Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC); Notice of Meeting, 16218-16219 [E9-8136]
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16218
Federal Register / Vol. 74, No. 67 / Thursday, April 9, 2009 / Notices
and Budget for review under the
Paperwork Reduction Act of 1995:
Proposed Project: Uncompensated
Services Assurance Report (OMB No.
0915–0077)—[Extension]
Under the Hill-Burton Act, the
government provides grants and loans
for construction or renovation of health
care facilities. As a condition of
receiving this construction assistance,
facilities are required to provide
services to persons unable to pay. A
condition of receiving this assistance
requires facilities to provide assurances
periodically that the required level of
Responses
per
respondent
Number of
respondents
Instrument
uncompensated care is being provided,
and that certain notification and record
keeping procedures are being followed.
These requirements are referred to as
the uncompensated services assurance.
The annual estimate of burden is as
follows:
Total
responses
Hours per
response
Total burden
hours
Disclosure Burden (42 CFR)
Published Notices (124.504(c)) ...........................................
Individual Notices (124.504(c)) ............................................
Determinations of Eligibility (124.507) .................................
86
86
86
1
1
99
86
86
8,514
0.75
43.6
0.75
64.5
3,749.6
6,385.50
Subtotal disclosure burden ...........................................
........................
........................
........................
........................
10,199.60
10
1
10
11.0
110
4
0
2
1
........................
1
4
........................
2
6.0
........................
6.0
24
........................
12
37
14
0
1
1
1
37
14
0
0.5
0.5
0.5
18.5
7
0
10
10
........................
1
1
........................
10
10
........................
0.25
0.5
........................
2.5
5
179
Number of
recordkeepers
Hours per year
Non-alternative Facilities (124.510(a)) ........................................................................................
86
50
4,300
Subtotal recordkeeping burden ............................................................................................
........................
........................
4,300
Reporting
Uncompensated Services Report—HRSA–710 Form
(124.509(a)) ......................................................................
Application for Compliance Alternatives:
Public Facilities (124.513) ............................................
Small Obligation Facilities (124.514(c)) ........................
Charitable Facilities (124.516(c)) ..................................
Annual Certification for Compliance Alternatives:
Public Facilities (124.509(b)) ........................................
Charitable Facilities (124.509(b)) .................................
Small Obligation Facilities (124.509(c)) ........................
Complaint Information (124.511(a)):
Individuals .....................................................................
Facilities ........................................................................
Subtotal reporting burden .............................................
Recordkeeping
The total burden for this project is
estimated to be 14,678.60 hours. Written
comments and recommendations
concerning the proposed information
collection should be sent within 30 days
of this notice to the desk officer for
HRSA, either by e-mail to
OIRA_submission@omb.eop.gov or by
fax to (202) 395–6974. Please direct all
correspondence to the ‘‘attention of the
desk officer for HRSA.’’
Dated: April 3, 2009.
Alexandra Huttinger,
Director, Division of Policy Review and
Coordination.
[FR Doc. E9–8141 Filed 4–8–09; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Advisory Committee on Heritable
Disorders in Newborns and Children
(ACHDNC); Notice of Meeting
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), notice is hereby given
of the following meeting:
Name: Advisory Committee on Heritable
Disorders in Newborns and Children.
Date and Time: May 12, 2009, 1 p.m.–5
p.m. EST.
Place: Web cast.
The ACHDNC will meet on Tuesday, May
12, 2009 from 1 p.m. to 5 p.m. EST. The
general public can join the meeting via
Webcast by logging onto https://
altarum.na3.acrobat.com/achdnc/; next
select ‘‘enter as a guest,’’ type in your full
name, and click ‘‘enter room.’’ Participants
must also dial the toll free phone number for
audio (listen only). The dial-in number is 1
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Total hour
burden
(877) 551–8166; when prompted say the
password ‘‘HRSA Genetics’’. Participants
should call no later than 12:50 p.m. EST in
order for the logistics to be established for
participation in the call. If there are technical
problems gaining access to the call, please
contact Alison Gary, Web Meetings
Coordinator, Altarum Institute, telephone
(202) 828–5100, or e-mail
webmeeting@altarum.org.
Meeting Registration: General public
participants are asked to register for the
conference by going to the meeting Web site
at https://events.SignUp4.com/achdnc0509.
The registration deadline is Monday, May 11,
2009.
Special Accommodations: Attendees
requiring special needs such as large print
materials or additional special needs may
make comments when registering at the
Online Web site. Or you may wish to contact
Tamar R. Shealy, Senior Meetings Manager,
Conference and Meetings Management,
Conference, Web and Communication
Services, Altarum Institute; telephone (202)
828–5100, or e-mail Tamar Shealy at
conferences@altarum.org.
