Agency Information Collection Activities: Submission for OMB Review; Comment Request, 60843-60845 [2011-25271]
Download as PDF
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Federal Register / Vol. 76, No. 190 / Friday, September 30, 2011 / Notices
the popHealth system related to
meaningful use measures; and/or target
patients with high disease burden in
need of early intervention.
Eligibility Rules for Participating in
the Competition: To be eligible to win
a prize under this challenge, an
individual or entity:
(1) Shall have registered to participate
in the competition under the rules
promulgated by Office of the National
Coordinator for Health Information
Technology;
(2) Shall have complied with all the
requirements under this section;
(3) In the case of a private entity, shall
be incorporated in and maintain a
primary place of business in the United
States, and in the case of an individual,
whether participating singly or in a
group, shall be a citizen or permanent
resident of the United States; and
(4) May not be a Federal entity or
Federal employee acting within the
scope of their employment.
An individual or entity shall not be
deemed ineligible because the
individual or entity used Federal
facilities or consulted with Federal
employees during a competition if the
facilities and employees are made
available to all individuals and entities
participating in the competition on an
equitable basis.
Registered participants shall be
required to agree to assume any and all
risks and waive claims against the
Federal Government and its related
entities, except in the case of willful
misconduct, for any injury, death,
damage, or loss of property, revenue, or
profits, whether direct, indirect, or
consequential, arising from their
participation in a competition, whether
the injury, death, damage, or loss arises
through negligence or otherwise.
Participants shall be required to
obtain liability insurance or
demonstrate financial responsibility, in
amounts determined by the head of the
Office of the National Coordinator for
Health Information Technology, for
claims by—
(1) A third party for death, bodily
injury, or property damage, or loss
resulting from an activity carried out in
connection with participation in a
competition, with the Federal
Government named as an additional
insured under the registered
participant’s insurance policy and
registered participants agreeing to
indemnify the Federal Government
against third party claims for damages
arising from or related to competition
activities; and
(2) the Federal Government for
damage or loss to Government property
resulting from such an activity.
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Participants must be teams of at least
two people.
All participants are required to
provide written consent to the rules
upon or before submitting an entry.
DATES:
• Submission Period Begins: 12:01
a.m., EDT, September 26, 2011.
• Submission Period Ends: 11:59
p.m., EDT, February 3, 2012.
Registration Process for Participants:
To register for this challenge
participants should:
• Access the https://
www.challenge.gov Web site and search
for the ‘‘popHealth Tools Development
Challenge’’.
• Access the ONC Investing in
Innovation (i2) Challenge Web site at:
Æ https://www.health2challenge.org/
category/onc/.
Æ A registration link for the challenge
can be found on the landing page under
the challenge description.
Amount of the Prize:
• First Prize: $75,000.
• Second Prize: $20,000.
• Third Prize: $5,000.
Awards may be subject to Federal
income taxes and HHS will comply with
IRS withholding and reporting
requirements, where applicable.
Basis Upon Which Winner Will Be
Selected:
The judging panel will make
selections based upon the following
criteria:
1. Ability to integrate with popHealth
system and build upon existing
functionality.
2. Impact on stakeholders.
3. Usability and design.
4. Creativity and Innovation.
Additional Information:
Ownership of intellectual property is
determined by the following:
• Each entrant retains title and full
ownership in and to their submission.
Entrants expressly reserve all
intellectual property rights not
expressly granted under the challenge
agreement.
• By participating in the challenge,
each entrant hereby irrevocably grants
to Sponsor and Administrator a limited,
non-exclusive, royalty free, worldwide,
license and right to reproduce,
publically perform, publically display,
and use the Submission to the extent
necessary to administer the challenge,
and to publically perform and
publically display the Submission,
including, without limitation, for
advertising and promotional purposes
relating to the challenge.
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60843
Dated: September 26, 2011.
Farzad Mostashari,
National Coordinator for Health Information
Technology.
[FR Doc. 2011–25295 Filed 9–29–11; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–9042, CMS–
10374, CMS–10385, CMS–10402 and CMS–
10396]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
and Human Services, is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this 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 function;
(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.
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Accelerated
Payments and Supporting Regulations
42 CFR, Section 412.116(f), 412.632(e),
413.64(g), 413.350(d), and 484.245; Use:
This information is used by the
contractor to determine the provider’s
eligibility for accelerated payments. If
this information were not furnished
with an accelerated payment request,
the contractor would not be able to
assess whether the provider’s financial
difficulties justified the accelerated
payment; Form Number: CMS–9042
(OMB # 0938–0269); Frequency: Yearly;
Affected Public: Private Sector; Business
or other for-profit and not-for-profit
institutions; Number of Respondents:
37,804; Total Annual Responses: 945;
Total Annual Hours: 473. (For policy
AGENCY:
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60844
Federal Register / Vol. 76, No. 190 / Friday, September 30, 2011 / Notices
questions regarding this collection
contact Leonard Fisher at 410–786–4574
TTY. For all other issues call 410–786–
1326.)
