Privacy Act of 1974; Report of a New System of Records, 58007-58011 [2011-23959]
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Federal Register / Vol. 76, No. 181 / Monday, September 19, 2011 / Notices
subcommittee was established by
SACHRP in October 2006. SOH was
established by SACHRP at its July 2009
meeting, and is charged with identifying
and prioritizing areas in which
regulations and/or guidelines for human
subjects research adopted by various
agencies or offices within HHS would
benefit from harmonization,
consistency, clarity, simplification and/
or coordination.
Public Comment will be heard on
both days.
Public attendance at the meeting is
limited to space available. Individuals
who plan to attend the meeting and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the designated contact persons.
Members of the public will have the
opportunity to provide comments on
both days of the meeting. Public
comment will be limited to five minutes
per speaker. Any members of the public
who wish to have printed materials
distributed to SACHRP members for this
scheduled meeting should submit
materials to the Executive Director,
SACHRP, prior to the close of business
September 30, 2011.
Dated: September 13, 2011.
Jerry Menikoff,
Director, Office for Human Research
Protections, Executive Secretary, Secretary’s
Advisory Committee on Human Research
Protections.
[FR Doc. 2011–23863 Filed 9–16–11; 8:45 am]
BILLING CODE 4150–36–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the Advisory Group on
Prevention, Health Promotion, and
Integrative and Public Health
Department of Health and
Human Services, Office of the Secretary,
Office of the Assistant Secretary for
Health, Office of the Surgeon General of
the United States Public Health Service.
ACTION: Notice.
AGENCY:
In accordance with Section
10(a) of the Federal Advisory Committee
Act, Public Law 92–463, as amended (5
U.S.C. App.), notice is hereby given that
a meeting is scheduled to be held for the
Advisory Group on Prevention, Health
Promotion, and Integrative and Public
Health (the ‘‘Advisory Group’’). The
meeting will be open to the public.
Information about the Advisory Group
can be obtained by accessing the
following Web site: https://
www.healthcare.gov/center/councils/
nphpphc/.
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SUMMARY:
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The meeting will be held on
October 3–4, 2011.
ADDRESSES: Will be announced on the
Web site: https://www.healthcare.gov/
center/councils/nphpphc/.
FOR FURTHER INFORMATION CONTACT:
Office of the Surgeon General, 200
Independence Ave., SW.; Hubert H.
Humphrey Building, Room 701H;
Washington, DC 20001; 202–205–9517;
prevention.council@hhs.gov.
SUPPLEMENTARY INFORMATION: On June
10, 2010, the President issued Executive
Order 13544 to comply with the statutes
under Section 4001 of the Patient
Protection and Affordable Care Act,
Public Law 111–148. This legislation
mandated that the Advisory Group was
to be established within the Department
of Health and Human Services. The
charter for the Advisory Group was
established by the Secretary of Health
and Human Services on June 23, 2010;
the charter was filed with the
appropriate Congressional committees
and Library of Congress on June 24,
2010. The Advisory Group has been
established as a non-discretionary
Federal advisory committee.
The Advisory Group has been
established to provide recommendations
and advice to the National Prevention,
Health Promotion and Public Health
Council (the ‘‘Council’’). The Advisory
Group shall provide assistance to the
Council in carrying out its mission.
The Advisory Group membership
shall consist of not more than 25 nonFederal members to be appointed by the
President. The membership shall
include a diverse group of licensed
health professionals, including
integrative health practitioners who
have expertise in (1) worksite health
promotion; (2) community services,
including community health centers; (3)
preventive medicine; (4) health
coaching; (5) public health education;
(6) geriatrics; and (7) rehabilitation
medicine. There are currently 16
members of the Advisory Group
appointed by the President. This will be
the third meeting of the Advisory
Group.
Public attendance at the meeting is
limited to the space available. Members
of the public who wish to attend must
register by 12 p.m. EST September 26,
2011. Individuals should register for
public attendance at
prevention.council@hhs.gov by
providing your full name and affiliation.
Individuals who plan to attend the
meeting and need special assistance
and/or accommodations, i.e., sign
language interpretation or other
reasonable accommodations, should
notify the designated point of contact
DATES:
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for the Advisory Group. The public will
have the opportunity to provide
comments to the Advisory Group on
October 3, 2011; public comment will
be limited to 3 minutes per speaker.
Registration through the designated
contact for the public comment session
is also required. Any member of the
public who wishes to have printed
materials distributed to the Advisory
Group for this scheduled meeting
should submit material to the designed
point of contact no later than 12 p.m.
EST September 26, 2011.
Dated: September 8, 2011.
Corinne M. Graffunder,
Acting Designated Federal Officer, Advisory
Group on Prevention, Health Promotion, and
Integrative and Public Health Office of the
Surgeon General.
[FR Doc. 2011–23869 Filed 9–16–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
Privacy Act of 1974; Report of a New
System of Records
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
ACTION: Notice to establish a new system
of records.
AGENCY:
In accordance with the
requirements of the Privacy Act of 1974,
CMS is establishing a new system of
records to support its shared savings
programs, the first of which are the
Medicare Shared Savings Program and
Pioneer ACO Model (collectively
referred to as the ACO program). The
ACO program implements recent health
care reform provisions of the Patient
Protection and Affordable Care Act
(PPACA), amending the Social Security
Act (the Act). The system of records will
contain personally identifiable
information (PII) about certain
individuals who participate in, or
whose PII is used to determine
eligibility of an Accountable Care
Organization (ACO) to participate in, a
shared savings program; i.e., Medicare
fee-for-service (FFS) beneficiaries, sole
proprietor health care ACO participants
and ACO suppliers/providers, key
leaders and managers of accountable
care organizations (ACOs), and contact
persons for ACOs. The program and the
system of records are more thoroughly
described in the Supplementary
Information section and System of
Records Notice (SORN), below.
SUMMARY:
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Federal Register / Vol. 76, No. 181 / Monday, September 19, 2011 / Notices
CMS filed a new system report
with the Chair of the House Committee
on Government Reform and Oversight,
the Chair of the Senate Committee on
Homeland Security & Governmental
Affairs, and the Administrator, Office of
Information and Regulatory Affairs,
Office of Management and Budget
(OMB) on September 14, 2011. To
ensure that all parties have adequate
time in which to comment, the new
system, including routine uses, will
become effective October 19, 2011. If
CMS receives comments that require
alterations to this notice, we will
publish a revised notice in the Federal
Register.
