Agency Information Collection Activities: Proposed Collection; Comment Request, 80247-80249 [2024-22578]
Download as PDF
Federal Register / Vol. 89, No. 191 / Wednesday, October 2, 2024 / Notices
comments received from the public and
other agencies.
During the comment period for this
proposal, a copy of the proposed PRA
OMB submission, including the draft
reporting form and instructions,
supporting statement (which contains
more detail about the information
collection and burden estimates than
this notice), and other documentation,
will be made available on the Board’s
public website at https://
www.federalreserve.gov/apps/
reportingforms/home/review or may be
requested from the agency clearance
officer, whose name appears above. On
the page displayed at the link above,
you can find the supporting information
by referencing the collection identifier,
FR 3052. Final versions of these
documents will be made available at
https://www.reginfo.gov/public/do/
PRAMain, if approved.
Request for Comment on Information
Collection Proposal
lotter on DSK11XQN23PROD with NOTICES1
The Board invites public comment on
the following information collection,
which is being reviewed under
authority delegated by the OMB under
the PRA. Comments are invited on the
following:
a. Whether the proposed collection of
information is necessary for the proper
performance of the Board’s functions,
including whether the information has
practical utility;
b. The accuracy of the Board’s
estimate of the burden of the proposed
information collection, including the
validity of the methodology and
assumptions used;
c. Ways to enhance the quality,
utility, and clarity of the information to
be collected;
d. Ways to minimize the burden of
information collection on respondents,
including through the use of automated
collection techniques or other forms of
information technology; and
e. Estimates of capital or startup costs
and costs of operation, maintenance,
and purchase of services to provide
information.
At the end of the comment period, the
comments and recommendations
received will be analyzed to determine
the extent to which the Board should
modify the proposal.
Proposal Under OMB Delegated
Authority To Extend for Three Years,
Without Revision, the Following
Information Collection
Collection title: Supervisory and
Regulatory Survey.
Collection identifier: FR 3052.
OMB control number: 7100–0322.
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General description of collection: This
survey collects information from
financial institutions specifically
tailored to the Federal Reserve’s
supervisory, regulatory, and operational
responsibilities. The frequency and
content of the questions may depend on
economic, regulatory, supervisory, and
legislative developments. The surveys
are conducted on a voluntary basis.
Frequency: On Occasion.
Respondents: Respondents may
include bank holding companies, state
member banks, savings and loan
holding companies, intermediate
holding companies, U.S. branches and
agencies of foreign banking
organizations (FBOs), Edge Act and
agreement corporations, non-bank
financial companies that the Financial
Stability Oversight Council has
determined should be supervised by the
Board, or the combined domestic
operations of FBOs.
Total estimated number of
respondents: 5,000.
Estimated average hours per response:
0.5.
Total estimated annual burden hours:
60,000.
Board of Governors of the Federal Reserve
System, September 27, 2024.
Benjamin W. McDonough,
Deputy Secretary and Ombuds of the Board.
[FR Doc. 2024–22634 Filed 10–1–24; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve extension of the
currently approved information
collection project: Medical Office
Survey on Patient Safety Culture
Database. This proposed information
collection was previously published in
the Federal Register on July 31, 2024
and allowed 60 days for public
comment. AHRQ received no
substantive comments from members of
the public. The purpose of this notice is
to allow an additional 30 days for public
comment.
SUMMARY:
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Fmt 4703
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80247
Comments on this notice must be
received by November 1, 2024.
ADDRESSES: Written 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. Copies of the proposed
collection plans, data collection
instruments, and specific details on the
estimated burden can be obtained from
the AHRQ Reports Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email REPORTSCLEARANCEOFFICER@
ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
DATES:
Proposed Project
Medical Office Survey on Patient Safety
Culture Database
In 1999, the Institute of Medicine
called for health care organizations to
develop a ‘‘culture of safety’’ such that
their workforce and processes focus on
improving the reliability and safety of
care for patients (IOM, 1999; To Err is
Human: Building a Safer Health
System). To respond to the need for
tools to assess patient safety culture in
health care, AHRQ developed and pilot
tested the Surveys on Patient Safety
Culture® (SOPS®) Medical Office
Survey with OMB approval (OMB NO.
