Notice of Meeting of the Advisory Committee on Organ Transplantation, 55494-55495 [06-8024]
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55494
Federal Register / Vol. 71, No. 184 / Friday, September 22, 2006 / Notices
Send comments to Susan G. Queen,
Ph.D., HRSA Reports Clearance Officer,
Room 10–33, Parklawn Building, 5600
Fishers Lane, Rockville, MD 20857.
Written comments should be received
within 60 days of this notice.
Dated: September 15, 2006.
Cheryl R. Dammons,
Director, Division of Policy Review and
Coordination.
[FR Doc. 06–8020 Filed 9–21–06; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: September 15, 2006.
Cheryl R. Dammons,
Director, Division of Policy Review and
Coordination.
[FR Doc. 06–8018 Filed 9–21–06; 8:45 am]
Health Resources and Services
Administration
Advisory Committee on Heritable
Disorders and Genetic Diseases in
Newborns and Children; Notice of
Meeting
BILLING CODE 4165–15–P
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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 and Genetic Diseases in Newborns
and Children (ACHDGDNC).
Dates and Times: November 2, 2006, 9 a.m.
to 5 p.m. November 3, 2006, 8:30 a.m. to 3
p.m.
Place: Hilton Washington Hotel,
Georgetown Room, 1919 Connecticut
Avenue, NW., Washington, DC 20009.
Status: The meeting will be open to the
public with attendance limited to space
availability.
Purpose: The Committee was established
specifically to advise and guide the Secretary
regarding the most appropriate application of
universal newborn screening tests,
technologies, policies, guidelines and
programs for effectively reducing morbidity
and mortality in newborns and children
having or at risk for heritable disorders. The
Committee also provides advice and
recommendations concerning the grants and
projects authorized under the Heritable
Disorders Program and technical information
to develop policies and priorities for this
program. The Heritable Disorders Program
was established to enhance the ability of
State and local health agencies to provide for
newborn and child screening, counseling and
health care services for newborns and
children having or at risk for heritable
disorders.
Agenda: The meeting will include a report
on the nomination process for newborn
screening candidate conditions, as well as
the continued work and reports by the
Committee’s subcommittees on laboratory
standards and procedures, follow-up and
treatment, and education and training.
Proposed agenda items are subject to
change.
Time will be provided each day for public
comment. Individuals who wish to provide
public comment or who plan to attend the
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20:37 Sep 21, 2006
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meeting and need special assistance, such as
sign language interpretation or other
reasonable accommodations, should notify
the ACHDGDNC Executive Secretary,
Michele A. Lloyd-Puryear, M.D., Ph.D.
(contact information provided below).
For Further Information Contact: Anyone
interested in obtaining a roster of members or
other relevant information should write or
contact Michele A. Lloyd-Puryear, M.D.,
Ph.D., Maternal and Child Health Bureau,
Health Resources and Services
Administration, Room 18A–19, Parklawn
Building, 5600 Fishers Lane, Rockville,
Maryland 20857, Telephone (301) 443–1080.
Information on the Advisory Committee is
available at https://mchb.hrsa.gov/programs/
genetics/committee.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Notice of Meeting of the Advisory
Committee on Organ Transplantation
Health Resources and Services
Administration, HHS.
SUMMARY: Pursuant to Public Law 92–
463, the Federal Advisory Committee
Act, as amended (5 U.S.C. Appendix 2),
notice is hereby given of the eleventh
meeting of the Advisory Committee on
Organ Transplantation (ACOT),
Department of Health and Human
Services (HHS). The meeting will be
held from approximately 9 a.m. to 5:30
p.m. on November 2, 2006, and from 9
a.m. to 3 p.m. on November 3, 2006, at
the Bethesda DoubleTree Hotel, 8120
Wisconsin Avenue, Bethesda, MD
20814. The meeting will be open to the
public; however, seating is limited and
pre-registration is encouraged (see
below).
