Medicare Program; Medicare Appeals; Adjustment to the Amount in Controversy Threshold Amounts for Calendar Year 2015, 57933-57935 [2014-22625]
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mstockstill on DSK4VPTVN1PROD with NOTICES
Federal Register / Vol. 79, No. 187 / Friday, September 26, 2014 / Notices
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by October 27, 2014:
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 OR, Email:
OIRA_submission@omb.eop.gov.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
VerDate Sep<11>2014
19:14 Sep 25, 2014
Jkt 232001
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Cost Sharing
Reduction Reconciliation; Use: Under
established Department of Health and
Human Services (HHS) regulations,
qualified health plan (QHP) issuers will
receive estimated advance payments of
cost-sharing reductions throughout the
year. Each issuer will then be subject to
a reconciliation process at the end of the
benefit year to ensure that HHS
reimburses each issuer only for actual
cost sharing. This proposed collection
establishes the data elements that a QHP
issuer would be required to report to
HHS in order to establish the costsharing reductions provided on behalf
of enrollees for the benefit year.
Comments were received and addressed
in a Response to Comments document.
Form Number: CMS–10526 (OMB
control number: 0938–NEW);
Frequency: Annually; Affected Public:
Private sector—Business or other forprofits; Number of Respondents: 295;
Total Annual Responses: 4 million;
Total Annual Hours: 2,469. (For policy
questions regarding this collection
contact Patricia Meisol at 410–786–
1917.)
2. Type of Information Collection
Request: Revision of a currently
approved information collection; Title
of Information Collection: Medicaid
Incentives for Prevention of Chronic
Disease (MIPCD) Demonstration; Use:
Under section 4108(d)(1) of the
Affordable Care Act, we are required to
contract with an independent entity or
organization to conduct an evaluation of
the Medicaid Incentives for Prevention
of Chronic Disease (MIPCD)
demonstration. The contractor will
conduct state site visits, two rounds of
focus group discussions, interviews
with key program stakeholders, and
field a beneficiary satisfaction survey.
Both the state site visits and interviews
with key program stakeholders will
entail one-on-one interviews; however
each set will have a unique data
collection form. Thus, each evaluation
task listed above has a separate data
collection form and this proposed
information collection encompasses six
PO 00000
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Sfmt 4703
57933
data collection forms. The purpose of
the evaluation and assessment includes
determining the following:
• The effect of such initiatives on the
use of health care services by Medicaid
beneficiaries participating in the
program;
• The extent to which special
populations (including adults with
disabilities, adults with chronic
illnesses, and children with special
health care needs) are able to participate
in the program;
• The level of satisfaction of
Medicaid beneficiaries with respect to
the accessibility and quality of health
care services provided through the
program; and
• The administrative costs incurred
by state agencies that are responsible for
administration of the program.
Subsequent to the initial OMB
approval issued January 23, 2014, we
have added two Administrative Cost
forms to the information collection. The
burden estimates for this information
collection have been revised to account
for the burden associated with the new
forms. Form Number: CMS–10477
(OMB control number: 0938–1219);
Frequency: Annually; Affected Public:
Individuals and Households, Private
sector—Business or other for-profits and
Not-for-profit institutions, State, Local
or Tribal Governments; Number of
Respondents: 4,706; Total Annual
Responses: 4,706; Total Annual Hours:
2,236. (For policy questions regarding
this collection contact Jean Scott at 410–
786–6327.)
Dated: September 23, 2014.
Martique Jones,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2014–22980 Filed 9–25–14; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–4175–N]
Medicare Program; Medicare Appeals;
Adjustment to the Amount in
Controversy Threshold Amounts for
Calendar Year 2015
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice announces the
annual adjustment in the amount in
controversy (AIC) threshold amounts for
Administrative Law Judge (ALJ)
SUMMARY:
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57934
Federal Register / Vol. 79, No. 187 / Friday, September 26, 2014 / Notices
hearings and judicial review under the
Medicare appeals process. The
adjustment to the AIC threshold
amounts will be effective for requests
for ALJ hearings and judicial review
filed on or after January 1, 2015. The
calendar year 2015 AIC threshold
amounts are $150 for ALJ hearings and
$1,460 for judicial review.
