Privacy Act of 1974; Report of a New System of Records, 10450-10454 [E8-3678]
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10450
Federal Register / Vol. 73, No. 39 / Wednesday, February 27, 2008 / Notices
Bank & Trust Company, all of Kansas
City, Kansas.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Board of Governors of the Federal Reserve
System, February 21, 2008.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. E8–3651 Filed 2–26–08; 8:45 am]
Centers for Medicare & Medicaid
Services
Privacy Act of 1974; Report of a New
System of Records
BILLING CODE 6210–01–S
Department of Health and
Human Services (HHS), Centers for
Medicare & Medicaid Services (CMS).
AGENCY:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Notice of a New System of
Records (SOR).
ACTION:
Centers for Medicare & Medicaid
Services
Privacy Act of 1974; Deletion of an
Existing System of Records
Department of Health and
Human Services (HHS), Centers for
Medicare & Medicaid Services (CMS).
AGENCY:
Notice to delete an existing CMS
system of records (SOR).
ACTION:
SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
CMS is deleting an existing system of
records titled the ‘‘Privacy
Accountability Database (PAD),’’ CMS
System No. 09–70–0540, established at
67 FR 62482 (October 7, 2002).
The deletion will be
effective on February 11, 2008.
EFFECTIVE DATE:
The public should address
comments to: CMS Privacy Officer,
Division of Privacy Compliance,
Enterprise Architecture and Strategy
Group, Office of Information Services,
CMS, Room N2–04–27, 7500 Security
Boulevard, Baltimore, Maryland 21244–
1850. The telephone number is (410)
786–5357. 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.
ADDRESSES:
The PAD
as a Privacy Act system of records is
being deleted because the database that
supported this collection is obsolete and
is no longer active. CMS will continue
to track disclosures and will provide the
necessary tracking, reporting, and
accounting of disclosures to be in
compliance with the Privacy Act of
1974 and the Health Insurance
Portability and Accountability Act of
1996.
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SUPPLEMENTARY INFORMATION:
Dated: February 20, 2008.
Charlene Frizzera,
Chief Operating Officer, Centers for Medicare
& Medicaid Services.
[FR Doc. 08–873 Filed 2–26–08; 8:45 am]
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SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
we are proposing to establish a new
system of records titled, ‘‘Medicare
Administrative Issue Tracker and
Reporting of Operations (MAISTRO)
System,’’ System No. 09–70–0598. The
purpose of the system is to capture and
track casework/inquiries pertaining to
Medicare Part A and Part B programs.
The system will also provide a
mechanism for recording data on a
national level and will serve as a tool to
leverage in performing analysis
including identification of systemic
trends. MAISTRO will record, track and
monitor beneficiary and provider level
inquiries & complaints. The system will
contain information needed to research
the inquiries, such as a beneficiary’s
health insurance claim number (HICN)
or a Provider Identification Number
(NPI).
The primary purpose of the system is
to collect and maintain information
needed to provide a mechanism for
CMS’ central and regional office to
capture, track, manage, report and trend
inquiries, complaints and issues related
to Fee-for-Service (FFS) programs.
Information maintained in this system
will also be disclosed to: (1) Support
regulatory, reimbursement, and policy
functions performed within the Agency
or by a contractor, consultant or CMS
grantee; (2) assist another Federal or
state agency, agency of a state
government, an agency established by
state law, or its fiscal agent; (3) facilitate
research on the quality and effectiveness
of care provided, as well as
epidemiological projects; (4) support
litigation involving the Agency; and (5)
combat fraud, waste, and abuse in
certain health benefits programs. We
have provided background information
about the modified system in the
SUPPLEMENTARY INFORMATION section
below. Although the Privacy Act
requires only that CMS provide an
opportunity for interested persons to
comment on the proposed routine uses,
CMS invites comments on all portions
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of this notice. See EFFECTIVE DATES
section for comment period.
EFFECTIVE DATES: CMS filed a new
system report with the Chair of the
House Committee on Oversight and
Government Reform, the Chair of the
Senate Committee on Homeland
Security and Governmental Affairs, and
the Administrator, Office of Information
and Regulatory Affairs, Office of
Management and Budget (OMB) on
2/11/2008. In any event, we will not
disclose any information under a
routine use until 30 days after
publication in the Federal Register or
40 days after mailings to Congress,
which ever is later. We may defer
implementation of this system or on one
or more of the routine uses listed below
if we receive comments that persuade us
to defer implementation.
ADDRESSES: The public should address
comments to: CMS Privacy Officer,
Division of Privacy Compliance,
Enterprise Architecture & Strategy
Group, Office of Information Services,
CMS, Mail Stop N2–04–27, 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:
Michele Livingston, Division of
Ombudsman Casework and Trends
Management, Medicare Ombudsman
Group, Office of External Affairs, CMS,
7500 Security Boulevard, Mail Stop S1–
20–21, Baltimore, Maryland 21244–
1850. The telephone number is 410–
786–6340 or contact
Michele.Livingston@cms.hhs.gov.
SUPPLEMENTARY INFORMATION: The CMS
Consortium for Financial Management
and Fee for Service Operations
(CFMFFSO) is responsible for handling
casework/inquiries, but not limited to:
(1) Coverage and payment policy; (2)
audit and reimbursement policy and
operations; (3) program integrity and
medical review policy; (4) Medicare
secondary payer and coordination of
benefits; (5) claims-related hearings,
appeals and grievances; (6) beneficiary
eligibility, enrollment, entitlement,
rights and protections, premium billing
and collection; and (7) dispute
resolution processes to assure the
effective administration of the Medicare
program. These types of inquiries
number in the tens of thousands
annually across the 10 CMS Regional
Offices.