ADDRESSES: The public should send
comments to: CMS Privacy Officer,
Division of Information Security &
Privacy Management, Enterprise
Architecture and Strategy Group, Office
of Information Services, CMS, Room
N1–24–08, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
Comments received will be available for
review at this location, by appointment,
during regular business hours, Monday
through Friday from 9 a.m.–3 p.m.,
Eastern Time zone.
FOR FURTHER INFORMATION CONTACT: For
Medicare Shared Savings Program:
Rebecca Weiss, Program Analyst,
Performance-Based Payment Policy
Staff, Center for Medicare, Centers for
Medicare & Medicaid Services, 7500
Security Boulevard, Mail-stop: C5–15–
12, Baltimore, MD 21244–1850. Office:
410–786–8084, Facsimile: (410) 786–
8005, E-mail address: aco@cms.hhs.gov.
For Pioneer Aco Model: Alli Chandra,
Health Insurance Specialist, Center for
Medicare and Medicaid Innovation,
Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Mailstop: S3–13–05, Baltimore, MD
21244–1850. Office Ph: 410–786–1132,
Facsimile: (410) 786–0487, E-mail
address: alli.chandra@cms.hhs.gov.
SUPPLEMENTARY INFORMATION: This
System of Records Notice (SORN)
addresses a new system which HHS is
establishing to support CMS shared
savings programs created as a result of
the Patient Protection and Affordable
Care Act (Pub. L. 111–148), the first of
which are the Medicare Shared Savings
Program and Pioneer ACO Model (ACO
program) described in more detail
below.
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DATES:
I. Medicare Shared Savings Program
The recently passed health care
reform bill, the Affordable Care Act
(PPACA) (Pub. L. 111–148), contains
provisions that seek to reward quality
care and takes steps toward paying for
high quality and efficient care. One of
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these provisions, Section 3022,
amended Title XVIII of the Social
Security Act (the Act) (42 U.S.C. 1395
et seq.) by adding new section 1899 to
the Act to establish a shared savings
program (SSP) that promotes
accountability for a patient population,
coordinates items and services under
Parts A and B, and encourages
investment in infrastructure and
redesigned care processes for high
quality and efficient service delivery.
Specifically:
• Section 1899(a)(1) of the Act
requires the Secretary to establish the
shared savings program no later than
January 1, 2012. Section 1899(a)(1) (A)
of the Act further provides that, ‘‘groups
of providers of services and suppliers
meeting criteria specified by the
Secretary may work together to manage
and coordinate care for Medicare feefor-service (FFS) beneficiaries through
an accountable care organization
(ACO).’’
• Section 1899(a)(1)(B) of the Act
provides that ACOs that meet quality
performance standards established by
the Secretary are eligible to receive
payments for ‘‘shared savings.’’
The Shared Savings Program is a
voluntary program. The statute provides
that, to participate in the program, an
ACO must ‘‘provide the Secretary with
such information regarding the ACO
professionals participating in the ACO
as the Secretary determines necessary to
support the assignment of Medicare feefor-service beneficiaries to an ACO, the
implementation of quality and other
reporting requirements * * * and the
determination of payments for shared
savings.’’ The statute requires an ACO to
meet certain eligibility criteria
including, but not limited to, having ‘‘a
formal legal structure that would allow
the organization to receive and
distribute payments for shared savings,’’
having ‘‘in place a leadership and
management structure that includes
clinical and administrative systems,’’
and demonstrating ‘‘to the Secretary that
it meets patient-centeredness criteria
specific by the Secretary.’’ In addition,
the ACO must agree to participate for
not less than 3 years, have a formal legal
structure including primary care
providers sufficient for the care of not
less than 5000 beneficiaries, and meet
others requirements.
The statute defines an ACO as
organization of health care providers
that agrees to become accountable for
the quality, cost, and overall care of
Medicare beneficiaries who are enrolled
in the traditional fee-for-service program
who are assigned to it. The statute states
that there are many types of
organizational arrangements for
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eligibility to become an ACO, as
determined appropriate by the
Secretary.
To qualify for shared savings
payments, the ACO must meet specific
cost and quality benchmarks. Quality
performance standards will be
determined by the Secretary and may
include measures of clinical processes
and outcomes, patient and/or caregiver
experience, and utilization measures.
An ACO will be eligible to receive a
share (a percentage, and any limits, to
be determined by the Secretary) of any
savings if the actual per capita
expenditures of its assigned Medicare
beneficiaries are a sufficient percentage
below its specified benchmark amount.
The benchmark for each ACO will be
based on the most recent available three
years of per-beneficiary expenditures for
Parts A and B services for Medicare FFS
beneficiaries assigned to the ACO. The
benchmark for each ACO will be
adjusted for beneficiary characteristics
and other factors as determined by the
Secretary, and updated by the projected
absolute amount of growth in national
per capita expenditures for Parts A and
B.
II. Pioneer ACO Model
Another provision of the Affordable
Care Act (PPACA), Section 3021,
amended Title XVIII of the Social
Security Act (the Act) (42 U.S.C. 1395
et seq.) by adding new section 1899 to
the Act to establish the Center for
Medicare and Medicaid Innovation
(Innovation Center). The Innovation
Center is tasked with development of
the Pioneer ACO Model. Under the
Pioneer ACO Model, the Innovation
Center will engage up to 30 highly
experienced provider organizations in
testing alternative payment models that
include escalating financial
accountability and substantial quality/
patient experience standards
(‘‘outcomes based arrangements’’). CMS
intends to pursue payment models that
(1) include escalating levels of financial
accountability through successive
performance periods during the
Participation Agreement; (2) provide a
transition to Population-Based Payment
by the third performance period, and (3)
are projected by CMS to generate
Medicare savings by the end of the
second performance period.
III. The Privacy Act
The Privacy Act (5 U.S.C. 552a)
governs the means by which the United
States Government collects, maintains,
and uses personally identifiable
information (PII) in a system of records.