DATES: This notice is effective on
January 1, 2015.
FOR FURTHER INFORMATION CONTACT: Liz
Hosna (Katherine.Hosna@cms.hhs.gov),
(410) 786–4993.
SUPPLEMENTARY INFORMATION:
I. Background
Section 1869(b)(1)(E) of the Social
Security Act (the Act), as amended by
section 521 of the Medicare, Medicaid,
and SCHIP Benefits Improvement and
Protection Act of 2000 (BIPA),
established the amount in controversy
(AIC) threshold amounts for
Administrative Law Judge (ALJ) hearing
requests and judicial review at $100 and
$1,000, respectively, for Medicare Part
A and Part B appeals. Section 940 of the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA), amended section
1869(b)(1)(E) of the Act to require the
AIC threshold amounts for ALJ hearings
and judicial review to be adjusted
annually. The AIC threshold amounts
are to be adjusted, as of January 2005,
by the percentage increase in the
medical care component of the
consumer price index (CPI) for all urban
consumers (U.S. city average) for July
2003 to July of the year preceding the
year involved and rounded to the
nearest multiple of $10. Section
940(b)(2) of the MMA provided
conforming amendments to apply the
AIC adjustment requirement to
Medicare Part C/Medicare Advantage
(MA) appeals and certain health
maintenance organization and
competitive health plan appeals. Health
care prepayment plans are also subject
to MA appeals rules, including the AIC
adjustment requirement. Section 101 of
the MMA provides for the application of
the AIC adjustment requirement to
Medicare Part D appeals.
mstockstill on DSK4VPTVN1PROD with NOTICES
A. Medicare Part A and Part B Appeals
The statutory formula for the annual
adjustment to the AIC threshold
amounts for ALJ hearings and judicial
review of Medicare Part A and Part B
appeals, set forth at section
1869(b)(1)(E) of the Act, is included in
the applicable implementing
regulations, 42 CFR 405.1006(b) and (c).
The regulations require the Secretary of
the Department of Health and Human
VerDate Sep<11>2014
19:14 Sep 25, 2014
Jkt 232001
Services (the Secretary) to publish
changes to the AIC threshold amounts
in the Federal Register
(§ 405.1006(b)(2)). In order to be entitled
to a hearing before an ALJ, a party to a
proceeding must meet the AIC
requirements at § 405.1006(b). Similarly,
a party must meet the AIC requirements
at § 405.1006(c) at the time judicial
review is requested for the court to have
jurisdiction over the appeal
(§ 405.1136(a)).
B. Medicare Part C/MA Appeals
Section 940(b)(2) of the MMA applies
the AIC adjustment requirement to
Medicare Part C appeals by amending
section 1852(g)(5) of the Act. The
implementing regulations for Medicare
Part C appeals are found at 42 CFR part
422, subpart M. Specifically, §§ 422.600
and 422.612 discuss the AIC threshold
amounts for ALJ hearings and judicial
review. Section 422.600 grants any party
to the reconsideration, except the MA
organization, who is dissatisfied with
the reconsideration determination, a
right to an ALJ hearing as long as the
amount remaining in controversy after
reconsideration meets the threshold
requirement established annually by the
Secretary. Section 422.612 states, in
part, that any party, including the MA
organization, may request judicial
review if the AIC meets the threshold
requirement established annually by the
Secretary.
