TRICARE; Reserve and Guard Family Member Benefits, 48864-48866 [E6-13720]
Download as PDF
48864
Federal Register / Vol. 71, No. 162 / Tuesday, August 22, 2006 / Proposed Rules
(7) A ‘‘veterinary feed directive’’ is a
written statement issued by a licensed
veterinarian in the course of the
veterinarian’s professional practice that
orders the use of a veterinary feed
directive (VFD) drug in or on an animal
feed. This written statement authorizes
the client (the owner of the animal or
animals or other caretaker) to obtain and
use the VFD drug in or on an animal
feed to treat the client’s animals only in
accordance with the directions for use
approved or indexed by the Food and
Drug Administration (FDA). A
veterinarian may issue a VFD only if a
valid veterinarian-client-patient
relationship exists, as defined in
§ 530.3(i) of this chapter.
*
*
*
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35. Amend § 558.5 by revising
paragraphs (c) and (d) to read as follows:
§ 558.5
feed.
Requirements for liquid medicated
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*
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(c) What is required for new animal
drugs intended for use in liquid feed?
Any new animal drug intended for use
in liquid feed must be approved for
such use under section 512 of the act or
index listed under section 572 of the
act. Such approvals under section 512 of
the act must be:
(1) An original NADA,
(2) A supplemental NADA, or
(3) An abbreviated NADA.
(d) What are the approval
requirements under section 512 of the
act for new animal drugs intended for
use in liquid feed? An approval under
section 512 of the act for a new animal
drug intended for use in liquid feed
must contain the following information:
(1) Data, or a reference to data in a
master file (MF), that shows the relevant
ranges of conditions under which the
drug will be chemically stable in liquid
feed under field use conditions; and
(2) Data, or a reference to data in an
MF, that shows that the drug is
physically stable in liquid feed under
field conditions; or
(3) Feed labeling with recirculation or
agitation directions as follows:
(i) For liquid feeds stored in
recirculating tank systems: Recirculate
immediately prior to use for not less
than 10 minutes, moving not less than
1 percent of the tank contents per
minute from the bottom of the tank to
the top. Recirculate daily as described
even when not used.
(ii) For liquid feeds stored in
mechanical, air, or other agitation-type
tank systems: Agitate immediately prior
to use for not less than 10 minutes,
creating a turbulence at the bottom of
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15:27 Aug 21, 2006
Jkt 208001
the tank that is visible at the top. Agitate
daily as described even when not used.
*
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*
*
*
36. Amend § 558.6 by revising
paragraphs (a)(4)(iv) and (a)(6) to read as
follows:
§ 558.6
Office of the Secretary
32 CFR Part 199
[DOD–2006–OS–0091]
Veterinary feed directive drugs.
(a) * * *
(4) * * *
(iv) Approved or index listed
indications for use.
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*
(6) You must issue a VFD only for the
approved or indexed conditions and
indications for use of the VFD drug.
*
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PART 589—SUBSTANCES
PROHIBITED FROM USE IN ANIMAL
FOOD OR FEED
37. The authority citation for 21 CFR
part 589 continues to read as follows:
Authority: 21 U.S.C. 321, 342, 343, 348,
371.
38. Revise § 589.1000 to read as
follows:
§ 589.1000
Gentian violet.
The Food and Drug Administration
has determined that gentian violet has
not been shown by adequate scientific
data to be safe for use in animal feed.
Use of gentian violet in animal feed
causes the feed to be adulterated and in
violation of the Federal Food, Drug, and
Cosmetic Act (the act), in the absence of
a regulation providing for its safe use as
a food additive under section 409 of the
act, unless it is subject to an effective
notice of claimed investigational
exemption for a food additive under
§ 570.17 of this chapter, or unless the
substance is intended for use as a new
animal drug and is subject to an
approved application under section 512
of the act, or an index listing under
section 572 of the act, or an effective
notice of claimed investigational
exemption for a new animal drug under
part 511 of this chapter or § 516.125 of
this chapter.
Dated: June 15, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 06–7070 Filed 8–21–06; 8:45 am]
BILLING CODE 4160–01–S
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DEPARTMENT OF DEFENSE
Frm 00027
Fmt 4702
Sfmt 4702
RIN 0720–AB00
TRICARE; Reserve and Guard Family
Member Benefits
ACTION:
Proposed rule.
