developmental studies include: 
(1) Within the National Ambulatory Medical Care Survey (NAMCS), new 
clinical groups may be expanded to include dentists, psychologists, 
podiatrists, chiropractors, optometrists), mid-level providers, and 
allied-health professionals (e.g., certified nursing aides, medical 
assistants, radiology technicians, laboratory technicians, pharmacists, 
dieticians/nutritionists). Current sampling frames such as those from 
the American Medical Association may be obtained and studied, as well 
as frames that are not currently in use by NAMCS, such as state and 
organizational listings of other licensed providers; (2) Within the 
National Study of Post-Acute and Long-Term Care Providers, additional 
new frames may be sought, developed, and evaluated and data items from 
home care agencies, long-term care hospitals, and facilities 
exclusively serving individuals with intellectual/developmental 
disability may be tested. Similarly, data may be obtained from lists 
compiled by states and other organizations. Data about the facilities 
as well as residents and their visits will be investigated; (3) In the 
inpatient and outpatient care settings, the National Hospital Care 
Survey (NHCS) may investigate the addition of facility and patient 
information especially as it relates to insurance and electronic 
medical records.
    The National Health Care Surveys collect critical, accurate data 
that are used to produce reliable national estimates--and in recent 
years, state-level estimates--of clinical services and of the providers 
who delivered those services in inpatient, outpatient, ambulatory, and 
long-term care settings. The data from these surveys are used by 
providers, policy makers and researchers to address important topics of 
interest, including the quality and disparities of care among 
populations, epidemiology of medical conditions, diffusion of 
technologies, effects of policies and practice guidelines, and changes 
in health care over time. Research studies need to be conducted to 
improve existing and proposed survey design and procedures of the 
National Health Care Surveys, as well as to evaluate alternative data 
collection approaches particularly due to the expansion of electronic 
health record use, and to develop new sample frames of currently out-
of-scope providers and settings of care.
    Average burdens are designed to cover 15-40 min interviews as well 
as 90-minute focus groups, longer on-site visits, and situations where 
organizations may be preparing electronic data files. CDC requests OMB 
approval for an estimated 3,000 annual burden hours. There is no cost 
to respondents other than their time to participate.

[[Page 59433]]



                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                      Average
                                                     Number of       Number of      burden per     Total burden
      Type of respondents           Form name       respondents    responses per   response (in        hours
                                                                    respondent        hours)
----------------------------------------------------------------------------------------------------------------
Health Care Providers and       Interviews,                2,582               1               1           2,582
 Business entities.              surveys, focus
                                 groups,
                                 experiments (in
                                 person, phone,
                                 internet,
                                 postal/
                                 electronic
                                 mail).
Health Care Providers, State/   Interviews,                  167               1             2.5             418
 local government agencies,      surveys, focus
 and business entities.          groups,
                                 experiments (in
                                 person, phone,
                                 internet,
                                 postal/
                                 electronic
                                 mail).
                               ---------------------------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............           3,000
----------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific 
Integrity, Office of Science, Centers for Disease Control and 
Prevention.
[FR Doc. 2022-21220 Filed 9-29-22; 8:45 am]
BILLING CODE 4163-18-P


This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.