C. Health Maintenance Organizations,
Competitive Medical Plans, and Health
Care Prepayment Plans
Section 1876(c)(5)(B) of the Act states
that the annual adjustment to the AIC
dollar amounts set forth in section
1869(b)(1)(E) of the Act applies to
certain beneficiary appeals within the
context of health maintenance
organizations and competitive medical
plans. The applicable implementing
regulations for Medicare Part C appeals
are set forth in 42 CFR part 422, subpart
M, and as discussed previously, apply
to these appeals. The Medicare Part C
appeals rules also apply to health care
prepayment plan appeals.
D. Medicare Part D (Prescription Drug
Plan) Appeals
The annually adjusted AIC threshold
amounts for ALJ hearings and judicial
review that apply to Medicare Parts A,
B, and C appeals also apply to Medicare
Part D appeals. Section 101 of the MMA
added section 1860D–4(h)(1) of the Act
regarding Part D appeals. This statutory
provision requires a prescription drug
plan sponsor to meet the requirements
set forth in sections 1852(g)(4) and (g)(5)
of the Act, in a similar manner as MA
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
organizations. As noted previously, the
annually adjusted AIC threshold
requirement was added to section
1852(g)(5) of the Act by section
940(b)(2)(A) of the MMA. The
implementing regulations for Medicare
Part D appeals can be found at 42 CFR
part 423, subparts M and U. The
regulations at § 423.562(c) prescribe
that, unless the Part D appeals rules
provide otherwise, the Part C appeals
rules (including the annually adjusted
AIC threshold amount) apply to Part D
appeals to the extent they are
appropriate. More specifically,
§§ 423.1970 and 423.1976 of the Part D
appeals rules discuss the AIC threshold
amounts for ALJ hearings and judicial
review. Section 423.1970(a) grants a Part
D enrollee, who is dissatisfied with the
independent review entity (IRE)
reconsideration determination, a right to
an ALJ hearing if the amount remaining
in controversy after the IRE
reconsideration meets the threshold
amount established annually by the
Secretary. Sections 423.1976(a) and (b)
allow a Part D enrollee to request
judicial review of an ALJ or MAC
decision if, in part, the AIC meets the
threshold amount established annually
by the Secretary.
II. Provisions of the Notice—Annual
AIC Adjustments
A. AIC Adjustment Formula and AIC
Adjustments
As previously noted, section 940 of
the MMA requires that the AIC
threshold amounts be adjusted
annually, beginning in January 2005, by
the percentage increase in the medical
care component of the CPI for all urban
consumers (U.S. city average) for July
2003 to July of the year preceding the
year involved and rounded to the
nearest multiple of $10.
B. Calendar Year 2015
The AIC threshold amount for ALJ
hearing requests will rise to $150 and
the AIC threshold amount for judicial
review will rise to $1,460 for CY 2015.
These amounts are based on the 46.480
percent increase in the medical care
component of the CPI level, which was
at 297.600 in July 2003 and rose to
435.924 in July 2014. The AIC threshold
amount for ALJ hearing requests
changes to $146.48 based on the 46.480
percent increase over the initial
threshold amount of $100 established in
2003. In accordance with section
1869(b)(1)(E)(iii) of the Act, the adjusted
threshold amounts are rounded to the
nearest multiple of $10. Therefore, the
CY 2015 AIC threshold amount for ALJ
hearings is $150.00. The AIC threshold
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57935
Federal Register / Vol. 79, No. 187 / Friday, September 26, 2014 / Notices
amount for judicial review changes to
$1,464.80 based on the 46.480 percent
increase over the initial threshold
amount of $1,000. This amount was
rounded to the nearest multiple of $10,
resulting in the CY 2015 AIC threshold
amount of $1,460.00 for judicial review.
CY 2011
ALJ Hearing .............................................................................................
Judicial Review ........................................................................................
III. Collection of Information
Requirements
This document does not impose
information collection and
recordkeeping requirements.
Consequently, it need not be reviewed
by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995 (44
U.S.C. 35).
Dated: September 11, 2014.
Marilyn Tavenner,
Administrator, Centers for Medicare &
Medicaid Services.
