Meeting on the Artificial Intelligence in Healthcare Safety Program, 86804-86805 [2024-25140]
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86804
Federal Register / Vol. 89, No. 211 / Thursday, October 31, 2024 / Notices
This Draft CII General Permit is
established pursuant to CWA sections
301, 402(a)(1), 402(p)(2)(E), and
402(p)(6).
1. Technology-Based Requirements
This Draft CII General Permit would
be available to authorize certain
stormwater discharges, as it is
authorized to do under CWA sections
301, 402(a)(1), 402(p)(2)(E) and
402(p)(6), by requiring the
implementation of BMPs. The Draft CII
Permit regulates Phosphorus, a nonconventional pollutant, as an indicator
parameter for all regulated pollutants.
As provided in section 402(a)(1) of the
CWA, EPA established TechnologyBased Effluent Limitations (TBELs) in
this Draft Permit utilizing Best
Professional Judgment (BPJ) to meet the
‘‘best available technology economically
achievable’’ (BAT), ‘‘best conventional
pollutant control technology’’ (BCT),
and ‘‘best practicable control technology
currently available’’ (BPT) standards
described in section 304(b) of the CWA.
TBELs in this Draft Permit are expressed
as requirements for implementation of
effective best management practices
(BMPs). 40 CFR 122.44(k). Section 2.1.1
of the Draft CII GP requires all
Permittees to develop and implement
Stormwater Pollution Control Plans
(SPCPs). The minimum BMPs specified
in this CII GP represent common
practices that can be implemented by
most CII facilities. Dischargers have
flexibility in designing their SPCP in
accordance with Section 2.2 of this Draft
CII GP.
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2. Water-Quality Based Requirements
Based on its scientific and technical
judgment, EPA has determined that the
following reductions of Phosphorus, as
an indicator pollutant, from CII sites are
necessary to meet water quality
standards: Charles River watershed,
65%; Mystic River watershed, 62%;
Neponset River watershed, 60%.
Permittees’ development and
implementation of SPCPs constitutes
compliance with the Water-Quality
Based Effluent Limitations (WQBELs)
contained in this Draft CII GP, including
the aforementioned reductions of
Phosphorus.
D. Provisions on Which EPA Is
Soliciting Comment
While EPA encourages the public to
review and comment on all provisions
in the Preliminary Determination and
the Draft CII GP, EPA has included in
the body of the Draft CII GP Fact Sheet
several proposed provisions on which
EPA specifically requests feedback. The
following list summarizes these specific
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18:18 Oct 30, 2024
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requests for comment, and where they
are included in the fact sheet. EPA notes
that these are only summaries of the
requests for comment. The Agency
recommends that the public see the
specific wording of each comment
request within the body of the fact
sheet.
1. Multifamily housing/tax codes
(Fact Sheet § 1.5): EPA is seeking
comment on whether to include MultiFamily Residential Properties in the
final designation and in the final CII GP.
2. Compliance schedule (Fact Sheet
§ 5.1.1): EPA is seeking comment on
whether the proposed compliance
schedule is appropriate.
3. Multiple non-contiguous properties
(Fact Sheet § 1.4): EPA is seeking
comment on how the permitting process
should work for owners with multiple
non-contiguous properties that are
subject to the CII GP.
4. Owner-operator (Fact Sheet § 1.4):
EPA is seeking comment on whether
EPA should regulate the operator with
control over a site instead of the owner,
including sites where multiple operators
may be tenants of a site (e.g., a shopping
plaza with one owner and multiple
tenants).
5. Contiguous properties (Fact Sheet
§ 1.4): EPA is seeking comment on its
regulation of contiguous sites, which
reflect EPAs interest in consolidating, to
the greatest extent possible,
responsibility for permit compliance.
6. Historic Properties (Fact Sheet
§ 9.3): EPA is seeking comment on the
Draft CII GP’s potential impact on
historic properties.
E. Procedures for Reaching a Final
Designation and Final Permit Decision
After the comment period closes, EPA
intends to issue a final permit and final
RDA determination. EPA will consider
all significant comments and make
appropriate changes before issuing this
permit. EPA’s responses to public
comments received will be included in
the docket as part of the final permit
issuance. Once the final permit becomes
effective, eligible dischargers may seek
authorization.
