Organization, Functions, and Delegations of Authority; Part G; Indian Health Service; Headquarters, Office of the Director, Office of Quality, 106537-106539 [2024-31273]

Download as PDF ddrumheller on DSK120RN23PROD with NOTICES1 Federal Register / Vol. 89, No. 249 / Monday, December 30, 2024 / Notices Committee (referred to as the ‘‘HITAC’’). The HITAC will be governed by the provisions of the Federal Advisory Committee Act (FACA) (Pub. L. 92– 463), as amended, (5 U.S.C. app.), which sets forth standards for the formation and use of federal advisory committees. Composition: The HITAC is comprised of at least 25 members, of which: • No fewer than 2 members are advocates for patients or consumers of health information technology; • 3 members are appointed by the HHS Secretary Æ 1 of whom shall be appointed to represent the Department of Health and Human Services; and Æ 1 of whom shall be a public health official; • 2 members are appointed by the majority leader of the Senate; • 2 members are appointed by the minority leader of the Senate; • 2 members are appointed by the Speaker of the House of Representatives; • 2 members are appointed by the minority leader of the House of Representatives; • Other members are appointed by the Comptroller General of the United States. Members serve for one-, two-, or three-year terms. All members may be reappointed for a subsequent three-year term. Each member is limited to two three-year terms, not to exceed six years of service. Members serve without pay but will be provided per-diem and travel costs for committee services, if warranted. Recommendations: The HITAC recommendations to the Assistant Secretary for Technology Policy/ National Coordinator for Health Information Technology are publicly available at https://www.healthit.gov/ topic/federal-advisory-committees/ recommendations-national-coordinatorhealth-it. Public Meetings: All HITAC meetings will be virtual. Please note that some HITAC meetings may also have an inperson meeting option. For web conference instructions and the most up-to-date information, including inperson meeting location (if applicable), please visit the HITAC calendar on the ONC website, www.healthit.gov/topic/ federal-advisory-committees/hitaccalendar. The schedule of meetings to be held in 2025 is as follows: • February 13, 2025, from approximately 10:00 a.m. to 3:00 p.m./ Eastern Time • March 20, 2025, from approximately 10:00 a.m. to 3:00 p.m./ Eastern Time VerDate Sep<11>2014 23:58 Dec 27, 2024 Jkt 265001 • April 10, 2025, from approximately 10:00 a.m. to 3:00 p.m./Eastern Time • May 8, 2025, from approximately 10:00 a.m. to 3:00 p.m./Eastern Time • June 12, 2025, from approximately 10:00 a.m. to 3:00 p.m./Eastern Time • July 17, 2025, from approximately 10:00 a.m. to 3:00 p.m./Eastern Time • August 14, 2025, from approximately 10:00 a.m. to 3:00 p.m./ Eastern Time • September 18, 2025, from approximately 10:00 a.m. to 3:00 p.m./ Eastern Time • October 16, 2025, from approximately 10:00 a.m. to 3:00 p.m./ Eastern Time • November 13, 2025, from approximately 10:00 a.m. to 3:00 p.m./ Eastern Time All meetings are open to the public. Additional meetings may be scheduled as needed. Contact Person for Meetings: Seth Pazinski, Seth.Pazinski@hhs.gov. A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Please email Seth Pazinski for the most current information about meetings. Agenda: As outlined in the 21st Century Cures Act, the HITAC will develop and submit recommendations to the Assistant Secretary for Technology Policy/National Coordinator on Health Information Technology on the topics of interoperability, privacy and security, patient access to information, use of technologies that support public health, design and use of technologies that advance health equity, and use of artificial intelligence that improves health and health care. In addition, the committee will also address any administrative matters and hear periodic reports from ASTP. ASTP intends to make background material available to the public no later than 24 hours prior to the meeting start time. If ASTP is unable to post the background material on its website prior to the meeting, the material will be made publicly available on ASTP’s website after the meeting, at www.healthit.gov/ hitac. Procedure: Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee. Written submissions may be made to the contact person prior to the meeting date. An oral public comment period will be scheduled at each meeting. Time allotted for each commenter will be limited to three minutes. If the number of speakers requesting to comment is PO 00000 Frm 00132 Fmt 4703 Sfmt 4703 106537 greater than can be reasonably accommodated during the scheduled public comment period, ASTP will take written comments after the meeting. ASTP welcomes the attendance of the public at its HITAC meetings. If you require special accommodations due to a disability, please contact Seth Pazinski at least seven (7) days in advance of the meeting. Notice of these meetings are