Healthcare Infection Control Practices Advisory Committee (HICPAC), 61573-61574 [2017-28072]
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Federal Register / Vol. 82, No. 248 / Thursday, December 28, 2017 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Office for State, Tribal, Local and
Territorial Support (OSTLTS), Tribal
Advisory Committee (TAC) Meeting
and 18th Biannual Tribal Consultation
Session
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of meeting.
AGENCY:
The Centers for Disease
Control and Prevention (CDC)/Agency
for Toxic Substances and Disease
Registry (ATSDR), announces the
following meeting and Tribal
Consultation Session. The meetings are
being hosted by CDC/ATSDR in-person
only and are open to the public.
Attendees must pre-register for the
event by March 2, 2018, at the following
link: www.cdc.gov/tribal/meetings.html.
DATES:
SUMMARY:
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March 13, 2018
• 8:00 a.m.–5:00 p.m., EDT—Tribal
Caucus (Open only to elected tribal
leaders and by invitation)
March 14, 2018
• 8:00 a.m.–5:00 p.m., EDT—TAC
Meeting (Open to the public)
ADDRESSES: CDC, Global
Communications Center Auditorium B3,
1600 Clifton Road NE, Atlanta, Georgia
30329.
FOR FURTHER INFORMATION CONTACT:
Carmen Clelland, PharmD, MPA, MPH,
Associate Director for Tribal Support,
Office for State, Tribal, Local and
Territorial Support, CDC, 4770 Buford
Highway, Mailstop E–70, Atlanta, GA
30341–3717; (404) 498–2205;
cclelland@cdc.gov.
SUPPLEMENTARY INFORMATION: This
meeting is being held in accordance
with Presidential Executive Order No.
13175, November 6, 2000, and the
Presidential Memorandum of November
5, 2009, and September 23, 2004,
Consultation and Coordination with
Indian Tribal Governments.
Purpose: The purpose of the TAC and
consultation meetings is to advance
CDC/ATSDR support for and
collaboration with American Indian and
Alaska Native (AI/AN) tribes and to
improve the health of AI/AN tribes by
pursuing goals that include assisting in
eliminating the health disparities faced
by AI/AN tribes; ensuring that access to
critical health and human services and
public health services is maximized to
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advance or enhance the social, physical,
and economic status of AI/ANs; and
promoting health equity for all Indian
people and communities. To advance
these goals, CDC/ATSDR conducts
government-to-government
consultations with elected tribal
officials or their authorized
representatives. Consultation is an
enhanced form of communication that
emphasizes trust, respect, and shared
responsibility. It is an open and free
exchange of information and opinion
among parties that leads to mutual
understanding.
Matters To Be Considered: The agenda
will include discussions on tribal
priorities for the CDC and ATSDR,
public health capacity in Indian
Country, AI/AN public health concerns,
budget and funding opportunities, and
programmatic highlights. Agenda items
are subject to change as priorities
dictate.
Tribal nations also will have an
opportunity to present testimony about
tribal health issues. All tribal leaders are
encouraged to submit written testimony
by 5:00 p.m. (EST) Friday, February 16,
2018, to CDC’s Tribal Support Unit via
mail to 4770 Buford Highway NE, MS
E–70, Atlanta, GA 30341–3717, or email
to TribalSupport@cdc.gov. Tribal
leaders can find guidance to assist in
developing tribal testimony for CDC and
ATSDR at www.cdc.gov/tribal/
consultation/.
Based on the number of tribal leaders
giving testimony and the time available,
it may be necessary to limit the time for
each.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention, and the Agency for Toxic
Substances and Disease Registry.
Claudette Grant,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
61573
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Advisory Committee on Immunization
Practices (ACIP); Notice of Charter
Amendment
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of charter amendment.
AGENCY:
This gives notice under (the
Federal Advisory Committee Act of
October 6, 1972, that the Advisory
Committee on Immunization Practices
(ACIP), Centers for Disease Control and
Prevention, Department of Health and
Human Services, has amended their
charter to include a non-voting liaison
representative; American Immunization
Registry Association. The amended
filing date is October 17, 2017.