The Office of the Medicare
Ombudsman was established as a result
of Section 923 of the Medicare
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Modernization Act and is responsible
for receiving complaints, grievances and
requests for information submitted by
individuals entitled to benefits under
Part A or enrolled under Part B, or both,
with respect to any aspect of the
Medicare program and providing
assistance with respect to complaints.
Over the last year the focus of inquiry
tracking has centered on the
implementation of Part D reporting.
Although each regional office has
developed its own system to track and
manage inquiries and complaints, these
systems are inconsistent and do not
utilize standardized operational
procedures or processes to guide how
inquiries are addressed or reported.
Standardization will improve
performance, reduce operating costs,
and enable statistical analysis of the
workload and trends among inquiries.
To address these issues, the following
tasks had to be accomplished: (1)
Identifying a system to track beneficiary
and provider inquiries, complaints and
issues specific to FFS operations; (2)
Ensuring that casework throughout each
region is consistently captured and
managed appropriately which ensures
the delivery of high quality customer
service to Medicare Part A and Part B
beneficiaries and providers; and (3)
Producing workload data statistics to
both account for the work and enable
improvement in CMS’ policies and
procedures.
When complete, the MAISTRO
system will provide a mechanism for
CMS’ central and regional office to
capture, track, manage, report and trend
inquiries, complaints and issues related
to Fee-for-Service. Additionally, the
goal of MAISTRO is to provide an easy
to use system that will provide
consistency when tracking, resolving,
and reporting FFS inquiries, complaints
and issues on a national level such that
trends, workloads and systemic issues
can be identified and managed
appropriately across the consortium.
I. Description of the Proposed System of
Records
A. Statutory and Regulatory Basis for
SOR
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Authority for maintenance of this
system is given under § 923 of the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA) (Public Law (Pub. L.) 108–
173).
B. Collection and Maintenance of Data
in the System
For purposes of this SOR, the system
contains information on Medicare
beneficiaries, providers and other
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individuals who have made inquiries
concerning the fee-for-service program.
The system contains information such
as a beneficiary’s name, address data,
health insurance claim number (HICN),
demographic information (gender, date
of birth), provider name, address data
and provider identification number
(NPI), provider organization
information, contact person
information, employer identification
numbers, and certain optional data such
as Social Security Numbers and other
provider identifiers used by these health
care providers.
II. Agency Policies, Procedures, and
Restrictions on the Routine Use
A. Agency Policies, Procedures, and
Restrictions Routine Uses
The Privacy Act permits us to disclose
information without an 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
data is known as a ‘‘routine use.’’ The
government will only release MAISTRO
information that can be associated with
an individual as provided for under
‘‘Section III. Proposed Routine Use
Disclosures of Data in the System.’’ Both
individually identifiable and nonindividually-identifiable data may be
disclosed under a routine use.
We will only disclose the minimum
personal data necessary to achieve the
purpose of MAISTRO. CMS has the
following policies and procedures
concerning disclosures of information
that is maintained in the system.
Disclosure of information from the
system will be approved only to the
extent necessary to accomplish the
purpose of the disclosure and only after
CMS:
1. Determines that the use or
disclosure is consistent with the reason
the data are being collected; e.g., to
collect and maintain information
needed to provide a mechanism for
CMS’ central and regional office to
capture, track, manage, report and trend
inquiries, complaints and issues related
to Fee-for-Service (FFS).
2. Determines that:
a. The purpose for which the
disclosure is to be made can only be
accomplished if the record is provided
in individually identifiable form;
b. The purpose for which the
disclosure is to be made is of sufficient
importance to warrant the effect and/or
risk on the privacy of the individual that
additional exposure of the record might
bring; and
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c. There is a strong probability that
the proposed use of the data would in
fact accomplish the stated purpose(s).
3. Requires the information recipient
to:
a. Establish administrative, technical,
and physical safeguards to prevent
unauthorized use or disclosure of the
record;
b. Remove or destroy at the earliest
time all individually-identifiable
information; and
c. Agree to not use or disclose the
information for any purpose other than
the stated purpose under which the
information was disclosed.
4. Determines that the data are valid
and reliable.
III. Proposed Routine Use Disclosures
of Data in the System
A. The Privacy Act allows us to
disclose information without an
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 compatible use of data is
known as a ‘‘routine use.’’ The proposed
routine uses in this system meet the
compatibility requirement of the Privacy
Act. We are proposing to establish the
following routine use disclosures of
information maintained in the system:
1. To support Agency contractors,
consultants, or CMS grantees that have
been contracted by the Agency to assist
in accomplishment of a CMS function
relating to the purposes for this system
and who need access to the records in
order to assist CMS.
We contemplate disclosing
information under this routine use only
in situations in which CMS may enter
into a contractual or similar agreement
with a third party to assist in
accomplishing a CMS function relating
to purposes for this system.
CMS occasionally contracts out
certain of its functions when doing so
would contribute to effective and
efficient operations. CMS must be able
to give a contractor, consultant, or
grantee whatever information is
necessary for the contractor, consultant,
or grantee to fulfill its duties. In these
situations, safeguards are provided in
the contract prohibiting the contractor,
consultant, or grantee from using or
disclosing the information for any
purpose other than that described in the
contract and requires the contractor or
consultant to return or destroy all
information at the completion of the
contract.
2. To assist another Federal or state
agency, agency of a state government, an
agency established by state law, or its
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fiscal agent pursuant to agreements with
CMS to:
a. Contribute to the accuracy of CMS’s
proper payment of Medicare benefits,
b. Enable such agency to administer a
Federal health benefits program, or as
necessary to enable such agency to
fulfill a requirement of a Federal statute
or regulation that implements a health
benefits program funded in whole or in
part with Federal funds, and/or
c. Assist Federal/state Medicaid
programs within the state.
