TRICARE; Rare Diseases Definition, 36639-36640 [E9-17650]
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Federal Register / Vol. 74, No. 141 / Friday, July 24, 2009 / Proposed Rules
PART 199—CIVILIAN HEALTH AND
MEDICAL PROGRAM OF THE
UNIFORMED SERVICES
1. The authority citation for part 199
continues to read as follows:
Authority: 5 U.S.C. 301; 10 U.S.C., chapter
55.
2. In § 199.4:
A. Revise paragraphs (g)(37)(viii) and
(ix).
B. Redesignate paragraphs (g)(27)(x)
through (g)(37)(xii) as (g)(37)(xi) through
(g)(37)(xiii).
C. Add a new paragraph (g)(37)(x).
The revisions and additions read as
follows:
§ 199.4
Basic program benefits.
*
*
*
*
*
(g) * * *
(37) * * *
(viii) Cancer screenings authorized by
10 U.S.C. 1079.
(ix) Health promotion and disease
preventions visits (which may include
all of the services provided pursuant to
§ 199.18(b)(2)) may include all of the
services provided pursuant to
§ 199.18(b)(2)) may be provided in
connection with immunizations and
cancer screening examinations
authorized by paragraphs (g)(37)(ii) or
(g)(37)(viii) of this section.
(x) Physical examinations for
beneficiaries ages 5–11 that are required
in connection with school enrollment.
*
*
*
*
*
Dated: July 17, 2009.
Patricia L. Toppings,
OSD Federal Register Liaison Officer,
Department of Defense.
[FR Doc. E9–17651 Filed 7–23–09; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF DEFENSE
Office of the Secretary
32 CFR Part 199
[DOD–2008–HA–0060]
RIN 0720–AB26
TRICARE; Rare Diseases Definition
Office of the Secretary, DoD.
Proposed rule.
AGENCY:
srobinson on DSKHWCL6B1PROD with PROPOSALS
ACTION:
SUMMARY: This proposed rule revises the
definition of rare diseases to adopt the
definition of a rare disease as
promulgated by the National Institutes
of Health, Office of Rare Diseases. The
rule modification will result in the
definition used by the TRICARE
program for a rare disease to be
consistent with the definition used by
VerDate Nov<24>2008
16:00 Jul 23, 2009
Jkt 217001
the National Institutes of Health and the
Food and Drug Administration.
TRICARE has generally been applying
the broader National Institutes of Health
and Food and Drug Administration
definitions when making coverage
decisions for treatments; therefore, there
will be no practical changes for
beneficiaries.
DATES: Written comments received at
the address indicated below by
September 22, 2009 will be accepted.
ADDRESSES: You may submit comments,
identified by docket number and/or
Regulatory Information Number (RIN)
number and title, by either of the
following methods:
• Federal Rulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Federal Docket Management
System Office, 1160 Defense Pentagon,
Washington, DC 20301–1160.
Instructions: All submissions received
must include the agency name and
docket number or RIN for this Federal
Register document. The general policy
for comments and other submissions
from members of the public is to make
these submissions available for public
viewing on the Internet at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
FOR FURTHER INFORMATION CONTACT:
LCDR James Ellzy, TRICARE
Management Activity, Office of the
Chief Medical Officer, telephone (703)
681–0064.
SUPPLEMENTARY INFORMATION: On
January 6, 1997, the Office of the
Secretary of Defense published a final
rule in the Federal Register (62 FR 627–
631) clarifying the TRICARE exclusion
of unproven drugs, devices and medical
treatments and procedures and adding a
definition of rare diseases to be used in
the TRICARE Program. TRICARE
defined a rare disease as one which
affects fewer than one in 200,000
Americans. Upon further review,
TRICARE proposes to revise the
definition to be in compliance with the
definition of other federal agencies. The
Office of Rare Diseases was initially
established as part of the National
Institutes of Health in 1993 to promote
research and collaboration on rare and
orphan diseases. The Rare Diseases Act
of 2002 (Pub. L. 107–280) codified the
establishment of the Office of Rare
Diseases by adding a section 404F to the
Public Health Service Act (42 U.S.C.
283h). This statute defines a rare disease
as ‘‘any disease or condition that affects
less than 200,000 persons in the United
PO 00000
Frm 00024
Fmt 4702
Sfmt 4702
36639
States.’’ Additionally, Section 526(a)(2)
of the Federal Food, Drug and Cosmetic
Act (21 U.S.C. 360bb(a)(2)), provides, in
part, that the term ‘‘rare disease or
condition’’ means any disease or
condition which affects less than
200,000 persons in the United States.