given under the Federal Advisory Committee Act (Pub. L. No. 92–463, 5 U.S.C., App. 2). Dated: November 22, 2024. Stanley S. Pazinski, Designated Federal Officer, Assistant Secretary for Technology Policy/Office of the National Coordinator for Health Information Technology. [FR Doc. 2024–31076 Filed 12–27–24; 8:45 am] BILLING CODE 4150–45–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Indian Health Service Organization, Functions, and Delegations of Authority; Part G; Indian Health Service; Headquarters, Office of the Director, Office of Quality Indian Health Service, Department of Health and Human Services. ACTION: Final notice. AGENCY: Part G of the Statement of Organization, Functions, and Delegations of Authority of the Department of Health and Human Services (HHS) is hereby amended to reflect a reorganization of the Indian Health Service (IHS). The purpose of this reorganization proposal is to update the current approved IHS, Office of the Director (GA), Congressional and Legislative Affairs Staff (GA1) and the Office of Quality (GAP) in their entirety and replace with the following: SUPPLEMENTARY INFORMATION: The IHS is an Operating Division within the Department of Health and Human Services (HHS) and is under the leadership and direction of a Director who is directly responsible to the Secretary of Health and Human Services. The IHS Headquarters is proposing to reorganize the following major component: Office the Office of Quality (OQ). Part G of the Statement of Organization, Functions, and Delegations of Authority was most recently amended at 89 FR 61126, July 30, 2024. SUMMARY: E:\FR\FM\30DEN1.SGM 30DEN1 106538 Federal Register / Vol. 89, No. 249 / Monday, December 30, 2024 / Notices Office of the Director, IHS (GA) ddrumheller on DSK120RN23PROD with NOTICES1 Congressional and Legislative Affairs Staff (CLAS) (GA1) (1) Serves as the principal advisor to the IHS Director on all legislative and congressional relations matters; (2) advises the IHS Director and other IHS officials on the need for changes in legislation and manages the development of IHS legislative initiatives; (3) serves as the IHS liaison office for congressional and legislative affairs with Congressional offices, the HHS, the Office of Management and Budget (OMB), the White House, and other federal agencies; (4) tracks all major legislative proposals in the Congress that would impact Indian health; (5) ensures that the IHS Director and appropriate IHS and HHS officials are briefed on the potential impact of proposed legislation; (6) develops legislative strategy for key policy and legislative initiatives; (7) provides technical assistance and advice relative to the effect that initiatives/ implementation would have on the IHS; (8) provides support and collaborates with the Office of Finance and Accounting relative to IHS appropriations efforts; (9) directs the development of IHS briefing materials for congressional hearings, testimony, and bill reports; (10) analyzes legislation for necessary action within the IHS; (11) develops appropriate legislative implementation plans; (12) coordinates with IHS HQ and Area Offices as appropriate to provide leadership, advocacy, and technical support to respond to requests from the public, including tribal governments, tribal organizations, and Indian community organizations regarding IHS legislative issues. Office of Quality (GAP) The Office of Quality (OQ) provides leadership and direction for quality improvement and patient safety activities and oversees compliance and risk management throughout the agency. Specifically, the office (1) advises the Indian Health Service (IHS) Director on assuring quality health care, maximizing the patient experience, and systematizing quality improvement activities to improve clinical outcomes and administrative processes; (2) develops and implements a strategic quality framework; (3) oversees accreditation readiness activities and compliance with accreditation requirements at all IHS Direct Service facilities; (4) conducts performance improvement, quality assurance, innovative thinking, and risk management trainings; (5) oversees IHS VerDate Sep<11>2014 23:58 Dec 27, 2024 Jkt 265001 facilities and staff in intra-agency quality improvement activities; (6) advises on development and monitoring of quality assurance and governance metrics for health care delivery processes and outcomes; (7) develops programs to assess, address, and improve systems and processes to improve health care quality; (8) advises on compliance with relevant federal regulations and accreditation and professional standards; (9) provides guidance for standardization of health care delivery policies, protocols, and governance; (10) advises and guides IHS patient-centered care processes, ensuring engagement of patients as partners in care; (11) oversees the IHS Enterprise Risk Management (ERM) vision, culture, strategy, and framework and clinical risk management; (12) oversees and coordinates the agency’s efforts to establish and