A ‘‘system of records’’ is a group of any
records under the control of a Federal
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agency from which information about
individuals is retrieved by name or
other personal identifier. The Privacy
Act requires each agency to publish in
the Federal Register a system of records
notice (SORN) identifying and
describing each system of records the
agency maintains, including the
purposes for which the agency uses PII
in the system, the routine uses for
which the agency discloses such
information outside the agency, and
how individual record subjects can
exercise their rights under the Privacy
Act (e.g., to determine if the system
contains information about them).
The Privacy Act permits an agency to
disclose information about an
individual (PII) without that
individual’s consent if the information
is to be used for a purpose that is
compatible with the purpose(s) for
which the information was collected.
Any such disclosure of PII is known as
a ‘‘routine use.’’ HHS/CMS will only
release PII from this system as provided
in the ‘‘Routine Uses’’ section below.
Both identifiable and non-identifiable
data may be disclosed under a routine
use. HHS/CMS will only disclose the
minimum PII necessary to achieve the
purpose of the routine use, after
determining that:
• The use or disclosure is consistent
with the reason that the PII was
collected;
• The purpose for which the
disclosure is to be made can only be
accomplished if the record is provided
in individually identifiable form;
• The purpose for which the
disclosure is to be made is of sufficient
importance to warrant the effect on and/
or risk to the privacy of the individual
that additional exposure of the record
might bring;
• There is a strong probability that
the proposed use of the data would in
fact accomplish the stated purpose(s);
and
• The data are valid and reliable.
Additionally, HHS/CMS will require
the information recipient to:
• Establish administrative, technical,
and physical safeguards to prevent
unauthorized use or disclosure of the
record;
• Remove or destroy at the earliest
time all individually-identifiable
information; and
• Agree to not use or disclose the
information for any purpose other than
the stated purpose under which the
information was disclosed.
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SYSTEM NUMBER:
09–70–0598
SYSTEM NAME:
ACO Database System HHS/CMS/CM
and HHS/CMS/CMMI.
SECURITY CLASSIFICATION:
Sensitive, unclassified.
SYSTEM LOCATION:
CMS Data Center, 7500 Security
Boulevard, North Building, First Floor,
Baltimore, Maryland 21244–1850 and at
various accountable care organization
(ACO) locations and contractor sites.
CATEGORIES OF INDIVIDUALS COVERED BY THE
SYSTEM:
The system will contain personally
identifiable information (PII) about the
following categories of individuals who
participate in, or whose PII is used to
determine eligibility of an ACO to
participate in, a Health and Human
Services (HHS) Centers for Medicare &
Medicaid Services (CMS) Medicare
shared savings program:
• Medicare fee-for-service (FFS)
beneficiaries who receive health care
services coordinated and managed by a
group of health care providers and
suppliers organized to receive shared
savings incentive payments, as an
accountable care organization (ACO).
• Any providers or suppliers
participating in an ACO who are sole
proprietorships, for whom certain
business-identifying information may
therefore constitute personally
identifiable information.
• Key leaders and managers of an
ACO who provide certain personally
identifiable information that is used to
determine the ACO’s eligibility to
participate in the program.
• Any contact persons for an ACO
who provide contact information for use
in contacting them for information
about the ACO.
CATEGORIES OF RECORDS IN THE SYSTEM:
This system may include, but will not
necessarily be limited to, the following
categories of records, containing PII (or
possible PII) data elements such as the
following:
• Medicare fee-for-service (FFS)
beneficiary claims records, containing
the beneficiary’s name, gender, Health
Insurance Claim Number (HICN) (which
could be the beneficiary’s Social
Security Number), address, date of birth
and description of provided services.
• ACO eligibility and contact records,
containing the ACO name and address
(which could be the home address of a
key leader or manager of the ACO); ACO
participant or ACO provider/supplier
names and addresses (which could
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include home addresses for any sole
proprietor providers/suppliers in the
ACO); ACO participant Tax
Identification Number (TIN) (which
could be a Social Security Number for
a sole proprietor ACO participant or
ACO provider/supplier in the ACO);
National Provider Identifier (NPI)
(which is considered PII for an
individual provider/supplier); and (for
individuals serving as key leaders or
managers of an ACO) the individual’s
name and address (which could be a
home address).
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
The Patient Protection and Affordable
Care Act (Pub. L. 111–148), which
amended Title XVIII of the Social
Security Act (the Act) (42 U.S.C. 1395
et seq.) to add new section 1899 to the
Act to establish a Medicare Shared
Savings Program (MSSP); and Section
3021 of the Patient Protection and
Affordable Care Act, which amended
Title XI of the Social Security Act (the
Act) (42 U.S.C. 1301 et seq.) to add new
section 1115A to the Act to establish the
Center for Medicare and Medicaid
Innovation.
PURPOSE(S) OF THE SYSTEM:
The system will enable the HHS
Centers for Medicare & Medicaid
Services (CMS) to administer the ACO
program. Relevant HHS personnel, and
any CMS contractors, grantees and
consultants assisting them, will use
personally identifiable information (PII)
from this system on a ‘‘need to know’’
basis for these purposes:
• Beneficiary claims information and
ACO eligibility and contact information
will be used to support the regulatory,
reimbursement and policy functions of
shared savings programs and to combat
fraud, waste and abuse in certain health
benefits programs.
ROUTINE USES OF RECORDS MAINTAINED IN THE
SYSTEM, INCLUDING CATEGORIES OR USERS AND
THE PURPOSES OF SUCH USES:
Any of the PII from this system may
be disclosed outside HHS for these
routine uses:
1. To obtain assistance from other
Federal agencies that help HHS,
pursuant to agreements with CMS, to
determine the eligibility of ACO
applicants to participate in the program.
For example, a TIN (which may be a
Social Security Number) may be shared
with the U.S. Federal Trade
Commission (FTC) and the U.S.
Department of Justice (DOJ) for purposes
of obtaining their assessment of the
ACO applicant’s market share status.
2. To provide ACOs with information
they need to meet requirements and
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implement quality and other reporting
requirements of the program.
3. To provide information to the U.S.
Department of Justice (DOJ), a court, or
an adjudicatory body when (a) the
Agency or any component thereof, or (b)
any employee of the Agency in his or
her official capacity, or (c) any
employee of the Agency in his or her
individual capacity where the DOJ has
agreed to represent the employee, or (d)
the United State Government, is a party
to litigation or has an interest in such
litigation, and by careful review, CMS
determines that the records are both
relevant and necessary to the litigation
and that the use of such records by the
DOJ, court, or adjudicatory body is
compatible with the purpose for which
the agency collected the records.