Agenda: The meeting will include (1) A
presentation of the external review
E:\FR\FM\09APN1.SGM
09APN1
dwashington3 on PROD1PC60 with NOTICES
Federal Register / Vol. 74, No. 67 / Thursday, April 9, 2009 / Notices
workgroup’s preliminary report on the
nomination of Krabbe disease to the uniform
newborn screening panel, (2) a discussion of
the Committee’s draft issue brief for
recommending policies to states for the use
and storage of newborn screening Residual
Blood Spots, and (3) a discussion of the
impact of the present economy on State
newborn screening program infrastructures.
Agenda items are subject to change as
priorities dictate. You can also locate the
Agenda, presentations, and meeting materials
at the home page of the meeting Web site at
https://events.SignUp4.com/achdnc0509.
Public Comments: Members of the public
may present oral comments during the public
comment session. Individuals must register
at the meeting Web site at https://
events.SignUp4.com/achdnc0509 by
Monday, May 11, 2009 to receive via e-mail
their assigned presentation time. Groups
having similar interests are requested to
combine their comments and present them
through a single representative. The
allocation of time may be adjusted to
accommodate the level of expressed interest.
Those presenting oral comments are
requested to submit their comments in
writing for distribution to Committee
members by Monday, May 11, 2009.
Comments should be submitted to Tamar R.
Shealy, Senior Meetings Manager,
Conference and Meetings Management,
Conference, Web and Communication
Services, Altarum Institute; telephone (202)
828–5100, fax (202) 785–3083, or e-mail
Tamar Shealy at conferences@altarum.org.
For Further Information Contact: Anyone
interested in obtaining other relevant
information should contact Alaina M. Harris,
Maternal and Child Health Bureau, Health
Resources and Services Administration,
Room 18A–19, Parklawn Building, 5600
Fishers Lane, Rockville, Maryland 20857,
Telephone (301) 443–0721, aharris@hrsa.gov.
More information on the Advisory
Committee is available at https://
www.hrsa.gov/heritabledisorderscommittee/.
Supplementary Information: The ACHDNC
was chartered originally under Section 1111
of the Public Health Service (PHS) Act, 42
U.S.C. 300b–10 in February 2003 to advise
the Secretary of the U.S. Department of
Health and Human Services and as amended
in the Newborn Screening Saves Lives Act.
The Committee is governed by the provisions
of Public Law 92–463, as amended (5 U.S.C.
App. 2), and 41 CFR part 102–3, which sets
forth standards for the formation and use of
advisory committees. The ACHDNC is
directed to review and report regularly on
newborn and childhood screening practices
for heritable disorders and to recommend
improvements in the national newborn and
childhood heritable screening programs.
Dated: April 3, 2009.
Alexandra Huttinger,
Director, Division of Policy Review and
Coordination.
[FR Doc. E9–8136 Filed ––; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Mental Health;
Notice of Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the
National Advisory Mental Health
Council.
The meeting will be open to the
public as indicated below, with
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the 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 Advisory
Mental Health Council.
Date: May 28–29, 2009.
Closed: May 28, 2009, 10:30 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Conference Room C/D/E,
Rockville, MD 20852.
Open: May 29, 2009, 8:30 a.m. to 12:30
p.m.
Agenda: Presentation of NIMH Director’s
report and discussion on NIMH program and
policy issues.
Place: National Institutes of Health,
Building 31, C Wing, 31 Center Drive, 6th
Floor, Conference Room 6, Bethesda, MD
20892.
Contact Person: Jane A. Steinberg, PhD,
Director, Division of Extramural Activities,
National Institute of Mental Health, NIH,
Neuroscience Center, 6001 Executive Blvd.,
Room 6154, MSC 9609, Bethesda, MD 20892–
9609, 301–443–5047.
Any member of the public interested in
presenting oral comments to the committee
may notify the Contact Person listed on this
notice at least 10 days in advance of the
meeting. Interested individuals and
representatives of organizations may submit
a letter of intent, a brief description of the
organization represented, and a short
description of the oral presentation. Only one
representative of an organization may be
allowed to present oral comments and if
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accepted by the committee, presentations
may be limited to five minutes. Both printed
and electronic copies are requested for the
record. In addition, any interested person
may file written comments with the
committee by forwarding their statement to
the Contact Person listed on this notice. The
statement should include the name, address,
telephone number and when applicable, the
business or professional affiliation of the
interested person.
In the interest of security, NIH has
instituted stringent procedures for entrance
onto the NIH campus. All visitor vehicles,
including taxicabs, hotel, and airport shuttles
will be inspected before being allowed on
campus. Visitors will be asked to show one
form of identification (for example, a
government-issued photo ID, driver’s license,
or passport) and to state the purpose of their
visit.
