Agency Information Collection Activities: Proposed Collection; Comment Request, 40482-40484 [2013-16085]
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40482
Federal Register / Vol. 78, No. 129 / Friday, July 5, 2013 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form
Number of
responses per
respondent
Number of
respondents
Respondents
Average
burden per
response
(in hours)
Total burden
(in hours)
Social and community service managers .......
TOTAL .........................
300
1
12/60
60
.........................................................................
........................
........................
........................
1,882
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2013–16106 Filed 7–3–13; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10316]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
ACTION:
Notice.
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
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 August 5, 2013.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
tkelley on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
17:06 Jul 03, 2013
Jkt 229001
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) 395–6974 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.
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: Revision of a currently
approved collection; Title of
Information Collection: Implementation
of the Medicare Prescription Drug Plan
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
(PDP) and Medicare Advantage (MA)
Plan Disenrollment Reasons Survey;
Use: This data collection complements
the satisfaction data collected through
the Medicare Consumer Assessment of
Healthcare Providers and Systems
survey by providing dissatisfaction data
in the form of reasons for disenrollment
from a Prescription Drug Plan. The data
collected in this survey can be used to
improve the operation of Medicare
Advantage (MA) (both MA and MA–PD)
contracts and standalone prescription
drug plans (PDPs) through the
identification of beneficiary
disenrollment reasons. Plans can use the
information to guide quality
improvement efforts. The data can also
be used by beneficiaries who need to
choose among the different MA and PDP
options. To the extent that these data
identify areas for improvement at the
contract level they can be used for
contract oversight. Form Number: CMS–
10316 (OCN: 0938–1113); Frequency:
Yearly; Affected Public: Individuals or
households; Number of Respondents:
88,492; Total Annual Responses:
88,492; Total Annual Hours: 22,887.
(For policy questions regarding this
collection contact Sai Ma at 410–786–
1479.)
Dated: June 28, 2013.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2013–16084 Filed 7–3–13; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10171, CMS–
10207, CMS–10476 and CMS–855(C)]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
E:\FR\FM\05JYN1.SGM
05JYN1
Federal Register / Vol. 78, No. 129 / Friday, July 5, 2013 / Notices
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
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
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates 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.
SUMMARY:
Comments must be received by
September 3, 2013.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number (OCN). To be
assured consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number llll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
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.
tkelley on DSK3SPTVN1PROD with NOTICES
DATES:
VerDate Mar<15>2010
17:06 Jul 03, 2013
Jkt 229001
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10171 Coordination of Benefits
Between Part D Plans and Other
Prescription Coverage Providers.
CMS–10207 Physician Self-Referral
Exceptions for Electronic Prescribing
and Electronic Health Records.
CMS–10476 Medical Loss Ratio
(MLR) Report for Medicare Advantage
(MA) Plans and Prescription Drug Plans
(PDP).
CMS–855(C) Medicare Enrollment
Application for Registration of Eligible
Entities That Provide Health Insurance
Coverage Complementary to Medicare
Part B
Under the Paperwork Reduction Act
(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
requires federal agencies to publish a
60-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.
Information Collections
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Coordination of
Benefits Between Part D Plans and
Other Prescription Coverage Providers;
Use: We will use the information along
with Part D plans, other health insurers
or payers, and pharmacies to coordinate
prescription drug benefits provided to
the Medicare beneficiary. Form Number:
CMS–10171 (OCN: 0938–0978):
Frequency: Occasionally; Affected
Public: Private sector—Business or other
for-profits; Number of Respondents:
PO 00000
Frm 00059
Fmt 4703
Sfmt 4703
40483
57,116; Total Annual Responses:
2,402,582; Total Annual Hours:
5,205,128. (For policy questions
regarding this collection contact Heather
Rudo at 410–786–7627.)
2. Type of Information Collection
Request: Reinstatement without change
of a previously approved collection;
Title of Information Collection:
Physician Self-Referral Exceptions for
Electronic Prescribing and Electronic
Health Records; Use: The collected
information would be used for
enforcement purposes. Specifically, if
we were investigating the financial
relationships between donors and
physicians to determine whether the
provisions in the exceptions at 42 CFR
411.357(v) and (w) were met, first, we
would review the written agreements
that indicate what items and services
each entity intended to provide. Form
Number: CMS–10207 (OCN: 0938–
1009); Frequency: Monthly; Affected
Public: Private sector—Business or other
for-profits and Not-for-profit
institutions; Number of Respondents:
9,409; Total Annual Responses: 17,744;
Total Annual Hours: 1,896. (For policy
questions regarding this collection
contact Michael Zleit at 410–786–2050.)
3. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Medical Loss
Ratio (MLR) Report for Medicare
Advantage (MA) Plans and Prescription
Drug Plans (PDP); Use: We will use the
data collection of annual reports
provided by plan sponsors for each
contract to ensure that beneficiaries are
receiving value for their premium dollar
by calculating each contract’s medical
loss ratio (MLR) and any remittances
due for the respective MLR reporting
year. The recordkeeping requirements
will be used to determine plan sponsors’
compliance with the MLR requirements,
including compliance with how plan
sponsors’ experience is to be reported,
and how their MLR and any remittances
are calculated. Form Number: CMS–
10476 (OCN: 0938-New); Frequency:
Yearly; Affected Public: Private sector—
Business or other for-profits and Notfor-profit institutions; Number of
Respondents: 616; Total Annual
Responses: 616; Total Annual Hours:
28,980. (For policy questions regarding
this collection contact Ilina Chaudhuri
at 410–786–8628.)
4. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Medicare
Enrollment Application for Registration
of Eligible Entities That Provide Health
Insurance Coverage Complementary to
Medicare Part B; Use: The primary
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05JYN1
tkelley on DSK3SPTVN1PROD with NOTICES
40484
Federal Register / Vol. 78, No. 129 / Friday, July 5, 2013 / Notices
function of a Medicare enrollment
application is to gather information
from a provider, supplier or other entity
that tells us who it is, whether it meets
certain qualifications to be a health care
provider, supplier or entity, where it
practices or renders its services, the
identity of the owners of the enrolling
entity, and information necessary to
establish correct claims payments. We
are adding a new CMS–855 Medicare
Registration Application, the CMS–
855C: Medicare Enrollment Application
for Registration of Eligible Entities That
Provide Health Insurance Coverage
Complementary to Medicare Part B.
This Medicare registration application is
to be completed by all entities that
provide a complimentary health benefit
plan and intend to bill Medicare as an
indirect payment procedure (IPP) biller
and the entity or health plan meets all
Medicare requirements to submit claims
for indirect payments. The entity must
furnish the name of at least one
authorized official, preferably the
administrator of the health plan, who
must sign this registration application
attesting that the registering entity meets
the requirements to register as an
indirect payment procedure biller and
will also abide by the requirements
stated in the Certification & Attestation
Statement in Section 10 of the
application.
The CMS–855C will be submitted at
the time the applicant first requests a
Medicare identification number for the
sole purpose of submitting claims under
the ‘‘Indirect Payment Procedure (IPP)’’
for reimbursement, and when necessary
to report any changes to information
previously submitted. The application
will be used by Medicare contractors to
collect data to ensure the applicant has
the necessary credentials to submit
Medicare claims for reimbursement,
including information that allows
Medicare contractors to ensure that the
entity and its owners and administrators
are not sanctioned from the Medicare
program, or debarred, suspended or
excluded from any other Federal agency
or program. Form Number: CMS–855(C)
(OCN: 0938-New); Frequency:
Occasionally; Affected Public: Private
sector—Business or other for-profits and
Not-for-profit institutions; Number of
Respondents: 440; Total Annual
Responses: 440; Total Annual Hours:
500. (For policy questions regarding this
collection contact Kim McPhillips at
410–786–5374.)
VerDate Mar<15>2010
17:06 Jul 03, 2013
Jkt 229001
Dated: June 28, 2013.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2013–16085 Filed 7–3–13; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–P–0303]
Determination That METADATE ER
(Methylphenidate Hydrochloride)
Extended-Release Tablet, 10
Milligrams, Was Not Withdrawn From
Sale for Reasons of Safety or
Effectiveness
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) has determined
that METADATE ER (methylphenidate
hydrochloride (HCl)) extended-release
tablet, 10 milligrams (mg), was not
withdrawn from sale for reasons of
safety or effectiveness. This
determination will allow FDA to
approve abbreviated new drug
applications (ANDAs) for
methylphenidate HCl extended-release
tablet, 10 mg, if all other legal and
regulatory requirements are met.
FOR FURTHER INFORMATION CONTACT:
Reena Raman, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, rm. 6238,
Silver Spring, MD 20993–0002, 301–
796–7577.
