Proposed Suspension of New Claims to the Federal Reviewing Official Review Level, Changes to the Role of the Medical and Vocational Expert System, and Future Demonstration Projects, 45701-45705 [E7-16071]
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Federal Register / Vol. 72, No. 157 / Wednesday, August 15, 2007 / Proposed Rules
The Proposed Amendment
SOCIAL SECURITY ADMINISTRATION
In consideration of the foregoing, the
Federal Aviation Administration
proposes to amend 14 CFR part 71 as
follows:
[Docket No. SSA–2007–0045]
PART 71—DESIGNATION OF CLASS A,
B, C, D, AND E AIRSPACE AREAS; AIR
TRAFFIC SERVICE ROUTES; AND
REPORTING POINTS
Proposed Suspension of New Claims
to the Federal Reviewing Official
Review Level, Changes to the Role of
the Medical and Vocational Expert
System, and Future Demonstration
Projects
1. The authority citation for part 71
continues to read as follows:
[Amended]
2. The incorporation by reference in
14 CFR 71.1 of Federal Aviation
Administration Order 7400.9P, Airspace
Designations and Reporting Points,
dated September 1, 2006, and effective
September 15, 2006, is amended as
follows:
Paragraph 6005 Class E Airspace Areas
Extending Upward from 700 feet or More
Above the Surface of the Earth
*
*
*
ASO AL E5
*
*
Scottsboro, AL [ADDED]
Scottsboro Municipal—Word Field Airport,
AL
(Lat. 34°41′19″ N., long. 86°00′21″ W.)
Jackson County Hospital Point In Space
Coordinates (Lat. 34°39′47″ N., long.
86°01′54″ W.)
That airspace extending upward from 700
feet above the surface within a 6.5-mile
radius of Scottsboro Municipal—Word Field
Airport extending from the 6.5-mile radius to
4.4 miles northeast of the airport and within
4 miles each side of the 218° bearing from the
Scottsboro Municipal—Word Field Airport
extending from the 6.5-mile radius to 4.5
miles southwest of the airport; and that
airspace within a 6-mile radius of the point
in space (Lat. 34°39′47″ N., long. 86°01′54″
W.) serving Jackson County Hospital.
*
*
*
*
*
Issued in College Park, Georgia, on July 2,
2007.
Lynda G. Otting,
Acting Group Manager, System Support
Group, Eastern Service Center.
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RIN 0960–AG53
Social Security Administration.
Notice of proposed rulemaking.
AGENCY:
Authority: 49 U.S.C. 106(g); 40103, 40113,
40120; E.O. 10854, 24 FR 9565, 3 CFR, 1959–
1963 Comp., p. 389.
§ 71.1
20 CFR Part 405
ACTION:
SUMMARY: We propose to modify our
disability administrative adjudication
processes to suspend new claims to the
Federal reviewing official (FedRO) level,
now operating in the Boston region.
Claims already received will continue to
be processed by the FedRO and a related
component of the disability
determination process, the Medical and
Vocational Expert System (MVES),
commonly known as the Office of
Medical and Vocational Expertise
(OMVE). We also propose to remove the
MVES/OMVE from the disability
adjudication process for new claims. We
are making these proposals to ensure
that we continually improve our
disability adjudication process. Lastly,
we are requesting comments on using
the MVES/OMVE to develop and
manage a national registry of experts.
DATES: To be sure that we consider your
comments on our proposed changes, we
must receive them no later than
September 14, 2007. However, we also
invite comments by November 13, 2007
on the merits of a national registry of
experts, including MVES/OMVE
management of the registry, and the
rates to be paid to the experts affiliated
with the registry.
ADDRESSES: You may give us your
comments by: Internet through the
Federal eRulemaking Portal at https://
www.regulations.gov; e-mail to
regulations@ssa.gov; telefax to (410)
966–2830; or letter to the Commissioner
of Social Security, P.O. Box 17703,
Baltimore, MD 21235–7703. You may
also deliver them to the Office of
Regulations, Social Security
Administration, 960 Altmeyer Building,
6401 Security Boulevard, Baltimore, MD
21235–6401, between 8 a.m. and 4:30
p.m. on regular business days.
Comments are posted on the Federal
eRulemaking Portal, or you may inspect
them on regular business days by
making arrangements with the contact
person shown in this preamble.
FOR FURTHER INFORMATION CONTACT:
James A. Winn, Social Security
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45701
Administration, 6401 Security
Boulevard, Baltimore, MD 21235–6401,
(410) 965–0600 for information about
this notice. For information on
eligibility or filing for benefits, call our
national toll-free number, 1–800–772–
1213 or TTY 1–800–325–0778, or visit
our Internet site, Social Security Online,
at https://www.socialsecurity.gov.
SUPPLEMENTARY INFORMATION:
Electronic Version
The electronic file of this document is
available on the date of publication in
the Federal Register at https://
www.gpoaccess.gov/fr/.
Introduction
We are dedicated to providing highquality service to the American public.
When in March 2006 we announced
changes to our administrative review
process for initial disability claims, we
explained that we expected that the
changes would improve disability
service. Our commitment to continuous
improvement in the way we process
disability claims did not end with the
publication of those rules as we
continually explore ways to improve
service to some of the most vulnerable
in our society. We face, now and in the
foreseeable future, significant challenges
to our ability to provide the level of
service that disability benefit claimants
deserve because of the increased
complexity of and growth in claims for
those benefits. Consequently, we
propose modifications to our
administrative review process that will
further help us evaluate changes put in
place in March 2006 and help us
provide accurate and timely service to
claimants for Social Security disability
benefits and supplemental security
income payments based on disability or
blindness.
The importance of these disability
benefits to the lives and subsistence of
many Americans cannot be
underestimated. Nearly 15 million
disabled Social Security beneficiaries
and supplemental security income
recipients receive over $10 billion in
Federal monthly payments. The
adjudication of disability claims
requires evaluating complex medical
and vocational evidence.
The number of claims and requests for
hearings that we receive has continued
to expand. In 2004–2006, we received
an annual average of 2.6 million
disability claims that required decisions
on medical grounds, the most time and
labor intensive basis for deciding such
claims. Along with this expansion in the
number of claims, there has been a
concomitant increase in the number of
hearing requests. Our hearing offices
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have received an average of over
564,000 titles II and XVI disability
hearing requests each year from 2002
through 2006, a significant increase
from the annual average of almost
472,000 hearing requests in 1997–2001.