Other Federal or state agencies in
their administration of a Federal health
program may require MAISTRO
information for the purposes of
collecting and maintaining information
needed to capture, track, manage, report
and trend inquiries, complaints and
issues related to Fee-for-Service (FFS).
Other Federal or state agencies, in
their administration of a Federal health
program, may require MAISTRO
information in order to support
evaluations and monitoring of Medicaid
claims information of beneficiaries,
including proper reimbursement for
services provided.
3. To an individual or organization for
a research project or in support of an
evaluation project related to the
prevention of disease or disability, the
restoration or maintenance of health, or
payment related projects.
The MAISTRO data will provide for
research or support of evaluation
projects and a broader, longitudinal,
national perspective of the status of
Medicaid beneficiaries. CMS anticipates
that researchers may have legitimate
requests to use these data in projects
that could ultimately improve the care
provided to Medicaid beneficiaries and
the policies that govern their care.
4. To assist the Department of Justice
(DOJ), court or 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 States 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.
Whenever CMS is involved in
litigation, or occasionally when another
party is involved in litigation and CMS’s
policies or operations could be affected
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by the outcome of the litigation, CMS
would be able to disclose information to
the DOJ, court, or adjudicatory body
involved.
5. To support a CMS contractor that
assists in the administration of a CMSadministered health benefits program,
or to a grantee of a CMS-administered
grant program, 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.
We contemplate disclosing
information under this routine use only
in situations in which CMS may enter
into a contract or grant with a third
party to assist in accomplishing CMS
functions relating to the purpose of
combating fraud, waste, and abuse.
CMS occasionally contracts out
certain of its functions when doing so
would contribute to effective and
efficient operations. CMS must be able
to give a contractor or CMS grantee
whatever information is necessary for
the contractor or CMS grantee to fulfill
its duties. In these situations, safeguards
are provided in the contract prohibiting
the contractor or grantee from using or
disclosing the information for any
purpose other than that described in the
contract and requiring the contractor or
grantee to return or destroy all
information.
6. To support another Federal agency
or to 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
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.
Other agencies may require MAISTRO
information for the purpose of
combating fraud, waste, and abuse in
such Federally-funded programs.
IV. Safeguards
CMS has safeguards in place for
authorized users and monitors such
users to ensure against excessive or
unauthorized use. 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
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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.
This system will conform to all
applicable Federal laws and regulations
and Federal, HHS, and CMS policies
and standards as they relate to
information security and data privacy.
These laws and regulations may apply
but are not limited to: The Privacy Act
of 1974; the Federal Information
Security Management Act of 2002; the
Computer Fraud and Abuse Act of 1986;
the Health Insurance Portability and
Accountability Act of 1996; the EGovernment Act of 2002, the ClingerCohen Act of 1996; the Medicare
Modernization Act of 2003, and the
corresponding implementing
regulations. OMB Circular A–130,
Management of Federal Resources,
Appendix III, Security of Federal
Automated Information Resources also
applies. Federal, HHS, and CMS
policies and standards include but are
not limited to: All pertinent National
Institute of Standards and Technology
publications; the HHS Information
Systems Program Handbook and the
CMS Information Security Handbook.
V. Effects of the Proposed System of
Records on Individual Rights
CMS proposes to establish this system
in accordance with the principles and
requirements of the Privacy Act and will
collect, use, and disseminate
information only as prescribed therein.
Data in this system will be subject to the
authorized releases in accordance with
the routine uses identified in this
system of records.
CMS will take precautionary
measures to minimize the risks of
unauthorized access to the records and
the potential harm to individual privacy
or other personal or property rights of
patients whose data are maintained in
the system. CMS will collect only that
information necessary to perform the
system’s functions. In addition, CMS
will make disclosure from the proposed
system only with consent of the subject
individual, or his/her legal
representative, or in accordance with an
applicable exception provision of the
Privacy Act. CMS, therefore, does not
anticipate an unfavorable effect on
individual privacy as a result of
information relating to individuals.
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Dated: February 20, 2008.
Charlene Frizzera,
Chief Operating Officer, Centers for Medicare
& Medicaid Services.
SYSTEM NUMBER: 09–70–0598
SYSTEM NAME:
‘‘Medicare Administrative Issue
Tracker and Reporting of Operations
(MAISTRO) System,’’ HHS/CMS/OEA.
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive
Data.
SYSTEM LOCATION:
Centers for Medicare & Medicaid
Services (CMS) Data Center, 7500
Security Boulevard, North Building,
First Floor, Baltimore, Maryland 21244.
CATEGORIES OF INDIVIDUALS COVERED BY THE
SYSTEM:
For purposes of this SOR, the system
contains information on Medicare
beneficiaries, providers and other
individuals who have made inquiries
concerning the fee-for-service program.
CATEGORIES OF RECORDS IN THE SYSTEM:
The system contains information such
as a beneficiary’s name, address data,
health insurance claim number (HICN),
demographic information, (gender, date
of birth), provider name, address data
and provider identification number
(NPI), provider organization
information, contact person
information, employer identification
numbers, and certain optional data such
as Social Security Numbers and other
provider identifiers used by these health
care providers.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for maintenance of this
system is given under § 923 of the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA) (Public Law (Pub. L.) 108–
173).
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PURPOSE(S) OF THE SYSTEM:
The primary purpose of the system is
to collect and maintain information
needed to provide a mechanism for
CMS’ central and regional office to
capture, track, manage, report and trend
inquiries, complaints and issues related
to Fee-for-Service (FFS) programs.