maintain proper internal controls; (13) ensures requirements are met under OMB Circular A–123; (14) develops programs to promote patient safety management and reporting systems and processes, sentinel event investigations/root cause analysis; and (15) participates in crosscutting issues and processes, including but not limited to, emergency preparedness/security, quality assurance, recruitment, budget formulation, self-determination issues, and resolution of audit findings as may be needed and appropriate. Division of Quality Assurance and Patient Safety (GAPA) (1) Develops and implements programs to promote sustained compliance with relevant federal regulations related to accreditation and professional standards for health care facilities; (2) manages and coordinates continuous accreditation compliance programs using multidisciplinary integration of survey readiness activities; (3) coordinates health care accreditation resource management; (4) tracks health care accreditation and certification survey reports; (5) develops and implements programs to manage credentialing standards and policy, acquires and maintains centralized credentialing software system, promotes unification of medical staff professionals (MSP), and promotes standardized training and support resources for MSP; (6) develops and implements policies and procedures to promote patient safety, infection control practices, and environment of care and life safety practices; (7) establishes policies and guidelines to reduce adverse events; (8) develops education and training related to the application of established patient safety and adverse PO 00000 Frm 00133 Fmt 4703 Sfmt 4703 event reporting systems and metrics; (9) establishes and maintains oversight mechanisms for incident identification and reporting, adverse events and good catches, comprehensive systemic analysis/root cause analysis process and documentation; (10) implements strategies to improve patient and workforce safety; (11) enhances collaborative communication to facilitate the sharing of best practices and learning related to identified risks and mitigation actions across the agency; (12) identifies IHS and National patient safety trends and investigates positive and negative patient safety outcomes across the agency; and (13) provides patient safety consultation regarding industry standards, best practices, and development of policy, processes, and procedures. Division of Enterprise Risk Management (GAPB) (1) Oversees and coordinates the IHS ERM vision, culture, strategy, and framework; (2) develops goals and objectives for the ERM program, integrated with broader IHS-wide strategic goals/objectives, and tracks progress toward achieving them; (3) coordinates the development of risk policy, including a risk appetite statement, to guide Agency decisionmaking and documentation related to risk; (4) advises and collaborates in the development of the IHS ERM portfolio of enterprise risks and ensures appropriate and effective management by accountable individual risk owners; (5) integrates risk assessment activities across the IHS risk portfolio; (6) advises on ERM and provides expertise, advice, and assistance to the agency leadership on compliance matters; (7) provides guidance and training on the risk management process and prioritization; (8) facilitates the governance policy, process, and reporting to establish consistency and quality of documentation of fiduciary responsibilities of governing bodies; (9) oversees tracking of high-risk administrative, clinical, or personnel incidents to ensure appropriate local and agency-wide response, timely closure, assessment of internal controls, and review of case studies to promote a safety culture based on risk-awareness; (10) collaborates with key HQ Offices to ensure consistency in cross-cutting agency strategic planning, ERM, and management of internal controls across IHS; (11) collaborates with strategic planning process to integrate risk management and strategic thinking; (12) reviews tort claims files; (13) represents the IHS when claims are presented for review by the Malpractice Claims E:\FR\FM\30DEN1.SGM 30DEN1 Federal Register / Vol. 89, No. 249 / Monday, December 30, 2024 / Notices Review Panel chartered by the HHS, and assists providers with Malpractice Claims Review Panel interactions; (14) submits payment reports to the National Practitioner Data Bank; (15) maintains case files and a malpractice claims database; (16) provides case summaries, peer review, outcome information, and feedback of risk management recommendations; (17) disseminates information about the review process; (18) responds to outside organizations requesting tort claim-involvement histories on former employees; and (19) responds to Tort Claims inquiries from governmental agencies, media, Tribal and Urban Indian organizations, and advocacy groups with the Office of General Council guidance. ddrumheller on DSK120RN23PROD with NOTICES1 Division of Innovation and Improvement (GAPC) (1) Provides trainings on innovative