The proposed rule modification will
result in the definition used by the
TRICARE program for a rare disease to
be consistent with the definition used
by the National Institutes of Health and
the Food and Drug Administration.
Regulatory Procedures
Executive Order 12866, ‘‘Regulatory
Planning and Review’’
Section 801 of title 5, United States
Code (U.S.C.), and Executive Order
(E.O.) 12866 requires certain regulatory
assessments and procedures for any
major rule or significant regulatory
action, defined as one that would result
in an annual effect of $100 million or
more on the national economy or which
would have other substantial impacts. It
has been certified that this rule is not an
economically significant rule, or a
significant regulatory action under the
provisions of E.O. 12866.
Section 202, Public Law 104–4,
‘‘Unfunded Mandates Reform Act’’
It has been certified that his rule does
not contain a Federal mandate that may
result in the expenditure by State, local
and tribal governments, in aggregate or
by the private sector, of $100 million or
more in any one year.
Public Law 96–354, ‘‘Regulatory
Flexibility Act’’ (5 U.S.C. 601)
The Regulatory Flexibility Act (RFA)
requires each Federal agency prepare,
and make available for public comment,
a regulatory flexibility analysis when
the agency issues a regulation which
would have a significant impact on a
substantial number of small entities.
This proposed rule will not significantly
affect a substantial number of small
entities for purposes of the RFA.
Public Law 96–511, ‘‘Paperwork
Reduction Act’’ (44 U.S.C. Chapter 35)
This rule will not impose additional
information collection requirements on
the public under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3511).
Executive Order 13132, ‘‘Federalism’’
This proposed rule has been
examined for its impact under E.O.
13132 and it does not contain policies
that have federalism implications that
would have substantial direct effects on
the States, on the relationship between
the national government and the States,
E:\FR\FM\24JYP1.SGM
24JYP1
36640
Federal Register / Vol. 74, No. 141 / Friday, July 24, 2009 / Proposed Rules
or on the distribution of power and
responsibilities among the various
levels of government; therefore,
consultation with State and local
officials is not required.
List of Subjects in 32 CFR Part 199
Claims, Dental health, Health care,
Health insurance, Individuals with
disabilities, Military personnel.
Accordingly, 32 CFR Part 199 is
amended as follows:
PART 199—[AMENDED]
1. The authority citation for Part 199
continues to read as follows:
Authority: 5 U.S.C. 301; 10 U.S.C. Chapter
55.
2. Section 199.2(b) is amended by
revising the definition of Rare Diseases
as follows:
§ 199.2
Definitions.
*
*
*
*
*
(b) * * *
Rare Diseases. TRICARE/CHAMPUS
defines a rare disease as any disease or
condition that has a prevalence of less
than 200,000 persons in the United
States.
*
*
*
*
*
Dated: July 17, 2009.
Patricia Toppings,
OSD Federal Register Liaison Officer,
Department of Defense.
[FR Doc. E9–17650 Filed 7–23–09; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF THE INTERIOR
National Park Service
36 CFR Part 7
RIN 1024–AD73
Special Regulations; Areas of the
National Park System
National Park Service, Interior.
Proposed rule; reopening of
comment period.
AGENCY:
srobinson on DSKHWCL6B1PROD with PROPOSALS
ACTION:
SUMMARY: The National Park Service
(NPS) announces the reopening of the
comment period on the proposed rules
to manage winter visitation and
recreational use in Yellowstone
National Park, Grand Teton National
Park, and the John D. Rockefeller, Jr.,
Memorial Parkway. The proposed rule
was published in the Federal Register
on November 5, 2008.
DATES: The comment period for the
proposed rule published on November
5, 2008 (73 FR 65784), is reopened.
Comments must be received by
September 8, 2009.
VerDate Nov<24>2008
16:00 Jul 23, 2009
Jkt 217001
You may submit your
comments, identified by Regulatory
Information Number 1024–AD73 (RIN),
by any of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Yellowstone National Park,
Winter Use Proposed Rule, P.O. Box
168, Yellowstone NP, WY 82190
All submissions received must
include the agency name and RIN. For
additional information see ‘‘Public
Comments’’ under SUPPLEMENTARY
INFORMATION below.
FOR FURTHER INFORMATION CONTACT: John
Sacklin, Management Assistant’s Office,
Headquarters Building, Yellowstone
National Park, 307–344–2019 or at the
address listed in the ADDRESSES section.