SUPPLEMENTARY INFORMATION: In 1984,
Congress enacted the Drug Price
Competition and Patent Term
Restoration Act of 1984 (Pub. L. 98–417)
(the 1984 amendments), which
authorized the approval of duplicate
versions of drug products under an
ANDA procedure. ANDA applicants
must, with certain exceptions, show that
the drug for which they are seeking
approval contains the same active
ingredient in the same strength and
dosage form as the ‘‘listed drug,’’ which
is a version of the drug that was
previously approved. ANDA applicants
do not have to repeat the extensive
clinical testing otherwise necessary to
gain approval of a new drug application
(NDA).
The 1984 amendments include what
is now section 505(j)(7) of the Federal
Food, Drug, and Cosmetic Act (21 U.S.C.
355(j)(7)), which requires FDA to
SUMMARY:
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
publish a list of all approved drugs.
FDA publishes this list as part of the
‘‘Approved Drug Products with
Therapeutic Equivalence Evaluations,’’
which is known generally as the
‘‘Orange Book.’’ Under FDA regulations,
drugs are removed from the list if the
Agency withdraws or suspends
approval of the drug’s NDA or ANDA
for reasons of safety or effectiveness or
if FDA determines that the listed drug
was withdrawn from sale for reasons of
safety or effectiveness (21 CFR 314.162).
A person may petition the Agency to
determine, or the Agency may
determine on its own initiative, whether
a listed drug was withdrawn from sale
for reasons of safety or effectiveness.
This determination may be made at any
time after the drug has been withdrawn
from sale, but must be made prior to
approving an ANDA that refers to the
listed drug (§ 314.161 (21 CFR 314.161)).
FDA may not approve an ANDA that
does not refer to a listed drug.
METADATE ER (methylphenidate
HCl) extended-release tablet, 10 mg, is
the subject of ANDA 40–306, held by
UCB, Inc., and initially approved on
October 20, 1999. METADATE ER is
indicated as an integral part of a total
treatment program which typically
includes other remedial measures
(psychological, educational, social) for a
stabilizing effect in children with a
behavioral syndrome characterized by
the following group of developmentally
inappropriate symptoms: Moderate-tosevere distractibility, short attention
span, hyperactivity, emotional lability,
and impulsivity.
In a letter dated November 4, 2011,
UCB, Inc., notified FDA that
METADATE ER (methylphenidate HCl)
extended-release tablet, 10 mg, had been
discontinued, and FDA moved the drug
product to the ‘‘Discontinued Drug
Product List’’ section of the Orange
Book.
Tedor Pharma Inc. submitted a citizen
petition dated March 6, 2013 (Docket
No. FDA–2013–P–0303), under 21 CFR
10.30, requesting that the Agency
determine whether METADATE ER
(methylphenidate HCl) extended-release
tablet, 10 mg, was withdrawn from sale
for reasons of safety or effectiveness.
After considering the citizen petition
and reviewing Agency records and
based on the information we have at this
time, FDA has determined under
§ 314.161 that METADATE ER
(methylphenidate HCl) extended-release
tablet, 10 mg, was not withdrawn for
reasons of safety or effectiveness. The
petitioner has identified no data or other
information suggesting that METADATE
ER (methylphenidate HCl) extendedrelease tablet, 10 mg, was withdrawn for
E:\FR\FM\05JYN1.SGM
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Agencies
[Federal Register Volume 78, Number 129 (Friday, July 5, 2013)]
[Notices]
[Pages 40482-40484]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-16085]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10171, CMS-10207, CMS-10476 and CMS-855(C)]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
[[Page 40483]]
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (PRA), federal agencies are required to 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 60 days for public comment on
the proposed action. Interested persons are invited to send comments
regarding our burden estimates 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 must be received by September 3, 2013.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number (OCN). To be assured consideration, comments and
recommendations must be submitted in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) that are accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number --------, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
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:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-10171 Coordination of Benefits Between Part D Plans and Other
Prescription Coverage Providers.
CMS-10207 Physician Self-Referral Exceptions for Electronic
Prescribing and Electronic Health Records.
CMS-10476 Medical Loss Ratio (MLR) Report for Medicare Advantage
(MA) Plans and Prescription Drug Plans (PDP).
CMS-855(C) Medicare Enrollment Application for Registration of
Eligible Entities That Provide Health Insurance Coverage Complementary
to Medicare Part B
Under the Paperwork Reduction Act (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 requires federal agencies to publish a 60-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.