4. To assist another Federal agency or
an instrumentality of any governmental
jurisdiction within or under the control
of the United States (including any state
or local governmental agency), that
administers or that has the authority to
investigate potential fraud, waste or
abuse in a health benefits program
funded in whole or in part by Federal
funds, when disclosure is deemed
reasonably necessary by CMS to
prevent, deter, discover, detect,
investigate, examine, prosecute, sue
with respect to, defend against, correct,
remedy, or otherwise combat fraud,
waste or abuse in such programs.
5. To assist appropriate Federal
agencies and HHS contractors that have
a need to know the information for the
purpose of assisting HHS’s efforts to
respond to a suspected or confirmed
breach of the security or confidentiality
of information maintained in this
system of records, provided that the
information disclosed is relevant and
necessary for that assistance.
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ADDITIONAL CIRCUMSTANCES AFFECTING
DISCLOSURE OF PII ABOUT BENEFICIARIES:
To the extent that the beneficiary
claims records in this system contain
Protected Health Information (PHI) as
defined by HHS regulation ‘‘Standards
for Privacy of Individually Identifiable
Health Information’’ (45 CFR parts 160
and 164, subparts A and E), disclosures
of such PHI that are otherwise
authorized by these routine uses may
only be made if, and as, permitted or
required by the ‘‘Standards for Privacy
of Individually Identifiable Health
Information’’ (see 45 CFR 164–512 (a)
(1)). In addition, HHS policy will be to
prohibit release even of data not directly
identifiable with a particular
beneficiary, except pursuant to one of
the routine uses or if required by law,
if HHS determines there is a possibility
that a particular beneficiary can be
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identified through implicit deduction
based on small cell sizes (instances
where the patient population is so small
that individuals could, because of the
small size, use this information to
deduce the identity of a particular
beneficiary).
POLICIES AND PRACTICES FOR STORING,
RETRIEVING, ACCESSING, RETAINING, AND
DISPOSING OF RECORDS IN THE SYSTEM—
STORAGE:
Electronic records will be stored on
both tape cartridges (magnetic storage
media) and in a in a DB2 and/or Oracle
relational database management
environment (DASD data storage
media). Any hard copies of ACO
program-related records containing PII
at HHS/CMS, ACO and contractor
locations will be kept in hard-copy file
folders locked in secure file cabinets
during non-duty hours.
RETRIEVABILITY:
Information may be retrieved by any
of these personal identifiers: ACO
participant TIN (which could be a sole
proprietor provider/supplier’s Social
Security Number), National Provider
Identifier (NPI), or beneficiary Health
Insurance Claim Number (HICN))
(which may be the beneficiary’s Social
Security Number).
SAFEGUARDS:
Personnel having access to the system
have been trained in the Privacy Act
and information security requirements.
Employees who maintain records in this
system are instructed not to release data
until the intended recipient agrees to
implement appropriate management,
operational and technical safeguards
sufficient to protect the confidentiality,
integrity and availability of the
information and information systems
and to prevent unauthorized access.
Access to records in the ACO
Database System will be limited to CMS
personnel, and any contractors, grantees
and consultants assisting them, through
password security, encryption,
firewalls, and secured operating system.
Future system enhancements may
allow for ACOs, ACO participants or
ACO provider/suppliers, and
beneficiaries to be external users of the
system, for purposes of viewing and
inputting their records in this system.
Access controls will ensure that each
external user is restricted to viewing
only the user’s own records, not records
pertaining to other users.
Any electronic or hard copies of ACO
program-related records containing PII
at HHS/CMS, an ACO, and any
contractor, grantee or consultant
locations will be kept in secure
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electronic files or in hard-copy file
folders locked in secure file cabinets
during non-duty hours.
RETENTION AND DISPOSAL:
Records containing PII will be
maintained for a period of up to 10
years after entry in the database. Any
records that are needed longer, such as
to resolve claims and audit exceptions
or to prosecute fraud, will be retained
until such matters are resolved.
Beneficiary claims records are currently
subject to a document preservation
order and will be preserved indefinitely
pending further notice from the U.S.
Department of Justice.
SYSTEM MANAGER AND ADDRESS:
Director, Performance-Based Payment
Policy Staff, Center for Medicare,
Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Mailstop: C5–15–12, Baltimore, MD
21244–1850; and
Director, Pioneer ACO Model, Center
for Medicare and Medicaid Innovation,
Centers for Medicare and Medicaid
Services, Mailstop: S3–13–05, 7500
Security Boulevard, Baltimore, MD
21244–1850.
NOTIFICATION PROCEDURE:
Individuals wishing to know if this
system contains records about them
should write to one of the system
managers and include the pertinent
personal identifier used for retrieval of
their records (i.e., TIN, NPI or
beneficiary Health Insurance Claim
Number).
RECORD ACCESS PROCEDURE:
Individuals seeking access to records
about them in this system should follow
the same instructions indicated under
‘‘Notification Procedure’’ and
reasonably specify the record contents
being sought. (These procedures are in
accordance with Department regulation
45 CFR 5b.5 (a)(2).)
CONTESTING RECORD PROCEDURES:
Individuals seeking to contest the
content of information about them in
this system should follow the same
instructions indicated under
‘‘Notification Procedure.’’ The request
should reasonably identify the record
and specify the information being
contested, state the corrective action
sought, and provide the reasons for the
correction, with supporting justification.
(These procedures are in accordance
with Department regulation 45 CFR
5b.7.)
RECORD SOURCE CATEGORIES:
Personally identifiable information in
this database is obtained from the
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Medicare Beneficiary Database (MBD)
(09–70–0536), from the National Claims
History File (NCH) (09–70–0558), and
from ACOs that provide the information
as required to perform the statutory
functions of beneficiary assignment,
implementation of quality and other
reporting requirements, and
determination of shared savings.
EXEMPTIONS CLAIMED FOR THIS SYSTEM:
None.
Dated: September 14, 2011.
Michelle Snyder,
Deputy Chief Operating Officer, Centers for
Medicare & Medicaid Services.