Authority: This action is being taken
pursuant to Clean Water Act sections
301, 402(a)(1), 402(p)(2)(E), and
402(p)(6).
Dated: October 24, 2024.
David W. Cash,
Administrator, EPA Region 1, Boston, MA.
[FR Doc. 2024–25219 Filed 10–30–24; 8:45 am]
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FEDERAL ELECTION COMMISSION
Sunshine Act Meetings
FEDERAL REGISTER CITATION OF PREVIOUS
ANNOUNCEMENT: 89 FR 85212.
PREVIOUSLY ANNOUNCED TIME AND DATE OF
THE MEETING: Wednesday, October 30,
2024 at 10:00 a.m., Hybrid Meeting:
1050 First Street NE, Washington, DC
(12th Floor) and virtual.
CHANGES IN THE MEETING: The October
30, 2024 Open Meeting has been
canceled.
CONTACT PERSON FOR MORE INFORMATION:
Judith Ingram, Press Officer, Telephone:
(202) 694–1220.
(Authority: Government in the Sunshine Act,
5 U.S.C. 552b)
Laura E. Sinram,
Secretary and Clerk of the Commission.
[FR Doc. 2024–25498 Filed 10–29–24; 4:15 pm]
BILLING CODE 6715–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Meeting on the Artificial Intelligence in
Healthcare Safety Program
Agency for Healthcare Research
and Quality (AHRQ), Department of
Health and Human Services (HHS).
ACTION: Notice of public meeting.
AGENCY:
HHS is directed by Executive
order (E.O.) to establish an Artificial
Intelligence (AI) in Healthcare Safety
Program in partnership with federally
listed Patient Safety Organizations
(PSOs). The purpose of this notice is to
announce a meeting to discuss
implementation of the Executive order
to establish the AI in Healthcare Safety
Program. This meeting is designed as an
interactive forum where participants
can provide input on the future of the
program.
DATES: The meeting will be held from
12:30 to 4 p.m. eastern on Friday,
November 15, 2024.
ADDRESSES: The meeting will be held
virtually.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Erofile Gripiotis, Program Analyst,
Center for Quality Improvement and
Patient Safety, AHRQ, 5600 Fishers
Lane, Rockville, MD 20857; Telephone
(toll free): (866) 403–3697; Telephone
(local): (301) 427–1111; TTY (toll free):
(866) 438–7231; TTY (local): (301) 427–
1130; Email: pso@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION:
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Federal Register / Vol. 89, No. 211 / Thursday, October 31, 2024 / Notices
Background
The Patient Safety and Quality
Improvement Act of 2005, 42 U.S.C.
299b–21 to 299b–26 (Patient Safety Act),
and the related Patient Safety and
Quality Improvement Final Rule, 42
CFR part 3 (Patient Safety Rule),
published in the Federal Register on
November 21, 2008, 73 FR 70731–
70814, provide for the Federal listing of
Patient Safety Organizations (PSOs),
which collect, aggregate, and analyze
confidential information (patient safety
work product) regarding the quality and
safety of healthcare delivery.
The Patient Safety Act also authorizes
the development of data standards,
known as the Common Formats, to
facilitate the aggregation and analysis of
non-identifiable patient safety work
product collected by PSOs and reported
to the Network of Patient Safety
Databases (NPSD). (42 U.S.C. 299b–
23(b)). The Patient Safety Act and
Patient Safety Rule can be accessed at:
https://www.pso.ahrq.gov/legislation/.
