[Federal Register: October 12, 2006 (Volume 71, Number 197)]
[Notices]
[Page 60153-60157]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr12oc06-58]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
Privacy Act of 1974; Report of a Modified or Altered System of
Records
AGENCY: Department of Health and Human Services (HHS), Centers for
Medicare & Medicaid Services (CMS).
ACTION: Notice of a Modified or Altered System of Records (SOR).
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SUMMARY: In accordance with the Privacy Act of 1974, we are proposing
to modify or alter an existing SOR, ``Medicare Managed Care Beneficiary
Reconsideration (RECON) System,'' System No. 09-70-4003, last published
at 67 Federal Register 48179 (July 23, 2002). We propose to assign a
new CMS identification number to this system to simplify the obsolete
and confusing numbering system originally designed to identify the
Bureau, Office, or Center within CMS that maintained the system of
records. The new assigned identifying number for this system should
read: System No. 09-70-0533.
We propose to modify existing routine use number 1 that permits
disclosure to agency contractors and consultants to include disclosure
to CMS grantees who perform a task for the agency. CMS grantees,
charged with completing projects or activities that require CMS data to
carry out that activity, are classified separate from CMS contractors
and/or consultants. The modified routine use will remain as routine use
number 1. We will delete routine use number 5 authorizing disclosure to
support constituent requests made to a congressional representative. If
an authorization for the disclosure has been obtained from the data
subject, then no routine use is needed. The Privacy Act allows for
disclosures with the ``prior written consent'' of the data subject. We
will broaden the scope of routine uses number 7 and 8, authorizing
disclosures to combat fraud and abuse in the Medicare and Medicaid
programs to include combating ``waste'' which refers to specific
beneficiary/recipient practices that result in unnecessary cost to all
Federally-funded health benefit programs
We are modifying the language in the remaining routine uses to
provide a proper explanation as to the need for the routine use and to
provide clarity to CMS' intention to disclose individual-specific
information contained in this system. The routine uses will then be
prioritized and reordered according to their usage. We will also take
the opportunity to update any sections of the system that were affected
by the recent reorganization or the Medicare Prescription Drug,
Improvement, and Modernization Act of 2003 (MMA) (Public Law 108-173)
provisions and to update language in the administrative sections to
correspond with language used in other CMS SORs.
The primary purpose of this modified system is to collect and
maintain information necessary to process requests for reconsideration
of service requests or claims by or on behalf of Medicare managed care
enrollees, promote the effectiveness and integrity of the Medicare
managed care program, and reply to future correspondence related to the
case. The information retrieved from this system of records will also
be disclosed to: (1) Support regulatory, reimbursement, and policy
functions performed within the agency or by a contractor or consultant;
(2) assist another Federal or state agency; (3) assist third party
contacts; (4) assist Quality Improvement Organizations; (5) support
litigation involving the agency; and (6) combat fraud, waste, and abuse
in Federally-funded health benefit 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
modified or altered routine uses, CMS invites comments on all portions
of this notice. See ``Effective Dates'' section for comment period.
DATES: Effective Date: CMS filed a modified or altered SOR 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 October 5, 2006. To
ensure that all parties have adequate time in which to comment, the new
system will become effective 30 days from the publication of the
notice, or 40 days from the date it was submitted to OMB and the
Congress, whichever is later. We may defer implementation of this
system or one or more of the routine use statements listed below if we
receive comments that persuade us to defer implementation.
ADDRESSES: The public should address comments to the CMS Privacy
Officer, Division of Privacy Compliance, Enterprise Architecture and
Strategy Group, Office of Information Services, 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 daylight time.
FOR FURTHER INFORMATION CONTACT: Beverly Sgroi, Health Insurance
Specialist, Division of Appeals Policy, Medicare Enrollment & Appeals
Group, Center for Beneficiary Choices, CMS, Mail Stop C2-12-16, 7500
Security Boulevard, Baltimore, Maryland 21244-1850. She can also be
reached by telephone at 410-786-7638, or via e-mail at
Beverly.Sgroi@cms.hhs.gov.
