Meeting of the Advisory Committee on Training in Primary Care Medicine and Dentistry, 64585-64586 [2018-27165]
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Federal Register / Vol. 83, No. 241 / Monday, December 17, 2018 / Notices
and 520 of the FD&C Act (21 U.S.C. 360
and 360j)), and their implementing
regulations as well as the provisions of
the FD&C Act (sections 531 through 542
of the FD&C Act (21 U.S.C. 360hh
through 360ss)) that apply to electronic
products, known as the Electronic
Product Radiation Control (EPRC) and
their implementing regulations. These
regulations pertain to the recordkeeping,
reporting, manufacturing, importing,
and installation of ‘‘electronic products’’
as defined under 21 CFR 1000.3(j). This
draft guidance, when finalized, will
supersede FDA’s guidance entitled
‘‘Clarification of Radiation Control
Regulations for Diagnostic X-Ray
Equipment’’ (HHS Publication FDA 89–
8221 issued in March 1989).
This draft guidance addresses only
the requirements that apply to
diagnostic x-ray equipment under the
EPRC provisions of the FD&C Act and
the regulations implementing those
provisions. This draft guidance does not
address requirements that may apply to
such equipment as medical devices
II. Significance of Guidance
This draft guidance is being issued
consistent with FDA’s good guidance
practices regulation (21 CFR 10.115).
The draft guidance, when finalized, will
represent the current thinking of FDA
on ‘‘Clarification of Radiation Control
Regulations for Manufacturers of
Diagnostic X-Ray Equipment.’’ It does
not establish any rights for any person
and is not binding on FDA or the public.
You can use an alternative approach if
it satisfies the requirements of the
applicable statutes and regulations. This
guidance is not subject to Executive
Order 12866.
III. Electronic Access
Persons interested in obtaining a copy
of the draft guidance may do so by
downloading an electronic copy from
the internet. A search capability for all
Center for Devices and Radiological
Health guidance documents is available
at https://www.fda.gov/MedicalDevices/
DeviceRegulationandGuidance/
GuidanceDocuments/default.htm. This
guidance document is also available at
https://www.regulations.gov. Persons
unable to download an electronic copy
of ‘‘Clarification of Radiation Control
Regulations for Manufacturers of
Diagnostic X-Ray Equipment’’ may send
an email request to CDRH-Guidance@
fda.hhs.gov to receive an electronic
copy of the document. Please use the
document number 1500029 to identify
the guidance you are requesting.
IV. Paperwork Reduction Act of 1995
This draft guidance refers to
previously approved collections of
information. These collections of
information are subject to review by the
Office of Management and Budget
(OMB) under the Paperwork Reduction
Act of 1995 (44 U.S.C. 3501–3520). The
collections of information in the
following FDA regulations have been
approved by OMB as listed in the
following table:
OMB control
No.
21 CFR part
Topic
1002, 1005, 1010, 1020, 1030, 1040, and 1050 .......................
Reporting and Recordkeeping for Electronic Products—General Requirements.
Dated: December 11, 2018.
Leslie Kux,
Associate Commissioner for Policy.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Meeting of the Advisory Committee on
Training in Primary Care Medicine and
Dentistry
Health Resources and Service
Administration (HRSA), Department of
Health and Human Services (HHS).
ACTION: Notice.
AGENCY:
The Advisory Committee on
Training in Primary Care Medicine and
Dentistry (ACTPCMD) has scheduled a
public meeting. Information about
ACTPCMD and the agenda for this
meeting can be found on the ACTPCMD
website at: https://www.hrsa.gov/
advisory-committees/primarycaredentist/.
DATES: January 9, 2019, 9 a.m.–5 p.m.
ET, and January 10, 2019, 8:30 a.m.–
2:30 p.m. ET.
SUMMARY:
VerDate Sep<11>2014
19:17 Dec 14, 2018
Jkt 247001
This meeting will be held in
person and will offer virtual access
through teleconference and webinar.
The address for the meeting is 5600
Fishers Lane, Rockville, Maryland
20857.
• Conference call-in number is: 1–
888–455–0640.
• Passcode is: HRSA COUNCIL.
• Webinar link is: https://
hrsa.connectsolutions.com/actpcmd.
FOR FURTHER INFORMATION CONTACT:
Kennita Carter, MD, Designated Federal
Official (DFO), Division of Medicine
and Dentistry, Bureau of Health
Workforce, HRSA, 5600 Fishers Lane,
15N–116, Rockville, Maryland 20857;
301–945–3505; or KCarter@hrsa.gov.
