Statement of Organization, Functions, and Delegations of Authority, 57457-57458 [2017-26148]
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Federal Register / Vol. 82, No. 232 / Tuesday, December 5, 2017 / Notices
immunization practices and policies in
the U.S and internationally; (7) provides
and supports public health training; (8)
responds to and assists internal and
external partners on other public health
problems of national and international
significance, as needed; (9) serves as the
National Reference Laboratory (rotavirus
and norovirus) and other agents of viral
gastroenteritis; and (10) serves as the
WHO Global Reference Center for
Rotavirus and other agents of viral
gastroenteritis.
Sherri Berger,
Chief Operating Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2017–26150 Filed 12–4–17; 8:45 am]
BILLING CODE 4160–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
sradovich on DSK3GMQ082PROD with NOTICES
Statement of Organization, Functions,
and Delegations of Authority
Part C (Centers for Disease Control
and Prevention) of the Statement of
Organization, Functions, and
Delegations of Authority of the
Department of Health and Human
Services (45 FR 67772–76, dated
October 14, 1980, and corrected at 45 FR
69296, October 20, 1980, as amended
most recently at 81 FR 84583–84591,
dated November 23, 2016) is amended
to reflect the reorganization of the
Center for Surveillance, Epidemiology
and Laboratory Services, Office of
Public Health Preparedness and
Response, Centers for Disease Control
and Prevention.
Section C–B, Organization and
Functions, is hereby amended as
follows:
Delete in its entirety the title for the
Center for Surveillance, Epidemiology
and Laboratory Service (CPN) and insert
the following title which includes the
Oxford comma: Center for Surveillance,
Epidemiology, and Laboratory Service
(CPN).
Delete in its entirety the title and the
mission and function statements for the
Division of Laboratory Systems (CPNB)
and insert the following:
Division of Laboratory Systems
(CPNB). The mission of the Division of
Laboratory Systems (DLS) is to
strengthen the nation’s clinical and
public health laboratory system by
continually improving quality and
safety, informatics and data science, and
workforce competency.
Office of the Director (CPNB1). (1)
Provides leadership and guidance on
VerDate Sep<11>2014
18:13 Dec 04, 2017
Jkt 244001
development of strategic goals,
objectives, and milestones to advance
the vision and mission of the Division
of Laboratory Systems (DLS), the Center
for Surveillance Epidemiology and
Laboratory Services (CSELS), and CDC;
(2) ensures optimal planning and
allocation of resources to achieve
program objectives, conducts
management and operations analyses,
and oversees required reporting; (3)
provides administrative management
support, advice, and guidance to DLS
regarding administrative policies, fiscal
management, property management,
human resources, and travel; (4) leads
coordination and stewardship of DLS
procurement, grants, cooperative
agreements, materials management,
interagency agreements, and extramural
resources; (5) fosters collaborations and
cross-cutting activities with other CDC
components and external organizations
to support the mission, activities, and
operations of DLS; (6) enhances internal
and external partnerships and partner/
stakeholder communication; (7)
provides leadership in evaluating and
improving program performance,
monitoring progress and
accomplishments to ensure that
programmatic goals are achieved with
measurable impact; (8) manages issues,
policy development, and tracks
regulatory and legislative activities; (9)
manages CDC Specimen Policy Board
and the CDC/ATSDR Specimen
Packaging, Inventory, and Repository
(CASPIR) Advisory Committee; (10)
collaborates with leadership of the
Centers for Medicare & Medicaid
Services (CMS) and the Food and Drug
Administration (FDA) in advancement
of the Clinical Laboratory Improvement
Amendments (CLIA) program and
oversees CDC responsibilities therein;
(11) provides scientific oversight for
DLS, performing scientific review and
clearance for DLS publications,
presentations, and reports; (12) provides
DLS communications, Web support,
responses to media requests, and
communication outreach efforts; and
(13) coordinates requests from other
CDC programs for international
technical assistance among DLS
capabilities.