FOR FURTHER INFORMATION CONTACT:
Stephanie Thomas, ACIP Committee
Management Specialist, CDC, NCIRD,
Email ACIP@cdc.gov.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
SUMMARY:
Claudette Grant,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2017–28069 Filed 12–27–17; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Healthcare Infection Control Practices
Advisory Committee (HICPAC)
[FR Doc. 2017–28071 Filed 12–27–17; 8:45 am]
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of meeting.
BILLING CODE 4160–18–P
SUMMARY:
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AGENCY:
In accordance with the
Federal Advisory Committee Act, the
CDC announces the following meeting
for the Healthcare Infection Control
Practices Advisory Committee
(HICPAC). This meeting is open to the
public, limited only by audio phone
lines available. The public is also
welcome to listen to the meeting by
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61574
Federal Register / Vol. 82, No. 248 / Thursday, December 28, 2017 / Notices
dialing 888–946–7207, passcode:
5023213. A total of 200 lines will be
available. To register for this call, please
go to www.cdc.gov/hicpac.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
The meeting will be held on
February 15, 2018, 12:00 p.m. to 2:00
p.m., EST.
[Docket No. FDA–2017–N–6888]
DATES:
Neurological Devices Panel of the
Medical Devices Advisory Committee;
Notice of Meeting
Teleconference Number:
888–946–7207, passcode: 5023213
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
AGENCY:
Erin
Stone, M.A., HICPAC, Division of
Healthcare Quality Promotion, NCEZID,
CDC, 1600 Clifton Road NE, Mailstop
A–31, Atlanta, Georgia 30333; Email:
HICPAC@cdc.gov.
SUPPLEMENTARY INFORMATION:
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Purpose: The Committee is charged
with providing advice and guidance to
the Director, Division of Healthcare
Quality Promotion (DHQP), the Director,
National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
the Director, CDC, the Secretary, Health
and Human Services regarding (1) the
practice of healthcare infection
prevention and control; (2) strategies for
surveillance, prevention, and control of
infections, antimicrobial resistance, and
related events in settings where
healthcare is provided; and (3) periodic
updating of CDC guidelines and other
policy statements regarding prevention
of healthcare-associated infections and
healthcare-related conditions.
Matters To Be Considered: The agenda
will include discussions from the
recommendation categorization update
workgroup, the guidelines for infection
prevention in healthcare personnel
workgroup, and the guidelines for
infection prevention in patients of
neonatal intensive care units
workgroup. Agenda items are subject to
change as priorities dictate.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Claudette Grant,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2017–28072 Filed 12–27–17; 8:45 am]
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Food and Drug Administration
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) announces a
forthcoming public advisory committee
meeting of the Neurological Devices
Panel of the Medical Devices Advisory
Committee. The general function of the
committee is to provide advice and
recommendations to the Agency on
FDA’s regulatory issues. The meeting
will be open to the public.
DATES: The meeting will be held on
March 1, 2018, from 8 a.m. to 6 p.m.
ADDRESSES: Hilton Washington, DC
North/Gaithersburg, 620 Perry Pkwy.,
Salons A, B, C, and D, Gaithersburg, MD
20877. The hotel’s telephone number is
301–977–8900. Answers to commonly
asked questions including information
regarding special accommodations due
to a disability, visitor parking, and
transportation may be accessed at:
https://www.fda.gov/Advisory
Committees/AboutAdvisoryCommittees/
ucm408555.htm.
FOR FURTHER INFORMATION CONTACT:
Aden Asefa, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. G642, Silver Spring,
MD 20993–0002, Aden.Asefa@
fda.hhs.gov, 301–796–0400, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area). 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.
Therefore, you should always check the
Agency’s website at https://
www.fda.gov/AdvisoryCommittees/
default.htm and scroll down to the
appropriate advisory committee meeting
link, or call the advisory committee
information line to learn about possible
modifications before coming to the
meeting.