BILLING CODE 4120–01–P
$130
1,300
$130
1,350
clearance under 44 U.S.C. 3507. An
Agency may not conduct or sponsor,
and a person is not required to respond
to, a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
information collection and has assigned
OMB control number 0910–0540. The
approval expires on August 31, 2017. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.reginfo.gov/
public/do/PRAMain.
[FR Doc. 2014–22981 Filed 9–25–14; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Docket No. FDA–2007–N–0037]
Food and Drug Administration
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Guidance for Industry: Animal Drug
User Fees and Fee Waivers and
Reductions
[Docket No. FDA–2011–N–0075]
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Guidance for Industry: Animal Drug
User Fees and Fee Waivers and
Reductions’’ has been approved by the
Office of Management and Budget
(OMB) under the Paperwork Reduction
Act of 1995.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
On July
08, 2014, the Agency submitted a
proposed collection of information
entitled ‘‘Guidance for Industry: Animal
Drug User Fees and Fee Waivers and
Reductions’’ to OMB for review and
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
19:14 Sep 25, 2014
Food and Drug Administration,
HHS.
SUMMARY:
mstockstill on DSK4VPTVN1PROD with NOTICES
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Good Laboratory
Practice Regulations for Nonclinical
Studies
AGENCY:
Notice.
Jkt 232001
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995
(PRA).
DATES: Fax written comments on the
collection of information by October 27,
2014.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to oira_
submission@omb.eop.gov. All
comments should be identified with the
SUMMARY:
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Frm 00067
Fmt 4703
Sfmt 4703
In the following table we list the CYs
2011 through 2015 threshold amounts.
CY 2012
Dated: September 23, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014–22625 Filed 9–25–14; 8:45 am]
C. Summary Table of Adjustments in
the AIC Threshold Amounts
CY 2013
$140
1,400
CY 2014
$140
1,430
CY 2015
$150
1,460
OMB control number 0910–0119. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Good Laboratory Practice Regulations
for Nonclinical Studies—21 CFR Part
58 (OMB Control Number 0910–0119)—
Extension
Sections 409, 505, 512, and 515 of the
Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 348, 355, 360b, 360e) and
related statutes require manufacturers of
food additives, human drugs and
biological products, animal drugs, and
medical devices to demonstrate the
safety and utility of their product by
submitting applications to FDA for
research or marketing permits. Such
applications contain, among other
important items, full reports of all
studies done to demonstrate product
safety in man and/or other animals. In
order to ensure adequate quality control
for these studies and to provide an
adequate degree of consumer protection,
the Agency issued good laboratory
practice (GLP) regulations for
nonclinical laboratory studies in part 58
(21 CFR part 58). The regulations
specify minimum standards for the
proper conduct of safety testing and
contain sections on facilities, personnel,
equipment, standard operating
procedures (SOPs), test and control
articles, quality assurance, protocol and
conduct of a safety study, records and
reports, and laboratory disqualification.
Part 58 requires testing facilities
engaged in conducting toxicological
studies to retain, and make available to
regulatory officials, records regarding
compliance with GLPs. Records are
maintained on file at each testing
facility and examined there periodically
by FDA inspectors. The GLP regulations
E:\FR\FM\26SEN1.SGM
26SEN1
Agencies
[Federal Register Volume 79, Number 187 (Friday, September 26, 2014)]
[Notices]
[Pages 57933-57935]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-22625]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[CMS-4175-N]
Medicare Program; Medicare Appeals; Adjustment to the Amount in
Controversy Threshold Amounts for Calendar Year 2015
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the annual adjustment in the amount in
controversy (AIC) threshold amounts for Administrative Law Judge (ALJ)
[[Page 57934]]
hearings and judicial review under the Medicare appeals process. The
adjustment to the AIC threshold amounts will be effective for requests
for ALJ hearings and judicial review filed on or after January 1, 2015.
The calendar year 2015 AIC threshold amounts are $150 for ALJ hearings
and $1,460 for judicial review.