As these figures show, over the 5-year
period from 2002 through 2006, we
received each year over 90,000 more
requests for titles II and XVI hearings
than we annually received during the
period from 1997 through 2001. The
vast number of disability claims now
filed each year, as well as other factors
such as the expected increase in
disability claims as the baby boomers
move into their disability-prone years,
probable limitations on our resources to
process these claims, and the projected
impending increase in filings for
retirement and survivors benefits as
baby boomers retire, will continue to
place an even greater strain on the
system.
We expected that the spring 2006
changes to the administrative review
process for initial disability claims
would ‘‘improve the accuracy,
consistency, and timeliness of decisionmaking throughout the disability
determination process.’’ 71 FR 16424
(March 31, 2006). We planned a gradual
roll-out of the changes so that we could
determine their effect on the disability
process overall. As we explained then,
‘‘Gradual implementation will allow us
to monitor the effects that our changes
are having on the entire disability
determination process * * * We will
carefully monitor the implementation
process in the Boston region and
quickly address any problems that may
arise.’’ 71 FR at 16440–41. Based on
initial reviews of the quick disability
determination (QDD) and FedRO
elements of that process, and mindful of
the workload challenges that we now
face—especially at the hearing level—
we believe we need to modify some of
the changes made last spring.
As we explain in our recently
published notice of proposed
rulemaking on the QDD process (July
10, 2007; 72 FR 37496), we are
proposing to retain and expand the QDD
process, and, as we explain here, we
propose to suspend new claims going
through the FedRO and the MVES,
organizationally known as the OMVE.
However, claims already received will
continue through the FedRO and MVES
so we can continue to evaluate their
effectiveness. These proposals are based
on our commitment to outstanding
service and to continuously improving
our service as we realign our resources
to ensure that we are capable of
processing the current and anticipated
number of disability claims and
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reducing the number of pending
hearings.
1. Suspending OFedRO and MVES/
OMVE Allows Reallocation of Resources
to the Backlog at the Hearings Level
In the March 2006 final rule, we
replaced the State agency
reconsideration level with a Federal
adjudicative level, called the FedRO.
Attorneys staff the FedRO positions, and
they, along with the managerial,
support, and administrative staff, make
up the Office of the FedRO (OFedRO).
OFedRO uses the MVES/OMVE to
develop the medical and vocational
evidence in the claims before them. The
goal of FedRO and OMVE is to have this
level of review help ensure more
accurate and consistent decision making
earlier in the process. We are continuing
to evaluate the effect of these new
components on our program and
administrative functions. Our
experience over the last year in the
Boston region demonstrates that the
administrative costs associated with
OFedRO and its consequent use of the
MVES/OMVE to develop medical and
vocational evidence is greater over the
foreseeable future than originally
anticipated. We do not yet have
sufficient results to fully evaluate the
potential improvements in program
efficacy that are the goals of the FedRO
and OMVE. Therefore, we propose to
suspend new claims going through the
FedRO and OMVE, so that we can
reallocate resources to reduce the
backlog at the hearing level, while we
evaluate the FedRO and OMVE through
the processing of claims already
received. Once this evaluation is
completed and alternative approaches
analyzed, we will make a decision
whether to reinstate the processing of
new claims at the FedRO or to pursue
an alternative approach to improving
the disability determination process.
Under this proposal, we are amending
part 405 with provisions that will
suspend new claims to the OFedRO and
MVES/OMVE. This change will allow
us to continue to evaluate the FedRO
and OMVE through the processing of
claims already received. We expect to
have approximately 15,500 cases
pending FedRO review when this rule
becomes effective. We will complete the
processing of those pending cases, but
will not assign to FedRO any more cases
originally filed under the new process
in Boston that otherwise would have
been slated for FedRO review. Instead,
if cases are at the initial level in Boston
or not assigned to FedRO on the
effective date of this rule, those cases
will be assigned to State agencies for
reconsidered determinations or to
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administrative law judges for hearing,
whichever is applicable in that
particular New England State. In other
words, States in the Boston region,
where the FedRO and MVES/OMVE are
currently functioning, would return to
the same process they were following
before August 2006, whether that
process was reconsideration under 20
CFR 404.907 and 416.1407 or the testing
procedures under 20 CFR 404.906 and
416.1406.
2. Request for Comments on a National
Registry of Experts
Even though we propose to suspend
new claims to the MVES/OMVE from
the administrative review process under
part 405 of our rules, we are considering
using the MVES/OMVE in a more
limited role to develop and manage a
national registry of medical,
psychological, and vocational experts to
assist disability adjudicators in
developing and/or clarifying
information within the record. Once the
MVES/OMVE has developed the
registry, the MVES/OMVE would
continue to manage the registry.
Disability adjudicators at the State and
Federal levels would be able to directly
access the experts affiliated with the
registry without having to go through
the MVES/OMVE to arrange for expert
assistance.
We ask for comments on the merits of
such a registry, including MVES/OMVE
management of the registry, and the
rates to be paid to the experts affiliated
with the registry. Questions upon which
you may wish to comment include, but
are not limited to: What qualifications
should experts on the national registry
have? Should experts be required to
have experience or training related to
our disability programs? Should
disability adjudicators be required to
use the registry when they require
expert assistance? Should we pay
experts flat rates nationally or should
the rates be based on locality? If rates
are based on locality, what factors
should we consider in setting those
rates? Regardless of whether the rates
we pay the experts are based on national
or local rates, should we vary rates to
account for the individual’s level of
expertise, and if so, how should that be
done? Should we build in an automatic
adjustment for inflation and, if so,
which measure would be most
appropriate for this function? We would
be very interested in your thoughts
regarding these issues and request that
they be submitted within 90 days of the
publication of this notice. We will
consider comments submitted within
this time period as we continue to
develop our plans for a national registry.
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We will not respond to these comments
until such time as we may publish a
notice of proposed rulemaking setting
out more detailed plans for such a
registry.
Clarity of These Proposed Rules
Executive Order 12866, as amended,
requires each agency to write all rules
in plain language. In addition to your
substantive comments on these final
rules, we invite your comments on how
to make them easier to understand. For
example:
• Have we organized the material to
suit your needs?
• Are the requirements in the rules
clearly stated?
• Do the rules contain technical
language or jargon that isn’t clear?