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HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0465]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Experimental
Study: Effect of Promotional Offers in
Direct-to-Consumer Prescription Drug
Print Advertisements on Consumer
Product Perceptions
Food and Drug Administration,
HHS.
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.
DATES: Fax written comments on the
collection of information by October 19,
2011.
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 e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–New and
title ‘‘Experimental Study: Effect of
Promotional Offers in Direct-toConsumer Prescription Drug Print
Advertisements on Consumer Product
Perceptions.’’ Also include the FDA
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Juanmanuel Vilela, Office of
mstockstill on DSK4VPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
15:46 Sep 16, 2011
Jkt 223001
SUPPLEMENTARY INFORMATION:
I. Background
In compliance with 44 U.S.C. 3507,
FDA has submitted the following
proposed collection of information to
OMB for review and clearance.
Experimental Study: Effect of
Promotional Offers in Direct-toConsumer Prescription Drug Print
Advertisements on Consumer Product
Perceptions—(OMB Control Number
0910–New)
[FR Doc. 2011–23959 Filed 9–15–11; 11:15 am]
AGENCY:
Information Management, Food and
Drug Administration, 1350 Piccard Dr.,
PI50–400B, Rockville, MD 20850, 301–
796–7651,
Juanmanuel.Vilela@fda.hhs.gov.
Section 502(n) of the Federal Food,
Drug, and Cosmetic Act (the FD&C Act)
(21 U.S.C. 352(n)) requires
advertisements for prescription drugs to
include, among other things, ‘‘such
information in brief summary relating to
side effects, contraindications, and
effectiveness as shall be required in
regulations.’’ Under this authority, FDA
has issued regulations to require most
prescription drug advertisements to
provide a ‘‘true statement of information
in brief summary relating to side effects,
contraindications, and effectiveness.’’
(§ 202.1(e) (1) (21 CFR 202.1(e)(1)). To
satisfy this requirement, an
advertisement that makes claims about
a prescription drug must also include a
‘‘fair balance’’ of information about the
benefits and risks of the advertised
product, in terms of both content and
presentation (§ 202.1(e)(5)(ii)). In part,
§ 202.1(e)(6)(i) states that [a]n
advertisement for a prescription drug is
false, lacking in fair balance, or
otherwise misleading, or otherwise
violative of section 502(n) of the act,
among other reasons, if it [c]ontains a
representation or suggestion, not
approved or permitted for use in the
labeling, that a drug is better, more
effective, useful in a broader range of
conditions or patients (as used in
§ 202.1 ’’patients’’ means humans and
in the case of veterinary drugs, other
animals) safer, has fewer, or less
incidence of, or less serious side effects
or contraindications than has been
demonstrated by substantial evidence or
substantial clinical experience (as
described in paragraphs (e)(4)(ii)(b) and
(e)(4)(ii)(c) of § 202.1) whether or not
such representations are made by
comparison with other drugs or
treatments, and whether or not such a
representation or suggestion is made
directly or through use of published or
unpublished literature, quotations, or
other references.
PO 00000
Frm 00065
Fmt 4703
Sfmt 4703
58011
FDA’s current regulations provide a
limited exception to the requirement in
§ 202.1(e)(1), of presenting a true
statement of information in brief
summary, for ‘‘reminder
advertisements’’ (‘‘reminder ads’’)—
advertisements that draw attention to
the name of the product but do not
make representations about the
product’s indication(s) or dosage
recommendations (§ 202.1(e)(2)(i)).
(Certain drugs are not permitted to
qualify for the reminder advertisement
exemption.) To meet the terms of this
exemption, reminders ads must in
general be limited to the proprietary and
established name of the product and the
established name of each active
ingredient in the drug product.
Reminder ads may also (optionally)
contain information about the product’s
quantitative ingredients, dosage form,
quantity, price, and manufacturer, as
well as other written, printed, or graphic
matter containing no representation or
suggestion relating to the product.
Further, reminder ads that are intended
to provide consumers with information
concerning the price charged for a
prescription drug product need not meet
the terms of § 202.1(e)(2)(i) in order to
be exempt from § 202.1(e)(1) if they
meet all of the conditions in § 200.200
(21 CFR 200.200). That regulation, in
turn, applies to prescription drug
reminders ads that are intended solely
to provide consumers with information
concerning the price charged for a
prescription for a particular drug
product, and the reminder ad contains
no representation or suggestion
concerning the drug product’s safety,
effectiveness, or indications for use
(§ 200.200(a)(1) and (b)).
A topic of ongoing interest for
consumer product manufacturers and
retailers is the use of consumer-oriented
sales promotions such as free trial
offers, discounts, money-back
guarantees, and rebates. Such
promotions are widely used in many
product categories, including
prescription drugs.
Prior research has demonstrated that
the type of promotion offered can affect
how consumers respond to the
promotion (Refs. 1, 2, and 3). Price
incentives 1 may act as cues about
product quality. For example, a price
incentive may not only act as an
economic incentive to buy the product,
it may also artificially enhance
consumers’ perceptions of the product’s
quality (Ref. 4). In the case that
1 In this document, we use the terms ‘‘price
incentive’’ and ‘‘coupon’’ interchangeably to refer to
the types of promotional offers to be addressed in
our study.
E:\FR\FM\19SEN1.SGM
19SEN1
Agencies
[Federal Register Volume 76, Number 181 (Monday, September 19, 2011)]
[Notices]
[Pages 58007-58011]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-23959]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
Privacy Act of 1974; Report of a New System of Records
AGENCY: Centers for Medicare & Medicaid Services (CMS), Department of
Health and Human Services (HHS).
ACTION: Notice to establish a new system of records.
-----------------------------------------------------------------------
SUMMARY: In accordance with the requirements of the Privacy Act of
1974, CMS is establishing a new system of records to support its shared
savings programs, the first of which are the Medicare Shared Savings
Program and Pioneer ACO Model (collectively referred to as the ACO
program). The ACO program implements recent health care reform
provisions of the Patient Protection and Affordable Care Act (PPACA),
amending the Social Security Act (the Act). The system of records will
contain personally identifiable information (PII) about certain
individuals who participate in, or whose PII is used to determine
eligibility of an Accountable Care Organization (ACO) to participate
in, a shared savings program; i.e., Medicare fee-for-service (FFS)
beneficiaries, sole proprietor health care ACO participants and ACO
suppliers/providers, key leaders and managers of accountable care
organizations (ACOs), and contact persons for ACOs. The program and the
system of records are more thoroughly described in the Supplementary
Information section and System of Records Notice (SORN), below.