DATES: This notice is effective on January 1, 2015.
FOR FURTHER INFORMATION CONTACT: Liz Hosna
(Katherine.Hosna@cms.hhs.gov), (410) 786-4993.
SUPPLEMENTARY INFORMATION:
I. Background
Section 1869(b)(1)(E) of the Social Security Act (the Act), as
amended by section 521 of the Medicare, Medicaid, and SCHIP Benefits
Improvement and Protection Act of 2000 (BIPA), established the amount
in controversy (AIC) threshold amounts for Administrative Law Judge
(ALJ) hearing requests and judicial review at $100 and $1,000,
respectively, for Medicare Part A and Part B appeals. Section 940 of
the Medicare Prescription Drug, Improvement, and Modernization Act of
2003 (MMA), amended section 1869(b)(1)(E) of the Act to require the AIC
threshold amounts for ALJ hearings and judicial review to be adjusted
annually. The AIC threshold amounts are to be adjusted, as of January
2005, by the percentage increase in the medical care component of the
consumer price index (CPI) for all urban consumers (U.S. city average)
for July 2003 to July of the year preceding the year involved and
rounded to the nearest multiple of $10. Section 940(b)(2) of the MMA
provided conforming amendments to apply the AIC adjustment requirement
to Medicare Part C/Medicare Advantage (MA) appeals and certain health
maintenance organization and competitive health plan appeals. Health
care prepayment plans are also subject to MA appeals rules, including
the AIC adjustment requirement. Section 101 of the MMA provides for the
application of the AIC adjustment requirement to Medicare Part D
appeals.
A. Medicare Part A and Part B Appeals
The statutory formula for the annual adjustment to the AIC
threshold amounts for ALJ hearings and judicial review of Medicare Part
A and Part B appeals, set forth at section 1869(b)(1)(E) of the Act, is
included in the applicable implementing regulations, 42 CFR 405.1006(b)
and (c). The regulations require the Secretary of the Department of
Health and Human Services (the Secretary) to publish changes to the AIC
threshold amounts in the Federal Register (Sec. 405.1006(b)(2)). In
order to be entitled to a hearing before an ALJ, a party to a
proceeding must meet the AIC requirements at Sec. 405.1006(b).
Similarly, a party must meet the AIC requirements at Sec. 405.1006(c)
at the time judicial review is requested for the court to have
jurisdiction over the appeal (Sec. 405.1136(a)).
B. Medicare Part C/MA Appeals
Section 940(b)(2) of the MMA applies the AIC adjustment requirement
to Medicare Part C appeals by amending section 1852(g)(5) of the Act.
The implementing regulations for Medicare Part C appeals are found at
42 CFR part 422, subpart M. Specifically, Sec. Sec. 422.600 and
422.612 discuss the AIC threshold amounts for ALJ hearings and judicial
review. Section 422.600 grants any party to the reconsideration, except
the MA organization, who is dissatisfied with the reconsideration
determination, a right to an ALJ hearing as long as the amount
remaining in controversy after reconsideration meets the threshold
requirement established annually by the Secretary. Section 422.612
states, in part, that any party, including the MA organization, may
request judicial review if the AIC meets the threshold requirement
established annually by the Secretary.
C. Health Maintenance Organizations, Competitive Medical Plans, and
Health Care Prepayment Plans
Section 1876(c)(5)(B) of the Act states that the annual adjustment
to the AIC dollar amounts set forth in section 1869(b)(1)(E) of the Act
applies to certain beneficiary appeals within the context of health
maintenance organizations and competitive medical plans. The applicable
implementing regulations for Medicare Part C appeals are set forth in
42 CFR part 422, subpart M, and as discussed previously, apply to these
appeals. The Medicare Part C appeals rules also apply to health care
prepayment plan appeals.