SUMMARY: This proposed rule would
implement sections 704 and 705 of the
Ronald W. Reagan National Defense
Authorization Act for Fiscal Year 2005.
These provisions would apply to
eligible family members who become
eligible for TRICARE as a result of their
Reserve Component (RC) sponsor
(including those with delayed effective
date orders up to 90 days) being called
or ordered to active duty for more than
30 days in support of a federal/
contingency operation and choose to
participate in TRICARE Standard or
Extra, rather than enroll in TRICARE
Prime. The first provision would
provide the Secretary the authority to
waive the annual TRICARE Standard (or
Extra) deductible, which is set by law
(10 U.S.C. 1079(b)) at $150 per
individual and $300 per family ($50/
$150 for families of members in pay
grades E–4 and below). The second
provision would provide the Secretary
the authority to increase TRICARE
payments up to 115 percent of the
TRICARE maximum allowable charge,
less the applicable patient cost share if
not previously waived under the first
provision, for covered outpatient health
services received from a provider that
does not participate (accept assignment)
with TRICARE. These provisions would
help ensure timely access to health care
and maintain clinically appropriate
continuity of health care to family
members of Reservists and Guardsmen
activated in support of a federal/
contingency operation; limit the out-ofpocket health care expenses for those
family members; and remove potential
barriers to health care access by Guard
and Reserve families.
DATES: Written comments received at
the address indicated below by October
23, 2006.
ADDRESSES: You may submit comments,
identified by docket number and or RIN
number and title, by any of the
following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
E:\FR\FM\22AUP1.SGM
22AUP1
Federal Register / Vol. 71, No. 162 / Tuesday, August 22, 2006 / Proposed Rules
• 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 Regulatory
Information Number (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://regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
LT
COL James Whitton, Strategic Initiatives
Division, TRICARE Operations,
TRICARE Management Activity,
telephone (703) 681–0039.
FOR FURTHER INFORMATION CONTACT:
SUPPLEMENTARY INFORMATION:
cprice-sewell on PROD1PC66 with PROPOSALS
I. Introduction and Background
On November 5, 2001, the Department
of Defense (DoD) published notice of a
nationwide TRICARE Demonstration
Project (66 FR 55928–55930). This
demonstration was conducted under the
authority of 10 U.S.C. 1092. In this
demonstration project, DoD addressed
unreasonable impediments to the
continuity of health care encountered by
certain family members of Reservists
and National Guard called to active duty
in support of a federal contingency
operation for more than 30 days. On
November 12, 2003, DoD published a
notice (68 FR 64087) to extend through
October 31, 2004, the demonstration
project which was scheduled to end on
November 1, 2003. On October 1, 2004,
the DoD published another notice (69
FR 58895) extending the demonstration
project, previously scheduled to end on
October 31, 2004, to October 31, 2005.
On October 12, 2005, DoD published a
notice (70 FR 59320) to extend the
demonstration project, previously
scheduled to end on October 31, 2005,
to October 31, 2007. The continued
deployment of RC members in support
of Operation Noble Eagle/Operation
Enduring Freedom and Operation Iraqi
Freedom warrants making permanent
the Secretary’s authority to exercise
certain components of this
demonstration project. Sections 704 and
705 of the Ronald W. Reagan National
Defense Authorization Act for Fiscal
Year 2005 provide DoD authority to
make two components of the
demonstration project permanent and
amend section 1095d(a) and section
1079(h) of Title 10, United States Code,
as appropriate. In accordance with these
two statutory provisions, DoD proposes
VerDate Aug<31>2005
15:27 Aug 21, 2006
Jkt 208001
to implement this discretionary
authority.
II. Permanent Benefits Offered to
Reserve Component Families
A. Waiver of deductible (paragraph
199.4(f)(2)(i)(H)). Eligible family
members of RC sponsors called or
ordered to active duty for more than 30
days in support of a federal contingency
operation, who choose to participate in
TRICARE Standard, may not be
responsible for paying the annual
TRICARE Standard deductible. By law,
the TRICARE Standard deductible for
active duty family members is $150 per
individual, $300 per family ($50/$150
for E–4s and below) each fiscal year.