• Would a different format (grouping
and order of sections, use of headings,
paragraphing) make the rules easier to
understand?
• Would more (but shorter) sections
be better?
• Could we improve clarity by adding
tables, lists, or diagrams?
• What else could we do to make the
rules easier to understand?
Regulatory Procedures
Pursuant to sections 205(a), 702(a)(5),
and 1631(d)(1) of the Social Security
Act, 42 U.S.C. 405(a), 902(a)(5), and
1383(d)(1), we follow the
Administrative Procedure Act (APA)
rulemaking procedures specified in 5
U.S.C. 553 in the development of our
regulations. We ordinarily publish a
notice of proposed rulemaking in the
Federal Register and permit a 60-day
comment period. This period, however,
may be shortened when the agency
finds good cause that a 60-day comment
period would be impracticable,
unnecessary, or contrary to the public
interest and incorporates a statement of
the finding and its reasons in the rule
issued. For this proposed rule, we find
that there is good cause for allowing a
30-day comment period on the issue of
suspending OFedRO and MVES/OMVE
(section 1 above) because we believe
that it would be contrary to the public
interest not to effectuate these rules as
quickly as we can. However, if it
appears that 30 days is not sufficient
time to comment—for example, if the
volume of comments indicates that
there is great public interest in this
rule—we will consider extending the
comment period to 60 days.
We intend to shift the resources
required for the FedRO and MVES/
OMVE to the effort to reduce the
pending hearing requests to a
manageable level. In order to shift those
resources as quickly as we can, we must
suspend new claims to the appeal
procedure to the FedRO, and thereby,
stem the flow of cases to the FedRO and
the MVES/OMVE. Upon the effective
date of the final rules, the first level of
appeal would be reconsideration for any
claimant who has not yet requested
FedRO review, unless the State is a part
of the prototype test in which case the
first level of review would be to an
administrative law judge. Claimants
who have not yet been issued an initial
determination would be advised in the
initial determination notice that their
first level of appeal would be
reconsideration or a hearing, whichever
applies. This would allow the FedRO
and the MVES/OMVE to complete the
processing of the cases in the pipeline,
allow us to redirect resources to other
tasks, including assisting us in reducing
the backlog at the hearing level.
However, we are providing a 90-day
comment period on the issue of a
national registry of experts (section 2
above).
Executive Order 12866, as Amended
We have consulted with the Office of
Management and Budget (OMB) and
determined that this proposed rule
meets the criteria for an economically
significant regulatory action under
Executive Order 12866, as amended.
Thus, it was reviewed by OMB.
The Office of the Chief Actuary
(OCACT) estimates that this rule will
result in program savings of roughly
$1.0 billion in OASDI benefit payments
and cost of $0.1 billion in Federal SSI
payments over the next 10 years, as
shown below (in millions of dollars):
TABLE 1.—ESTIMATED EFFECT ON OASDI AND FEDERAL SSI BENEFIT PAYMENTS OF A PROPOSED REGULATION ELIMINATING NEW CLAIMS TO THE FEDERAL REVIEWING OFFICIAL AND MODIFYING THE ROLE OF THE MEDICAL AND VOCATIONAL EXPERT SYSTEM, FISCAL YEARS 2008–17
[In millions]
Fiscal year
OASDI
2008 .............................................................................................................................................
2009 .............................................................................................................................................
2010 .............................................................................................................................................
2011 .............................................................................................................................................
2012 .............................................................................................................................................
2013 .............................................................................................................................................
2014 .............................................................................................................................................
2015 .............................................................................................................................................
2016 .............................................................................................................................................
2017 .............................................................................................................................................
Totals:
2008–12 ................................................................................................................................
2008–17 ................................................................................................................................
SSI
Total
¥$14
¥42
¥51
¥57
¥45
¥53
¥122
¥192
¥248
¥219
¥$3
¥9
¥8
¥15
¥6
9
22
29
40
82
¥$18
¥51
¥60
¥72
¥51
¥44
¥100
¥163
¥208
¥137
¥209
¥1,042
¥41
140
¥251
¥902
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Notes:
1. The estimates are based on the assumptions underlying the President’s FY 2008 Budget.
2. Federal SSI payments due on October 1st in fiscal years 2012, 2017 and 2018 are included with payments for the prior fiscal year.
3. Totals may not equal sum of components due to rounding.
Table 1 above presents the estimated
short-range effects on OASDI benefit
payments and Federal SSI payments
that would result from implementation
of this NPRM, measured relative to the
baseline used for the President’s Fiscal
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Year 2008 Budget and assuming that a
final rule implementing these changes
would become effective for initial
determinations made on or after April 1,
2008. The FY 2008 Budget assumed that
DSI would be gradually implemented at
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the pace of one region per year and be
fully implemented for new claims in all
regions by the beginning of FY 2016. For
the 10 States where the Prototype
determination process has been or is
being tested, the effect of this NPRM
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would be to retain or restore the
Prototype process so that the first level
of appeal of an initial disability decision
would be to an administrative law
judge.
As required by OMB Circular A–4
(available at https://
www.whitehouse.gov/omb/circulars/
a004/a-4.pdf), in Table 2, we have
prepared an accounting statement
showing the annualized economic
impact of suspending new claims to the
FedRO level. All estimated impacts are
classified as transfers.
TABLE 2.—ACCOUNTING STATEMENT: ESTIMATED ECONOMIC IMPACT OF SUSPENDING NEW CLAIMS TO THE FEDRO LEVEL
FROM 2008–2016 IN 2007 DOLLARS
Category
Transfers
Annualized Monetized Transfers ..............................................................
$81.3 million (7% discount rate).
$86.4 million (3% discount rate).
From SSA beneficiaries to the Social Security trust fund and the general fund.
From Whom To Whom? ...........................................................................
Suspending new claims going through
the FedRO and OMVE will allow us to
reallocate resources to reduce the
backlog at the hearing level by holding
more hearings and making system
improvements to increase the efficiency
of our hearings process.
We will also continue to evaluate the
FedRO and OMVE through the
processing of claims already received.
This evaluation will include an
assessment of DSI, as the pilot is
currently implemented in the Boston
region, with existing claims. In the
analysis we will analyze DSI’s impact
on the timeliness of disability
determinations, on overall program
costs, as well as its impact on the
administrative costs required to
implement this new process. Once this
evaluation is complete and alternative
approaches analyzed, we will make a
decision whether to reinstate the
processing of new claims into the
FedRO or pursue an alternative
approach to improving the disability
determination process.