SUPPLEMENTARY INFORMATION:
ACTPCMD provides advice and
recommendations to the Secretary of
HHS (Secretary) on policy, program
development, and other matters of
significance concerning the activities
under section 747 of Title VII of the
Public Health Service (PHS) Act, as it
existed upon the enactment of Section
749 of the PHS Act in 1998. ACTPCMD
prepares an annual report describing the
activities of the Committee, including
findings and recommendations made by
the Committee concerning the activities
under section 747, as well as training
ADDRESSES:
[FR Doc. 2018–27236 Filed 12–14–18; 8:45 am]
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under provisions of the FD&C Act and
its implementing regulations.
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64585
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programs in oral health and dentistry.
The annual report is submitted to the
Secretary and Chairman and ranking
members of the Senate Committee on
Health, Education, Labor and Pensions,
and the House of Representatives
Committee on Energy and Commerce.
The Committee is also charged with
developing, publishing, and
implementing performance measures
and guidelines for longitudinal
evaluations of programs authorized
under Title VII, part C of the PHS Act,
and recommending appropriation levels
for programs under this part. During the
January 9–10, 2019, meeting, ACTPCMD
will discuss innovations in primary care
and oral health training. Agenda items
are subject to change as priorities
dictate. Refer to the ACTPCMD website
for any updated information concerning
the meeting. The meeting agenda will be
available on the ACTPCMD website at
least 14 days prior to the meeting.
Members of the public will have the
opportunity to provide comments.
Public participants may submit written
statements in advance of the scheduled
meeting. Oral comments will be
honored in the order they are requested
and may be limited as time allows.
Requests to make oral comments or
submit a written statement to
ACTPCMD should be sent to Kennita
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64586
Federal Register / Vol. 83, No. 241 / Monday, December 17, 2018 / Notices
Carter, DFO, using the contact
information above at least 3 business
days prior to the meeting.
Individuals who plan to attend and
need special assistance or another
reasonable accommodation should
notify Kennita Carter at the address and
phone number listed above at least 10
business days prior to the meeting.
Since this meeting occurs in a federal
government building, attendees must go
through a security check to enter the
building. Non-U.S. Citizen attendees
must notify HRSA of their planned
attendance at least 10 business days
prior to the meeting in order to facilitate
their entry into the building. All
attendees are required to present
government-issued identification prior
to entry.
Amy P. McNulty,
Acting Director, Division of the Executive
Secretariat.
[FR Doc. 2018–27165 Filed 12–14–18; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Human Genome Research
Institute; Notice of Closed Meeting
amozie on DSK3GDR082PROD with NOTICES1
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of a
meeting of the Center for Inherited
Disease Research Access Committee.
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: Center for Inherited
Disease Research Access Committee.
Date: January 11, 2019.
Time: 11:30 a.m. to 1:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Rockledge 6700, Suite 3100, Room 3185,
6700B Rockledge Drive, Bethesda, MD 20817
(Telephone Conference Call).
Contact Person: Barbara J. Thomas, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, National Human Genome Research
Institute, National Institutes of Health, 5635
Fishers Lane, Ste. 4076, MSC 9306, Bethesda,
MD 20892–9306, 301–402–0838,
barbara.thomas@nih.gov.
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19:17 Dec 14, 2018
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(Catalogue of Federal Domestic Assistance
Program Nos. 93.172, Human Genome
Research, National Institutes of Health, HHS)
Dated: December 11, 2018.
Sylvia L. Neal,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2018–27179 Filed 12–14–18; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Aging; Notice of
Closed Meeting
Pursuant to section 10(d) 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 on
Aging Special Emphasis Panel; ‘‘2019 Beeson
Review’’.
Date: January 17–18, 2019.
Time: 4:00 p.m. to 2:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hilton Garden Inn, 7301 Waverly
St., Bethesda, MD 20892.
Contact Person: Alexander Parsadanian,
Ph.D., Scientific Review Officer, National
Institute on Aging, Gateway Building 2c/212,
7201 Wisconsin Avenue, Bethesda, MD
20892, 301–496–9666, PARSADANIANA@
NIA.NIH.GOV.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.866, Aging Research,
National Institutes of Health, HHS)
Dated: December 11, 2018.
Melanie J. Pantoja,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2018–27180 Filed 12–14–18; 8:45 am]
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DEPARTMENT OF HOUSING AND
URBAN DEVELOPMENT
[Docket No. FR–7001–N–60]
30-Day Notice of Proposed Information
Collection: Builder’s Certification of
Plans, Specifications and Site
Office of the Chief Information
Officer, HUD.
ACTION: Notice.
AGENCY:
HUD submitted the proposed
information collection requirement
described below to the Office of
Management and Budget (OMB) for
review, in accordance with the
Paperwork Reduction Act. The purpose
of this notice is to allow for 30 days of
public comment.
DATES: Comments Due Date: January 16,
2019.
ADDRESSES: Interested persons are
invited to submit comments regarding
this proposal. Comments should refer to
the proposal by name and/or OMB
Control Number and should be sent to:
HUD Desk Officer, Office of
Management and Budget, New
Executive Office Building, Washington,
DC 20503; fax: 202–395–5806, Email:
OIRA Submission@omb.eop.gov.