SUPPLEMENTARY INFORMATION: The
proposed rule was originally published
with a 15-day comment period. The
NPS has now determined that there is
sufficient time to provide for an
additional 45-day comment period to
ensure that the public has had an
opportunity for review and comment.
The NPS intends for final rules to be
published on or before November 15,
2009, and to be in effect for the winter
season commencing on December 15,
2009. Under the proposed rule, up to
318 snowmobiles would be allowed in
Yellowstone each day.
The proposed regulatory provisions
regarding the duration of this rule
remain as published last year. The NPS
intends that this rule would be in effect
in Yellowstone National Park for the
winter seasons ending with the 2010–
2011 winter season. During the period
this rule is in effect, the NPS will work
with all interested parties to complete a
new environmental impact statement
using the best information available, a
new long-term plan, and permanent
regulations governing winter use in
Yellowstone National Park. The
proposed rules for Grand Teton National
Park and the John D. Rockefeller, Jr.,
Memorial Parkway, if adopted, will be
permanent for these two units.
If you have already commented on the
rule, you do not have to resend your
comment. We will consider it in
preparing the final rule. We will also
consider any comments that may have
been received between the close of the
comment period on November 20, 2008
and the re-opening of this comment
period.
Before including your address, phone
number, e-mail address, or other
personal identifying information in your
comment, you should be aware that
your entire comment—including your
personal identifying information—may
ADDRESSES:
PO 00000
Frm 00025
Fmt 4702
Sfmt 4702
be made publicly available at any time.
While you can ask us in your comment
to withhold your personal identifying
information from public review, we
cannot guarantee that we will be able to
do so.
Dated: July 21, 2009.
Will Shafroth,
Principal Deputy Assistant Secretary of the
Interior for Fish and Wildlife and Parks.
[FR Doc. E9–17778 Filed 7–23–09; 8:45 am]
BILLING CODE 4312–52–P
DEPARTMENT OF VETERANS
AFFAIRS
38 CFR Parts 3, 17, and 21
RIN 2900–AN27
Herbicide Exposure and Veterans With
Covered Service in Korea
Department of Veterans Affairs.
Proposed rule.
AGENCY:
ACTION:
SUMMARY: The Department of Veterans
Affairs (VA) proposes to amend its
adjudication, medical, and vocational
rehabilitation and employment
regulations to incorporate relevant
provisions from the Veterans Benefits
Act of 2003. Specifically, this document
proposes to amend VA’s regulations
regarding herbicide exposure of certain
veterans who served in or near the
Korean demilitarized zone and
regulations regarding spina bifida in
their children. It also proposes to amend
VA’s medical regulations by correcting
the Health Administration Center’s
hand-delivery address.
DATES: Comments must be received by
VA on or before September 22, 2009.
ADDRESSES: Written comments may be
submitted through https://
www.Regulations.gov; by mail or handdelivery to the Office of General
Counsel (02REG), Department of
Veterans Affairs, 810 Vermont Ave.,
NW., Room 1068, Washington, DC
20420; or by fax to (202) 273–9026.
Comments should indicate that they are
submitted in response to ‘‘RIN 2900–
AN27—Herbicide Exposure and
Veterans with Covered Service in
Korea.’’ Copies of comments received
will be available for public inspection in
the Office of General Counsel, Room
1063B, between the hours of 8 a.m. and
4:30 p.m., Monday through Friday
(except holidays). Please call (202) 461–
4902 for an appointment. (This is not a
toll-free number.) In addition, during
the comment period, comments may be
viewed online through the Federal
Docket Management System (FDMS) at
https://www.Regulations.gov.
E:\FR\FM\24JYP1.SGM
24JYP1
Agencies
[Federal Register Volume 74, Number 141 (Friday, July 24, 2009)]
[Proposed Rules]
[Pages 36639-36640]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-17650]
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Office of the Secretary
32 CFR Part 199
[DOD-2008-HA-0060]
RIN 0720-AB26
TRICARE; Rare Diseases Definition
AGENCY: Office of the Secretary, DoD.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule revises the definition of rare diseases to
adopt the definition of a rare disease as promulgated by the National
Institutes of Health, Office of Rare Diseases. The rule modification
will result in the definition used by the TRICARE program for a rare
disease to be consistent with the definition used by the National
Institutes of Health and the Food and Drug Administration. TRICARE has
generally been applying the broader National Institutes of Health and
Food and Drug Administration definitions when making coverage decisions
for treatments; therefore, there will be no practical changes for
beneficiaries.
DATES: Written comments received at the address indicated below by
September 22, 2009 will be accepted.