thinking and performance improvement techniques; (2) provides training on empathy and relational intelligence to better understand colleagues and stakeholders and maximize teamwork; (3) integrates innovative thinking into quality improvement and policy formation processes to stimulate rapid idea generation; (4) oversees training programs to increase quality improvement capacity and standardize improvement methodology to test smallscale changes at the local level; (5) reviews use of health information technology and data to improve performance, quality and service; (6) monitors patient and staff satisfaction with health care service delivery; (7) leads change management for practice transformation to embrace new models of care delivery and to enhance efficiency of the care delivery process; (8) develops programs to promote the implementation of patient-centered care models; (9) coordinates sharing of best practices between Area Quality Managers and Service Unit Quality Assurance and Performance Improvement officers; and (10) supports and promotes patient-centered care including Patient and Family Engagement, and promotes unification of Area Quality Managers and Service Unit Quality Assurance and Performance Improvement Officers. Division of Compliance (GAPD) (1) Coordinates the IHS’s compliance program; (2) administers the agency’s internal control program in accordance with the Federal Managers’ Financial Integrity Act, OMB Circular No. A–123, GAO Green Book, and other applicable requirements; (3) oversees and coordinates the agency’s efforts to establish and maintain proper internal VerDate Sep<11>2014 23:58 Dec 27, 2024 Jkt 265001 controls; (4) oversees and institutionalizes a continuous compliance review process; (5) manages goals and objectives for the Compliance program, integrates them with broader IHS-wide strategic goals/objectives, and tracks progress toward achieving them; (6) evaluates and monitors systems of internal control across IHS and uses the assessments of the internal control program as an integral part of ERM to effectively manage risks across IHS; (7) Serves as the IHS liaison office to the Government Accountability Office (GAO) and Office of Inspector General (OIG); (8) coordinates the development, clearance, and transmittal of IHS responses and follow-up to reports issued by the OIG, the GAO, and other federal internal and external authorities reviewing risk management and internal controls; (9) provides leadership and direction on activities for continuous improvement of management accountability and administrative systems for effective and efficient program support services IHS-wide; and (10) oversees and coordinates the annual development and submission of the agency’s federal Activities Inventory Reform Act report to the HHS. Section GA–30, Indian Health Service— Delegations of Authority All delegations of authority and redelegations of authority made to IHS officials that were in effect immediately prior to this reorganization, and that are consistent with this reorganization, shall continue in effect pending further re-delegation. Roselyn Tso, Director, Indian Health Service. [FR Doc. 2024–31273 Filed 12–27–24; 8:45 am] BILLING CODE 4166–14–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Aging; Notice of Closed Meeting Pursuant to section 1009 of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant PO 00000 Frm 00134 Fmt 4703 Sfmt 4703 106539 applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute on Aging Special Emphasis Panel; NHP Review. Date: January 31, 2025. Time: 10:30 a.m. to 1:00 p.m. Agenda: To review and evaluate grant applications. Address: National Institute on Aging, 5601 Fishers Lane, Suite 8B, Rockville, MD 20892. Meeting Format: Virtual Meeting. Contact Person: Bita Nakhai, Ph.D., Scientific Review Officer, National Institute on Aging, National Institutes of Health, 5601 Fishers Lane, Suite 8B, Rockville, MD 20852, (301) 402–7701, nakhaib@nia.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.866, Aging Research, National Institutes of Health, HHS) Dated: December 19, 2024. Miguelina Perez, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2024–30880 Filed 12–27–24; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of General Medical Sciences; Notice of Closed Meeting Pursuant to section 1009 of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute of General Medical Sciences Initial Review Group Training and Workforce Development Study Section—C Training & Workforce Development Study Section C (TWD–C) Review of applications for the B2B & IRACDA Programs and Scientific Meetings & Conferences. Date: February 20–21, 2025. Time: 10:00 a.m. to 6:00 p.m. Agenda: To review and evaluate grant applications. Address: National Institutes of Health, National Institute of General Medical Sciences, Natcher Building, 45 Center Drive, Bethesda, Maryland 20892. Meeting Format: Virtual Meeting. Contact Person: Sonia Ivette OrtizMiranda, Ph.D., Scientific Review Officer, E:\FR\FM\30DEN1.SGM 30DEN1