Exercise of the authority to waive this
annual deductible would appropriately
limit out-of-pocket expenses for many
Reserve and Guard family members, in
consideration of the fact that many may
have already paid annual deductibles
under their civilian health plan.
B. Increased payment to providers
(paragraph 199.14(j)). Executive of the
authority contained in this program
would allow an increase in TRICARE
payments up to 115 percent of the
TRICARE maximum allowable charge,
less the applicable patient cost share if
not previously waived under the first
provision, for outpatient care received
from a provider that does not participate
(acept assignment) under TRICARE.
This would help Reserve and Guard
family members be able to continue to
see civilian providers with whom they
would ahve established relations and
would promote access and clinically
appropriate continuity of care.
III. Regulatory Procedures
Executive Order 12866 requires
certain regulatory assessments for any
significant regulatory action that would
result in an annual effect on the
economy of $100 million or more. The
Congressional Review Act establishes
certain procedures for major rules,
defined as those with similar major
impacts. The Regulatory Flexibility Act
(RFA) requires that each Federal agency
prepare, and make available for public
comment, a regulatory flexibility
analysis when the agency issues a
regulation that would have significant
impact on a substantial number of small
entities. This proposed rule would not
have an annual effect on the economy
of $100 million or more. An IGCE
estimates the annual cost for both of
these provisions at less than $30
million.
This rule, however, does address a
novel policy issues relating to waiving
the deductibles for one category of
family member beneficiaries and not
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Fmt 4702
Sfmt 4702
48865
others, as well as allowing providers
who treat this same group of
beneficiaries to receive reimbursement
at a higher rate than providers who treat
similar beneficiaries. Thus this rule has
been reviewed by the Office of
Management and Budget under E.O.
12866.
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).
We have examined the impact(s) of
the proposed rule under Executive
Order 13132 and it does not have
policies that have federalism
implications that would have
substantial direct effects on the States,
on the relationship between the national
government and the States, 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
proposed to be 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 199.4 is proposed to be
amended by revising paragraph
(f)(2)(i)(H) to read as follows:
§ 199.4
Basic program benefits.
*
*
*
*
*
(f) * * *
(2) * * *
(i) * * *
(H) The Director, TRICARE
Management Activity, may waive the
annual individual or family fiscal year
deductible for dependents of a Reserve
Component member who is called or
ordered to active duty for a period of
more than 30 days or a National Guard
member who is called or ordered to fulltime federal National Guard duty for a
period of more than 30 days in support
of a contingency operation (as defined
in 10 U.S.C. 101(a)(13)). For purposes of
this paragraph, a dependent is a lawful
husband or wife of the member and a
child as defined in paragraphs
(b)(2)(ii)(A) through (F) and
(b)(2)(ii)(H)(1), (2), and (4) of § 199.3.
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*
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48866
Federal Register / Vol. 71, No. 162 / Tuesday, August 22, 2006 / Proposed Rules
3. Section 199.14 is proposed to be
amended by adding paragraph (j)(1)(i)(E)
to read as follows:
§ 199.14 Provider reimbursement
methods.
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*
*
*
*
(j) * * *
(1) * * *
(i) * * *
(E) Special rule for certain TRICARE
Standard Beneficiaries. In the case of a
dependent spouse or child, as defined
in paragraphs (b)(2)(ii)(A) through (F)
and (b)(2)(ii)(H)(1), (2), and (4) of
§ 199.3, of a Reserve component
member serving on active duty pursuant
to a call or order to active duty for a
period of more than 30 days in support
of a contingency operation under a
provision of law referred to in section
101(a)(13)(B) of title 10, United States
Code, the Director, TRICARE
Management Activity, may authorize for
non-participating providers the
allowable charge to be the lower of the
billed amount or 115% of the applicable
balance billing limit under paragraph
(j)(1)(i)(C) of this section, less the
applicable beneficiary cost share.
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*
August 15, 2006.
L.M. Bynum,
OSD Federal Register Liaison Officer,
Department of Defense.
[FR Doc. E6–13720 Filed 8–21–06; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF EDUCATION
34 CFR Part 280
Magnet Schools Assistance Program
Office of Innovation and
Improvement, Department of Education.