SUPPLEMENTARY INFORMATION: Under the
authority of 42 U.S.C. 217a, section 222
of the Public Health Service Act, as
amended, and 42 CFR 121.12 (2000),
ACOT was established to assist the
Secretary in enhancing organ donation,
ensuring that the system of organ
transplantation is grounded in the best
available medical science, and assuring
the public that the system is as effective
and equitable as possible, and, thereby,
increasing public confidence in the
integrity and effectiveness of the
transplantation system. ACOT is
composed of up to 25 members,
including the Chair. Members are
AGENCY:
PO 00000
Frm 00079
Fmt 4703
Sfmt 4703
serving as Special Government
Employees and have diverse
backgrounds in fields such as organ
donation, health care public policy,
transplantation medicine and surgery,
critical care medicine and other medical
specialties involved in the identification
and referral of donors, non-physician
transplant professions, nursing,
epidemiology, immunology, law and
bioethics, behavioral sciences,
economics and statistics, as well as
representatives of transplant candidates,
transplant recipients, organ donors, and
family members.
ACOT will hear presentations on the
revised Uniform Anatomical Gift Act;
the United Network for Organ Sharing
Department of Evaluation and Quality;
the Hollywood Health and Society
Project; new developments in
immunosuppression; and payment for
organs.
The draft meeting agenda will be
available on October 16 on the
Department’s donation Web site at
https://www.organdonor.gov/acot.html.
A registration form will be available
on October 2 on the Department’s
donation Web site at https://
www.organdonor.gov/acot.html. The
completed registration form should be
submitted by facsimile to Professional
and Scientific Associates (PSA), the
logistical support contractor for the
meeting, at fax number (703) 234–1701.
Individuals without access to the
Internet who wish to register may call
Sowjanya Kotakonda with PSA at (703)
234–1737. Registration can also be
completed electronically at https://
www.psava.com/dot/acot2006/.
Individuals who plan to attend the
meeting and need special assistance,
such as sign language interpretation or
other reasonable accommodations,
should notify the ACOT Executive
Secretary, Remy Aronoff, in advance of
the meeting. Mr. Aronoff may be
reached by telephone at 301–443–3264,
e-mail: Remy.Aronoff@hrsa.hhs.gov or
in writing at the address provided
below. Management and support
services for ACOT functions are
provided by the Division of
Transplantation, Healthcare Systems
Bureau, Health Resources and Services
Administration, 5600 Fishers Lane,
Parklawn Building, Room 12C–06,
Rockville, Maryland 20857; telephone
number 301–443–7577.
After the presentations and ACOT
discussions, members of the public will
have an opportunity to provide
comments. Because of the Committee’s
full agenda and the timeframe in which
to cover the agenda topics, public
comment will be limited. All public
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55495
Federal Register / Vol. 71, No. 184 / Friday, September 22, 2006 / Notices
comments will be included in the
record of the ACOT meeting.
Dated: September 12, 2006.
Elizabeth M. Duke,
Administrator.
[FR Doc. 06–8024 Filed 9–21–06; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Indian Health Service
Request for Public Comment: 30-day
Proposed Information Collection:
Indian Health Service Contract Health
Service Report
Indian Health Service, HHS.
The Indian Health Service
(IHS), as part of its continuing effort to
reduce paperwork and respondent
burden, conducts a pre-clearance
consultation program to provide the
general public and Federal agencies
with an opportunity to comment on
proposed and/or continuing collections
of information in accordance with the
Paperwork Reduction Act of 1995 (44
U.S.C. 3506(c)(2)(A)). This program
helps to ensure that requested data can
be provided in the desired format,
reporting burden (time and financial
resources) is minimized, collection
instruments are clearly understood, and
the impact of collection requirements on
respondents can be properly assessed.
As required by section 3507(a)(1)(D) of
the Act, the proposed information
collection has been submitted to the
AGENCY:
SUMMARY:
Office of Management and Budget
(OMB) for review and approval.