FOR FURTHER INFORMATION CONTACT:
Colette Pollard, Reports Management
Officer, QMAC, Department of Housing
and Urban Development, 451 7th Street
SW, Washington, DC 20410; email
Colette.Pollard@hud.gov, or telephone
202–402–3400. This is not a toll-free
number. Person with hearing or speech
impairments may access this number
through TTY by calling the toll-free
Federal Relay Service at (800) 877–8339.
Copies of available documents
submitted to OMB may be obtained
from Ms. Pollard.
SUPPLEMENTARY INFORMATION: This
notice informs the public that HUD is
seeking approval from OMB for the
information collection described in
Section A. The Federal Register notice
that solicited public comment on the
information collection for a period of 60
days was published on August 21, 2018
at 83 FR 42312.
SUMMARY:
A. Overview of Information Collection
Title of Information Collection:
Builder’s Certification of Plans,
Specifications, and Site.
OMB Approved Number: 2502–0496.
Type of Request: Revision.
Form Number: HUD–92541.
Description of the need for the
information and proposed use: Builders
use the form to certify that a property
does not have adverse conditions and is
not located in a special flood hazard
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Agencies
[Federal Register Volume 83, Number 241 (Monday, December 17, 2018)]
[Notices]
[Pages 64585-64586]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-27165]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Meeting of the Advisory Committee on Training in Primary Care
Medicine and Dentistry
AGENCY: Health Resources and Service Administration (HRSA), Department
of Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Advisory Committee on Training in Primary Care Medicine
and Dentistry (ACTPCMD) has scheduled a public meeting. Information
about ACTPCMD and the agenda for this meeting can be found on the
ACTPCMD website at: https://www.hrsa.gov/advisory-committees/primarycare-dentist/.
DATES: January 9, 2019, 9 a.m.-5 p.m. ET, and January 10, 2019, 8:30
a.m.-2:30 p.m. ET.
ADDRESSES: This meeting will be held in person and will offer virtual
access through teleconference and webinar. The address for the meeting
is 5600 Fishers Lane, Rockville, Maryland 20857.
Conference call-in number is: 1-888-455-0640.
Passcode is: HRSA COUNCIL.
Webinar link is: https://hrsa.connectsolutions.com/actpcmd.
FOR FURTHER INFORMATION CONTACT: Kennita Carter, MD, Designated Federal
Official (DFO), Division of Medicine and Dentistry, Bureau of Health
Workforce, HRSA, 5600 Fishers Lane, 15N-116, Rockville, Maryland 20857;
301-945-3505; or KCarter@hrsa.gov.
SUPPLEMENTARY INFORMATION: ACTPCMD provides advice and recommendations
to the Secretary of HHS (Secretary) on policy, program development, and
other matters of significance concerning the activities under section
747 of Title VII of the Public Health Service (PHS) Act, as it existed
upon the enactment of Section 749 of the PHS Act in 1998. ACTPCMD
prepares an annual report describing the activities of the Committee,
including findings and recommendations made by the Committee concerning
the activities under section 747, as well as training programs in oral
health and dentistry. The annual report is submitted to the Secretary
and Chairman and ranking members of the Senate Committee on Health,
Education, Labor and Pensions, and the House of Representatives
Committee on Energy and Commerce. The Committee is also charged with
developing, publishing, and implementing performance measures and
guidelines for longitudinal evaluations of programs authorized under
Title VII, part C of the PHS Act, and recommending appropriation levels
for programs under this part. During the January 9-10, 2019, meeting,
ACTPCMD will discuss innovations in primary care and oral health
training. Agenda items are subject to change as priorities dictate.
Refer to the ACTPCMD website for any updated information concerning the
meeting. The meeting agenda will be available on the ACTPCMD website at
least 14 days prior to the meeting.
Members of the public will have the opportunity to provide
comments. Public participants may submit written statements in advance
of the scheduled meeting. Oral comments will be honored in the order
they are requested and may be limited as time allows. Requests to make
oral comments or submit a written statement to ACTPCMD should be sent
to Kennita
[[Page 64586]]
Carter, DFO, using the contact information above at least 3 business
days prior to the meeting.
Individuals who plan to attend and need special assistance or
another reasonable accommodation should notify Kennita Carter at the
address and phone number listed above at least 10 business days prior
to the meeting. Since this meeting occurs in a federal government
building, attendees must go through a security check to enter the
building. Non-U.S. Citizen attendees must notify HRSA of their planned
attendance at least 10 business days prior to the meeting in order to
facilitate their entry into the building. All attendees are required to
present government-issued identification prior to entry.
Amy P. McNulty,
Acting Director, Division of the Executive Secretariat.
[FR Doc. 2018-27165 Filed 12-14-18; 8:45 am]
BILLING CODE 4165-15-P