2. Type of Information Collection
Request: New collection of information;
Title of Information Collection: Training
Needs Assessment, Evaluation/Survey—
Question Compilation; Use: The intent
of this information collection is to assist
in the creation and enhancement of
training for Federal and State health
care surveyors and certification
specialists. The purpose of the
collection is to gather information for
training needs assessment, training
analysis, related demographic,
psychographics and technographics to
support the development and
enhancement of training and training
aids; Form Number: CMS–10374 (OMB
# 0938–New); Frequency: Half-year (2
per year); Affected Public: State, Local,
or Tribal Governments; Number of
Respondents: 2,161; Total Annual
Responses: 4,322; Total Annual Hours:
1,430. (For policy questions regarding
this collection contact Etolia Biggs at
410–786–8664. For all other issues call
410–786–1326.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Expedited
Checklist: Medicaid Eligibility &
Enrollment Systems—Advance Planning
Document (E&E–APD); Use: Under
sections 1903(a)(3)(A)(i) and
1903(a)(3)(B) of the Social Security Act,
CMS has issued new standards and
conditions that must be met by States
for Medicaid technology investments
(including traditional claims processing
systems, as well as eligibility systems)
to be eligible for enhanced match
funding. The Checklist will be
submitted by States to the E&E APD
National Coordinator for review and
coordination in the Eligibility/
Enrollment Systems APD approval
assignment. The information requested
on the Checklist will be used to
determine and approve enhanced FFP to
States and to determine how States are
complying with the seven standards and
conditions; Form Number: CMS–10385
(OMB#: 0938–1125); Frequency:
Occasionally; Affected Public: State,
Local, or Tribal Governments; Number
of Respondents: 56; Total Annual
Responses: 168; Total Annual Hours:
204. (For policy questions regarding this
collection contact Richard Friedman at
410–786–4451. For all other issues call
410–786–1326.)
4. Type of Information Collection
Request: New collection; Title of
Information Collection: Medicaid State
Plan Preprint for Use by States When
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Implementing Section 6401 of the
Patient Protection and Affordable Care
Act under the Medicaid Program; Use:
The Secretary, in consultation with the
Department of Health of Human
Services’ Office of the Inspector
General, is required to establish
procedures under which screening is
conducted with respect to providers of
medical or other items or services and
suppliers under Medicare, Medicaid,
and CHIP. The Secretary is also required
to impose a fee on each institutional
provider of medical or other items or
services or supplier that would be used
by the Secretary for program integrity
efforts. States are required to comply
with the process of screening providers
and suppliers as established by the
Secretary under 1866(j)(2) of the
Affordable Care Act. The Office of
General Counsel through guidance, is
requiring that States use the Medicaid
State Plan Preprint to assure CMS
compliance with the law. CMS will use
the information to review and approve
the State plan. States would refer to the
State plan on an as needed basis to
manage and operate their Medicaid
programs under Title XIX of the Social
Security Act; Form Number: CMS–
10402 (OMB # 0938–New); Frequency:
Once; Affected Public: State, Local, or
Tribal Governments; Number of
Respondents: 56; Total Annual
Responses: 56; Total Annual Hours: 14.
(For policy questions regarding this
collection contact Richard Friedman. at
410–786–4451. For all other issues call
410–786–1326.)
5. Type of Information Collection
Request: New collection; Title of
Information Collection: Medication
Therapy Management Program
Improvements—Standardized Format.
Use: The Medicare Modernization Act
of 2003 (MMA) under title 42 CFR Part
423, Subpart D, established the
requirements that Part D sponsors must
meet with regard to medication therapy
management (MTM) programs.
Beginning in 2010, sponsors must offer
an interactive, person-to-person
comprehensive medication review
(CMR) by a pharmacist or other
qualified provider at least annually. A
CMR is a review of a beneficiary’s
medications, including prescription and
over-the-counter (OTC) medications,
herbal therapies, and dietary
supplements, which is intended to aid
in assessing medication therapy and
optimizing patient outcomes. Sponsors
must summarize the CMR and provide
an individualized written or printed
summary to the beneficiary. The burden
associated with the time and effort
necessary for Part D sponsors to conduct
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
CMRs with written summaries was
estimated previously under OMB
Control Number 0938–0964 as 937,500
hours with total labor cost of $112.5
million.