Training and Workforce Development
Branch (CPNBC). (1) Provides
leadership and support of laboratory
workforce through initiatives that
strengthen recruitment, retention,
management, and training; (2) supports
the development, promotion, adoption,
and implementation of competencies
relevant to the laboratory workforce; (3)
develops frameworks, models, and
resources that support competency-
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57457
based laboratory training, fellowships,
and education; (4) engages agency and
laboratory community experts to
collaboratively assess and develop
effective training products to maintain a
competent, prepared, and sustainable
national and global laboratory
workforce; (5) designs and implements
training pertaining to clinical and
public health laboratory methodology,
technology, quality and safety and
practice for public health, clinical, CDC,
and other federal agency laboratory
professionals; and (6) evaluates the
efficiency and effectiveness of public
health laboratory education and
training, including measuring the
outcomes of all training to ensure the
effective transfer of knowledge and
skills to improved laboratory practice.
Quality and Safety Systems Branch
(CPNBD). (1) Develops, promotes,
implements, and evaluates intervention
strategies to improve quality and safety
in clinical and public health laboratory
systems; (2) provides scientific and
technical support for the Clinical
Laboratory Improvement Amendments
(CLIA) program to assure the quality,
including safety, of clinical and public
health laboratory testing nationwide; (3)
facilitates and conducts studies to
provide scientific evidence and assess
the impact of CLIA regulations and
voluntary guidelines for laboratory
quality and safety; (4) provides expertise
and guidance in the development or
revision of CLIA technical standards
and voluntary guidelines for laboratory
quality and safety, especially in light of
new and evolving laboratory technology
and practices; (5) develops,
disseminates, promotes, and evaluates
the impact of educational materials to
support the understanding of and
compliance with CLIA regulations and
voluntary quality and safety guidelines;
(6) hosts and manages the Clinical
Laboratory Improvement Advisory
Committee (CLIAC) and its workgroups
on behalf of a tri-agency partnership
among CDC, CMS, and FDA; (7)
provides information to the laboratory
medicine and public health
communities, as well as policy makers,
regarding the interpretation and
application of the CLIA technical
standards and other issues of laboratory
quality and safety; (8) provides
technical assistance in the review of
laboratory accreditation and state
licensure programs, and CLIA-approved
proficiency testing programs; (9)
facilitates and supports collaborations
with federal partners and other
stakeholders (including other CDC
programs upon request) for the
exchange of information about
E:\FR\FM\05DEN1.SGM
05DEN1
sradovich on DSK3GMQ082PROD with NOTICES
57458
Federal Register / Vol. 82, No. 232 / Tuesday, December 5, 2017 / Notices
laboratory quality and safety practices,
research, standards, and guidelines, and
coordinates clinical and public health
laboratory improvement efforts among
all; (10) provides safety and quality
subject matter expertise to the Training
and Workforce Development Branch for
the development of training courses for
internal CDC laboratories and external
clinical and public health laboratories;
(11) provides advice and oversight of
safety and quality measures, controls,
practices and documents to ensure
compliance of DLS laboratory areas with
CDC policies, regulations, and
guidelines for laboratory quality and
safety (e.g., Roybal campus—Building
18 Training Laboratory and
Lawrenceville campus laboratories); (12)
provides scientific and technical
support and guidance for CDC
initiatives, programs, committees, work
groups, and task forces involving use,
handling, shipping, import/export,
transport or storage of biological
specimens and their support materials;
(13) provides safety and quality-related
content expertise for the development of
the Laboratory Leadership Service (LLS)
Fellows curriculum and serve as course
instructors for LLS training classes (and
to other laboratory-related workforce
efforts as may be requested by other
programs); and (14) serves as quality
and safety advisors and liaisons to other
CDC programs and offices involving
clinical laboratory activities upon
request.