SUPPLEMENTARY INFORMATION: In 1988, CMS established a SOR under the
authority of Sec. 1874 of the Social Security Act (the Act) (Title 42
United States Code (U.S.C.) section 1395mm). Notice of this system,
RECON, was published in the Federal Register (FR) 53 FR 35914
(September 15, 1988), a routine use was added for the Social Security
Administration at 61 FR 6645 (February 21, 1996), three new fraud and
abuse routine uses were added at 63 FR 38414 (July 16, 1998), two fraud
and abuse routine uses were revised and a third deleted at 65 FR 50552
(August 18, 2000), and the name and security classification were
changed as well as deleting a routine use for the state insurance
administrator at 67 FR 48179 (July 23, 2002).
I. Description of the Modified or Altered System of Records
A. Statutory and Regulatory Basis for SOR
Authority for maintenance of the system is given under Sec. Sec.
1852, and 1876
[[Page 60154]]
of the Social Security Act (Title 42 U.S.C. 1395w-22, and 1395mm).
B. Collection and Maintenance of Data in the System
RECON contains information concerning Medicare beneficiaries who
have been enrolled in a managed care program and who have requested an
appeal by CMS, or any person who acts on behalf of these beneficiaries.
Information in this system includes, but is not limited to, name,
address, social security number, health insurance claim number, health
insurance plan name and address, health insurance plan number, medical
records and statement of fact, service request/claims data, date of
service request/claim received by the health plan, dates of service,
beneficiary enrollment form and disenrollment form, verification of
enrollment status, date reconsideration request submitted to CMS, and
dates of determination by plan and CMS.
II. Agency Policies, Procedures, and Restrictions on the Routine Use
A. Agency Policies, Procedures, and Restrictions on the Routine Use
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 RECON information that can be
associated with an individual as provided for under ``Section III.
Proposed Routine Use Disclosures of Data in the System.'' Both
identifiable and non-identifiable data may be disclosed under a routine
use.
We will only collect the minimum personal data necessary to achieve
the purpose of RECON. CMS has the following policies and procedures
concerning disclosures of information that will be maintained in the
system. Disclosure of information from this 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 that the data is being collected, e.g., to collect and maintain
information necessary to process requests for reconsideration of
service requests or claims by or on behalf of Medicare managed care
enrollees, promote the effectiveness and integrity of the Medicare
managed care program, and reply to future correspondence related to the
case.
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 of disclosure of the record;
b. remove or destroy at the earliest time all patient-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 a grantee of a
CMS-administered grant program, who have been engaged by the agency to
assist in the accomplishment of a CMS function relating to the purposes
for this system and who need to have access to the records in order to
assist CMS.
We contemplate disclosing this 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, consultant or grantee to
return or destroy all information at the completion of the contract.
2. To another Federal or state agency to:
a. contribute to the accuracy of CMS' 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 RECON information in order to
support evaluations and monitoring of Medicare claims information of
beneficiaries, including proper reimbursement for services provided.
In addition, other state agencies in their administration of a
Federal health program may require RECON information for the purposes
of determining, evaluating and/or assessing cost, effectiveness, and/or
the quality of health care services provided in the state.
SSA requires RECON data to enable them to assist in the
implementation and maintenance of the Medicare program.
State Insurance Commissioners or other state regulators with
similar authority acting in a manner consistent with maintaining the
integrity of the Medicare program may require RECON data to assist in
accomplishing their activities.
3. To assist a third party contact in situations where the party to
be contacted has, or is expected to have information relating to the
individual's capacity to manage his or her affairs or to his or her
eligibility for, or an entitlement to, benefits under the Medicare
program.
a. The individual is unable to provide the information being sought
(an individual is considered to be unable to provide certain types of
information when any of the following conditions exist: the individual
is confined to a mental institution, a court of competent jurisdiction
has appointed a guardian to manage the affairs of that individual, a
court of competent jurisdiction has declared the individual to be
mentally incompetent, or the individual's attending physician has
certified that the individual is not sufficiently
[[Page 60155]]
mentally competent to manage his or her own affairs or to provide the
information being sought, the individual cannot read or write, cannot
afford the cost of obtaining the information, a language barrier
exists, or the custodian of the information will not, as a matter of
policy, provide it to the individual), or
b. The data are needed to establish the validity of evidence or to
verify the accuracy of information presented by the individual, and it
concerns one or more of the following: The individual's entitlement to
benefits under the Medicare program, the amount of reimbursement, or
any case in which the evidence is being reviewed as a result of
suspected fraud and abuse, program integrity, quality appraisal, or
evaluation and measurement of activities.