The Affordable Care Act (ACA) under
Section 10328 specifies that the
Secretary, in consultation with relevant
stakeholders, develop a standardized
format for the action plan and written or
printed summary that are given to
beneficiaries as a result of their CMRs.
The standardized format will replace
whatever formats Part D sponsors are
using for their written CMR summaries
and action plans prior to 2013.
Beginning in January, 2013, Part D
sponsors will collect information
required by the new standardized
format, and provide that information to
Medicare beneficiaries after their CMRs
on forms that comply with the
requirements specified by CMS for the
standardized format. The use of the
standardized format will increase the
burden associated with providing the
CMRs with written summaries and
action plans as described in this
submission. The use of the standardized
format will support a uniform and
consistent level of MTMP
communications with beneficiaries,
improve the ability of beneficiaries to
understand and manage their
medications safely and effectively, and
support improved healthcare outcomes
and lower overall healthcare costs. The
final standardized format will be posted
in the 2013 Call Letter for
implementation by Part D sponsors in
January 2013. Form Number: CMS–
10396 (OCN: 0938–New); Frequency:
Yearly; Affected Public: Private Sector—
Business or other For-profits; Number of
Respondents: 673; Number of
Responses: 1,875,000; Total Annual
Hours: 1,179,894. (For policy questions
regarding this collection, contact Gary
Wirth at 410–786–3997. For all other
issues call (410) 786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS Web Site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
To be assured consideration,
comments for the proposed information
collections must be received by the
OMB desk officer at the address below,
no later than 5 p.m. on October 31,
2011.
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OMB, Office of Information and
Regulatory Affairs, Attention: CMS
Desk Officer, Fax Number: (202) 395–
6974, E-mail:
OIRA_submission@omb.eop.gov.
Dated: September 27, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–25271 Filed 9–29–11; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10241, CMS–
10412, CMS–R–263, CMS–R–262, CMS–
10142 and CMS–855(O)]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this 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.
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Survey of Retail
Prices: Payment and Utilization Rates,
and Performance Rankings; Use: CMS
will develop a National Average Drug
Acquisition Cost (NADAC) for States to
consider when developing
reimbursement methodology. The
NADAC is a new pricing benchmark
that will be based on the national
average costs that pharmacies pay to
acquire Medicaid covered outpatient
drugs. It is intended to provide States
with a more accurate reference price to
base reimbursement for prescription
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drugs and will be based on drug
acquisition costs collected directly from
pharmacies through a nationwide
survey process. This survey will be
conducted on a monthly basis to ensure
that the NADAC reference file remains
current and up-to-date. A NADAC
Survey Request for Information has been
developed to send to random
pharmacies for voluntary completion.
CMS proposes to add the survey to an
existing collection, ‘‘Annual State
Report and Annual State Performance
Rankings.’’ The requirements and
burden associated with the annual
report/rankings are unaffected by this
proposed action; Form Number: CMS–
10241 (OCN: 0938–1041); Frequency:
Biennially, Once; Affected Public:
Private Sector; Business or other forprofits; Number of Respondents: 30,000;
Total Annual Responses: 30,000; Total
Annual Hours: 15,000. (For policy
questions regarding this collection
contact Lisa Ferrandi at 410–786–5445.
For all other issues call 410–786–1326.)
2. Type of Information Collection
Request: New collection; Title of
Information Collection: Section 1115
Demonstration: Long Term Services and
Supports and Other Service Models for
Individuals with Disabilities and
Chronic Conditions; Use: Section 1115
of the Social Security Act provides the
Secretary of Health and Human Services
broad authority to authorize
experimental, pilot, or demonstration
projects likely to assist in promoting the
objectives of the Medicaid statute.
Flexibility under Section 1115 is
sufficiently broad to allow states to test
substantially new ideas of policy merit.
States seeking interventions for
individuals needing LTSS to lower
costs, improve care and improve health
can utilize the 1115 demonstration to
test and deliver innovative services and
approaches to better and more
efficiently meet the needs of this
population. Section 1115
demonstrations provide a vehicle for
innovations in both care delivery and
payment methodologies.
Demonstrations must be ‘‘budget
neutral’’ over the life of the project,
meaning they cannot be expected to cost
the Federal government more than it
would cost without the waiver. State
Medicaid agencies are responsible for
developing section 1115 demonstration
applications and submitting them to
CMS; Form Number: CMS–10412 (OCN:
0938–New); Frequency: Once; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
56; Total Annual Responses: 56; Total
Annual Hours: 2,240. (For policy
questions regarding this collection
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
60845
contact Adrienne Delozer at 410–786–
0278. For all other issues call 410–786–
1326.)