ACTION: Notice of proposed rulemaking.
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AGENCY:
SUMMARY: The Secretary proposes to
amend the regulations governing the
Magnet Schools Assistance Program
(MSAP) in 34 CFR part 280. These
proposed amendments would allow the
MSAP to use an approach similar to that
in 34 CFR 75.200 for establishing
selection criteria in grant competitions.
Under this approach the MSAP would
have the flexibility to use selection
criteria from its program regulations,
from the menu of general selection
criteria in the Education Department
General Administrative Regulations
(EDGAR) in 34 CFR 75.210, based on
statutory provisions in accordance with
34 CFR 75.209, or from any combination
of these.
DATES: We must receive your comments
on or before September 21, 2006.
VerDate Aug<31>2005
15:27 Aug 21, 2006
Jkt 208001
Address all comments about
these proposed regulations to Steven L.
Brockhouse, U.S. Department of
Education, 400 Maryland Avenue, SW.,
room 4W229, Washington, DC 20202–
5970. If you prefer to send your
comments through the Internet, you
may address them to us at the U.S.
Government Web site: https://
www.regulations.gov.
Or you may send your Internet
comments to us at the following
address: steve.brockhouse@ed.gov.
You must include the term ‘‘MSAP
NPRM’’ in the subject line of your
electronic message.
FOR FURTHER INFORMATION CONTACT:
Steven L. Brockhouse. Telephone: (202)
260–2476 or via Internet:
steve.brockhouse@ed.gov.
If you use a telecommunications
device for the deaf (TDD), you may call
the Federal Relay Service (FRS) at 1–
800–877–8339.
Individuals with disabilities may
obtain this document in an alternative
format (e.g., Braille, large print,
audiotape, or computer diskette) on
request to the contact person listed
under FOR FURTHER INFORMATION
CONTACT.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
Invitation To Comment
We invite you to submit comments
regarding these proposed regulations.
To ensure that your comments have
maximum effect in developing the final
regulations, we urge you to identify
clearly the specific section or sections of
the proposed regulations that each of
your comments addresses and to arrange
your comments in the same order as the
proposed regulations.
We invite you to assist us in
complying with the specific
requirements of Executive Order 12866
and its overall requirement of reducing
regulatory burden that might result from
these proposed regulations. Please let us
know of any further opportunities we
should take to reduce potential costs or
increase potential benefits while
preserving the effective and efficient
administration of the program.
During and after the comment period,
you may inspect all public comments
about these proposed regulations in
room 4W229, 400 Maryland Avenue,
SW., Washington, DC, between the
hours of 8:30 a.m. and 4:00 p.m.,
Eastern time, Monday through Friday of
each week except Federal holidays.
Assistance to Individuals With
Disabilities in Reviewing the
Rulemaking Record
On request, we will supply an
appropriate aid to an individual with a
PO 00000
Frm 00029
Fmt 4702
Sfmt 4702
disability who needs assistance to
review the comments or other
documents in the public rulemaking
record for these proposed regulations. If
you want to schedule an appointment
for this type of aid, please contact the
person listed under FOR FURTHER
INFORMATION CONTACT.
Background
On March 6, 1997, the Secretary
published final regulations (62 FR
10398) amending the provisions of
EDGAR governing discretionary grant
programs administered directly by us.
These amendments established an
approach by which the Secretary could
use different types of selection criteria
when evaluating a grant application.
Specifically, § 75.200 was amended to
permit the Secretary to use selection
criteria based on statutory provisions in
accordance with 34 CFR 75.209,
selection criteria in program-specific
regulations, selection criteria
established under 34 CFR 75.210, or any
combination of these. Section 75.210
provides a menu of selection criteria.
For a competition, the Secretary selects
from the menu one or more criteria that
best enable us to identify the highestquality applications consistent with the
program purpose, statutory
requirements, and any priorities
established. Within each criterion, the
Secretary may further define the
criterion by selecting one or more
specific factors.
At the time that these final regulations
were published, we also amended,
through notice and comment
rulemaking, the regulations for a
number of Department programs that
contained program-specific selection
criteria, so that these programs could
use the criteria in 34 CFR 75.210,
criteria based on statutory provisions, or
the criteria in their program regulations
for grant competitions. The MSAP
regulations were not amended at that
time.