Information Collections
1. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Coordination of
Benefits Between Part D Plans and Other Prescription Coverage
Providers; Use: We will use the information along with Part D plans,
other health insurers or payers, and pharmacies to coordinate
prescription drug benefits provided to the Medicare beneficiary. Form
Number: CMS-10171 (OCN: 0938-0978): Frequency: Occasionally; Affected
Public: Private sector--Business or other for-profits; Number of
Respondents: 57,116; Total Annual Responses: 2,402,582; Total Annual
Hours: 5,205,128. (For policy questions regarding this collection
contact Heather Rudo at 410-786-7627.)
2. Type of Information Collection Request: Reinstatement without
change of a previously approved collection; Title of Information
Collection: Physician Self-Referral Exceptions for Electronic
Prescribing and Electronic Health Records; Use: The collected
information would be used for enforcement purposes. Specifically, if we
were investigating the financial relationships between donors and
physicians to determine whether the provisions in the exceptions at 42
CFR 411.357(v) and (w) were met, first, we would review the written
agreements that indicate what items and services each entity intended
to provide. Form Number: CMS-10207 (OCN: 0938-1009); Frequency:
Monthly; Affected Public: Private sector--Business or other for-profits
and Not-for-profit institutions; Number of Respondents: 9,409; Total
Annual Responses: 17,744; Total Annual Hours: 1,896. (For policy
questions regarding this collection contact Michael Zleit at 410-786-
2050.)
3. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection: Medical
Loss Ratio (MLR) Report for Medicare Advantage (MA) Plans and
Prescription Drug Plans (PDP); Use: We will use the data collection of
annual reports provided by plan sponsors for each contract to ensure
that beneficiaries are receiving value for their premium dollar by
calculating each contract's medical loss ratio (MLR) and any
remittances due for the respective MLR reporting year. The
recordkeeping requirements will be used to determine plan sponsors'
compliance with the MLR requirements, including compliance with how
plan sponsors' experience is to be reported, and how their MLR and any
remittances are calculated. Form Number: CMS-10476 (OCN: 0938-New);
Frequency: Yearly; Affected Public: Private sector--Business or other
for-profits and Not-for-profit institutions; Number of Respondents:
616; Total Annual Responses: 616; Total Annual Hours: 28,980. (For
policy questions regarding this collection contact Ilina Chaudhuri at
410-786-8628.)
4. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection:
Medicare Enrollment Application for Registration of Eligible Entities
That Provide Health Insurance Coverage Complementary to Medicare Part
B; Use: The primary
[[Page 40484]]
function of a Medicare enrollment application is to gather information
from a provider, supplier or other entity that tells us who it is,
whether it meets certain qualifications to be a health care provider,
supplier or entity, where it practices or renders its services, the
identity of the owners of the enrolling entity, and information
necessary to establish correct claims payments. We are adding a new
CMS-855 Medicare Registration Application, the CMS-855C: Medicare
Enrollment Application for Registration of Eligible Entities That
Provide Health Insurance Coverage Complementary to Medicare Part B.
This Medicare registration application is to be completed by all
entities that provide a complimentary health benefit plan and intend to
bill Medicare as an indirect payment procedure (IPP) biller and the
entity or health plan meets all Medicare requirements to submit claims
for indirect payments. The entity must furnish the name of at least one
authorized official, preferably the administrator of the health plan,
who must sign this registration application attesting that the
registering entity meets the requirements to register as an indirect
payment procedure biller and will also abide by the requirements stated
in the Certification & Attestation Statement in Section 10 of the
application.
The CMS-855C will be submitted at the time the applicant first
requests a Medicare identification number for the sole purpose of
submitting claims under the ``Indirect Payment Procedure (IPP)'' for
reimbursement, and when necessary to report any changes to information
previously submitted. The application will be used by Medicare
contractors to collect data to ensure the applicant has the necessary
credentials to submit Medicare claims for reimbursement, including
information that allows Medicare contractors to ensure that the entity
and its owners and administrators are not sanctioned from the Medicare
program, or debarred, suspended or excluded from any other Federal
agency or program. Form Number: CMS-855(C) (OCN: 0938-New); Frequency:
Occasionally; Affected Public: Private sector--Business or other for-
profits and Not-for-profit institutions; Number of Respondents: 440;
Total Annual Responses: 440; Total Annual Hours: 500. (For policy
questions regarding this collection contact Kim McPhillips at 410-786-
5374.)
Dated: June 28, 2013.
Martique Jones,
Deputy Director, Regulations Development Group, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2013-16085 Filed 7-3-13; 8:45 am]
BILLING CODE 4120-01-P