[[Page 58008]]
DATES: CMS filed a new system report with the Chair of the House
Committee on Government Reform and Oversight, the Chair of the Senate
Committee on Homeland Security & Governmental Affairs, and the
Administrator, Office of Information and Regulatory Affairs, Office of
Management and Budget (OMB) on September 14, 2011. To ensure that all
parties have adequate time in which to comment, the new system,
including routine uses, will become effective October 19, 2011. If CMS
receives comments that require alterations to this notice, we will
publish a revised notice in the Federal Register.
ADDRESSES: The public should send comments to: CMS Privacy Officer,
Division of Information Security & Privacy Management, Enterprise
Architecture and Strategy Group, Office of Information Services, CMS,
Room N1-24-08, 7500 Security Boulevard, Baltimore, Maryland 21244-1850.
Comments received will be available for review at this location, by
appointment, during regular business hours, Monday through Friday from
9 a.m.-3 p.m., Eastern Time zone.
FOR FURTHER INFORMATION CONTACT: For Medicare Shared Savings Program:
Rebecca Weiss, Program Analyst, Performance-Based Payment Policy Staff,
Center for Medicare, Centers for Medicare & Medicaid Services, 7500
Security Boulevard, Mail-stop: C5-15-12, Baltimore, MD 21244-1850.
Office: 410-786-8084, Facsimile: (410) 786-8005, E-mail address:
aco@cms.hhs.gov.
For Pioneer Aco Model: Alli Chandra, Health Insurance Specialist,
Center for Medicare and Medicaid Innovation, Centers for Medicare &
Medicaid Services, 7500 Security Boulevard, Mailstop: S3-13-05,
Baltimore, MD 21244-1850. Office Ph: 410-786-1132, Facsimile: (410)
786-0487, E-mail address: alli.chandra@cms.hhs.gov.
SUPPLEMENTARY INFORMATION: This System of Records Notice (SORN)
addresses a new system which HHS is establishing to support CMS shared
savings programs created as a result of the Patient Protection and
Affordable Care Act (Pub. L. 111-148), the first of which are the
Medicare Shared Savings Program and Pioneer ACO Model (ACO program)
described in more detail below.
I. Medicare Shared Savings Program
The recently passed health care reform bill, the Affordable Care
Act (PPACA) (Pub. L. 111-148), contains provisions that seek to reward
quality care and takes steps toward paying for high quality and
efficient care. One of these provisions, Section 3022, amended Title
XVIII of the Social Security Act (the Act) (42 U.S.C. 1395 et seq.) by
adding new section 1899 to the Act to establish a shared savings
program (SSP) that promotes accountability for a patient population,
coordinates items and services under Parts A and B, and encourages
investment in infrastructure and redesigned care processes for high
quality and efficient service delivery. Specifically:
Section 1899(a)(1) of the Act requires the Secretary to
establish the shared savings program no later than January 1, 2012.
Section 1899(a)(1) (A) of the Act further provides that, ``groups of
providers of services and suppliers meeting criteria specified by the
Secretary may work together to manage and coordinate care for Medicare
fee-for-service (FFS) beneficiaries through an accountable care
organization (ACO).''
Section 1899(a)(1)(B) of the Act provides that ACOs that
meet quality performance standards established by the Secretary are
eligible to receive payments for ``shared savings.''
The Shared Savings Program is a voluntary program. The statute
provides that, to participate in the program, an ACO must ``provide the
Secretary with such information regarding the ACO professionals
participating in the ACO as the Secretary determines necessary to
support the assignment of Medicare fee-for-service beneficiaries to an
ACO, the implementation of quality and other reporting requirements * *
* and the determination of payments for shared savings.'' The statute
requires an ACO to meet certain eligibility criteria including, but not
limited to, having ``a formal legal structure that would allow the
organization to receive and distribute payments for shared savings,''
having ``in place a leadership and management structure that includes
clinical and administrative systems,'' and demonstrating ``to the
Secretary that it meets patient-centeredness criteria specific by the
Secretary.'' In addition, the ACO must agree to participate for not
less than 3 years, have a formal legal structure including primary care
providers sufficient for the care of not less than 5000 beneficiaries,
and meet others requirements.
The statute defines an ACO as organization of health care providers
that agrees to become accountable for the quality, cost, and overall
care of Medicare beneficiaries who are enrolled in the traditional fee-
for-service program who are assigned to it. The statute states that
there are many types of organizational arrangements for eligibility to
become an ACO, as determined appropriate by the Secretary.
To qualify for shared savings payments, the ACO must meet specific
cost and quality benchmarks. Quality performance standards will be
determined by the Secretary and may include measures of clinical
processes and outcomes, patient and/or caregiver experience, and
utilization measures. An ACO will be eligible to receive a share (a
percentage, and any limits, to be determined by the Secretary) of any
savings if the actual per capita expenditures of its assigned Medicare
beneficiaries are a sufficient percentage below its specified benchmark
amount. The benchmark for each ACO will be based on the most recent
available three years of per-beneficiary expenditures for Parts A and B
services for Medicare FFS beneficiaries assigned to the ACO. The
benchmark for each ACO will be adjusted for beneficiary characteristics
and other factors as determined by the Secretary, and updated by the
projected absolute amount of growth in national per capita expenditures
for Parts A and B.
II. Pioneer ACO Model
Another provision of the Affordable Care Act (PPACA), Section 3021,
amended Title XVIII of the Social Security Act (the Act) (42 U.S.C.
1395 et seq.) by adding new section 1899 to the Act to establish the
Center for Medicare and Medicaid Innovation (Innovation Center). The
Innovation Center is tasked with development of the Pioneer ACO Model.
Under the Pioneer ACO Model, the Innovation Center will engage up to 30
highly experienced provider organizations in testing alternative
payment models that include escalating financial accountability and
substantial quality/patient experience standards (``outcomes based
arrangements''). CMS intends to pursue payment models that (1) include
escalating levels of financial accountability through successive
performance periods during the Participation Agreement; (2) provide a
transition to Population-Based Payment by the third performance period,
and (3) are projected by CMS to generate Medicare savings by the end of
the second performance period.