Agencies

[Federal Register Volume 89, Number 249 (Monday, December 30, 2024)]
[Notices]
[Pages 106537-106539]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-31273]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Indian Health Service


Organization, Functions, and Delegations of Authority; Part G; 
Indian Health Service; Headquarters, Office of the Director, Office of 
Quality

AGENCY: Indian Health Service, Department of Health and Human Services.

ACTION: Final notice.

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

SUMMARY: Part G of the Statement of Organization, Functions, and 
Delegations of Authority of the Department of Health and Human Services 
(HHS) is hereby amended to reflect a reorganization of the Indian 
Health Service (IHS). The purpose of this reorganization proposal is to 
update the current approved IHS, Office of the Director (GA), 
Congressional and Legislative Affairs Staff (GA1) and the Office of 
Quality (GAP) in their entirety and replace with the following:

SUPPLEMENTARY INFORMATION: The IHS is an Operating Division within the 
Department of Health and Human Services (HHS) and is under the 
leadership and direction of a Director who is directly responsible to 
the Secretary of Health and Human Services. The IHS Headquarters is 
proposing to reorganize the following major component: Office the 
Office of Quality (OQ).
    Part G of the Statement of Organization, Functions, and Delegations 
of Authority was most recently amended at 89 FR 61126, July 30, 2024.

[[Page 106538]]

Office of the Director, IHS (GA)

Congressional and Legislative Affairs Staff (CLAS) (GA1)

    (1) Serves as the principal advisor to the IHS Director on all 
legislative and congressional relations matters; (2) advises the IHS 
Director and other IHS officials on the need for changes in legislation 
and manages the development of IHS legislative initiatives; (3) serves 
as the IHS liaison office for congressional and legislative affairs 
with Congressional offices, the HHS, the Office of Management and 
Budget (OMB), the White House, and other federal agencies; (4) tracks 
all major legislative proposals in the Congress that would impact 
Indian health; (5) ensures that the IHS Director and appropriate IHS 
and HHS officials are briefed on the potential impact of proposed 
legislation; (6) develops legislative strategy for key policy and 
legislative initiatives; (7) provides technical assistance and advice 
relative to the effect that initiatives/implementation would have on 
the IHS; (8) provides support and collaborates with the Office of 
Finance and Accounting relative to IHS appropriations efforts; (9) 
directs the development of IHS briefing materials for congressional 
hearings, testimony, and bill reports; (10) analyzes legislation for 
necessary action within the IHS; (11) develops appropriate legislative 
implementation plans; (12) coordinates with IHS HQ and Area Offices as 
appropriate to provide leadership, advocacy, and technical support to 
respond to requests from the public, including tribal governments, 
tribal organizations, and Indian community organizations regarding IHS 
legislative issues.