Regulatory Flexibility Act
We certify that this proposed rule,
when published in final, will not have
a significant economic impact on a
substantial number of small entities as
it affects only States and individuals.
Therefore, a regulatory flexibility
analysis as provided in the Regulatory
Flexibility Act, as amended, is not
required.
Paperwork Reduction Act
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These rules impose no new reporting
or recordkeeping requirements requiring
OMB clearance.
Federalism Impact and Unfunded
Mandates Impact
We have reviewed this proposed rule
under the threshold criteria of Executive
Order 13132 and the Unfunded
Mandates Reform Act and have
determined that it does not have
substantial direct effects on the States,
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on the relationship between the national
government and the States, on the
distribution of power and
responsibilities among the various
levels of government, or on imposing
any costs on State, local, or tribal
governments. This proposed rule does
not affect the roles of the State, local, or
tribal governments. However, the
proposed rule takes administrative
notice of existing statutes governing the
roles and relationships of the State
agencies with us with respect to
disability determinations under the Act.
(Catalog of Federal Domestic Assistance
Program Nos. 96.001, Social Security—
Disability Insurance; 96.002, Social
Security—Retirement Insurance; 96.004,
Social Security—Survivors Insurance;
96.006, Supplemental Security Income)
List of Subjects in 20 CFR Part 405
Administrative practice and
procedure; Blind, Disability benefits;
Old-Age, Survivors, and Disability
Insurance; Public assistance programs,
Reporting and recordkeeping
requirements; Social Security;
Supplemental Security Income (SSI).
Dated: August 7, 2007.
Michael J. Astrue,
Commissioner of Social Security.
For the reasons set out in the
preamble, we are amending subparts A
and C of part 405 as set forth below:
PART 405—ADMINISTRATIVE REVIEW
PROCESS FOR ADJUDICATING
INITIAL DISABILITY CLAIMS
1. The authority citation for part 405
continues to read as follows:
Authority: Secs. 201(j), 205(a)–(b), (d)–(h),
and (s), 221, 223(a)–(b), 702(a)(5), 1601, 1602,
1631, and 1633 of the Social Security Act (42
U.S.C. 401(j), 405(a)–(b), (d)–(h), and (s), 421,
423(a)–(b), 902(a)(5), 1381, 1381a, 1383, and
1383b).
Subpart A—[Amended]
2. Amend § 405.10 by adding
paragraph (d) to read as follows:
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§ 405.10 Medical and Vocational Expert
System.
*
*
*
*
*
(d) This section will no longer be
effective on the same date as described
in § 405.240(c) of this part unless the
Commissioner decides that the Medical
and Vocational Expert System should be
continued and extends the sunset date
as described in § 405.240(d) of this part
by publishing a notice of proposed
rulemaking in the Federal Register
before that date.
3. Revise the appendix to subpart A
of part 405 to read as follows:
Appendix to Subpart A of Part 405—
Claims That Will Be Handled Under the
Procedures in This Part
(a) We will apply the procedures in this
part to disability claims (as defined in
§ 405.5) filed in Maine, New Hampshire,
Vermont, Massachusetts, Rhode Island, or
Connecticut.
(b) If you move from one State to another
after your disability claim has been filed,
adjudicators at subsequent levels of review
will apply the regulations that initially
applied to the disability claim. For example,
if you file a claim in a State in which we
apply the procedures in this part, the
procedures in this part will apply to the
disability claim at subsequent levels of
review, even if you move to a State where we
would otherwise not apply these procedures.
Conversely, if you file a claim in a State
where we do not apply the procedures in this
part, we will adjudicate the claim using the
procedures in part 404 or 416 of this chapter,
as appropriate, even if you subsequently
move to a State where we would otherwise
apply the procedures in this part.
Subpart C—[Amended]
4. Add § 405.240 to read as follows:
§ 405.240
Sunset of this Subpart.
(a) If you have filed a request for
review by a Federal reviewing official
on or before the effective date of this
section, the Federal reviewing official
will review and issue a decision on your
claim.
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(b) If you have not filed a request for
review by a Federal reviewing official
on or before the effective date of this
section and you have received an initial
determination under subpart B of this
part, we will process any request for
additional administrative review filed
after the effective date as either a
request for reconsideration by the State
agency or a request for hearing before an
administrative law judge if your State
uses the testing procedures under
§§ 404.906 and 416.1406 of this title.
(c) This subpart will no longer be
effective the day after a Federal
reviewing official issues a decision on
the last of the claims accepted for
review under paragraph (a) of this
section.
(d) If compelling evidence shows that
the Federal reviewing official process is
efficient, effective, and sustainable
given available Agency resources, the
Commissioner may reinstate the Federal
reviewing official process by publishing
a notice of proposed rulemaking in the
Federal Register.
[FR Doc. E7–16071 Filed 8–14–07; 8:45 am]
BILLING CODE 4191–02–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 52 and 97
[EPA–R06–OAR–2007–0651; FRL–8455–1]
Approval and Promulgation of
Implementation Plans; Louisiana;
Clean Air Interstate Rule Nitrogen
Oxides Trading Programs
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
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AGENCY:
SUMMARY: EPA is proposing to approve
a revision to the Louisiana State
Implementation Plan (SIP) submitted by
the State of Louisiana on July 12, 2007,
as the Louisiana Clean Air Interstate
Rule (CAIR) Nitrogen Oxides (NOX)
Trading Programs abbreviated SIP. We
are proposing to approve Louisiana’s
CAIR NOX Annual and Ozone Season
Abbreviated SIP revision in parallel
with the Louisiana Department of
Environmental Quality’s (LDEQ)
rulemaking activities (‘‘parallel
processing’’). The abbreviated SIP
revision includes the Louisiana
methodology for allocation of annual
and ozone season NOX allowances. EPA
is proposing to determine that the
Louisiana CAIR NOX Trading Programs
abbreviated SIP revision satisfies the
applicable requirements of a CAIR
abbreviated SIP revision. EPA is also
VerDate Aug<31>2005
14:58 Aug 14, 2007
Jkt 211001
proposing to approve revisions to the
Louisiana SIP that establish
administrative reporting requirements
for all Louisiana CAIR programs; these
revisions were submitted on September
22, 2006, as part of the Louisiana CAIR
Sulfur Dioxide (SO2) Trading Program
SIP. EPA is also proposing that the
Louisiana CAIR NOX Annual and Ozone
Season Abbreviated SIP will satisfy
Louisiana’s Clean Air Act (CAA) Section
110(a)(2)(D)(i) obligations to submit a
SIP revision that contains adequate
provisions to prohibit air emissions
from adversely affecting another State’s
air quality through interstate transport.