III. The Privacy Act
The Privacy Act (5 U.S.C. 552a) governs the means by which the
United States Government collects, maintains, and uses personally
identifiable information (PII) in a system of records. A ``system of
records'' is a group of any records under the control of a Federal
[[Page 58009]]
agency from which information about individuals is retrieved by name or
other personal identifier. The Privacy Act requires each agency to
publish in the Federal Register a system of records notice (SORN)
identifying and describing each system of records the agency maintains,
including the purposes for which the agency uses PII in the system, the
routine uses for which the agency discloses such information outside
the agency, and how individual record subjects can exercise their
rights under the Privacy Act (e.g., to determine if the system contains
information about them).
The Privacy Act permits an agency to disclose information about an
individual (PII) without that individual's consent if the information
is to be used for a purpose that is compatible with the purpose(s) for
which the information was collected. Any such disclosure of PII is
known as a ``routine use.'' HHS/CMS will only release PII from this
system as provided in the ``Routine Uses'' section below. Both
identifiable and non-identifiable data may be disclosed under a routine
use. HHS/CMS will only disclose the minimum PII necessary to achieve
the purpose of the routine use, after determining that:
The use or disclosure is consistent with the reason that
the PII was collected;
The purpose for which the disclosure is to be made can
only be accomplished if the record is provided in individually
identifiable form;
The purpose for which the disclosure is to be made is of
sufficient importance to warrant the effect on and/or risk to the
privacy of the individual that additional exposure of the record might
bring;
There is a strong probability that the proposed use of the
data would in fact accomplish the stated purpose(s); and
The data are valid and reliable.
Additionally, HHS/CMS will require the information recipient to:
Establish administrative, technical, and physical
safeguards to prevent unauthorized use or disclosure of the record;
Remove or destroy at the earliest time all individually-
identifiable information; and
Agree to not use or disclose the information for any
purpose other than the stated purpose under which the information was
disclosed.
SYSTEM NUMBER:
09-70-0598
SYSTEM NAME:
ACO Database System HHS/CMS/CM and HHS/CMS/CMMI.
SECURITY CLASSIFICATION:
Sensitive, unclassified.
SYSTEM LOCATION:
CMS Data Center, 7500 Security Boulevard, North Building, First
Floor, Baltimore, Maryland 21244-1850 and at various accountable care
organization (ACO) locations and contractor sites.
CATEGORIES OF INDIVIDUALS COVERED BY THE SYSTEM:
The system will contain personally identifiable information (PII)
about the following categories of individuals who participate in, or
whose PII is used to determine eligibility of an ACO to participate in,
a Health and Human Services (HHS) Centers for Medicare & Medicaid
Services (CMS) Medicare shared savings program:
Medicare fee-for-service (FFS) beneficiaries who receive
health care services coordinated and managed by a group of health care
providers and suppliers organized to receive shared savings incentive
payments, as an accountable care organization (ACO).
Any providers or suppliers participating in an ACO who are
sole proprietorships, for whom certain business-identifying information
may therefore constitute personally identifiable information.
Key leaders and managers of an ACO who provide certain
personally identifiable information that is used to determine the ACO's
eligibility to participate in the program.
Any contact persons for an ACO who provide contact
information for use in contacting them for information about the ACO.
CATEGORIES OF RECORDS IN THE SYSTEM:
This system may include, but will not necessarily be limited to,
the following categories of records, containing PII (or possible PII)
data elements such as the following:
Medicare fee-for-service (FFS) beneficiary claims records,
containing the beneficiary's name, gender, Health Insurance Claim
Number (HICN) (which could be the beneficiary's Social Security
Number), address, date of birth and description of provided services.
ACO eligibility and contact records, containing the ACO
name and address (which could be the home address of a key leader or
manager of the ACO); ACO participant or ACO provider/supplier names and
addresses (which could include home addresses for any sole proprietor
providers/suppliers in the ACO); ACO participant Tax Identification
Number (TIN) (which could be a Social Security Number for a sole
proprietor ACO participant or ACO provider/supplier in the ACO);
National Provider Identifier (NPI) (which is considered PII for an
individual provider/supplier); and (for individuals serving as key
leaders or managers of an ACO) the individual's name and address (which
could be a home address).
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
The Patient Protection and Affordable Care Act (Pub. L. 111-148),
which amended Title XVIII of the Social Security Act (the Act) (42
U.S.C. 1395 et seq.) to add new section 1899 to the Act to establish a
Medicare Shared Savings Program (MSSP); and Section 3021 of the Patient
Protection and Affordable Care Act, which amended Title XI of the
Social Security Act (the Act) (42 U.S.C. 1301 et seq.) to add new
section 1115A to the Act to establish the Center for Medicare and
Medicaid Innovation.
PURPOSE(S) OF THE SYSTEM:
The system will enable the HHS Centers for Medicare & Medicaid
Services (CMS) to administer the ACO program. Relevant HHS personnel,
and any CMS contractors, grantees and consultants assisting them, will
use personally identifiable information (PII) from this system on a
``need to know'' basis for these purposes:
Beneficiary claims information and ACO eligibility and
contact information will be used to support the regulatory,
reimbursement and policy functions of shared savings programs and to
combat fraud, waste and abuse in certain health benefits programs.
ROUTINE USES OF RECORDS MAINTAINED IN THE SYSTEM, INCLUDING CATEGORIES
OR USERS AND THE PURPOSES OF SUCH USES:
Any of the PII from this system may be disclosed outside HHS for
these routine uses:
1. To obtain assistance from other Federal agencies that help HHS,
pursuant to agreements with CMS, to determine the eligibility of ACO
applicants to participate in the program. For example, a TIN (which may
be a Social Security Number) may be shared with the U.S. Federal Trade
Commission (FTC) and the U.S. Department of Justice (DOJ) for purposes
of obtaining their assessment of the ACO applicant's market share
status.
2. To provide ACOs with information they need to meet requirements
and
[[Page 58010]]
implement quality and other reporting requirements of the program.