0935–0131; Approved July 5, 2007).
The survey is designed to enable
medical offices to assess provider and
staff perspectives about patient safety
issues, medical error, and error
reporting. The survey includes 38 items
that measure 10 composites of patient
safety culture. In addition to the
composite items, 14 items measure staff
perceptions of how often medical offices
have problems exchanging information
with other settings as well as other
patient safety and quality issues. AHRQ
made the survey publicly available
along with a Survey User’s Guide and
other toolkit materials in January 2009,
on the AHRQ website.
The AHRQ SOPS Medical Office
Database consists of data from the
AHRQ Medical Office Survey on Patient
Safety Culture and may include
reportable, non-required supplemental
items. Medical offices in the U.S. can
voluntarily submit data from the survey
to AHRQ, through its contractor, Westat.
The SOPS Medical Office Database
(OMB NO. 0935–0196, last approved on
September 24, 2021) was developed by
AHRQ in 2011 in response to requests
E:\FR\FM\02OCN1.SGM
02OCN1
80248
Federal Register / Vol. 89, No. 191 / Wednesday, October 2, 2024 / Notices
from medical offices interested in
tracking their own survey results. Those
organizations submitting data receive a
feedback report, as well as a report of
the aggregated, de-identified findings of
the other medical offices submitting
data. These reports are used to assist
medical office staff in their efforts to
improve patient safety culture in their
organizations.
The goal of the Medical Office Survey
on Patient Safety Culture Database is to
promote improvements in the quality
and safety of healthcare in medical
office settings. The survey, toolkit
materials, and database results are all
made publicly available on AHRQ’s
website. Technical assistance is
provided by AHRQ through its
contractor at no charge to medical
offices, to facilitate the use of these
materials for medical office patient
safety and quality improvement.
This database:
(1) Presents results from medical
offices that voluntarily submit their
data,
(2) Provides data to medical offices to
facilitate internal assessment and
learning in the patient safety
improvement process, and
(3) Provides supplemental
information to help medical offices
identify their strengths and areas with
potential for improvement in patient
safety culture.
To achieve the goal of this project, the
following activities and data collections
will be implemented:
(1) Eligibility and Registration Form—
The medical office point-of-contact
(POC) completes several data
submission steps and forms, beginning
with the completion of an online
Eligibility and Registration Form. The
purpose of this form is to collect basic
demographic information about the
medical office and initiate the
registration process.
(2) Medical Office Site Information
Form—The purpose of the site
information form, also completed by the
medical office POC, is to collect
background characteristics of the
medical office. This information will be
used to analyze data collected with
SOPS Medical Office Survey.
(3) Data Use Agreement—The purpose
of the data use agreement, completed by
the medical office POC, is to state how
data submitted by medical offices will
be used and provides privacy
assurances.
(4) Data File(s) Submission—POCs
upload their data file(s), using the
medical office data file specifications, to
ensure that users submit their data in a
standardized way (e.g., variable names,
order, coding, formatting). The number
of submissions to the database is likely
to vary from submission period to
submission period because medical
offices do not administer the survey and
submit data every year. Data submission
is typically handled by one POC who is
either an office manager or a survey
vendor who contracts with a medical
office to collect their data. POCs submit
data on behalf of 30 medical offices, on
average, because many medical offices
are part of a health system that includes
many medical office sites, or the POC is
a vendor that is submitting data for
multiple medical offices.
This study is being conducted by
AHRQ through its contractor, Westat,
pursuant to AHRQ’s statutory authority
to conduct and support research on
healthcare and on systems for the
delivery of such care, including
activities with respect to: the quality,
effectiveness, efficiency,
appropriateness and value of healthcare
services; quality measurement and
improvement; and database
development. 42 U.S.C. 299a(a)(1), (2),
and (8).