The intended effect of this action is to
reduce NOX emissions from the State of
Louisiana that are contributing to
nonattainment of the 8-hour ozone and
PM2.5 National Ambient Air Quality
Standards (NAAQS or standard) in
downwind states. This action is being
taken under section 110 of the CAA.
DATES: Comments must be received on
or before September 14, 2007.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–R06–
OAR–2007–0651, by one of the
following methods:
(1) www.regulations.gov: Follow the
on-line instructions for submitting
comments.
(2) E-mail: Mr. Jeff Robinson at
robinson.jeffrey@epa.gov. Please also cc
the person listed in the FOR FURTHER
INFORMATION CONTACT paragraph below.
(3) U.S. EPA Region 6 ‘‘Contact Us’’
Web site: https://epa.gov/region6/
r6coment.htm. Please click on ‘‘6PD’’
(Multimedia) and select ‘‘Air’’ before
submitting comments.
(4) Fax: Mr. Jeff Robinson, Chief, Air
Permits Section (6PD–R), at fax number
214–665–6762.
(5) Mail: Mr. Jeff Robinson, Chief, Air
Permits Section (6PD–R), Environmental
Protection Agency, 1445 Ross Avenue,
Suite 1200, Dallas, Texas 75202–2733.
(6) Hand or Courier Delivery: Mr. Jeff
Robinson, Chief, Air Permits Section
(6PD–R), Environmental Protection
Agency, 1445 Ross Avenue, Suite 1200,
Dallas, Texas 75202–2733. Such
deliveries are accepted only between the
hours of 8:30 a.m. and 4:30 p.m.
weekdays except for legal holidays.
Special arrangements should be made
for deliveries of boxed information.
Instructions: Direct your comments to
Docket ID No. EPA–R06–OAR–2007–
0651. EPA’s policy is that all comments
received will be included in the public
docket without change and may be
made available online at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
PO 00000
Frm 00007
Fmt 4702
Sfmt 4702
45705
claimed to be Confidential Business
Information (CBI) or other information
the disclosure of which is restricted by
statute. Do not submit information
through https://www.regulations.gov or
e-mail, if you believe that it is CBI or
otherwise protected from disclosure.
The https://www.regulations.gov Web
site is an ‘‘anonymous access’’ system,
which means that EPA will not know
your identity or contact information
unless you provide it in the body of
your comment. If you send an e-mail
comment directly to EPA without going
through https://www.regulations.gov,
your e-mail address will be
automatically captured and included as
part of the comment that is placed in the
public docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment along with any disk or CDROM submitted. If EPA cannot read
your comment due to technical
difficulties and cannot contact you for
clarification, EPA may not be able to
consider your comment. Electronic files
should avoid the use of special
characters and any form of encryption
and should be free of any defects or
viruses. For additional information
about EPA’s public docket, visit the EPA
Docket Center homepage at https://
www.epa.gov/epahome/dockets.htm.
Docket: All documents in the docket
are listed in the https://
www.regulations.gov index. Although
listed in the index, some information is
not publicly available, e.g., CBI or other
information the disclosure of which is
restricted by statute. Certain other
material, such as copyrighted material,
will be publicly available only in hard
copy. Publicly available docket
materials are available either
electronically in https://
www.regulations.gov or in hard copy at
the Air Permits Section (6PD–R),
Environmental Protection Agency, 1445
Ross Avenue, Suite 700, Dallas, Texas
75202–2733. The file will be made
available by appointment for public
inspection in the Region 6 FOIA Review
Room between the hours of 8:30 a.m.
and 4:30 p.m. weekdays except for legal
holidays. Contact the person listed in
the FOR FURTHER INFORMATION CONTACT
paragraph below to make an
appointment. If possible, please make
the appointment at least two working
days in advance of your visit. A 15 cent
per page fee will be charged for making
photocopies of documents. On the day
of the visit, please check in at the EPA
Region 6 reception area on the seventh
E:\FR\FM\15AUP1.SGM
15AUP1
Agencies
[Federal Register Volume 72, Number 157 (Wednesday, August 15, 2007)]
[Proposed Rules]
[Pages 45701-45705]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-16071]
=======================================================================
-----------------------------------------------------------------------
SOCIAL SECURITY ADMINISTRATION
[Docket No. SSA-2007-0045]
20 CFR Part 405
RIN 0960-AG53
Proposed Suspension of New Claims to the Federal Reviewing
Official Review Level, Changes to the Role of the Medical and
Vocational Expert System, and Future Demonstration Projects
AGENCY: Social Security Administration.
ACTION: Notice of proposed rulemaking.
-----------------------------------------------------------------------
SUMMARY: We propose to modify our disability administrative
adjudication processes to suspend new claims to the Federal reviewing
official (FedRO) level, now operating in the Boston region. Claims
already received will continue to be processed by the FedRO and a
related component of the disability determination process, the Medical
and Vocational Expert System (MVES), commonly known as the Office of
Medical and Vocational Expertise (OMVE). We also propose to remove the
MVES/OMVE from the disability adjudication process for new claims. We
are making these proposals to ensure that we continually improve our
disability adjudication process. Lastly, we are requesting comments on
using the MVES/OMVE to develop and manage a national registry of
experts.
DATES: To be sure that we consider your comments on our proposed
changes, we must receive them no later than September 14, 2007.
However, we also invite comments by November 13, 2007 on the merits of
a national registry of experts, including MVES/OMVE management of the
registry, and the rates to be paid to the experts affiliated with the
registry.
ADDRESSES: You may give us your comments by: Internet through the
Federal eRulemaking Portal at https://www.regulations.gov; e-mail to
regulations@ssa.gov; telefax to (410) 966-2830; or letter to the
Commissioner of Social Security, P.O. Box 17703, Baltimore, MD 21235-
7703. You may also deliver them to the Office of Regulations, Social
Security Administration, 960 Altmeyer Building, 6401 Security
Boulevard, Baltimore, MD 21235-6401, between 8 a.m. and 4:30 p.m. on
regular business days. Comments are posted on the Federal eRulemaking
Portal, or you may inspect them on regular business days by making
arrangements with the contact person shown in this preamble.