Informatics and Data Science Branch
(CPNBE). (1) Supports the CDC
Specimen Policy Board and OADLSS in
the development of CDC specimen
management and collection policies,
and oversees implementation of those
policies at CASPIR in collaboration with
the CASPIR Advisory Committee; (2)
develops, promotes, implements, and
evaluates data science approaches for
improved research of large and complex
data sets in support of CLIA standards
and laboratory practice; (3) maintains
and leverages data acquired from
national laboratory systems and other
large health databases to evaluate
laboratory testing events, capabilities,
capacity, and public health outcomes;
(4) develops solutions to strengthen the
management of laboratory test service
capability and capacity data,
biorepositories, access to materials for
standardizing laboratory testing, as well
as support laboratory preparedness and
workforce development activities; (5)
develops and implements solutions,
often with external partners and
collaborators, to strengthen clinical and
public health laboratory information
systems, reporting of laboratory results
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18:13 Dec 04, 2017
Jkt 244001
between diagnostic facilities and
healthcare providers, electronic
reporting of laboratory information to
electronic health records, and general
preparedness of the laboratory system to
respond to public health emergencies;
(6) develops and implements computerbased decision support tools and mobile
applications that help to inform better
laboratory-related decision-making by
healthcare providers; and (7)
collaborates with other CDC programs to
develop and promote informatics
solutions for improving laboratory
management, practice, and
preparedness.
Sherri A. Berger,
Chief Operating Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2017–26148 Filed 12–4–17; 8:45 am]
BILLING CODE 4160–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection; Public
Comments Request; New Data
Collection; National Center on Law and
Elder Rights (NCLER)
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) is announcing
an opportunity for the public to
comment on ACL’s intention to collect
information from legal and aging/
disability service professionals. Under
the Paperwork Reduction Act of 1995
(the PRA), Federal agencies are required
to publish a notice in the Federal
Register concerning each proposed
collection of Information and to allow
60 days for public comment in response
on the proposed action. This notice
solicits comments on proposed
information collection requirements
relating to ACL funded training, case
consultation, and technical assistance
for aging/disability networks assisting
older adults in social or economic need
facing legal issues.
DATES: Submit written or electronic
comments on the collection of
information by February 5, 2018.
ADDRESSES: Submit electronic
comments on the collection of
information to Omar Valverde at
omar.valverde@acl.hhs.gov. Submit
written comments on the collection of
information by mail to Omar Valverde,
Administration for Community Living,
Washington, DC 20201.
SUMMARY:
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Fmt 4703
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FOR FURTHER INFORMATION CONTACT:
Omar Valverde at omar.valverde@
acl.hhs.gov or (202) 795–7460.
SUPPLEMENTARY INFORMATION: Under the
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.
‘‘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 provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension or
update of an existing collection of
information, before submitting the
collection to OMB for approval. The
proposed collection of information
represents new information requested
from aging/disability networks to fulfill
requirements regarding the provision of
services and overall performance of ACL
legal assistance programs.
To comply with the above
requirement, ACL is publishing a notice
regarding the proposed collection of
information set forth in this document.
ACL contracts with a national legal
assistance resource center, the National
Center on Law and Elder Rights, to
provide the required services. Through
the contract, ACL provides aging,
disability, and related legal
professionals with training and complex
case consultations and support for
demonstration projects regarding
contractually identified priority legal
topics.
The purpose of the information
requested is for ACL to ensure that the
resource center creates and prioritizes
the training, case consultations and
technical assistance resources it was
contracted to provide and to ensure that
the center targets the contractually
designated aging network practitioners
about the priority subject matters. This
approach enables ACL to make datainformed decisions about the
deployment of its resource center assets.
These data are necessary for ACL to
evaluate contractual compliance with
established performance indicators.