Method of Collection
All information collection for the
SOPS Medical Office Database is done
electronically, except the Data Use
Agreement (DUA) that medical offices
print, sign and return (either via fax, by
scanning and emailing or uploading to
a secure website, or by mailing back).
Registration, submission of medical
office information, and data upload is
handled online through a secure
website. Customized feedback reports
are delivered electronically (the person
submitting the data will enter a
username and password for access to a
secure website from which to download
their reports).
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondents’ time to participate in the
database. An estimated 85 POCs, each
representing an average of 30 individual
medical offices each, will complete the
database submission steps and forms.
Each POC will submit the following:
1. Eligibility and Registration Form—
Estimated to take 3 minutes to complete.
2. Medical Office Site Information
Form—Estimated to take 5 minutes to
complete.
3. Data Use Agreement—Estimated to
take 3 minutes to complete.
4. Survey Data File(s) Submission—
Estimated to take 1 hour to complete.
The total burden is estimated to be
308 hours.
Exhibit 2 shows the estimated
annualized cost burden based on the
respondents’ time to submit their data.
The cost burden is estimated to be
$19,891 annually.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
lotter on DSK11XQN23PROD with NOTICES1
1.
2.
3.
4.
Number of
responses
per POC
Hours per
response
Total burden
hours
Eligibility/Registration Form .........................................................................
Medical Office Site Information Form ..........................................................
Data Use Agreement ...................................................................................
Data File(s) Submission ..............................................................................
85
85
85
85
1
30
1
1
3/60
5/60
3/60
1
5
213
5
85
Total ..........................................................................................................
NA
NA
NA
308
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Total burden
hours
Form name
1. Eligibility/Registration Form .................................................................................................
2. Medical Office Site Information Form ..................................................................................
3. Data Use Agreement ...........................................................................................................
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E:\FR\FM\02OCN1.SGM
Average hourly
wage rate *
5
213
5
02OCN1
$64.58
64.58
64.58
Total cost
burden
$323
13,756
323
80249
Federal Register / Vol. 89, No. 191 / Wednesday, October 2, 2024 / Notices
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN—Continued
Total burden
hours
Form name
Average hourly
wage rate *
Total cost
burden
4. Data File(s) Submission ......................................................................................................
85
64.58
5,489
Total ..................................................................................................................................
308
NA
19,891
* Mean hourly wage rate of $64.58 for Medical and Health Services Managers (SOC code 11–9111) was obtained from the May 2023 National
Industry-Specific Occupational Employment and Wage Estimates, NAICS 621100—Offices of Physicians located at https://www.bls.gov/oes/current/naics4_621100.htm.
Request for Comments
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) whether the
proposed collection of information is
necessary for the proper performance of
AHRQ’s health care research and health
care information dissemination
functions, including whether the
information will have practical utility;
(b) the accuracy of AHRQ’s estimate of
burden (including hours and costs) of
the proposed collection(s) 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 upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: September 26, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024–22578 Filed 10–1–24; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10844 and CMS–
10157]
lotter on DSK11XQN23PROD with NOTICES1
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
SUMMARY:
VerDate Sep<11>2014
18:16 Oct 01, 2024
Jkt 262001
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Comments on the collection(s) of
information must be received by the
OMB desk officer by November 1, 2024.
ADDRESSES: Written 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.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, please access the CMS PRA
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing
DATES:
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
SUPPLEMENTARY INFORMATION:
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Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Small Biotech
Exception and Biosimilar Delay
Information Collection Request (ICR) for
Initial Price Applicability Year 2027;
Use: Under the authority in sections
11001 and 11002 of the Inflation
Reduction Act of 2022 (Pub. L. 117–
169), the Centers for Medicare &
Medicaid Services (CMS) is
implementing the Medicare Drug Price
Negotiation Program, codified in
sections 1191 through 1198 of the Social
Security Act (the Act). The Information
Collection Request Forms for the Small
Biotech Exception and Biosimilar Delay
Information Collection Request for
Initial Price Applicability Year 2027
must be submitted to CMS before CMS
establishes the selected drug list for
initial price applicability year 2027.