Section 8(iv) of E.O. 14110 requires
the Secretary of HHS, in consultation
with the Secretaries of Defense and
Veterans Affairs, to establish an AI
safety program that, in partnership with
PSOs, will:
• establish a common framework for
approaches to identifying and capturing
clinical errors resulting from AI
deployed in healthcare settings as well
as specifications for a central tracking
repository for associated incidents that
cause harm, including through bias or
discrimination, to patients, caregivers,
or other parties;
• analyze captured data and
generated evidence to develop,
wherever appropriate,
recommendations, best practices, or
other informal guidelines aimed at
avoiding these harms; and
• disseminate those
recommendations, best practices, or
other informal guidelines to appropriate
stakeholders, including healthcare
providers.
lotter on DSK11XQN23PROD with NOTICES1
Agenda, Registration, and Other
Information About the Meeting
AHRQ will be hosting this fully
virtual meeting to discuss
implementation of the AI in Healthcare
Safety Program with members of the
public, including PSOs and other
interested parties. Agenda topics will
include recent AI-related analyses from
the NPSD, available program resources,
and speakers from the Assistant
Secretary for Technology Policy/Office
of the National Coordinator for Health
Information Technology and the
Coalition for Health AI. Active
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participation and discussion by meeting
participants is encouraged, including
through breakout sessions.
AHRQ requests that interested
persons send an email to SDMeetings@
infinityconferences.com for registration
information. Before the meeting, an
agenda and logistical information will
be provided to registrants.
Dated: October 24, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024–25140 Filed 10–30–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[CDC–2024–0065; Docket Number NIOSH–
352–A]
Draft Hazard Review: Wildland Fire
Smoke Exposure Among Farmworkers
and Other Outdoor Workers
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Extension of comment period
and announcement of informational
webinar.
AGENCY:
On September 13, 2024,
NIOSH published a notice in the
Federal Register announcing public
comment and technical review on the
draft Hazard Review: Wildland Fire
Smoke Exposure Among Farmworkers
and Other Outdoor Workers. Written
comments were to be received by
November 12, 2024. NIOSH is extending
the public comment period to January
10, 2025. NIOSH will also convene an
informational webinar to present an
overview about the draft Hazard Review
document, describe its content and
purpose, and provide information about
the public comment period. The
webinar is scheduled to occur on
Tuesday, December 3, 2024, at 1:00 p.m.
Eastern Time (US and Canada).
Attendees are requested to register in
advance for this webinar.
DATES: Registration for the webinar must
occur on or before the date of the
webinar, December 3, 2024. The
comment period for the draft Hazard
Review: Wildland Fire Smoke Exposure
Among Farmworkers and Other Outdoor
Workers, published September 13, 2024
at 89 FR 74960, is extended. Electronic
or written comments must be received
by January 10, 2025, at 11:59 p.m.
ADDRESSES: Register in advance for the
webinar at the following link.
SUMMARY:
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86805
Attendance for the webinar is limited to
3,000 participants: https://
cdc.zoomgov.com/webinar/register/WN_
lnOhz1wMTNyr_06z1hYgRw.
You may submit comments on the
draft Hazard Review: Wildland Fire
Smoke Exposure Among Farmworkers
and Other Outdoor Workers, identified
by CDC–2024–0065 and Docket Number
NIOSH–352–A, by either of the
following two methods:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: National Institute for
Occupational Safety and Health, NIOSH
Docket Office, 1090 Tusculum Avenue,
MS C–34, Cincinnati, Ohio 45226–1998.
Instructions: All information received
in response to this notice must include
the agency name and docket number
(CDC–2024–0065; NIOSH–352–A). All
relevant comments, including any
personal information provided, will be
posted without change to https://
www.regulations.gov. Do not submit
comments by email. CDC does not
accept comments by email. For access to
the docket to read the draft Hazard
Review document or comments
received, go to https://
www.regulations.gov.
R.
Todd Niemeier, Ph.D., National Institute
for Occupational Safety and Health,
MS–C15, 1090 Tusculum Avenue,
Cincinnati, OH 45226. Telephone: (513)
533–8166.
SUPPLEMENTARY INFORMATION: NIOSH is
requesting public comment and
technical review of the draft Hazard
Review: Wildland Fire Smoke Exposure
Among Farmworkers and Other Outdoor
Workers, which is accessible in the
docket (CDC–2024–0065; NIOSH–352–
A). NIOSH is extending the public
comment period to January 10, 2025.
The comment period is being extended
to provide an informational webinar and
allow additional time for comment.
Specific review questions to be
considered are included in the initial
Federal Register notice published on
September 13, 2024 at 89 FR 74960.