FOR FURTHER INFORMATION CONTACT: James A. Winn, Social Security
Administration, 6401 Security Boulevard, Baltimore, MD 21235-6401,
(410) 965-0600 for information about this notice. For information on
eligibility or filing for benefits, call our national toll-free number,
1-800-772-1213 or TTY 1-800-325-0778, or visit our Internet site,
Social Security Online, at https://www.socialsecurity.gov.
SUPPLEMENTARY INFORMATION:
Electronic Version
The electronic file of this document is available on the date of
publication in the Federal Register at https://www.gpoaccess.gov/fr/
index.html.
Introduction
We are dedicated to providing high-quality service to the American
public. When in March 2006 we announced changes to our administrative
review process for initial disability claims, we explained that we
expected that the changes would improve disability service. Our
commitment to continuous improvement in the way we process disability
claims did not end with the publication of those rules as we
continually explore ways to improve service to some of the most
vulnerable in our society. We face, now and in the foreseeable future,
significant challenges to our ability to provide the level of service
that disability benefit claimants deserve because of the increased
complexity of and growth in claims for those benefits. Consequently, we
propose modifications to our administrative review process that will
further help us evaluate changes put in place in March 2006 and help us
provide accurate and timely service to claimants for Social Security
disability benefits and supplemental security income payments based on
disability or blindness.
The importance of these disability benefits to the lives and
subsistence of many Americans cannot be underestimated. Nearly 15
million disabled Social Security beneficiaries and supplemental
security income recipients receive over $10 billion in Federal monthly
payments. The adjudication of disability claims requires evaluating
complex medical and vocational evidence.
The number of claims and requests for hearings that we receive has
continued to expand. In 2004-2006, we received an annual average of 2.6
million disability claims that required decisions on medical grounds,
the most time and labor intensive basis for deciding such claims. Along
with this expansion in the number of claims, there has been a
concomitant increase in the number of hearing requests. Our hearing
offices
[[Page 45702]]
have received an average of over 564,000 titles II and XVI disability
hearing requests each year from 2002 through 2006, a significant
increase from the annual average of almost 472,000 hearing requests in
1997-2001. As these figures show, over the 5-year period from 2002
through 2006, we received each year over 90,000 more requests for
titles II and XVI hearings than we annually received during the period
from 1997 through 2001. The vast number of disability claims now filed
each year, as well as other factors such as the expected increase in
disability claims as the baby boomers move into their disability-prone
years, probable limitations on our resources to process these claims,
and the projected impending increase in filings for retirement and
survivors benefits as baby boomers retire, will continue to place an
even greater strain on the system.
We expected that the spring 2006 changes to the administrative
review process for initial disability claims would ``improve the
accuracy, consistency, and timeliness of decision-making throughout the
disability determination process.'' 71 FR 16424 (March 31, 2006). We
planned a gradual roll-out of the changes so that we could determine
their effect on the disability process overall. As we explained then,
``Gradual implementation will allow us to monitor the effects that our
changes are having on the entire disability determination process * * *
We will carefully monitor the implementation process in the Boston
region and quickly address any problems that may arise.'' 71 FR at
16440-41. Based on initial reviews of the quick disability
determination (QDD) and FedRO elements of that process, and mindful of
the workload challenges that we now face--especially at the hearing
level--we believe we need to modify some of the changes made last
spring.
As we explain in our recently published notice of proposed
rulemaking on the QDD process (July 10, 2007; 72 FR 37496), we are
proposing to retain and expand the QDD process, and, as we explain
here, we propose to suspend new claims going through the FedRO and the
MVES, organizationally known as the OMVE. However, claims already
received will continue through the FedRO and MVES so we can continue to
evaluate their effectiveness. These proposals are based on our
commitment to outstanding service and to continuously improving our
service as we realign our resources to ensure that we are capable of
processing the current and anticipated number of disability claims and
reducing the number of pending hearings.
1. Suspending OFedRO and MVES/OMVE Allows Reallocation of Resources to
the Backlog at the Hearings Level
In the March 2006 final rule, we replaced the State agency
reconsideration level with a Federal adjudicative level, called the
FedRO. Attorneys staff the FedRO positions, and they, along with the
managerial, support, and administrative staff, make up the Office of
the FedRO (OFedRO). OFedRO uses the MVES/OMVE to develop the medical
and vocational evidence in the claims before them. The goal of FedRO
and OMVE is to have this level of review help ensure more accurate and
consistent decision making earlier in the process. We are continuing to
evaluate the effect of these new components on our program and
administrative functions. Our experience over the last year in the
Boston region demonstrates that the administrative costs associated
with OFedRO and its consequent use of the MVES/OMVE to develop medical
and vocational evidence is greater over the foreseeable future than
originally anticipated. We do not yet have sufficient results to fully
evaluate the potential improvements in program efficacy that are the
goals of the FedRO and OMVE. Therefore, we propose to suspend new
claims going through the FedRO and OMVE, so that we can reallocate
resources to reduce the backlog at the hearing level, while we evaluate
the FedRO and OMVE through the processing of claims already received.
Once this evaluation is completed and alternative approaches analyzed,
we will make a decision whether to reinstate the processing of new
claims at the FedRO or to pursue an alternative approach to improving
the disability determination process.
Under this proposal, we are amending part 405 with provisions that
will suspend new claims to the OFedRO and MVES/OMVE. This change will
allow us to continue to evaluate the FedRO and OMVE through the
processing of claims already received. We expect to have approximately
15,500 cases pending FedRO review when this rule becomes effective. We
will complete the processing of those pending cases, but will not
assign to FedRO any more cases originally filed under the new process
in Boston that otherwise would have been slated for FedRO review.
Instead, if cases are at the initial level in Boston or not assigned to
FedRO on the effective date of this rule, those cases will be assigned
to State agencies for reconsidered determinations or to administrative
law judges for hearing, whichever is applicable in that particular New
England State. In other words, States in the Boston region, where the
FedRO and MVES/OMVE are currently functioning, would return to the same
process they were following before August 2006, whether that process
was reconsideration under 20 CFR 404.907 and 416.1407 or the testing
procedures under 20 CFR 404.906 and 416.1406.