Small Biotech Exception: In
accordance with section 1192(d)(2) of
the Act, the term ‘‘negotiation-eligible
drug’’ excludes, with respect to the
initial price applicability years 2026,
2027, and 2028, a qualifying single
source drug that meets the requirements
for the exception for small biotech drugs
(the ‘‘Small Biotech Exception,’’ or
‘‘SBE’’).
E:\FR\FM\02OCN1.SGM
02OCN1
Agencies
[Federal Register Volume 89, Number 191 (Wednesday, October 2, 2024)]
[Notices]
[Pages 80247-80249]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-22578]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) approve extension of the currently approved
information collection project: Medical Office Survey on Patient Safety
Culture Database. This proposed information collection was previously
published in the Federal Register on July 31, 2024 and allowed 60 days
for public comment. AHRQ received no substantive comments from members
of the public. The purpose of this notice is to allow an additional 30
days for public comment.
DATES: Comments on this notice must be received by November 1, 2024.
ADDRESSES: Written 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. Copies of
the proposed collection plans, data collection instruments, and
specific details on the estimated burden can be obtained from the AHRQ
Reports Clearance Officer.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email
[email protected].
SUPPLEMENTARY INFORMATION:
Proposed Project
Medical Office Survey on Patient Safety Culture Database
In 1999, the Institute of Medicine called for health care
organizations to develop a ``culture of safety'' such that their
workforce and processes focus on improving the reliability and safety
of care for patients (IOM, 1999; To Err is Human: Building a Safer
Health System). To respond to the need for tools to assess patient
safety culture in health care, AHRQ developed and pilot tested the
Surveys on Patient Safety Culture[supreg] (SOPS[supreg]) Medical Office
Survey with OMB approval (OMB NO. 0935-0131; Approved July 5, 2007).
The survey is designed to enable medical offices to assess provider
and staff perspectives about patient safety issues, medical error, and
error reporting. The survey includes 38 items that measure 10
composites of patient safety culture. In addition to the composite
items, 14 items measure staff perceptions of how often medical offices
have problems exchanging information with other settings as well as
other patient safety and quality issues. AHRQ made the survey publicly
available along with a Survey User's Guide and other toolkit materials
in January 2009, on the AHRQ website.
The AHRQ SOPS Medical Office Database consists of data from the
AHRQ Medical Office Survey on Patient Safety Culture and may include
reportable, non-required supplemental items. Medical offices in the
U.S. can voluntarily submit data from the survey to AHRQ, through its
contractor, Westat. The SOPS Medical Office Database (OMB NO. 0935-
0196, last approved on September 24, 2021) was developed by AHRQ in
2011 in response to requests
[[Page 80248]]
from medical offices interested in tracking their own survey results.
Those organizations submitting data receive a feedback report, as well
as a report of the aggregated, de-identified findings of the other
medical offices submitting data. These reports are used to assist
medical office staff in their efforts to improve patient safety culture
in their organizations.
The goal of the Medical Office Survey on Patient Safety Culture
Database is to promote improvements in the quality and safety of
healthcare in medical office settings. The survey, toolkit materials,
and database results are all made publicly available on AHRQ's website.
Technical assistance is provided by AHRQ through its contractor at no
charge to medical offices, to facilitate the use of these materials for
medical office patient safety and quality improvement.
This database:
(1) Presents results from medical offices that voluntarily submit
their data,
(2) Provides data to medical offices to facilitate internal
assessment and learning in the patient safety improvement process, and
(3) Provides supplemental information to help medical offices
identify their strengths and areas with potential for improvement in
patient safety culture.
To achieve the goal of this project, the following activities and
data collections will be implemented:
(1) Eligibility and Registration Form--The medical office point-of-
contact (POC) completes several data submission steps and forms,
beginning with the completion of an online Eligibility and Registration
Form. The purpose of this form is to collect basic demographic
information about the medical office and initiate the registration
process.
(2) Medical Office Site Information Form--The purpose of the site
information form, also completed by the medical office POC, is to
collect background characteristics of the medical office. This
information will be used to analyze data collected with SOPS Medical
Office Survey.