The final document will be used as
the scientific evidence base to inform
the development of supplementary
educational materials for workers,
employers, and other relevant audiences
to support the implementation of the
recommendations. Therefore, comments
that focus on the understandability,
accessibility, and feasibility of the
recommendations are requested.
The draft Hazard Review was
developed to provide the scientific
rationale for characterizing hazards of
exposure to wildland fire smoke for
FOR FURTHER INFORMATION CONTACT:
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Agencies
[Federal Register Volume 89, Number 211 (Thursday, October 31, 2024)]
[Notices]
[Pages 86804-86805]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-25140]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Meeting on the Artificial Intelligence in Healthcare Safety
Program
AGENCY: Agency for Healthcare Research and Quality (AHRQ), Department
of Health and Human Services (HHS).
ACTION: Notice of public meeting.
-----------------------------------------------------------------------
SUMMARY: HHS is directed by Executive order (E.O.) to establish an
Artificial Intelligence (AI) in Healthcare Safety Program in
partnership with federally listed Patient Safety Organizations (PSOs).
The purpose of this notice is to announce a meeting to discuss
implementation of the Executive order to establish the AI in Healthcare
Safety Program. This meeting is designed as an interactive forum where
participants can provide input on the future of the program.
DATES: The meeting will be held from 12:30 to 4 p.m. eastern on Friday,
November 15, 2024.
ADDRESSES: The meeting will be held virtually.
FOR FURTHER INFORMATION CONTACT: Erofile Gripiotis, Program Analyst,
Center for Quality Improvement and Patient Safety, AHRQ, 5600 Fishers
Lane, Rockville, MD 20857; Telephone (toll free): (866) 403-3697;
Telephone (local): (301) 427-1111; TTY (toll free): (866) 438-7231; TTY
(local): (301) 427-1130; Email: [email protected].
SUPPLEMENTARY INFORMATION:
[[Page 86805]]
Background
The Patient Safety and Quality Improvement Act of 2005, 42 U.S.C.
299b-21 to 299b-26 (Patient Safety Act), and the related Patient Safety
and Quality Improvement Final Rule, 42 CFR part 3 (Patient Safety
Rule), published in the Federal Register on November 21, 2008, 73 FR
70731-70814, provide for the Federal listing of Patient Safety
Organizations (PSOs), which collect, aggregate, and analyze
confidential information (patient safety work product) regarding the
quality and safety of healthcare delivery.
The Patient Safety Act also authorizes the development of data
standards, known as the Common Formats, to facilitate the aggregation
and analysis of non-identifiable patient safety work product collected
by PSOs and reported to the Network of Patient Safety Databases (NPSD).
(42 U.S.C. 299b-23(b)). The Patient Safety Act and Patient Safety Rule
can be accessed at: https://www.pso.ahrq.gov/legislation/.
Section 8(iv) of E.O. 14110 requires the Secretary of HHS, in
consultation with the Secretaries of Defense and Veterans Affairs, to
establish an AI safety program that, in partnership with PSOs, will:
establish a common framework for approaches to identifying
and capturing clinical errors resulting from AI deployed in healthcare
settings as well as specifications for a central tracking repository
for associated incidents that cause harm, including through bias or
discrimination, to patients, caregivers, or other parties;
analyze captured data and generated evidence to develop,
wherever appropriate, recommendations, best practices, or other
informal guidelines aimed at avoiding these harms; and
disseminate those recommendations, best practices, or
other informal guidelines to appropriate stakeholders, including
healthcare providers.
Agenda, Registration, and Other Information About the Meeting
AHRQ will be hosting this fully virtual meeting to discuss
implementation of the AI in Healthcare Safety Program with members of
the public, including PSOs and other interested parties. Agenda topics
will include recent AI-related analyses from the NPSD, available
program resources, and speakers from the Assistant Secretary for
Technology Policy/Office of the National Coordinator for Health
Information Technology and the Coalition for Health AI. Active
participation and discussion by meeting participants is encouraged,
including through breakout sessions.
AHRQ requests that interested persons send an email to
[email protected] for registration information. Before
the meeting, an agenda and logistical information will be provided to
registrants.
Dated: October 24, 2024.
Marquita Cullom,
Associate Director.
[FR Doc. 2024-25140 Filed 10-30-24; 8:45 am]
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