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Site
Investigation for Durable Medical
Equipment (DME) Suppliers; Use: CMS
is mandated to identify and implement
measures to prevent fraud and abuse in
the Medicare program. To meet this
challenge, CMS has moved forward to
improve the quality of the process for
enrolling suppliers into the Medicare
program by establishing a uniform
application for enumerating suppliers of
durable medical equipment, prosthetics,
orthotics, and supplies (DMEPOS).
Implementation of enhanced procedures
for verifying the enrollment information
has also improved the enrollment
process. As part of this process,
verification of compliance with supplier
standards is necessary. The site
investigation form has been used in the
past to aid the Medicare contractor (the
National Supplier Clearinghouse and/or
its subcontractors) in verifying
compliance with the required supplier
standards found in 42 CFR 424.57(c).
The primary function of the site
investigation form is to provide a
standardized, uniform tool to gather
information from a DMEPOS supplier
that tells us whether it meets certain
qualifications to be a DMEPOS supplier
(as found in 42 CFR 424.57(c)) and
where it practices or renders its
services.
This site investigation form collects
the same information as its predecessor,
with the exception of one new yes/no
question under the ‘‘Records and
Telephone’’ section (question 11(a))
used to verify if the DMEPOS supplier
maintains physician ordering/referring
records for the supplies and/or services
it renders to Medicare beneficiaries (if
applicable). This information is required
by Section 1833(q) of the Social Security
Act which states that all physicians and
non-physician practitioners that meet
the definitions at section 1861(r) and
1842(b)(18)(C) be uniquely identified for
all claims for services that are ordered
or referred. Other information collected
on this site investigation remains
unchanged, but has been reformatted for
greater functionality. Form Number:
CMS–R–263 (OCN: 0938–0749);
Frequency: Once; Affected Public:
Private Sector—Business or other forprofits and not-for-profit institutions;
Number of Respondents: 30,000; Total
Annual Responses: 30,000; Total
Annual Hours: 15,000. (For policy
questions regarding this collection
contact Kimberly McPhillips at 410–
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Agencies
[Federal Register Volume 76, Number 190 (Friday, September 30, 2011)]
[Notices]
[Pages 60843-60845]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-25271]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-9042, CMS-10374, CMS-10385, CMS-10402 and
CMS-10396]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS), Department of Health and Human Services, is publishing
the following summary of proposed collections for public comment.
Interested persons are invited to send comments regarding this 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 function; (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.
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Accelerated
Payments and Supporting Regulations 42 CFR, Section 412.116(f),
412.632(e), 413.64(g), 413.350(d), and 484.245; Use: This information
is used by the contractor to determine the provider's eligibility for
accelerated payments. If this information were not furnished with an
accelerated payment request, the contractor would not be able to assess
whether the provider's financial difficulties justified the accelerated
payment; Form Number: CMS-9042 (OMB 0938-0269); Frequency:
Yearly; Affected Public: Private Sector; Business or other for-profit
and not-for-profit institutions; Number of Respondents: 37,804; Total
Annual Responses: 945; Total Annual Hours: 473. (For policy
[[Page 60844]]
questions regarding this collection contact Leonard Fisher at 410-786-
4574 TTY. For all other issues call 410-786-1326.)
2. Type of Information Collection Request: New collection of
information; Title of Information Collection: Training Needs
Assessment, Evaluation/Survey--Question Compilation; Use: The intent of
this information collection is to assist in the creation and
enhancement of training for Federal and State health care surveyors and
certification specialists. The purpose of the collection is to gather
information for training needs assessment, training analysis, related
demographic, psychographics and technographics to support the
development and enhancement of training and training aids; Form Number:
CMS-10374 (OMB 0938-New); Frequency: Half-year (2 per year);
Affected Public: State, Local, or Tribal Governments; Number of
Respondents: 2,161; Total Annual Responses: 4,322; Total Annual Hours:
1,430. (For policy questions regarding this collection contact Etolia
Biggs at 410-786-8664. For all other issues call 410-786-1326.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Expedited
Checklist: Medicaid Eligibility & Enrollment Systems--Advance Planning
Document (E&E-APD); Use: Under sections 1903(a)(3)(A)(i) and
1903(a)(3)(B) of the Social Security Act, CMS has issued new standards
and conditions that must be met by States for Medicaid technology
investments (including traditional claims processing systems, as well
as eligibility systems) to be eligible for enhanced match funding. The
Checklist will be submitted by States to the E&E APD National
Coordinator for review and coordination in the Eligibility/Enrollment
Systems APD approval assignment. The information requested on the
Checklist will be used to determine and approve enhanced FFP to States
and to determine how States are complying with the seven standards and
conditions; Form Number: CMS-10385 (OMB: 0938-1125);
Frequency: Occasionally; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 56; Total Annual Responses: 168;
Total Annual Hours: 204. (For policy questions regarding this
collection contact Richard Friedman at 410-786-4451. For all other
issues call 410-786-1326.)