These metrics include quantifiable
increases in uptake by stakeholders of
training, case consultation and technical
assistance, and measures of satisfaction
with and perceived benefit from these
services. For example, the metrics
measure successful problem resolution
as a result of the services provided,
E:\FR\FM\05DEN1.SGM
05DEN1
Agencies
[Federal Register Volume 82, Number 232 (Tuesday, December 5, 2017)]
[Notices]
[Pages 57457-57458]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-26148]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Statement of Organization, Functions, and Delegations of
Authority
Part C (Centers for Disease Control and Prevention) of the
Statement of Organization, Functions, and Delegations of Authority of
the Department of Health and Human Services (45 FR 67772-76, dated
October 14, 1980, and corrected at 45 FR 69296, October 20, 1980, as
amended most recently at 81 FR 84583-84591, dated November 23, 2016) is
amended to reflect the reorganization of the Center for Surveillance,
Epidemiology and Laboratory Services, Office of Public Health
Preparedness and Response, Centers for Disease Control and Prevention.
Section C-B, Organization and Functions, is hereby amended as
follows:
Delete in its entirety the title for the Center for Surveillance,
Epidemiology and Laboratory Service (CPN) and insert the following
title which includes the Oxford comma: Center for Surveillance,
Epidemiology, and Laboratory Service (CPN).
Delete in its entirety the title and the mission and function
statements for the Division of Laboratory Systems (CPNB) and insert the
following:
Division of Laboratory Systems (CPNB). The mission of the Division
of Laboratory Systems (DLS) is to strengthen the nation's clinical and
public health laboratory system by continually improving quality and
safety, informatics and data science, and workforce competency.
Office of the Director (CPNB1). (1) Provides leadership and
guidance on development of strategic goals, objectives, and milestones
to advance the vision and mission of the Division of Laboratory Systems
(DLS), the Center for Surveillance Epidemiology and Laboratory Services
(CSELS), and CDC; (2) ensures optimal planning and allocation of
resources to achieve program objectives, conducts management and
operations analyses, and oversees required reporting; (3) provides
administrative management support, advice, and guidance to DLS
regarding administrative policies, fiscal management, property
management, human resources, and travel; (4) leads coordination and
stewardship of DLS procurement, grants, cooperative agreements,
materials management, interagency agreements, and extramural resources;
(5) fosters collaborations and cross-cutting activities with other CDC
components and external organizations to support the mission,
activities, and operations of DLS; (6) enhances internal and external
partnerships and partner/stakeholder communication; (7) provides
leadership in evaluating and improving program performance, monitoring
progress and accomplishments to ensure that programmatic goals are
achieved with measurable impact; (8) manages issues, policy
development, and tracks regulatory and legislative activities; (9)
manages CDC Specimen Policy Board and the CDC/ATSDR Specimen Packaging,
Inventory, and Repository (CASPIR) Advisory Committee; (10)
collaborates with leadership of the Centers for Medicare & Medicaid
Services (CMS) and the Food and Drug Administration (FDA) in
advancement of the Clinical Laboratory Improvement Amendments (CLIA)
program and oversees CDC responsibilities therein; (11) provides
scientific oversight for DLS, performing scientific review and
clearance for DLS publications, presentations, and reports; (12)
provides DLS communications, Web support, responses to media requests,
and communication outreach efforts; and (13) coordinates requests from
other CDC programs for international technical assistance among DLS
capabilities.
Training and Workforce Development Branch (CPNBC). (1) Provides
leadership and support of laboratory workforce through initiatives that
strengthen recruitment, retention, management, and training; (2)
supports the development, promotion, adoption, and implementation of
competencies relevant to the laboratory workforce; (3) develops
frameworks, models, and resources that support competency-based
laboratory training, fellowships, and education; (4) engages agency and
laboratory community experts to collaboratively assess and develop
effective training products to maintain a competent, prepared, and
sustainable national and global laboratory workforce; (5) designs and
implements training pertaining to clinical and public health laboratory
methodology, technology, quality and safety and practice for public
health, clinical, CDC, and other federal agency laboratory
professionals; and (6) evaluates the efficiency and effectiveness of
public health laboratory education and training, including measuring
the outcomes of all training to ensure the effective transfer of
knowledge and skills to improved laboratory practice.