2. Request for Comments on a National Registry of Experts
Even though we propose to suspend new claims to the MVES/OMVE from
the administrative review process under part 405 of our rules, we are
considering using the MVES/OMVE in a more limited role to develop and
manage a national registry of medical, psychological, and vocational
experts to assist disability adjudicators in developing and/or
clarifying information within the record. Once the MVES/OMVE has
developed the registry, the MVES/OMVE would continue to manage the
registry. Disability adjudicators at the State and Federal levels would
be able to directly access the experts affiliated with the registry
without having to go through the MVES/OMVE to arrange for expert
assistance.
We ask for comments on the merits of such a registry, including
MVES/OMVE management of the registry, and the rates to be paid to the
experts affiliated with the registry. Questions upon which you may wish
to comment include, but are not limited to: What qualifications should
experts on the national registry have? Should experts be required to
have experience or training related to our disability programs? Should
disability adjudicators be required to use the registry when they
require expert assistance? Should we pay experts flat rates nationally
or should the rates be based on locality? If rates are based on
locality, what factors should we consider in setting those rates?
Regardless of whether the rates we pay the experts are based on
national or local rates, should we vary rates to account for the
individual's level of expertise, and if so, how should that be done?
Should we build in an automatic adjustment for inflation and, if so,
which measure would be most appropriate for this function? We would be
very interested in your thoughts regarding these issues and request
that they be submitted within 90 days of the publication of this
notice. We will consider comments submitted within this time period as
we continue to develop our plans for a national registry.
[[Page 45703]]
We will not respond to these comments until such time as we may publish
a notice of proposed rulemaking setting out more detailed plans for
such a registry.
Clarity of These Proposed Rules
Executive Order 12866, as amended, requires each agency to write
all rules in plain language. In addition to your substantive comments
on these final rules, we invite your comments on how to make them
easier to understand. For example:
Have we organized the material to suit your needs?
Are the requirements in the rules clearly stated?
Do the rules contain technical language or jargon that
isn't clear?
Would a different format (grouping and order of sections,
use of headings, paragraphing) make the rules easier to understand?
Would more (but shorter) sections be better?
Could we improve clarity by adding tables, lists, or
diagrams?
What else could we do to make the rules easier to
understand?
Regulatory Procedures
Pursuant to sections 205(a), 702(a)(5), and 1631(d)(1) of the
Social Security Act, 42 U.S.C. 405(a), 902(a)(5), and 1383(d)(1), we
follow the Administrative Procedure Act (APA) rulemaking procedures
specified in 5 U.S.C. 553 in the development of our regulations. We
ordinarily publish a notice of proposed rulemaking in the Federal
Register and permit a 60-day comment period. This period, however, may
be shortened when the agency finds good cause that a 60-day comment
period would be impracticable, unnecessary, or contrary to the public
interest and incorporates a statement of the finding and its reasons in
the rule issued. For this proposed rule, we find that there is good
cause for allowing a 30-day comment period on the issue of suspending
OFedRO and MVES/OMVE (section 1 above) because we believe that it would
be contrary to the public interest not to effectuate these rules as
quickly as we can. However, if it appears that 30 days is not
sufficient time to comment--for example, if the volume of comments
indicates that there is great public interest in this rule--we will
consider extending the comment period to 60 days.
We intend to shift the resources required for the FedRO and MVES/
OMVE to the effort to reduce the pending hearing requests to a
manageable level. In order to shift those resources as quickly as we
can, we must suspend new claims to the appeal procedure to the FedRO,
and thereby, stem the flow of cases to the FedRO and the MVES/OMVE.
Upon the effective date of the final rules, the first level of appeal
would be reconsideration for any claimant who has not yet requested
FedRO review, unless the State is a part of the prototype test in which
case the first level of review would be to an administrative law judge.
Claimants who have not yet been issued an initial determination would
be advised in the initial determination notice that their first level
of appeal would be reconsideration or a hearing, whichever applies.
This would allow the FedRO and the MVES/OMVE to complete the processing
of the cases in the pipeline, allow us to redirect resources to other
tasks, including assisting us in reducing the backlog at the hearing
level.
However, we are providing a 90-day comment period on the issue of a
national registry of experts (section 2 above).
Executive Order 12866, as Amended
We have consulted with the Office of Management and Budget (OMB)
and determined that this proposed rule meets the criteria for an
economically significant regulatory action under Executive Order 12866,
as amended. Thus, it was reviewed by OMB.
The Office of the Chief Actuary (OCACT) estimates that this rule
will result in program savings of roughly $1.0 billion in OASDI benefit
payments and cost of $0.1 billion in Federal SSI payments over the next
10 years, as shown below (in millions of dollars):
Table 1.--Estimated Effect on OASDI and Federal SSI Benefit Payments of a Proposed Regulation Eliminating New
Claims to the Federal Reviewing Official and Modifying the Role of the Medical and Vocational Expert System,
Fiscal Years 2008-17
[In millions]
----------------------------------------------------------------------------------------------------------------
Fiscal year OASDI SSI Total
----------------------------------------------------------------------------------------------------------------
2008............................................................ -$14 -$3 -$18
2009............................................................ -42 -9 -51
2010............................................................ -51 -8 -60
2011............................................................ -57 -15 -72
2012............................................................ -45 -6 -51
2013............................................................ -53 9 -44
2014............................................................ -122 22 -100
2015............................................................ -192 29 -163
2016............................................................ -248 40 -208
2017............................................................ -219 82 -137
Totals:
2008-12..................................................... -209 -41 -251
2008-17..................................................... -1,042 140 -902
----------------------------------------------------------------------------------------------------------------
Notes:
1. The estimates are based on the assumptions underlying the President's FY 2008 Budget.
2. Federal SSI payments due on October 1st in fiscal years 2012, 2017 and 2018 are included with payments for
the prior fiscal year.
3. Totals may not equal sum of components due to rounding.
Table 1 above presents the estimated short-range effects on OASDI
benefit payments and Federal SSI payments that would result from
implementation of this NPRM, measured relative to the baseline used for
the President's Fiscal Year 2008 Budget and assuming that a final rule
implementing these changes would become effective for initial
determinations made on or after April 1, 2008. The FY 2008 Budget
assumed that DSI would be gradually implemented at the pace of one
region per year and be fully implemented for new claims in all regions
by the beginning of FY 2016. For the 10 States where the Prototype
determination process has been or is being tested, the effect of this
NPRM
[[Page 45704]]
would be to retain or restore the Prototype process so that the first
level of appeal of an initial disability decision would be to an
administrative law judge.