This notice of proposed rulemaking
would conform the MSAP regulations to
those of the majority of other
discretionary grant programs in the
Department. We believe that by
expanding the range of selection criteria
that could be used in a specific grant
competition, we will be able to
administer the MSAP more effectively
to best meet the program’s statutory
purposes and requirements and to better
ensure that MSAP projects are
effectively integrated with State and
local reform activities.
We intend that the MSAP will use the
selection criteria in 34 CFR 75.210 in
conjunction with criteria based on the
statute and in the program-specific
E:\FR\FM\22AUP1.SGM
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Agencies
[Federal Register Volume 71, Number 162 (Tuesday, August 22, 2006)]
[Proposed Rules]
[Pages 48864-48866]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-13720]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Office of the Secretary
32 CFR Part 199
[DOD-2006-OS-0091]
RIN 0720-AB00
TRICARE; Reserve and Guard Family Member Benefits
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule would implement sections 704 and 705 of the
Ronald W. Reagan National Defense Authorization Act for Fiscal Year
2005. These provisions would apply to eligible family members who
become eligible for TRICARE as a result of their Reserve Component (RC)
sponsor (including those with delayed effective date orders up to 90
days) being called or ordered to active duty for more than 30 days in
support of a federal/contingency operation and choose to participate in
TRICARE Standard or Extra, rather than enroll in TRICARE Prime. The
first provision would provide the Secretary the authority to waive the
annual TRICARE Standard (or Extra) deductible, which is set by law (10
U.S.C. 1079(b)) at $150 per individual and $300 per family ($50/$150
for families of members in pay grades E-4 and below). The second
provision would provide the Secretary the authority to increase TRICARE
payments up to 115 percent of the TRICARE maximum allowable charge,
less the applicable patient cost share if not previously waived under
the first provision, for covered outpatient health services received
from a provider that does not participate (accept assignment) with
TRICARE. These provisions would help ensure timely access to health
care and maintain clinically appropriate continuity of health care to
family members of Reservists and Guardsmen activated in support of a
federal/contingency operation; limit the out-of-pocket health care
expenses for those family members; and remove potential barriers to
health care access by Guard and Reserve families.
DATES: Written comments received at the address indicated below by
October 23, 2006.
ADDRESSES: You may submit comments, identified by docket number and or
RIN number and title, by any of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
[[Page 48865]]
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 Regulatory Information Number (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://regulations.gov
as they are received without change, including any personal identifiers
or contact information.
FOR FURTHER INFORMATION CONTACT: LT COL James Whitton, Strategic
Initiatives Division, TRICARE Operations, TRICARE Management Activity,
telephone (703) 681-0039.
SUPPLEMENTARY INFORMATION:
I. Introduction and Background
On November 5, 2001, the Department of Defense (DoD) published
notice of a nationwide TRICARE Demonstration Project (66 FR 55928-
55930). This demonstration was conducted under the authority of 10
U.S.C. 1092. In this demonstration project, DoD addressed unreasonable
impediments to the continuity of health care encountered by certain
family members of Reservists and National Guard called to active duty
in support of a federal contingency operation for more than 30 days. On
November 12, 2003, DoD published a notice (68 FR 64087) to extend
through October 31, 2004, the demonstration project which was scheduled
to end on November 1, 2003. On October 1, 2004, the DoD published
another notice (69 FR 58895) extending the demonstration project,
previously scheduled to end on October 31, 2004, to October 31, 2005.
On October 12, 2005, DoD published a notice (70 FR 59320) to extend the
demonstration project, previously scheduled to end on October 31, 2005,
to October 31, 2007. The continued deployment of RC members in support
of Operation Noble Eagle/Operation Enduring Freedom and Operation Iraqi
Freedom warrants making permanent the Secretary's authority to exercise
certain components of this demonstration project. Sections 704 and 705
of the Ronald W. Reagan National Defense Authorization Act for Fiscal
Year 2005 provide DoD authority to make two components of the
demonstration project permanent and amend section 1095d(a) and section
1079(h) of Title 10, United States Code, as appropriate. In accordance
with these two statutory provisions, DoD proposes to implement this
discretionary authority.