The IHS received no comments in
response to the 60-day Federal Register
notice (71 FR 39686) published on July
13, 2006. The purpose of this notice is
to allow an additional 30 days for public
comment to be submitted directly to
OMB.
Proposed Collection: Title: 0917–
0002, ‘‘Indian Health Service Contract
Health Service Report.’’ Type of
Information Collection Request:
Extension of a currently approved
information collection, 0917–0002,
‘‘Indian Health Service Contract Health
Service Report.’’ Form Number: IHS
843–1A. Need and Use of Information
Collection: The purpose for the
collection is to authorize contract health
care providers to provide health care
services to eligible IHS patients. The
IHS form 843–1A ‘‘Order for Health
Services’’ was developed specifically for
this collection of information. Other
than revising the title ‘‘PurchaseDelivery Order for Health Services’’ to
read ‘‘Order for Health Services’’,
acquisition terms on the front of the
form, the contract clauses contained on
the back of copy 3 of the form, the form
has not been revised and there is no
change in the substance or in the use of
the form. A copy of the form is at
Attachment 2.
The majority of the information
contained in this form is completed by
IHS staff from existing IHS automated
patient and vendor data files. Contract
health care providers complete and sign
the streamlined form and submit it,
Est. No. of respondents
Data collection instrument
Responses
per respondent
along with a completed standard
Centers for Medicare & Medicaid
Services (CMS) health claim form (CMS
1450 (UB 92) and CMS 1500), to the IHS
for verification and payment. The CMS
forms are used and accepted nationwide by the health care industry and
IHS is an approved user.
The information collected is needed
to administer and manage the contract
health care services provided to eligible
American Indian and Alaska Native
patients. The form is used to: Authorize
contract health care services for eligible
patients; certify that the health care
services requested and authorized have
been performed by the contract
provider(s); process payments for health
care services performed by such
providers; obtain program data; and,
serve as a legal document for health and
medical care authorized by the IHS and
rendered by health care providers under
contract with the IHS.
The information collected is also used
for: Planning for further care of the
patient; for keeping an accurate record
of the patient’s health status and health
services received and recommended; for
planning future health care programs;
for communicating among members of
the health care team; for evaluating the
health care rendered; for research and
continuing education; and, for the
provision of program health statistics.
Affected Public: Individuals and
households.
Type of Respondents: Individuals.
The table below provides the
estimated burden hours for this
information collection:
Annual number of responses
Burden per response
Total annual
burden hrs.
IHS–843–1A .........................................................................
IDS* ......................................................................................
7,399
13,717
42
1
272,506
13,717
0.05
0.05
13,625.3
685.8
Total ..............................................................................
21,116
........................
........................
........................
14,311.1
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*Inpatient Discharge Summary (IDS)
There are no capital costs, operating
costs and/or maintenance costs to
respondents.
Request for Comments: Your written
comments and/or suggestions are
invited on one or more of the following
points: (a) Whether the information
collection activity is necessary to carry
out an agency function; (b) whether the
agency processes the information
collected in a useful and timely fashion;
(c) the accuracy of public burden
estimate (the estimated amount of time
needed for individual respondents to
provide the requested information); (d)
whether the methodology and
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assumptions used to determine the
estimate are logical; (e) ways to enhance
the quality, utility, and clarity of the
information being collected; and (f)
ways to minimize the public burden
through the use of automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology.
Direct Comments to OMB: Send your
written comments and suggestions
regarding the proposed information
collection contained in this notice,
especially regarding the estimated
public burden and associated response
time, to: Office of Management and
PO 00000
Frm 00080
Fmt 4703
Sfmt 4703
Budget, Office of Regulatory Affairs,
New Executive Office Building, Room
10235, Washington, DC 20503,
Attention: Allison Eydt, Desk Office for
IHS.