Information maintained in this system
will also be disclosed to: (1) Support
regulatory, reimbursement, and policy
functions performed within the Agency
or by a contractor, consultant or CMS
grantee; (2) assist another Federal or
state agency, agency of a state
government, an agency established by
state law, or its fiscal agent; (3) facilitate
research on the quality and effectiveness
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of care provided, as well as
epidemiological projects; (4) support
litigation involving the Agency; and (5)
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:
A. The Privacy Act allows us to
disclose information without an
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 compatible use of data is
known as a ‘‘routine use.’’ The proposed
routine uses in this system meet the
compatibility requirement of the Privacy
Act. We are proposing to establish the
following routine use disclosures of
information maintained in the system:
1. To support Agency contractors,
consultants, or grantees that have been
contracted by the Agency to assist in
accomplishment of a CMS function
relating to the purposes for this system
and who need access to the records in
order to assist CMS.
2. To assist another Federal or state
agency, agency of a state government, an
agency established by state law, or its
fiscal agent pursuant to agreements with
CMS to:
a. Contribute to the accuracy of CMS’s
proper payment of Medicare benefits,
b. Enable such agency to administer a
Federal health benefits program, or as
necessary to enable such agency to
fulfill a requirement of a Federal statute
or regulation that implements a health
benefits program funded in whole or in
part with Federal funds, and/or
c. Assist Federal/state Medicaid
programs within the state.
3. To an individual or organization for
a research project or in support of an
evaluation project related to the
prevention of disease or disability, the
restoration or maintenance of health, or
payment related projects.
4. To assist the Department of Justice
(DOJ), court or 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 States 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
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the purpose for which the agency
collected the records.
5. To support a CMS contractor that
assists in the administration of a CMSadministered health benefits program,
or to a grantee of a CMS-administered
grant program, 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.
6. To support another Federal agency
or to 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
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.
POLICIES AND PRACTICES FOR STORING,
RETRIEVING, ACCESSING, RETAINING, AND
DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
All records are stored on magnetic
media.
RETRIEVABILITY:
All records are accessible by
individual name or identification
number.
SAFEGUARDS:
CMS has safeguards in place for
authorized users and monitors such
users to ensure against excessive or
unauthorized use. 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.
This system will conform to all
applicable Federal laws and regulations
and Federal, HHS, and CMS policies
and standards as they relate to
information security and data privacy.
These laws and regulations may apply
but are not limited to: The Privacy Act
of 1974; the Federal Information
Security Management Act of 2002; the
Computer Fraud and Abuse Act of 1986;
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the Health Insurance Portability and
Accountability Act of 1996; the
E-Government Act of 2002, the ClingerCohen Act of 1996; the Medicare
Modernization Act of 2003, and the
corresponding implementing
regulations. OMB Circular A–130,
Management of Federal Resources,
Appendix III, Security of Federal
Automated Information Resources also
applies. Federal, HHS, and CMS
policies and standards include but are
not limited to: All pertinent National
Institute of Standards and Technology
publications; the HHS Information
Systems Program Handbook and the
CMS Information Security Handbook.
RECORD SOURCE CATEGORIES:
RETENTION AND DISPOSAL:
Request for Notification From Industry
Organizations Interested in
Participating in the Selection Process
for a Nonvoting Industry
Representative on the Pediatric
Advisory Committee and Request for
Nominations for a Nonvoting Industry
Representative on the Pediatric
Advisory Committee
Records are maintained for a period of
six years and three months. All claimsrelated records are encompassed by the
document preservation order and will
be retained until notification is received
by DOJ.
SYSTEM MANAGER AND ADDRESS:
Director, Division of Ombudsman
Casework and Trends Management,
Medicare Ombudsman Group, Office of
External Affairs, CMS, 7500 Security
Boulevard, Mail Stop S1–11–21,
Baltimore, Maryland 21244–1850.
NOTIFICATION PROCEDURE:
For purpose of access, the subject
individual health care provider should
write to the system manager who will
require the system name, National
Provider Identifier, address, date of
birth, and gender, and for verification
purposes, the subject individual health
care provider’s name (woman’s maiden
name, if applicable), and Social Security
number (SSN). Furnishing the SSN is
voluntary, but it may make searching for
a record easier and prevent delay.
RECORD ACCESS PROCEDURE:
For purpose of access, use the same
procedures outlined in Notification
Procedures above. Requestors should
also reasonably specify the record
contents being sought. (These
procedures are in accordance with
department regulation 45 CFR 5b.5(a)
(2)).
jlentini on PROD1PC65 with NOTICES
CONTESTING RECORD PROCEDURES:
The subject individual health care
provider should contact the systems
manager named above, and reasonably
identify the record and specify the
information to be contested. State the
corrective action sought and the reasons
for the correction with supporting
justification. (These procedures are in
accordance with department regulation
45 CFR 5b.7).
VerDate Aug<31>2005
19:49 Feb 26, 2008
Jkt 214001
The data contained in this system of
records are obtained from the
individuals who communicate or
correspond with CMS.
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS
OF THE ACT:
None.
[FR Doc. E8–3678 Filed 2–26–08; 8:45 am]
BILLING CODE 4120–03–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is requesting that
any industry organizations interested in
participating in the selection of a
nonvoting industry representative to
serve on its Pediatric Advisory
Committee notify FDA in writing. A
nominee may either be self-nominated
or nominated by an organization to
serve as a nonvoting industry
representative. Nominations will be
accepted for an upcoming vacancy on
June 30, 2008, effective with this notice.