Office of Quality (GAP)

    The Office of Quality (OQ) provides leadership and direction for 
quality improvement and patient safety activities and oversees 
compliance and risk management throughout the agency. Specifically, the 
office (1) advises the Indian Health Service (IHS) Director on assuring 
quality health care, maximizing the patient experience, and 
systematizing quality improvement activities to improve clinical 
outcomes and administrative processes; (2) develops and implements a 
strategic quality framework; (3) oversees accreditation readiness 
activities and compliance with accreditation requirements at all IHS 
Direct Service facilities; (4) conducts performance improvement, 
quality assurance, innovative thinking, and risk management trainings; 
(5) oversees IHS facilities and staff in intra-agency quality 
improvement activities; (6) advises on development and monitoring of 
quality assurance and governance metrics for health care delivery 
processes and outcomes; (7) develops programs to assess, address, and 
improve systems and processes to improve health care quality; (8) 
advises on compliance with relevant federal regulations and 
accreditation and professional standards; (9) provides guidance for 
standardization of health care delivery policies, protocols, and 
governance; (10) advises and guides IHS patient-centered care 
processes, ensuring engagement of patients as partners in care; (11) 
oversees the IHS Enterprise Risk Management (ERM) vision, culture, 
strategy, and framework and clinical risk management; (12) oversees and 
coordinates the agency's efforts to establish and maintain proper 
internal controls; (13) ensures requirements are met under OMB Circular 
A-123; (14) develops programs to promote patient safety management and 
reporting systems and processes, sentinel event investigations/root 
cause analysis; and (15) participates in cross-cutting issues and 
processes, including but not limited to, emergency preparedness/
security, quality assurance, recruitment, budget formulation, self-
determination issues, and resolution of audit findings as may be needed 
and appropriate.

Division of Quality Assurance and Patient Safety (GAPA)

    (1) Develops and implements programs to promote sustained 
compliance with relevant federal regulations related to accreditation 
and professional standards for health care facilities; (2) manages and 
coordinates continuous accreditation compliance programs using 
multidisciplinary integration of survey readiness activities; (3) 
coordinates health care accreditation resource management; (4) tracks 
health care accreditation and certification survey reports; (5) 
develops and implements programs to manage credentialing standards and 
policy, acquires and maintains centralized credentialing software 
system, promotes unification of medical staff professionals (MSP), and 
promotes standardized training and support resources for MSP; (6) 
develops and implements policies and procedures to promote patient 
safety, infection control practices, and environment of care and life 
safety practices; (7) establishes policies and guidelines to reduce 
adverse events; (8) develops education and training related to the 
application of established patient safety and adverse event reporting 
systems and metrics; (9) establishes and maintains oversight mechanisms 
for incident identification and reporting, adverse events and good 
catches, comprehensive systemic analysis/root cause analysis process 
and documentation; (10) implements strategies to improve patient and 
workforce safety; (11) enhances collaborative communication to 
facilitate the sharing of best practices and learning related to 
identified risks and mitigation actions across the agency; (12) 
identifies IHS and National patient safety trends and investigates 
positive and negative patient safety outcomes across the agency; and 
(13) provides patient safety consultation regarding industry standards, 
best practices, and development of policy, processes, and procedures.

Division of Enterprise Risk Management (GAPB)

    (1) Oversees and coordinates the IHS ERM vision, culture, strategy, 
and framework; (2) develops goals and objectives for the ERM program, 
integrated with broader IHS-wide strategic goals/objectives, and tracks 
progress toward achieving them; (3) coordinates the development of risk 
policy, including a risk appetite statement, to guide Agency decision-
making and documentation related to risk; (4) advises and collaborates 
in the development of the IHS ERM portfolio of enterprise risks and 
ensures appropriate and effective management by accountable individual 
risk owners; (5) integrates risk assessment activities across the IHS 
risk portfolio; (6) advises on ERM and provides expertise, advice, and 
assistance to the agency leadership on compliance matters; (7) provides 
guidance and training on the risk management process and 
prioritization; (8) facilitates the governance policy, process, and 
reporting to establish consistency and quality of documentation of 
fiduciary responsibilities of governing bodies; (9) oversees tracking 
of high-risk administrative, clinical, or personnel incidents to ensure 
appropriate local and agency-wide response, timely closure, assessment 
of internal controls, and review of case studies to promote a safety 
culture based on risk-awareness; (10) collaborates with key HQ Offices 
to ensure consistency in cross-cutting agency strategic planning, ERM, 
and management of internal controls across IHS; (11) collaborates with 
strategic planning process to integrate risk management and strategic 
thinking; (12) reviews tort claims files; (13) represents the IHS when 
claims are presented for review by the Malpractice Claims