FOR FURTHER INFORMATION CONTACT:
Send requests for more information on
the proposed collection or to obtain a
copy of the data collection instrument(s)
and instructions to Mrs. Christina
Rouleau, IHS Reports Clearance Officer,
801 Thompson Avenue, TMP, Suite 450,
Rockville, MD 20852, call non-toll free
(301) 443–5938, send via facsimile to
(301) 443–2316, or send your e-mail
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Agencies
[Federal Register Volume 71, Number 184 (Friday, September 22, 2006)]
[Notices]
[Pages 55494-55495]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-8024]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Notice of Meeting of the Advisory Committee on Organ
Transplantation
AGENCY: Health Resources and Services Administration, HHS.
SUMMARY: Pursuant to Public Law 92-463, the Federal Advisory Committee
Act, as amended (5 U.S.C. Appendix 2), notice is hereby given of the
eleventh meeting of the Advisory Committee on Organ Transplantation
(ACOT), Department of Health and Human Services (HHS). The meeting will
be held from approximately 9 a.m. to 5:30 p.m. on November 2, 2006, and
from 9 a.m. to 3 p.m. on November 3, 2006, at the Bethesda DoubleTree
Hotel, 8120 Wisconsin Avenue, Bethesda, MD 20814. The meeting will be
open to the public; however, seating is limited and pre-registration is
encouraged (see below).
SUPPLEMENTARY INFORMATION: Under the authority of 42 U.S.C. 217a,
section 222 of the Public Health Service Act, as amended, and 42 CFR
121.12 (2000), ACOT was established to assist the Secretary in
enhancing organ donation, ensuring that the system of organ
transplantation is grounded in the best available medical science, and
assuring the public that the system is as effective and equitable as
possible, and, thereby, increasing public confidence in the integrity
and effectiveness of the transplantation system. ACOT is composed of up
to 25 members, including the Chair. Members are serving as Special
Government Employees and have diverse backgrounds in fields such as
organ donation, health care public policy, transplantation medicine and
surgery, critical care medicine and other medical specialties involved
in the identification and referral of donors, non-physician transplant
professions, nursing, epidemiology, immunology, law and bioethics,
behavioral sciences, economics and statistics, as well as
representatives of transplant candidates, transplant recipients, organ
donors, and family members.
ACOT will hear presentations on the revised Uniform Anatomical Gift
Act; the United Network for Organ Sharing Department of Evaluation and
Quality; the Hollywood Health and Society Project; new developments in
immunosuppression; and payment for organs.
The draft meeting agenda will be available on October 16 on the
Department's donation Web site at https://www.organdonor.gov/acot.html.
A registration form will be available on October 2 on the
Department's donation Web site at https://www.organdonor.gov/acot.html.
The completed registration form should be submitted by facsimile to
Professional and Scientific Associates (PSA), the logistical support
contractor for the meeting, at fax number (703) 234-1701. Individuals
without access to the Internet who wish to register may call Sowjanya
Kotakonda with PSA at (703) 234-1737. Registration can also be
completed electronically at https://www.psava.com/dot/acot2006/.
Individuals who plan to attend the meeting and need special assistance,
such as sign language interpretation or other reasonable
accommodations, should notify the ACOT Executive Secretary, Remy
Aronoff, in advance of the meeting. Mr. Aronoff may be reached by
telephone at 301-443-3264, e-mail: Remy.Aronoff@hrsa.hhs.gov or in
writing at the address provided below. Management and support services
for ACOT functions are provided by the Division of Transplantation,
Healthcare Systems Bureau, Health Resources and Services
Administration, 5600 Fishers Lane, Parklawn Building, Room 12C-06,
Rockville, Maryland 20857; telephone number 301-443-7577.
After the presentations and ACOT discussions, members of the public
will have an opportunity to provide comments. Because of the
Committee's full agenda and the timeframe in which to cover the agenda
topics, public comment will be limited. All public
[[Page 55495]]
comments will be included in the record of the ACOT meeting.
Dated: September 12, 2006.
Elizabeth M. Duke,
Administrator.
[FR Doc. 06-8024 Filed 9-21-06; 8:45 am]
BILLING CODE 4165-15-P