3. To provide information to the U.S. Department of Justice (DOJ),
a court, or an adjudicatory body when (a) the Agency or any component
thereof, or (b) any employee of the Agency in his or her official
capacity, or (c) any employee of the Agency in his or her individual
capacity where the DOJ has agreed to represent the employee, or (d) the
United State Government, is a party to litigation or has an interest in
such litigation, and by careful review, CMS determines that the records
are both relevant and necessary to the litigation and that the use of
such records by the DOJ, court, or adjudicatory body is compatible with
the purpose for which the agency collected the records.
4. To assist another Federal agency or an instrumentality of any
governmental jurisdiction within or under the control of the United
States (including any state or local governmental agency), that
administers or that has the authority to investigate potential fraud,
waste or abuse in a health benefits program funded in whole or in part
by Federal funds, when disclosure is deemed reasonably necessary by CMS
to prevent, deter, discover, detect, investigate, examine, prosecute,
sue with respect to, defend against, correct, remedy, or otherwise
combat fraud, waste or abuse in such programs.
5. To assist appropriate Federal agencies and HHS contractors that
have a need to know the information for the purpose of assisting HHS's
efforts to respond to a suspected or confirmed breach of the security
or confidentiality of information maintained in this system of records,
provided that the information disclosed is relevant and necessary for
that assistance.
Additional Circumstances Affecting Disclosure of PII About
Beneficiaries:
To the extent that the beneficiary claims records in this system
contain Protected Health Information (PHI) as defined by HHS regulation
``Standards for Privacy of Individually Identifiable Health
Information'' (45 CFR parts 160 and 164, subparts A and E), disclosures
of such PHI that are otherwise authorized by these routine uses may
only be made if, and as, permitted or required by the ``Standards for
Privacy of Individually Identifiable Health Information'' (see 45 CFR
164-512 (a) (1)). In addition, HHS policy will be to prohibit release
even of data not directly identifiable with a particular beneficiary,
except pursuant to one of the routine uses or if required by law, if
HHS determines there is a possibility that a particular beneficiary can
be identified through implicit deduction based on small cell sizes
(instances where the patient population is so small that individuals
could, because of the small size, use this information to deduce the
identity of a particular beneficiary).
POLICIES AND PRACTICES FOR STORING, RETRIEVING, ACCESSING, RETAINING,
AND DISPOSING OF RECORDS IN THE SYSTEM--
STORAGE:
Electronic records will be stored on both tape cartridges (magnetic
storage media) and in a in a DB2 and/or Oracle relational database
management environment (DASD data storage media). Any hard copies of
ACO program-related records containing PII at HHS/CMS, ACO and
contractor locations will be kept in hard-copy file folders locked in
secure file cabinets during non-duty hours.
RETRIEVABILITY:
Information may be retrieved by any of these personal identifiers:
ACO participant TIN (which could be a sole proprietor provider/
supplier's Social Security Number), National Provider Identifier (NPI),
or beneficiary Health Insurance Claim Number (HICN)) (which may be the
beneficiary's Social Security Number).
SAFEGUARDS:
Personnel having access to the system have been trained in the
Privacy Act and information security requirements. Employees who
maintain records in this system are instructed not to release data
until the intended recipient agrees to implement appropriate
management, operational and technical safeguards sufficient to protect
the confidentiality, integrity and availability of the information and
information systems and to prevent unauthorized access.
Access to records in the ACO Database System will be limited to CMS
personnel, and any contractors, grantees and consultants assisting
them, through password security, encryption, firewalls, and secured
operating system.
Future system enhancements may allow for ACOs, ACO participants or
ACO provider/suppliers, and beneficiaries to be external users of the
system, for purposes of viewing and inputting their records in this
system. Access controls will ensure that each external user is
restricted to viewing only the user's own records, not records
pertaining to other users.
Any electronic or hard copies of ACO program-related records
containing PII at HHS/CMS, an ACO, and any contractor, grantee or
consultant locations will be kept in secure electronic files or in
hard-copy file folders locked in secure file cabinets during non-duty
hours.
RETENTION AND DISPOSAL:
Records containing PII will be maintained for a period of up to 10
years after entry in the database. Any records that are needed longer,
such as to resolve claims and audit exceptions or to prosecute fraud,
will be retained until such matters are resolved. Beneficiary claims
records are currently subject to a document preservation order and will
be preserved indefinitely pending further notice from the U.S.
Department of Justice.
SYSTEM MANAGER AND ADDRESS:
Director, Performance-Based Payment Policy Staff, Center for
Medicare, Centers for Medicare & Medicaid Services, 7500 Security
Boulevard, Mailstop: C5-15-12, Baltimore, MD 21244-1850; and
Director, Pioneer ACO Model, Center for Medicare and Medicaid
Innovation, Centers for Medicare and Medicaid Services, Mailstop: S3-
13-05, 7500 Security Boulevard, Baltimore, MD 21244-1850.
NOTIFICATION PROCEDURE:
Individuals wishing to know if this system contains records about
them should write to one of the system managers and include the
pertinent personal identifier used for retrieval of their records
(i.e., TIN, NPI or beneficiary Health Insurance Claim Number).
RECORD ACCESS PROCEDURE:
Individuals seeking access to records about them in this system
should follow the same instructions indicated under ``Notification
Procedure'' and reasonably specify the record contents being sought.
(These procedures are in accordance with Department regulation 45 CFR
5b.5 (a)(2).)
CONTESTING RECORD PROCEDURES:
Individuals seeking to contest the content of information about
them in this system should follow the same instructions indicated under
``Notification Procedure.'' The request should reasonably identify the
record and specify the information being contested, state the
corrective action sought, and provide the reasons for the correction,
with supporting justification. (These procedures are in accordance with
Department regulation 45 CFR 5b.7.)
RECORD SOURCE CATEGORIES:
Personally identifiable information in this database is obtained
from the
[[Page 58011]]
Medicare Beneficiary Database (MBD) (09-70-0536), from the National
Claims History File (NCH) (09-70-0558), and from ACOs that provide the
information as required to perform the statutory functions of
beneficiary assignment, implementation of quality and other reporting
requirements, and determination of shared savings.
EXEMPTIONS CLAIMED FOR THIS SYSTEM:
None.
Dated: September 14, 2011.
Michelle Snyder,
Deputy Chief Operating Officer, Centers for Medicare & Medicaid
Services.
[FR Doc. 2011-23959 Filed 9-15-11; 11:15 am]
BILLING CODE 4120-03-P