II. Permanent Benefits Offered to Reserve Component Families
A. Waiver of deductible (paragraph 199.4(f)(2)(i)(H)). Eligible
family members of RC sponsors called or ordered to active duty for more
than 30 days in support of a federal contingency operation, who choose
to participate in TRICARE Standard, may not be responsible for paying
the annual TRICARE Standard deductible. By law, the TRICARE Standard
deductible for active duty family members is $150 per individual, $300
per family ($50/$150 for E-4s and below) each fiscal year. Exercise of
the authority to waive this annual deductible would appropriately limit
out-of-pocket expenses for many Reserve and Guard family members, in
consideration of the fact that many may have already paid annual
deductibles under their civilian health plan.
B. Increased payment to providers (paragraph 199.14(j)). Executive
of the authority contained in this program would allow an increase in
TRICARE payments up to 115 percent of the TRICARE maximum allowable
charge, less the applicable patient cost share if not previously waived
under the first provision, for outpatient care received from a provider
that does not participate (acept assignment) under TRICARE. This would
help Reserve and Guard family members be able to continue to see
civilian providers with whom they would ahve established relations and
would promote access and clinically appropriate continuity of care.
III. Regulatory Procedures
Executive Order 12866 requires certain regulatory assessments for
any significant regulatory action that would result in an annual effect
on the economy of $100 million or more. The Congressional Review Act
establishes certain procedures for major rules, defined as those with
similar major impacts. The Regulatory Flexibility Act (RFA) requires
that each Federal agency prepare, and make available for public
comment, a regulatory flexibility analysis when the agency issues a
regulation that would have significant impact on a substantial number
of small entities. This proposed rule would not have an annual effect
on the economy of $100 million or more. An IGCE estimates the annual
cost for both of these provisions at less than $30 million.
This rule, however, does address a novel policy issues relating to
waiving the deductibles for one category of family member beneficiaries
and not others, as well as allowing providers who treat this same group
of beneficiaries to receive reimbursement at a higher rate than
providers who treat similar beneficiaries. Thus this rule has been
reviewed by the Office of Management and Budget under E.O. 12866.
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).
We have examined the impact(s) of the proposed rule under Executive
Order 13132 and it does not have policies that have federalism
implications that would have substantial direct effects on the States,
on the relationship between the national government and the States, 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 proposed to be 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 199.4 is proposed to be amended by revising paragraph
(f)(2)(i)(H) to read as follows:
Sec. 199.4 Basic program benefits.
* * * * *
(f) * * *
(2) * * *
(i) * * *
(H) The Director, TRICARE Management Activity, may waive the annual
individual or family fiscal year deductible for dependents of a Reserve
Component member who is called or ordered to active duty for a period
of more than 30 days or a National Guard member who is called or
ordered to full-time federal National Guard duty for a period of more
than 30 days in support of a contingency operation (as defined in 10
U.S.C. 101(a)(13)). For purposes of this paragraph, a dependent is a
lawful husband or wife of the member and a child as defined in
paragraphs (b)(2)(ii)(A) through (F) and (b)(2)(ii)(H)(1), (2), and (4)
of Sec. 199.3.
* * * * *
[[Page 48866]]
3. Section 199.14 is proposed to be amended by adding paragraph
(j)(1)(i)(E) to read as follows:
Sec. 199.14 Provider reimbursement methods.
* * * * *
(j) * * *
(1) * * *
(i) * * *
(E) Special rule for certain TRICARE Standard Beneficiaries. In the
case of a dependent spouse or child, as defined in paragraphs
(b)(2)(ii)(A) through (F) and (b)(2)(ii)(H)(1), (2), and (4) of Sec.
199.3, of a Reserve component member serving on active duty pursuant to
a call or order to active duty for a period of more than 30 days in
support of a contingency operation under a provision of law referred to
in section 101(a)(13)(B) of title 10, United States Code, the Director,
TRICARE Management Activity, may authorize for non-participating
providers the allowable charge to be the lower of the billed amount or
115% of the applicable balance billing limit under paragraph
(j)(1)(i)(C) of this section, less the applicable beneficiary cost
share.
* * * * *
August 15, 2006.
L.M. Bynum,
OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. E6-13720 Filed 8-21-06; 8:45 am]
BILLING CODE 5001-06-P