DATES: Any industry organization
interested in participating in the
selection of an appropriate nonvoting
member to represent industry interests
must send a letter stating the interest to
FDA by March 28, 2008, for vacancies
listed in this notice. Concurrently,
nomination material for prospective
candidates should be sent to FDA by
March 28, 2008.
ADDRESSES: All letters of interest and
nominations should be submitted in
˜
writing to Carlos Pena (see FOR FURTHER
INFORMATION CONTACT).
FOR FURTHER INFORMATION CONTACT:
˜
Carlos Pena, Office of Science and
Health Coordination, Office of the
Commissioner (HF–33), Food and Drug
Administration, 5600 Fishers Lane (for
express delivery, rm. 14B–08),
Rockville, MD 20857, 301–827–3340, or
˜
by e-mail: Carlos.Pena@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: The
agency requests nominations for a
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
nonvoting industry representative on
the Pediatric Advisory Committee.
I. Function
The committee advises and makes
recommendations to the Commissioner
of Food and Drugs (the Commissioner)
regarding: (1) Pediatric research
conducted under sections 351, 409I, and
499 of the Public Health Service Act (42
U.S.C. 262, 284m, and 290b) and
sections 501, 502, 505, 505A, and 505B
of the Federal Food, Drug, and Cosmetic
Act (21 U.S.C. 351, 352, 355, 355a, and
355c); (2) identification of research
priorities related to pediatric
therapeutics and the need for additional
treatments of specific pediatric diseases
or conditions; (3) the ethics, design, and
analysis of clinical trials related to
pediatric therapeutics; (4) pediatric
labeling disputes as specified in section
3 of the Best Pharmaceuticals for
Children Act (Public Law 107–109); (5)
pediatric labeling changes as specified
in section 5 of the Best Pharmaceuticals
for Children Act; (6) adverse event
reports for drugs granted pediatric
exclusivity and any safety issues that
may occur as specified in section 17 of
the Best Pharmaceuticals for Children
Act; (7) any other pediatric issue or
pediatric labeling dispute involving
FDA-regulated products; (8) research
involving children as subjects as
specified in 21 CFR 50.54; and (9) any
other matter involving pediatrics for
which FDA has regulatory
responsibility. The committee also
advises and makes recommendations to
the Secretary of Health and Human
Services (the Secretary) directly or to
the Secretary through the Commissioner
on research involving children as
subjects that is conducted or supported
by the Department of Health and Human
Services as specified in 45 CFR 46.407.
II. Selection Procedure
Any pediatric products industry,
association, or organization interested in
the selection of an appropriate
nonvoting member to represent industry
interests should send a letter stating that
interest to the FDA contact (see FOR
FURTHER INFORMATION CONTACT) within
30 days of publication of this document
(see DATES). Within the subsequent 30
days, FDA will send a letter to each
organization that has expressed an
interest, attaching a complete list of all
such organizations, and a list of all
nominees along with their current
resumes. The letter will also state that
it is the responsibility of the interested
organizations to confer with one another
and to select an industry representative,
within 60 days after the receipt of the
FDA letter, and the industry
E:\FR\FM\27FEN1.SGM
27FEN1
Agencies
[Federal Register Volume 73, Number 39 (Wednesday, February 27, 2008)]
[Notices]
[Pages 10450-10454]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-3678]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
Privacy Act of 1974; Report of a New System of Records
AGENCY: Department of Health and Human Services (HHS), Centers for
Medicare & Medicaid Services (CMS).
ACTION: Notice of a New System of Records (SOR).
-----------------------------------------------------------------------
SUMMARY: In accordance with the requirements of the Privacy Act of
1974, we are proposing to establish a new system of records titled,
``Medicare Administrative Issue Tracker and Reporting of Operations
(MAISTRO) System,'' System No. 09-70-0598. The purpose of the system is
to capture and track casework/inquiries pertaining to Medicare Part A
and Part B programs. The system will also provide a mechanism for
recording data on a national level and will serve as a tool to leverage
in performing analysis including identification of systemic trends.
MAISTRO will record, track and monitor beneficiary and provider level
inquiries & complaints. The system will contain information needed to
research the inquiries, such as a beneficiary's health insurance claim
number (HICN) or a Provider Identification Number (NPI).
The primary purpose of the system is to collect and maintain
information needed to provide a mechanism for CMS' central and regional
office to capture, track, manage, report and trend inquiries,
complaints and issues related to Fee-for-Service (FFS) programs.
Information maintained in this system will also be disclosed to: (1)
Support regulatory, reimbursement, and policy functions performed
within the Agency or by a contractor, consultant or CMS grantee; (2)
assist another Federal or state agency, agency of a state government,
an agency established by state law, or its fiscal agent; (3) facilitate
research on the quality and effectiveness of care provided, as well as
epidemiological projects; (4) support litigation involving the Agency;
and (5) combat fraud, waste, and abuse in certain health benefits
programs. We have provided background information about the modified
system in the Supplementary Information section below. Although the
Privacy Act requires only that CMS provide an opportunity for
interested persons to comment on the proposed routine uses, CMS invites
comments on all portions of this notice. See EFFECTIVE DATES section
for comment period.
EFFECTIVE DATES: CMS filed a new system report with the Chair of the
House Committee on Oversight and Government Reform, the Chair of the
Senate Committee on Homeland Security and Governmental Affairs, and the
Administrator, Office of Information and Regulatory Affairs, Office of
Management and Budget (OMB) on 2/11/2008. In any event, we will not
disclose any information under a routine use until 30 days after
publication in the Federal Register or 40 days after mailings to
Congress, which ever is later. We may defer implementation of this
system or on one or more of the routine uses listed below if we receive
comments that persuade us to defer implementation.