(3) Data Use Agreement--The purpose of the data use agreement,
completed by the medical office POC, is to state how data submitted by
medical offices will be used and provides privacy assurances.
(4) Data File(s) Submission--POCs upload their data file(s), using
the medical office data file specifications, to ensure that users
submit their data in a standardized way (e.g., variable names, order,
coding, formatting). The number of submissions to the database is
likely to vary from submission period to submission period because
medical offices do not administer the survey and submit data every
year. Data submission is typically handled by one POC who is either an
office manager or a survey vendor who contracts with a medical office
to collect their data. POCs submit data on behalf of 30 medical
offices, on average, because many medical offices are part of a health
system that includes many medical office sites, or the POC is a vendor
that is submitting data for multiple medical offices.
This study is being conducted by AHRQ through its contractor,
Westat, pursuant to AHRQ's statutory authority to conduct and support
research on healthcare and on systems for the delivery of such care,
including activities with respect to: the quality, effectiveness,
efficiency, appropriateness and value of healthcare services; quality
measurement and improvement; and database development. 42 U.S.C.
299a(a)(1), (2), and (8).
Method of Collection
All information collection for the SOPS Medical Office Database is
done electronically, except the Data Use Agreement (DUA) that medical
offices print, sign and return (either via fax, by scanning and
emailing or uploading to a secure website, or by mailing back).
Registration, submission of medical office information, and data upload
is handled online through a secure website. Customized feedback reports
are delivered electronically (the person submitting the data will enter
a username and password for access to a secure website from which to
download their reports).
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours for the
respondents' time to participate in the database. An estimated 85 POCs,
each representing an average of 30 individual medical offices each,
will complete the database submission steps and forms. Each POC will
submit the following:
1. Eligibility and Registration Form--Estimated to take 3 minutes
to complete.
2. Medical Office Site Information Form--Estimated to take 5
minutes to complete.
3. Data Use Agreement--Estimated to take 3 minutes to complete.
4. Survey Data File(s) Submission--Estimated to take 1 hour to
complete.
The total burden is estimated to be 308 hours.
Exhibit 2 shows the estimated annualized cost burden based on the
respondents' time to submit their data. The cost burden is estimated to
be $19,891 annually.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Total burden
respondents POC response hours
----------------------------------------------------------------------------------------------------------------
1. Eligibility/Registration Form................ 85 1 3/60 5
2. Medical Office Site Information Form......... 85 30 5/60 213
3. Data Use Agreement........................... 85 1 3/60 5
4. Data File(s) Submission...................... 85 1 1 85
---------------------------------------------------------------
Total....................................... NA NA NA 308
----------------------------------------------------------------------------------------------------------------
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Total burden Average hourly Total cost
Form name hours wage rate * burden
----------------------------------------------------------------------------------------------------------------
1. Eligibility/Registration Form.............................. 5 $64.58 $323
2. Medical Office Site Information Form....................... 213 64.58 13,756
3. Data Use Agreement......................................... 5 64.58 323
[[Page 80249]]
4. Data File(s) Submission.................................... 85 64.58 5,489
-------------------------------------------------
Total..................................................... 308 NA 19,891
----------------------------------------------------------------------------------------------------------------
* Mean hourly wage rate of $64.58 for Medical and Health Services Managers (SOC code 11-9111) was obtained from
the May 2023 National Industry-Specific Occupational Employment and Wage Estimates, NAICS 621100--Offices of
Physicians located at https://www.bls.gov/oes/current/naics4_621100.htm.
Request for Comments
In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-
3520, comments on AHRQ's information collection are requested with
regard to any of the following: (a) whether the proposed collection of
information is necessary for the proper performance of AHRQ's health
care research and health care information dissemination functions,
including whether the information will have practical utility; (b) the
accuracy of AHRQ's estimate of burden (including hours and costs) of
the proposed collection(s) 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 upon
the respondents, including the use of automated collection techniques
or other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
Dated: September 26, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024-22578 Filed 10-1-24; 8:45 am]
BILLING CODE 4160-90-P