[[Page 106539]]

Review Panel chartered by the HHS, and assists providers with 
Malpractice Claims Review Panel interactions; (14) submits payment 
reports to the National Practitioner Data Bank; (15) maintains case 
files and a malpractice claims database; (16) provides case summaries, 
peer review, outcome information, and feedback of risk management 
recommendations; (17) disseminates information about the review 
process; (18) responds to outside organizations requesting tort claim-
involvement histories on former employees; and (19) responds to Tort 
Claims inquiries from governmental agencies, media, Tribal and Urban 
Indian organizations, and advocacy groups with the Office of General 
Council guidance.

Division of Innovation and Improvement (GAPC)

    (1) Provides trainings on innovative thinking and performance 
improvement techniques; (2) provides training on empathy and relational 
intelligence to better understand colleagues and stakeholders and 
maximize teamwork; (3) integrates innovative thinking into quality 
improvement and policy formation processes to stimulate rapid idea 
generation; (4) oversees training programs to increase quality 
improvement capacity and standardize improvement methodology to test 
small-scale changes at the local level; (5) reviews use of health 
information technology and data to improve performance, quality and 
service; (6) monitors patient and staff satisfaction with health care 
service delivery; (7) leads change management for practice 
transformation to embrace new models of care delivery and to enhance 
efficiency of the care delivery process; (8) develops programs to 
promote the implementation of patient-centered care models; (9) 
coordinates sharing of best practices between Area Quality Managers and 
Service Unit Quality Assurance and Performance Improvement officers; 
and (10) supports and promotes patient-centered care including Patient 
and Family Engagement, and promotes unification of Area Quality 
Managers and Service Unit Quality Assurance and Performance Improvement 
Officers.

Division of Compliance (GAPD)

    (1) Coordinates the IHS's compliance program; (2) administers the 
agency's internal control program in accordance with the Federal 
Managers' Financial Integrity Act, OMB Circular No. A-123, GAO Green 
Book, and other applicable requirements; (3) oversees and coordinates 
the agency's efforts to establish and maintain proper internal 
controls; (4) oversees and institutionalizes a continuous compliance 
review process; (5) manages goals and objectives for the Compliance 
program, integrates them with broader IHS-wide strategic goals/
objectives, and tracks progress toward achieving them; (6) evaluates 
and monitors systems of internal control across IHS and uses the 
assessments of the internal control program as an integral part of ERM 
to effectively manage risks across IHS; (7) Serves as the IHS liaison 
office to the Government Accountability Office (GAO) and Office of 
Inspector General (OIG); (8) coordinates the development, clearance, 
and transmittal of IHS responses and follow-up to reports issued by the 
OIG, the GAO, and other federal internal and external authorities 
reviewing risk management and internal controls; (9) provides 
leadership and direction on activities for continuous improvement of 
management accountability and administrative systems for effective and 
efficient program support services IHS-wide; and (10) oversees and 
coordinates the annual development and submission of the agency's 
federal Activities Inventory Reform Act report to the HHS.

Section GA-30, Indian Health Service--Delegations of Authority

    All delegations of authority and re-delegations of authority made 
to IHS officials that were in effect immediately prior to this 
reorganization, and that are consistent with this reorganization, shall 
continue in effect pending further re-delegation.

Roselyn Tso,
Director, Indian Health Service.
[FR Doc. 2024-31273 Filed 12-27-24; 8:45 am]
BILLING CODE 4166-14-P
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