As required by OMB Circular A-4 (available at https://
www.whitehouse.gov/omb/circulars/a004/a-4.pdf), in Table 2, we have
prepared an accounting statement showing the annualized economic impact
of suspending new claims to the FedRO level. All estimated impacts are
classified as transfers.
Table 2.--Accounting Statement: Estimated Economic Impact of Suspending
New Claims to the FedRO Level From 2008-2016 in 2007 Dollars
------------------------------------------------------------------------
Category Transfers
------------------------------------------------------------------------
Annualized Monetized Transfers......... $81.3 million (7% discount
rate).
$86.4 million (3% discount
rate).
From Whom To Whom?..................... From SSA beneficiaries to the
Social Security trust fund and
the general fund.
------------------------------------------------------------------------
Suspending new claims going through the FedRO and OMVE will allow
us to reallocate resources to reduce the backlog at the hearing level
by holding more hearings and making system improvements to increase the
efficiency of our hearings process.
We will also continue to evaluate the FedRO and OMVE through the
processing of claims already received. This evaluation will include an
assessment of DSI, as the pilot is currently implemented in the Boston
region, with existing claims. In the analysis we will analyze DSI's
impact on the timeliness of disability determinations, on overall
program costs, as well as its impact on the administrative costs
required to implement this new process. Once this evaluation is
complete and alternative approaches analyzed, we will make a decision
whether to reinstate the processing of new claims into the FedRO or
pursue an alternative approach to improving the disability
determination process.
Regulatory Flexibility Act
We certify that this proposed rule, when published in final, will
not have a significant economic impact on a substantial number of small
entities as it affects only States and individuals. Therefore, a
regulatory flexibility analysis as provided in the Regulatory
Flexibility Act, as amended, is not required.
Paperwork Reduction Act
These rules impose no new reporting or recordkeeping requirements
requiring OMB clearance.
Federalism Impact and Unfunded Mandates Impact
We have reviewed this proposed rule under the threshold criteria of
Executive Order 13132 and the Unfunded Mandates Reform Act and have
determined that it does not have substantial direct effects on the
States, on the relationship between the national government and the
States, on the distribution of power and responsibilities among the
various levels of government, or on imposing any costs on State, local,
or tribal governments. This proposed rule does not affect the roles of
the State, local, or tribal governments. However, the proposed rule
takes administrative notice of existing statutes governing the roles
and relationships of the State agencies with us with respect to
disability determinations under the Act.
(Catalog of Federal Domestic Assistance Program Nos. 96.001, Social
Security--Disability Insurance; 96.002, Social Security--Retirement
Insurance; 96.004, Social Security--Survivors Insurance; 96.006,
Supplemental Security Income)
List of Subjects in 20 CFR Part 405
Administrative practice and procedure; Blind, Disability benefits;
Old-Age, Survivors, and Disability Insurance; Public assistance
programs, Reporting and recordkeeping requirements; Social Security;
Supplemental Security Income (SSI).
Dated: August 7, 2007.
Michael J. Astrue,
Commissioner of Social Security.
For the reasons set out in the preamble, we are amending subparts A
and C of part 405 as set forth below:
PART 405--ADMINISTRATIVE REVIEW PROCESS FOR ADJUDICATING INITIAL
DISABILITY CLAIMS
1. The authority citation for part 405 continues to read as
follows:
Authority: Secs. 201(j), 205(a)-(b), (d)-(h), and (s), 221,
223(a)-(b), 702(a)(5), 1601, 1602, 1631, and 1633 of the Social
Security Act (42 U.S.C. 401(j), 405(a)-(b), (d)-(h), and (s), 421,
423(a)-(b), 902(a)(5), 1381, 1381a, 1383, and 1383b).
Subpart A--[Amended]
2. Amend Sec. 405.10 by adding paragraph (d) to read as follows:
Sec. 405.10 Medical and Vocational Expert System.
* * * * *
(d) This section will no longer be effective on the same date as
described in Sec. 405.240(c) of this part unless the Commissioner
decides that the Medical and Vocational Expert System should be
continued and extends the sunset date as described in Sec. 405.240(d)
of this part by publishing a notice of proposed rulemaking in the
Federal Register before that date.
3. Revise the appendix to subpart A of part 405 to read as follows:
Appendix to Subpart A of Part 405--Claims That Will Be Handled Under
the Procedures in This Part
(a) We will apply the procedures in this part to disability
claims (as defined in Sec. 405.5) filed in Maine, New Hampshire,
Vermont, Massachusetts, Rhode Island, or Connecticut.
(b) If you move from one State to another after your disability
claim has been filed, adjudicators at subsequent levels of review
will apply the regulations that initially applied to the disability
claim. For example, if you file a claim in a State in which we apply
the procedures in this part, the procedures in this part will apply
to the disability claim at subsequent levels of review, even if you
move to a State where we would otherwise not apply these procedures.
Conversely, if you file a claim in a State where we do not apply the
procedures in this part, we will adjudicate the claim using the
procedures in part 404 or 416 of this chapter, as appropriate, even
if you subsequently move to a State where we would otherwise apply
the procedures in this part.
Subpart C--[Amended]
4. Add Sec. 405.240 to read as follows:
Sec. 405.240 Sunset of this Subpart.
(a) If you have filed a request for review by a Federal reviewing
official on or before the effective date of this section, the Federal
reviewing official will review and issue a decision on your claim.
[[Page 45705]]
(b) If you have not filed a request for review by a Federal
reviewing official on or before the effective date of this section and
you have received an initial determination under subpart B of this
part, we will process any request for additional administrative review
filed after the effective date as either a request for reconsideration
by the State agency or a request for hearing before an administrative
law judge if your State uses the testing procedures under Sec. Sec.
404.906 and 416.1406 of this title.
(c) This subpart will no longer be effective the day after a
Federal reviewing official issues a decision on the last of the claims
accepted for review under paragraph (a) of this section.
(d) If compelling evidence shows that the Federal reviewing
official process is efficient, effective, and sustainable given
available Agency resources, the Commissioner may reinstate the Federal
reviewing official process by publishing a notice of proposed
rulemaking in the Federal Register.
[FR Doc. E7-16071 Filed 8-14-07; 8:45 am]
BILLING CODE 4191-02-P