ADDRESSES: The public should address comments to: CMS Privacy Officer,
Division of Privacy Compliance, Enterprise Architecture & Strategy
Group, Office of Information Services, CMS, Mail Stop N2-04-27, 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: Michele Livingston, Division of
Ombudsman Casework and Trends Management, Medicare Ombudsman Group,
Office of External Affairs, CMS, 7500 Security Boulevard, Mail Stop S1-
20-21, Baltimore, Maryland 21244-1850. The telephone number is 410-786-
6340 or contact Michele.Livingston@cms.hhs.gov.
SUPPLEMENTARY INFORMATION: The CMS Consortium for Financial Management
and Fee for Service Operations (CFMFFSO) is responsible for handling
casework/inquiries, but not limited to: (1) Coverage and payment
policy; (2) audit and reimbursement policy and operations; (3) program
integrity and medical review policy; (4) Medicare secondary payer and
coordination of benefits; (5) claims-related hearings, appeals and
grievances; (6) beneficiary eligibility, enrollment, entitlement,
rights and protections, premium billing and collection; and (7) dispute
resolution processes to assure the effective administration of the
Medicare program. These types of inquiries number in the tens of
thousands annually across the 10 CMS Regional Offices.
The Office of the Medicare Ombudsman was established as a result of
Section 923 of the Medicare
[[Page 10451]]
Modernization Act and is responsible for receiving complaints,
grievances and requests for information submitted by individuals
entitled to benefits under Part A or enrolled under Part B, or both,
with respect to any aspect of the Medicare program and providing
assistance with respect to complaints. Over the last year the focus of
inquiry tracking has centered on the implementation of Part D
reporting.
Although each regional office has developed its own system to track
and manage inquiries and complaints, these systems are inconsistent and
do not utilize standardized operational procedures or processes to
guide how inquiries are addressed or reported. Standardization will
improve performance, reduce operating costs, and enable statistical
analysis of the workload and trends among inquiries. To address these
issues, the following tasks had to be accomplished: (1) Identifying a
system to track beneficiary and provider inquiries, complaints and
issues specific to FFS operations; (2) Ensuring that casework
throughout each region is consistently captured and managed
appropriately which ensures the delivery of high quality customer
service to Medicare Part A and Part B beneficiaries and providers; and
(3) Producing workload data statistics to both account for the work and
enable improvement in CMS' policies and procedures.
When complete, the MAISTRO system will provide a mechanism for CMS'
central and regional office to capture, track, manage, report and trend
inquiries, complaints and issues related to Fee-for-Service.
Additionally, the goal of MAISTRO is to provide an easy to use system
that will provide consistency when tracking, resolving, and reporting
FFS inquiries, complaints and issues on a national level such that
trends, workloads and systemic issues can be identified and managed
appropriately across the consortium.
I. Description of the Proposed System of Records
A. Statutory and Regulatory Basis for SOR
Authority for maintenance of this system is given under Sec. 923
of the Medicare Prescription Drug, Improvement, and Modernization Act
of 2003 (MMA) (Public Law (Pub. L.) 108-173).
B. Collection and Maintenance of Data in the System
For purposes of this SOR, the system contains information on
Medicare beneficiaries, providers and other individuals who have made
inquiries concerning the fee-for-service program. The system contains
information such as a beneficiary's name, address data, health
insurance claim number (HICN), demographic information (gender, date of
birth), provider name, address data and provider identification number
(NPI), provider organization information, contact person information,
employer identification numbers, and certain optional data such as
Social Security Numbers and other provider identifiers used by these
health care providers.
II. Agency Policies, Procedures, and Restrictions on the Routine Use
A. Agency Policies, Procedures, and Restrictions Routine Uses
The Privacy Act permits us to disclose information without an
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 data is known as a ``routine use.''
The government will only release MAISTRO information that can be
associated with an individual as provided for under ``Section III.
Proposed Routine Use Disclosures of Data in the System.'' Both
individually identifiable and non-individually-identifiable data may be
disclosed under a routine use.
We will only disclose the minimum personal data necessary to
achieve the purpose of MAISTRO. CMS has the following policies and
procedures concerning disclosures of information that is maintained in
the system. Disclosure of information from the system will be approved
only to the extent necessary to accomplish the purpose of the
disclosure and only after CMS:
1. Determines that the use or disclosure is consistent with the
reason the data are being collected; e.g., to collect and maintain
information needed to provide a mechanism for CMS' central and regional
office to capture, track, manage, report and trend inquiries,
complaints and issues related to Fee-for-Service (FFS).
2. Determines that:
a. The purpose for which the disclosure is to be made can only be
accomplished if the record is provided in individually identifiable
form;
b. The purpose for which the disclosure is to be made is of
sufficient importance to warrant the effect and/or risk on the privacy
of the individual that additional exposure of the record might bring;
and
c. There is a strong probability that the proposed use of the data
would in fact accomplish the stated purpose(s).
3. Requires the information recipient to:
a. Establish administrative, technical, and physical safeguards to
prevent unauthorized use or disclosure of the record;
b. Remove or destroy at the earliest time all individually-
identifiable information; and
c. Agree to not use or disclose the information for any purpose
other than the stated purpose under which the information was
disclosed.
4. Determines that the data are valid and reliable.
III. Proposed Routine Use Disclosures of Data in the System
A. The Privacy Act allows us to disclose information without an
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 compatible use of data is known as a ``routine
use.'' The proposed routine uses in this system meet the compatibility
requirement of the Privacy Act. We are proposing to establish the
following routine use disclosures of information maintained in the
system:
1. To support Agency contractors, consultants, or CMS grantees that
have been contracted by the Agency to assist in accomplishment of a CMS
function relating to the purposes for this system and who need access
to the records in order to assist CMS.