D. Medicare Part D (Prescription Drug Plan) Appeals
The annually adjusted AIC threshold amounts for ALJ hearings and
judicial review that apply to Medicare Parts A, B, and C appeals also
apply to Medicare Part D appeals. Section 101 of the MMA added section
1860D-4(h)(1) of the Act regarding Part D appeals. This statutory
provision requires a prescription drug plan sponsor to meet the
requirements set forth in sections 1852(g)(4) and (g)(5) of the Act, in
a similar manner as MA organizations. As noted previously, the annually
adjusted AIC threshold requirement was added to section 1852(g)(5) of
the Act by section 940(b)(2)(A) of the MMA. The implementing
regulations for Medicare Part D appeals can be found at 42 CFR part
423, subparts M and U. The regulations at Sec. 423.562(c) prescribe
that, unless the Part D appeals rules provide otherwise, the Part C
appeals rules (including the annually adjusted AIC threshold amount)
apply to Part D appeals to the extent they are appropriate. More
specifically, Sec. Sec. 423.1970 and 423.1976 of the Part D appeals
rules discuss the AIC threshold amounts for ALJ hearings and judicial
review. Section 423.1970(a) grants a Part D enrollee, who is
dissatisfied with the independent review entity (IRE) reconsideration
determination, a right to an ALJ hearing if the amount remaining in
controversy after the IRE reconsideration meets the threshold amount
established annually by the Secretary. Sections 423.1976(a) and (b)
allow a Part D enrollee to request judicial review of an ALJ or MAC
decision if, in part, the AIC meets the threshold amount established
annually by the Secretary.
II. Provisions of the Notice--Annual AIC Adjustments
A. AIC Adjustment Formula and AIC Adjustments
As previously noted, section 940 of the MMA requires that the AIC
threshold amounts be adjusted annually, beginning in January 2005, by
the percentage increase in the medical care component of the CPI for
all urban consumers (U.S. city average) for July 2003 to July of the
year preceding the year involved and rounded to the nearest multiple of
$10.
B. Calendar Year 2015
The AIC threshold amount for ALJ hearing requests will rise to $150
and the AIC threshold amount for judicial review will rise to $1,460
for CY 2015. These amounts are based on the 46.480 percent increase in
the medical care component of the CPI level, which was at 297.600 in
July 2003 and rose to 435.924 in July 2014. The AIC threshold amount
for ALJ hearing requests changes to $146.48 based on the 46.480 percent
increase over the initial threshold amount of $100 established in 2003.
In accordance with section 1869(b)(1)(E)(iii) of the Act, the adjusted
threshold amounts are rounded to the nearest multiple of $10.
Therefore, the CY 2015 AIC threshold amount for ALJ hearings is
$150.00. The AIC threshold
[[Page 57935]]
amount for judicial review changes to $1,464.80 based on the 46.480
percent increase over the initial threshold amount of $1,000. This
amount was rounded to the nearest multiple of $10, resulting in the CY
2015 AIC threshold amount of $1,460.00 for judicial review.
C. Summary Table of Adjustments in the AIC Threshold Amounts
In the following table we list the CYs 2011 through 2015 threshold
amounts.
----------------------------------------------------------------------------------------------------------------
CY 2011 CY 2012 CY 2013 CY 2014 CY 2015
----------------------------------------------------------------------------------------------------------------
ALJ Hearing.................................... $130 $130 $140 $140 $150
Judicial Review................................ 1,300 1,350 1,400 1,430 1,460
----------------------------------------------------------------------------------------------------------------
III. Collection of Information Requirements
This document does not impose information collection and
recordkeeping requirements. Consequently, it need not be reviewed by
the Office of Management and Budget under the authority of the
Paperwork Reduction Act of 1995 (44 U.S.C. 35).
Dated: September 11, 2014.
Marilyn Tavenner,
Administrator, Centers for Medicare & Medicaid Services.
[FR Doc. 2014-22625 Filed 9-25-14; 8:45 am]
BILLING CODE 4120-01-P