Information is also available on the
Institute’s/Center’s home page: https://
www.nimh.nih.gov/about/advisory-boardsand-groups/namhc/index.shtml where an
agenda and any additional information for
the meeting will be posted when available.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.242, Mental Health Research
Grants; 93.281, Scientist Development
Award, Scientist Development Award for
Clinicians, and Research Scientist Award;
93.282, Mental Health National Research
Service Awards for Research Training,
National Institutes of Health, HHS)
Dated: April 2, 2009.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. E9–8015 Filed 4–8–09; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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: Center for Scientific
Review Special Emphasis; Panel Member
Conflicts: Sensory Neurophysiology.
Date: April 13, 2009.
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Agencies
[Federal Register Volume 74, Number 67 (Thursday, April 9, 2009)]
[Notices]
[Pages 16218-16219]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-8136]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Advisory Committee on Heritable Disorders in Newborns and
Children (ACHDNC); Notice of Meeting
In accordance with section 10(a)(2) of the Federal Advisory
Committee Act (Pub. L. 92-463), notice is hereby given of the following
meeting:
Name: Advisory Committee on Heritable Disorders in Newborns and
Children.
Date and Time: May 12, 2009, 1 p.m.-5 p.m. EST.
Place: Web cast.
The ACHDNC will meet on Tuesday, May 12, 2009 from 1 p.m. to 5
p.m. EST. The general public can join the meeting via Webcast by
logging onto https://altarum.na3.acrobat.com/achdnc/; next select
``enter as a guest,'' type in your full name, and click ``enter
room.'' Participants must also dial the toll free phone number for
audio (listen only). The dial-in number is 1 (877) 551-8166; when
prompted say the password ``HRSA Genetics''. Participants should
call no later than 12:50 p.m. EST in order for the logistics to be
established for participation in the call. If there are technical
problems gaining access to the call, please contact Alison Gary, Web
Meetings Coordinator, Altarum Institute, telephone (202) 828-5100,
or e-mail webmeeting@altarum.org.
Meeting Registration: General public participants are asked to
register for the conference by going to the meeting Web site at
https://events.SignUp4.com/achdnc0509. The registration deadline is
Monday, May 11, 2009.
Special Accommodations: Attendees requiring special needs such
as large print materials or additional special needs may make
comments when registering at the Online Web site. Or you may wish to
contact Tamar R. Shealy, Senior Meetings Manager, Conference and
Meetings Management, Conference, Web and Communication Services,
Altarum Institute; telephone (202) 828-5100, or e-mail Tamar Shealy
at conferences@altarum.org.
Agenda: The meeting will include (1) A presentation of the
external review
[[Page 16219]]
workgroup's preliminary report on the nomination of Krabbe disease
to the uniform newborn screening panel, (2) a discussion of the
Committee's draft issue brief for recommending policies to states
for the use and storage of newborn screening Residual Blood Spots,
and (3) a discussion of the impact of the present economy on State
newborn screening program infrastructures. Agenda items are subject
to change as priorities dictate. You can also locate the Agenda,
presentations, and meeting materials at the home page of the meeting
Web site at https://events.SignUp4.com/achdnc0509.
Public Comments: Members of the public may present oral comments
during the public comment session. Individuals must register at the
meeting Web site at https://events.SignUp4.com/achdnc0509 by Monday,
May 11, 2009 to receive via e-mail their assigned presentation time.
Groups having similar interests are requested to combine their
comments and present them through a single representative. The
allocation of time may be adjusted to accommodate the level of
expressed interest. Those presenting oral comments are requested to
submit their comments in writing for distribution to Committee
members by Monday, May 11, 2009. Comments should be submitted to
Tamar R. Shealy, Senior Meetings Manager, Conference and Meetings
Management, Conference, Web and Communication Services, Altarum
Institute; telephone (202) 828-5100, fax (202) 785-3083, or e-mail
Tamar Shealy at conferences@altarum.org.
For Further Information Contact: Anyone interested in obtaining
other relevant information should contact Alaina M. Harris, Maternal
and Child Health Bureau, Health Resources and Services
Administration, Room 18A-19, Parklawn Building, 5600 Fishers Lane,
Rockville, Maryland 20857, Telephone (301) 443-0721,
aharris@hrsa.gov. More information on the Advisory Committee is
available at https://www.hrsa.gov/heritabledisorderscommittee/.
Supplementary Information: The ACHDNC was chartered originally
under Section 1111 of the Public Health Service (PHS) Act, 42 U.S.C.
300b-10 in February 2003 to advise the Secretary of the U.S.
Department of Health and Human Services and as amended in the
Newborn Screening Saves Lives Act. The Committee is governed by the
provisions of Public Law 92-463, as amended (5 U.S.C. App. 2), and
41 CFR part 102-3, which sets forth standards for the formation and
use of advisory committees. The ACHDNC is directed to review and
report regularly on newborn and childhood screening practices for
heritable disorders and to recommend improvements in the national
newborn and childhood heritable screening programs.
Dated: April 3, 2009.
Alexandra Huttinger,
Director, Division of Policy Review and Coordination.
[FR Doc. E9-8136 Filed --; 8:45 am]
BILLING CODE 4165-15-P