4. Type of Information Collection Request: New collection; Title of
Information Collection: Medicaid State Plan Preprint for Use by States
When Implementing Section 6401 of the Patient Protection and Affordable
Care Act under the Medicaid Program; Use: The Secretary, in
consultation with the Department of Health of Human Services' Office of
the Inspector General, is required to establish procedures under which
screening is conducted with respect to providers of medical or other
items or services and suppliers under Medicare, Medicaid, and CHIP. The
Secretary is also required to impose a fee on each institutional
provider of medical or other items or services or supplier that would
be used by the Secretary for program integrity efforts. States are
required to comply with the process of screening providers and
suppliers as established by the Secretary under 1866(j)(2) of the
Affordable Care Act. The Office of General Counsel through guidance, is
requiring that States use the Medicaid State Plan Preprint to assure
CMS compliance with the law. CMS will use the information to review and
approve the State plan. States would refer to the State plan on an as
needed basis to manage and operate their Medicaid programs under Title
XIX of the Social Security Act; Form Number: CMS-10402 (OMB
0938-New); Frequency: Once; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 56; Total Annual Responses: 56;
Total Annual Hours: 14. (For policy questions regarding this collection
contact Richard Friedman. at 410-786-4451. For all other issues call
410-786-1326.)
5. Type of Information Collection Request: New collection; Title of
Information Collection: Medication Therapy Management Program
Improvements--Standardized Format. Use: The Medicare Modernization Act
of 2003 (MMA) under title 42 CFR Part 423, Subpart D, established the
requirements that Part D sponsors must meet with regard to medication
therapy management (MTM) programs. Beginning in 2010, sponsors must
offer an interactive, person-to-person comprehensive medication review
(CMR) by a pharmacist or other qualified provider at least annually. A
CMR is a review of a beneficiary's medications, including prescription
and over-the-counter (OTC) medications, herbal therapies, and dietary
supplements, which is intended to aid in assessing medication therapy
and optimizing patient outcomes. Sponsors must summarize the CMR and
provide an individualized written or printed summary to the
beneficiary. The burden associated with the time and effort necessary
for Part D sponsors to conduct CMRs with written summaries was
estimated previously under OMB Control Number 0938-0964 as 937,500
hours with total labor cost of $112.5 million.
The Affordable Care Act (ACA) under Section 10328 specifies that
the Secretary, in consultation with relevant stakeholders, develop a
standardized format for the action plan and written or printed summary
that are given to beneficiaries as a result of their CMRs. The
standardized format will replace whatever formats Part D sponsors are
using for their written CMR summaries and action plans prior to 2013.
Beginning in January, 2013, Part D sponsors will collect information
required by the new standardized format, and provide that information
to Medicare beneficiaries after their CMRs on forms that comply with
the requirements specified by CMS for the standardized format. The use
of the standardized format will increase the burden associated with
providing the CMRs with written summaries and action plans as described
in this submission. The use of the standardized format will support a
uniform and consistent level of MTMP communications with beneficiaries,
improve the ability of beneficiaries to understand and manage their
medications safely and effectively, and support improved healthcare
outcomes and lower overall healthcare costs. The final standardized
format will be posted in the 2013 Call Letter for implementation by
Part D sponsors in January 2013. Form Number: CMS-10396 (OCN: 0938-
New); Frequency: Yearly; Affected Public: Private Sector--Business or
other For-profits; Number of Respondents: 673; Number of Responses:
1,875,000; Total Annual Hours: 1,179,894. (For policy questions
regarding this collection, contact Gary Wirth at 410-786-3997. For all
other issues call (410) 786-1326.)
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS Web
Site address at https://www.cms.hhs.gov/PaperworkReductionActof1995, or
E-mail your request, including your address, phone number, OMB number,
and CMS document identifier, to Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786-1326.
To be assured consideration, comments for the proposed information
collections must be received by the OMB desk officer at the address
below, no later than 5 p.m. on October 31, 2011.
[[Page 60845]]
OMB, Office of Information and Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395-6974, E-mail: OIRA_submission@omb.eop.gov.
Dated: September 27, 2011.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2011-25271 Filed 9-29-11; 8:45 am]
BILLING CODE 4120-01-P