SUPPLEMENTARY INFORMATION:
Agenda: On March 1, 2018, the
committee will discuss, make
recommendations, and advise FDA
regarding the evaluation of clinical
study data to support the safety and
SUMMARY:
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effectiveness of intracranial aneurysm
treatment devices and factors that can
affect clinical outcomes such as
aneurysm morphology, size, and
location in the neurovasculature. FDA is
also convening this committee to seek
expert opinion on the scientific and
clinical considerations relating to the
clinical trial design that may be relevant
to the determination of safety and
effectiveness for these devices.
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
material on its website prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s website after
the meeting. Background material is
available at https://www.fda.gov/
AdvisoryCommittees/Calendar/
default.htm. Scroll down to the
appropriate advisory committee meeting
link.
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 on or before January 19, 2018.
Oral presentations from the public will
be scheduled between approximately 1
p.m. and 2 p.m. Those individuals
interested in making formal oral
presentations should notify the contact
person and submit a brief statement of
the general nature of the evidence or
arguments they wish to present, the
names and addresses of proposed
participants, and an indication of the
approximate time requested to make
their presentation on or before January
12, 2018. Time allotted for each
presentation may be limited. If the
number of registrants requesting to
speak is greater than can be reasonably
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by January 16, 2018.
Persons attending FDA’s advisory
committee meetings are advised that the
Agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with disabilities.
If you require accommodations due to a
disability, please contact AnnMarie
Williams at Annmarie.Williams@
fda.hhs.gov or 301–796–5966 at least 7
days in advance of the meeting.
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Agencies
[Federal Register Volume 82, Number 248 (Thursday, December 28, 2017)]
[Notices]
[Pages 61573-61574]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-28072]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Healthcare Infection Control Practices Advisory Committee
(HICPAC)
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice of meeting.
-----------------------------------------------------------------------
SUMMARY: In accordance with the Federal Advisory Committee Act, the CDC
announces the following meeting for the Healthcare Infection Control
Practices Advisory Committee (HICPAC). This meeting is open to the
public, limited only by audio phone lines available. The public is also
welcome to listen to the meeting by
[[Page 61574]]
dialing 888-946-7207, passcode: 5023213. A total of 200 lines will be
available. To register for this call, please go to www.cdc.gov/hicpac.
DATES: The meeting will be held on February 15, 2018, 12:00 p.m. to
2:00 p.m., EST.
ADDRESSES: Teleconference Number: 888-946-7207, passcode: 5023213
FOR FURTHER INFORMATION CONTACT: Erin Stone, M.A., HICPAC, Division of
Healthcare Quality Promotion, NCEZID, CDC, 1600 Clifton Road NE,
Mailstop A-31, Atlanta, Georgia 30333; Email: [email protected].
SUPPLEMENTARY INFORMATION:
Purpose: The Committee is charged with providing advice and
guidance to the Director, Division of Healthcare Quality Promotion
(DHQP), the Director, National Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), the Director, CDC, the Secretary, Health
and Human Services regarding (1) the practice of healthcare infection
prevention and control; (2) strategies for surveillance, prevention,
and control of infections, antimicrobial resistance, and related events
in settings where healthcare is provided; and (3) periodic updating of
CDC guidelines and other policy statements regarding prevention of
healthcare-associated infections and healthcare-related conditions.
Matters To Be Considered: The agenda will include discussions from
the recommendation categorization update workgroup, the guidelines for
infection prevention in healthcare personnel workgroup, and the
guidelines for infection prevention in patients of neonatal intensive
care units workgroup. Agenda items are subject to change as priorities
dictate.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register notices pertaining to
announcements of meetings and other committee management activities,
for both the Centers for Disease Control and Prevention and the Agency
for Toxic Substances and Disease Registry.
Claudette Grant,
Acting Director, Management Analysis and Services Office, Centers for
Disease Control and Prevention.
[FR Doc. 2017-28072 Filed 12-27-17; 8:45 am]
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