Third party contacts require RECON information in order to provide
support for the individual's entitlement to benefits under the Medicare
program, to establish the validity of evidence or to verify the
accuracy of information presented by the individual, and assist in the
monitoring of Medicare claims information of beneficiaries, including
proper reimbursement of services provided.
4. To support Quality Improvement Organizations (QIO) in order to
assist the QIO to perform Title XI and Title XVIII functions relating
to assessing and improving quality of care.
The QIO will work to implement quality improvement programs,
provide consultation to CMS, its contractors, and to state agencies.
The QIO will assist state agencies in related monitoring and
enforcement efforts, assist CMS and intermediaries in program integrity
assessment, and prepare summary information for release to CMS.
5. 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, and 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.
6. To assist a CMS contractor (including, but not necessarily
limited to fiscal intermediaries and carriers) 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
program.
We contemplate disclosing information under this routine use only
in situations in which CMS may enter into a contractual relationship 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 and makes
grants when doing so would contribute to effective and efficient
operations. CMS must be able to give a contractor or grantee whatever
information is necessary for the contractor or 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.
7. To assist 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 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.
Other agencies may require RECON information for the purpose of
combating fraud, waste, and abuse in such Federally-funded programs.
B. Additional Provisions Affecting Routine Use Disclosures
To the extent this system contains 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) 65 FR 82462 (12-28-00). 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, our policy will be to prohibit release even of data
not directly identifiable, except pursuant to one of the routine uses
or if required by law, if we determine there is a possibility that an
individual can be identified through implicit deduction based on small
cell sizes (instances where the patient population is so small that an
individual could, because of the small size, use this information to
deduce the identity of the beneficiary).
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
[[Page 60156]]
Institute of Standards and Technology publications; the HHS Information
Systems Program Handbook and the CMS Information Security Handbook.
V. Effects of the Modified System of Records on Individual Rights
CMS proposes to modify 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.
Dated: October 4, 2006.
Charlene Frizzera,
Acting Chief Operating Officer, Centers for Medicare & Medicaid
Services.
SYSTEM NO. 09-70-0533
SYSTEM NAME:
``Medicare Managed Care Beneficiary Reconsideration (RECON)
System,'' HHS/CMS/CBC.
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive Data.
SYSTEM LOCATION:
The Centers for Medicare & Medicaid Services (CMS) Data Center,
7500 Security Boulevard, North Building, First Floor, Baltimore,
Maryland 21244-1850 and at various contractor sites and at CMS Regional
Offices.
CATEGORIES OF INDIVIDUALS COVERED BY THE SYSTEM:
RECON contains information concerning Medicare beneficiaries who
have been enrolled in a managed care program and who have requested an
appeal by CMS, or any person who acts on behalf of these beneficiaries.
CATEGORIES OF RECORDS IN THE SYSTEM:
Information in this system includes, but is not limited to, name,
address, social security number (SSN), health insurance claim number
(HICN), health insurance plan name and address, health insurance plan
number, medical records and statement of fact, service request/claims
data, date of service request/claim received by the health plan, dates
of service, beneficiary enrollment form and disenrollment form,
verification of enrollment status, date reconsideration request
submitted to CMS, and dates of determination by plan and CMS.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for maintenance of the system is given under Sec. Sec.
1852, and 1876 of the Social Security Act (Title 42 U.S.C. 1395w-22,
and 1395mm).
PURPOSE(S) OF THE SYSTEM:
The primary purpose of this modified system is to collect and
maintain information necessary to process requests for reconsideration
of service requests or claims by or on behalf of Medicare managed care
enrollees, promote the effectiveness and integrity of the Medicare
managed care program, and reply to future correspondence related to the
case. The information retrieved from this system of records will also
be disclosed to: (1) Support regulatory, reimbursement, and policy
functions performed within the agency or by a contractor or consultant;
(2) assist another Federal or state agency; (3) assist third party
contacts; (4) assist Quality Improvement Organizations; (5) support
litigation involving the agency; and (6) combat fraud, waste, and abuse
in Federally-funded health benefit 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 a grantee of a
CMS-administered grant program, who have been engaged by the agency to
assist in the accomplishment of a CMS function relating to the purposes
for this system and who need to have access to the records in order to
assist CMS.