Quality and Safety Systems Branch (CPNBD). (1) Develops, promotes,
implements, and evaluates intervention strategies to improve quality
and safety in clinical and public health laboratory systems; (2)
provides scientific and technical support for the Clinical Laboratory
Improvement Amendments (CLIA) program to assure the quality, including
safety, of clinical and public health laboratory testing nationwide;
(3) facilitates and conducts studies to provide scientific evidence and
assess the impact of CLIA regulations and voluntary guidelines for
laboratory quality and safety; (4) provides expertise and guidance in
the development or revision of CLIA technical standards and voluntary
guidelines for laboratory quality and safety, especially in light of
new and evolving laboratory technology and practices; (5) develops,
disseminates, promotes, and evaluates the impact of educational
materials to support the understanding of and compliance with CLIA
regulations and voluntary quality and safety guidelines; (6) hosts and
manages the Clinical Laboratory Improvement Advisory Committee (CLIAC)
and its workgroups on behalf of a tri-agency partnership among CDC,
CMS, and FDA; (7) provides information to the laboratory medicine and
public health communities, as well as policy makers, regarding the
interpretation and application of the CLIA technical standards and
other issues of laboratory quality and safety; (8) provides technical
assistance in the review of laboratory accreditation and state
licensure programs, and CLIA-approved proficiency testing programs; (9)
facilitates and supports collaborations with federal partners and other
stakeholders (including other CDC programs upon request) for the
exchange of information about
[[Page 57458]]
laboratory quality and safety practices, research, standards, and
guidelines, and coordinates clinical and public health laboratory
improvement efforts among all; (10) provides safety and quality subject
matter expertise to the Training and Workforce Development Branch for
the development of training courses for internal CDC laboratories and
external clinical and public health laboratories; (11) provides advice
and oversight of safety and quality measures, controls, practices and
documents to ensure compliance of DLS laboratory areas with CDC
policies, regulations, and guidelines for laboratory quality and safety
(e.g., Roybal campus--Building 18 Training Laboratory and Lawrenceville
campus laboratories); (12) provides scientific and technical support
and guidance for CDC initiatives, programs, committees, work groups,
and task forces involving use, handling, shipping, import/export,
transport or storage of biological specimens and their support
materials; (13) provides safety and quality-related content expertise
for the development of the Laboratory Leadership Service (LLS) Fellows
curriculum and serve as course instructors for LLS training classes
(and to other laboratory-related workforce efforts as may be requested
by other programs); and (14) serves as quality and safety advisors and
liaisons to other CDC programs and offices involving clinical
laboratory activities upon request.
Informatics and Data Science Branch (CPNBE). (1) Supports the CDC
Specimen Policy Board and OADLSS in the development of CDC specimen
management and collection policies, and oversees implementation of
those policies at CASPIR in collaboration with the CASPIR Advisory
Committee; (2) develops, promotes, implements, and evaluates data
science approaches for improved research of large and complex data sets
in support of CLIA standards and laboratory practice; (3) maintains and
leverages data acquired from national laboratory systems and other
large health databases to evaluate laboratory testing events,
capabilities, capacity, and public health outcomes; (4) develops
solutions to strengthen the management of laboratory test service
capability and capacity data, biorepositories, access to materials for
standardizing laboratory testing, as well as support laboratory
preparedness and workforce development activities; (5) develops and
implements solutions, often with external partners and collaborators,
to strengthen clinical and public health laboratory information
systems, reporting of laboratory results between diagnostic facilities
and healthcare providers, electronic reporting of laboratory
information to electronic health records, and general preparedness of
the laboratory system to respond to public health emergencies; (6)
develops and implements computer-based decision support tools and
mobile applications that help to inform better laboratory-related
decision-making by healthcare providers; and (7) collaborates with
other CDC programs to develop and promote informatics solutions for
improving laboratory management, practice, and preparedness.
Sherri A. Berger,
Chief Operating Officer, Centers for Disease Control and Prevention.
[FR Doc. 2017-26148 Filed 12-4-17; 8:45 am]
BILLING CODE 4160-18-P