We contemplate disclosing information under this routine use only
in situations in which CMS may enter into a contractual or similar
agreement with a third party to assist in accomplishing a CMS function
relating to purposes for this system.
CMS occasionally contracts out certain of its functions when doing
so would contribute to effective and efficient operations. CMS must be
able to give a contractor, consultant, or grantee whatever information
is necessary for the contractor, consultant, or grantee to fulfill its
duties. In these situations, safeguards are provided in the contract
prohibiting the contractor, consultant, or grantee from using or
disclosing the information for any purpose other than that described in
the contract and requires the contractor or consultant to return or
destroy all information at the completion of the contract.
2. To assist another Federal or state agency, agency of a state
government, an agency established by state law, or its
[[Page 10452]]
fiscal agent pursuant to agreements with CMS to:
a. Contribute to the accuracy of CMS's proper payment of Medicare
benefits,
b. Enable such agency to administer a Federal health benefits
program, or as necessary to enable such agency to fulfill a requirement
of a Federal statute or regulation that implements a health benefits
program funded in whole or in part with Federal funds, and/or
c. Assist Federal/state Medicaid programs within the state.
Other Federal or state agencies in their administration of a
Federal health program may require MAISTRO information for the purposes
of collecting and maintaining information needed to capture, track,
manage, report and trend inquiries, complaints and issues related to
Fee-for-Service (FFS).
Other Federal or state agencies, in their administration of a
Federal health program, may require MAISTRO information in order to
support evaluations and monitoring of Medicaid claims information of
beneficiaries, including proper reimbursement for services provided.
3. To an individual or organization for a research project or in
support of an evaluation project related to the prevention of disease
or disability, the restoration or maintenance of health, or payment
related projects.
The MAISTRO data will provide for research or support of evaluation
projects and a broader, longitudinal, national perspective of the
status of Medicaid beneficiaries. CMS anticipates that researchers may
have legitimate requests to use these data in projects that could
ultimately improve the care provided to Medicaid beneficiaries and the
policies that govern their care.
4. To assist the Department of Justice (DOJ), court or 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 States 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.
Whenever CMS is involved in litigation, or occasionally when
another party is involved in litigation and CMS's policies or
operations could be affected by the outcome of the litigation, CMS
would be able to disclose information to the DOJ, court, or
adjudicatory body involved.
5. To support a CMS contractor that assists in the administration
of a CMS-administered health benefits program, or to a grantee of a
CMS-administered grant program, 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.
We contemplate disclosing information under this routine use only
in situations in which CMS may enter into a contract or grant with a
third party to assist in accomplishing CMS functions relating to the
purpose of combating fraud, waste, and abuse.
CMS occasionally contracts out certain of its functions when doing
so would contribute to effective and efficient operations. CMS must be
able to give a contractor or CMS grantee whatever information is
necessary for the contractor or CMS grantee to fulfill its duties. In
these situations, safeguards are provided in the contract prohibiting
the contractor or grantee from using or disclosing the information for
any purpose other than that described in the contract and requiring the
contractor or grantee to return or destroy all information.
6. To support another Federal agency or to 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 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.
Other agencies may require MAISTRO information for the purpose of
combating fraud, waste, and abuse in such Federally-funded programs.
IV. Safeguards
CMS has safeguards in place for authorized users and monitors such
users to ensure against excessive or unauthorized use. 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.
This system will conform to all applicable Federal laws and
regulations and Federal, HHS, and CMS policies and standards as they
relate to information security and data privacy. These laws and
regulations may apply but are not limited to: The Privacy Act of 1974;
the Federal Information Security Management Act of 2002; the Computer
Fraud and Abuse Act of 1986; the Health Insurance Portability and
Accountability Act of 1996; the E-Government Act of 2002, the Clinger-
Cohen Act of 1996; the Medicare Modernization Act of 2003, and the
corresponding implementing regulations. OMB Circular A-130, Management
of Federal Resources, Appendix III, Security of Federal Automated
Information Resources also applies. Federal, HHS, and CMS policies and
standards include but are not limited to: All pertinent National
Institute of Standards and Technology publications; the HHS Information
Systems Program Handbook and the CMS Information Security Handbook.
V. Effects of the Proposed System of Records on Individual Rights
CMS proposes to establish this system in accordance with the
principles and requirements of the Privacy Act and will collect, use,
and disseminate information only as prescribed therein. Data in this
system will be subject to the authorized releases in accordance with
the routine uses identified in this system of records.
CMS will take precautionary measures to minimize the risks of
unauthorized access to the records and the potential harm to individual
privacy or other personal or property rights of patients whose data are
maintained in the system. CMS will collect only that information
necessary to perform the system's functions. In addition, CMS will make
disclosure from the proposed system only with consent of the subject
individual, or his/her legal representative, or in accordance with an
applicable exception provision of the Privacy Act. CMS, therefore, does
not anticipate an unfavorable effect on individual privacy as a result
of information relating to individuals.
[[Page 10453]]
Dated: February 20, 2008.
Charlene Frizzera,
Chief Operating Officer, Centers for Medicare & Medicaid Services.
SYSTEM NUMBER: 09-70-0598
SYSTEM NAME:
``Medicare Administrative Issue Tracker and Reporting of Operations
(MAISTRO) System,'' HHS/CMS/OEA.
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive Data.
SYSTEM LOCATION:
Centers for Medicare & Medicaid Services (CMS) Data Center, 7500
Security Boulevard, North Building, First Floor, Baltimore, Maryland
21244.