ADDRESSES: You may submit comments, identified by docket number and/or
Regulatory Information Number (RIN) number and title, by either of the
following methods:
Federal Rulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Mail: Federal Docket Management System Office, 1160
Defense Pentagon, Washington, DC 20301-1160.
Instructions: All submissions received must include the agency name
and docket number or RIN for this Federal Register document. The
general policy for comments and other submissions from members of the
public is to make these submissions available for public viewing on the
Internet at https://www.regulations.gov as they are received without
change, including any personal identifiers or contact information.
FOR FURTHER INFORMATION CONTACT: LCDR James Ellzy, TRICARE Management
Activity, Office of the Chief Medical Officer, telephone (703) 681-
0064.
SUPPLEMENTARY INFORMATION: On January 6, 1997, the Office of the
Secretary of Defense published a final rule in the Federal Register (62
FR 627-631) clarifying the TRICARE exclusion of unproven drugs, devices
and medical treatments and procedures and adding a definition of rare
diseases to be used in the TRICARE Program. TRICARE defined a rare
disease as one which affects fewer than one in 200,000 Americans. Upon
further review, TRICARE proposes to revise the definition to be in
compliance with the definition of other federal agencies. The Office of
Rare Diseases was initially established as part of the National
Institutes of Health in 1993 to promote research and collaboration on
rare and orphan diseases. The Rare Diseases Act of 2002 (Pub. L. 107-
280) codified the establishment of the Office of Rare Diseases by
adding a section 404F to the Public Health Service Act (42 U.S.C.
283h). This statute defines a rare disease as ``any disease or
condition that affects less than 200,000 persons in the United
States.'' Additionally, Section 526(a)(2) of the Federal Food, Drug and
Cosmetic Act (21 U.S.C. 360bb(a)(2)), provides, in part, that the term
``rare disease or condition'' means any disease or condition which
affects less than 200,000 persons in the United States. The proposed
rule modification will result in the definition used by the TRICARE
program for a rare disease to be consistent with the definition used by
the National Institutes of Health and the Food and Drug Administration.
Regulatory Procedures
Executive Order 12866, ``Regulatory Planning and Review''
Section 801 of title 5, United States Code (U.S.C.), and Executive
Order (E.O.) 12866 requires certain regulatory assessments and
procedures for any major rule or significant regulatory action, defined
as one that would result in an annual effect of $100 million or more on
the national economy or which would have other substantial impacts. It
has been certified that this rule is not an economically significant
rule, or a significant regulatory action under the provisions of E.O.
12866.
Section 202, Public Law 104-4, ``Unfunded Mandates Reform Act''
It has been certified that his rule does not contain a Federal
mandate that may result in the expenditure by State, local and tribal
governments, in aggregate or by the private sector, of $100 million or
more in any one year.
Public Law 96-354, ``Regulatory Flexibility Act'' (5 U.S.C. 601)
The Regulatory Flexibility Act (RFA) requires each Federal agency
prepare, and make available for public comment, a regulatory
flexibility analysis when the agency issues a regulation which would
have a significant impact on a substantial number of small entities.
This proposed rule will not significantly affect a substantial number
of small entities for purposes of the RFA.
Public Law 96-511, ``Paperwork Reduction Act'' (44 U.S.C. Chapter 35)
This rule will not impose additional information collection
requirements on the public under the Paperwork Reduction Act of 1995
(44 U.S.C. 3501-3511).
Executive Order 13132, ``Federalism''
This proposed rule has been examined for its impact under E.O.
13132 and it does not contain policies that have federalism
implications that would have substantial direct effects on the States,
on the relationship between the national government and the States,
[[Page 36640]]
or on the distribution of power and responsibilities among the various
levels of government; therefore, consultation with State and local
officials is not required.
List of Subjects in 32 CFR Part 199
Claims, Dental health, Health care, Health insurance, Individuals
with disabilities, Military personnel.
Accordingly, 32 CFR Part 199 is amended as follows:
PART 199--[AMENDED]
1. The authority citation for Part 199 continues to read as
follows:
Authority: 5 U.S.C. 301; 10 U.S.C. Chapter 55.
2. Section 199.2(b) is amended by revising the definition of Rare
Diseases as follows:
Sec. 199.2 Definitions.
* * * * *
(b) * * *
Rare Diseases. TRICARE/CHAMPUS defines a rare disease as any
disease or condition that has a prevalence of less than 200,000 persons
in the United States.
* * * * *
Dated: July 17, 2009.
Patricia Toppings,
OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. E9-17650 Filed 7-23-09; 8:45 am]
BILLING CODE 5001-06-P