2. To assist another Federal and/or state agency to:
a. contribute to the accuracy of CMS' 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 assist a third party contact in situations where the party to
be contacted has, or is expected to have information relating to the
individual's capacity to manage his or her affairs or to his or her
eligibility for, or an entitlement to, benefits under the Medicare
program.
a. The individual is unable to provide the information being sought
(an individual is considered to be unable to provide certain types of
information when any of the following conditions exist: the individual
is confined to a mental institution, a court of competent jurisdiction
has appointed a guardian to manage the affairs of that individual, a
court of competent jurisdiction has declared the individual to be
mentally incompetent, or the individual's attending physician has
certified that the individual is not sufficiently mentally competent to
manage his or her own affairs or to provide the information being
sought, the individual cannot read or write, cannot afford the cost of
obtaining the information, a language barrier exists, or the custodian
of the information will not, as a matter of policy, provide it to the
individual), or
b. The data are needed to establish the validity of evidence or to
verify the accuracy of information presented by the individual, and it
concerns one or more of the following: The individual's entitlement to
benefits under the Medicare program, the amount of reimbursement, or
any case in which the evidence is being reviewed as a result of
suspected fraud and abuse, program integrity, quality appraisal, or
evaluation and measurement of activities.
4. To assist Quality Improvement Organizations (QIO) in order to
assist the QIO to perform Title XI and Title XVIII functions relating
to assessing and improving quality of care.
5. To support 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
[[Page 60157]]
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.
6. To assist a CMS contractor (including, but not necessarily
limited to fiscal intermediaries and carriers) 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
program.
7. 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.
B. Additional Provisions Affecting Routine Use Disclosures.
To the extent this system contains 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) 65 FR 82462 (12-28-00). 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, our policy will be to prohibit release even of data
not directly identifiable, except pursuant to one of the routine uses
or if required by law, if we determine there is a possibility that an
individual can be identified through implicit deduction based on small
cell sizes (instances where the patient population is so small that an
individual could, because of the small size, use this information to
deduce the identity of the beneficiary).
POLICIES AND PRACTICES FOR STORING, RETRIEVING, ACCESSING, RETAINING,
AND DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
All records are stored on computer diskette and magnetic media.
RETRIEVABILITY:
Information can be retrieved by the name, SSN, and/or HICN of
claimant.
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.
RETENTION AND DISPOSAL:
CMS will transfer to and maintain in an archival file for a total
period not to exceed 7 years. All claims-related records are
encompassed by the document preservation order and will be retained
until notification is received from DOJ.
SYSTEM MANAGER(S) AND ADDRESS:
Director, Division of Appeals Policy, Medicare Enrollment & Appeals
Group, Center for Beneficiary Choices, CMS, Mail Stop C2-12-16, 7500
Security Boulevard, Baltimore, Maryland 21244-1850.
NOTIFICATION PROCEDURE:
For purpose of access, the subject individual should write to the
system manager who will require the system name, HICN, address, date of
birth, and gender, and for verification purposes, the subject
individual's name (woman's maiden name, if applicable), and 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 specify the
record contents being sought. (These procedures are in accordance with
department regulation 45 CFR 5b.5(a)(2)).
CONTESTING RECORDS PROCEDURES:
The subject individual should contact the system manager named
above, and reasonably identify the records 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).
RECORDS SOURCE CATEGORIES:
Sources on information contained in this records system is obtained
from the reconsideration requests made by or on behalf of Medicare
beneficiaries and from inquiries from congressional offices, health
plans, providers, state insurance commissioners, state regulators,
disenrollment surveys, Medicare carriers or intermediaries, and QIO
records.
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS OF THE ACT:
None.
[FR Doc. E6-16852 Filed 10-11-06; 8:45 am]
BILLING CODE 4120-03-P