CATEGORIES OF INDIVIDUALS COVERED BY THE SYSTEM:
For purposes of this SOR, the system contains information on
Medicare beneficiaries, providers and other individuals who have made
inquiries concerning the fee-for-service program.
CATEGORIES OF RECORDS IN THE SYSTEM:
The system contains information such as a beneficiary's name,
address data, health insurance claim number (HICN), demographic
information, (gender, date of birth), provider name, address data and
provider identification number (NPI), provider organization
information, contact person information, employer identification
numbers, and certain optional data such as Social Security Numbers and
other provider identifiers used by these health care providers.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for maintenance of this system is given under Sec. 923
of the Medicare Prescription Drug, Improvement, and Modernization Act
of 2003 (MMA) (Public Law (Pub. L.) 108-173).
PURPOSE(S) OF THE SYSTEM:
The primary purpose of the system is to collect and maintain
information needed to provide a mechanism for CMS' central and regional
office to capture, track, manage, report and trend inquiries,
complaints and issues related to Fee-for-Service (FFS) programs.
Information maintained in this system will also be disclosed to: (1)
Support regulatory, reimbursement, and policy functions performed
within the Agency or by a contractor, consultant or CMS grantee; (2)
assist another Federal or state agency, agency of a state government,
an agency established by state law, or its fiscal agent; (3) facilitate
research on the quality and effectiveness of care provided, as well as
epidemiological projects; (4) support litigation involving the Agency;
and (5) 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:
A. The Privacy Act allows us to disclose information without an
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 compatible use of data is known as a ``routine
use.'' The proposed routine uses in this system meet the compatibility
requirement of the Privacy Act. We are proposing to establish the
following routine use disclosures of information maintained in the
system:
1. To support Agency contractors, consultants, or grantees that
have been contracted by the Agency to assist in accomplishment of a CMS
function relating to the purposes for this system and who need access
to the records in order to assist CMS.
2. To assist another Federal or state agency, agency of a state
government, an agency established by state law, or its fiscal agent
pursuant to agreements with CMS to:
a. Contribute to the accuracy of CMS's proper payment of Medicare
benefits,
b. Enable such agency to administer a Federal health benefits
program, or as necessary to enable such agency to fulfill a requirement
of a Federal statute or regulation that implements a health benefits
program funded in whole or in part with Federal funds, and/or
c. Assist Federal/state Medicaid programs within the state.
3. To an individual or organization for a research project or in
support of an evaluation project related to the prevention of disease
or disability, the restoration or maintenance of health, or payment
related projects.
4. To assist the Department of Justice (DOJ), court or 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 States 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.
5. To support a CMS contractor that assists in the administration
of a CMS-administered health benefits program, or to a grantee of a
CMS-administered grant program, 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.
6. To support another Federal agency or to 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 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.
POLICIES AND PRACTICES FOR STORING, RETRIEVING, ACCESSING, RETAINING,
AND DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
All records are stored on magnetic media.
RETRIEVABILITY:
All records are accessible by individual name or identification
number.
SAFEGUARDS:
CMS has safeguards in place for authorized users and monitors such
users to ensure against excessive or unauthorized use. 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.
This system will conform to all applicable Federal laws and
regulations and Federal, HHS, and CMS policies and standards as they
relate to information security and data privacy. These laws and
regulations may apply but are not limited to: The Privacy Act of 1974;
the Federal Information Security Management Act of 2002; the Computer
Fraud and Abuse Act of 1986;
[[Page 10454]]
the Health Insurance Portability and Accountability Act of 1996; the E-
Government Act of 2002, the Clinger-Cohen Act of 1996; the Medicare
Modernization Act of 2003, and the corresponding implementing
regulations. OMB Circular A-130, Management of Federal Resources,
Appendix III, Security of Federal Automated Information Resources also
applies. Federal, HHS, and CMS policies and standards include but are
not limited to: All pertinent National Institute of Standards and
Technology publications; the HHS Information Systems Program Handbook
and the CMS Information Security Handbook.
RETENTION AND DISPOSAL:
Records are maintained for a period of six years and three months.
All claims-related records are encompassed by the document preservation
order and will be retained until notification is received by DOJ.
SYSTEM MANAGER AND ADDRESS:
Director, Division of Ombudsman Casework and Trends Management,
Medicare Ombudsman Group, Office of External Affairs, CMS, 7500
Security Boulevard, Mail Stop S1-11-21, Baltimore, Maryland 21244-1850.
NOTIFICATION PROCEDURE:
For purpose of access, the subject individual health care provider
should write to the system manager who will require the system name,
National Provider Identifier, address, date of birth, and gender, and
for verification purposes, the subject individual health care
provider's name (woman's maiden name, if applicable), and Social
Security number (SSN). Furnishing the SSN is voluntary, but it may make
searching for a record easier and prevent delay.
RECORD ACCESS PROCEDURE:
For purpose of access, use the same procedures outlined in
Notification Procedures above. Requestors should also reasonably
specify the record contents being sought. (These procedures are in
accordance with department regulation 45 CFR 5b.5(a) (2)).
CONTESTING RECORD PROCEDURES:
The subject individual health care provider should contact the
systems manager named above, and reasonably identify the record and
specify the information to be contested. State the corrective action
sought and the reasons for the correction with supporting
justification. (These procedures are in accordance with department
regulation 45 CFR 5b.7).
RECORD SOURCE CATEGORIES:
The data contained in this system of records are obtained from the
individuals who communicate or correspond with CMS.
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS OF THE ACT:
None.
[FR Doc. E8-3678 Filed 2-26-08; 8:45 am]
BILLING CODE 4120-03-P