Office of the Assistant Secretary for Planning and Evaluation; Privacy Act of 1974; Report of New System of Records, 77027-77029 [E8-28345]
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Federal Register / Vol. 73, No. 244 / Thursday, December 18, 2008 / Notices
77027
studies to assess the carcinogenic
potency of a class of agents with dioxinlike activity
• TR 558 3,3′,4,4′Tetrachloroazobenzene (CASRN 14047–
09–7)
Æ Impurity in dichloroaniline and in
herbicides derived from dichloroaniline;
evaluated as part of the Dioxin Toxic
Equivalency Factor Evaluation for
compounds with dioxin-like activity
• TR 560 Androstenedione (CASRN
63–05–8)
Æ Dietary supplement that was used
by athletes during training, but now is
banned for over-the-counter sale
• TR 557 b-Myrcene (CASRN 123–
35–3)
Æ Intermediate in the commercial
production of terpene alcohols, which
are intermediates in the production of
aroma and flavoring chemicals; used as
a scent in cosmetics and soaps and as
a flavoring additive in food and
beverages; major constituent of hop and
bay oils
• TR 555 Tetralin (CASRN 119–64–2)
Æ Used as an industrial solvent for
paints, waxes, polishes, pesticides,
rubber, asphalt, and aromatic
hydrocarbons; used as an insecticide;
derived from naphthalene
• TR 562 Goldenseal Root Powder
(CASRN goldensealRT)
Æ Natural herbal remedy for which
there is little or no toxicity data
portion of the system be published for
comment, ASPE invites comments on
all portions of this notice. Elsewhere in
today’s Federal Register, a related final
rulemaking establishing the State Long
Term Care Partnership: Reporting
Requirements for Insurers.
Dated: November 21, 2008.
Mary M. McGeein,
Principal Deputy Assistant Secretary for
Planning and Evaluation.
DATES: Effective Date: The new system
of records, including routine uses, will
become effective January 27, 2009
unless ASPE receives comments that
require alteration to this notice.
SYSTEM NAME:
[FR Doc. E8–30024 Filed 12–17–08; 8:45 am]
The Partnership for Long Term Care
initiative was mandated by Section 6021
of Public Law 109–171, the Deficit
Reduction Act of 2005 (DRA). The
Partnership allows states to offer special
Medicaid asset disregards to persons
purchasing specially certified long term
care insurance policies. The asset
disregards allow program participants to
keep additional assets should they need
to apply for Medicaid coverage of long
term care. DRA also mandates the use of
a standard reporting system for all
insurers participating in a state
Partnership for Long Term Care program
through a Medicaid State Plan
Amendment approved after May 14,
1993. Participating insurers are required
to report data on Partnership policy
purchasers, features of the policies they
purchase, and, selected claims
information.
The Privacy Act permits us to disclose
information without the consent of
individuals under a ‘‘routine use.’’ A
routine use is a disclosure outside of the
Department of Health and Human
Services that is compatible with the
purpose for which we collected the
information. The proposed routine uses
in the new system of records meet the
compatibility criterion of the statute.
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Assistant Secretary for
Planning and Evaluation; Privacy Act
of 1974; Report of New System of
Records
mstockstill on PROD1PC66 with NOTICES
AGENCY: Office of the Assistant
Secretary for Planning and Evaluation
(ASPE).
ACTION: Notice of new System of
Records (SOR).
SUMMARY: In accordance with the
requirements of the Privacy Act of 1974,
the Office of Assistant Secretary for
Planning and Evaluation (ASPE) is
proposing to establish a new system of
records, called the Partnership for Long
Term Care Data Set. The Partnership
allows states to offer special Medicaid
asset disregards to persons purchasing
specially certified long term care
insurance policies. This program and
the data collection were established by
the Deficit Reduction Act of 2005—
Section 6021. Although the Privacy Act
requires only that the ‘‘routine uses’’
VerDate Aug<31>2005
17:51 Dec 17, 2008
Jkt 217001
Address comments to the
Privacy Act Officer, Office of Assistant
Secretary for Planning and Evaluation,
U.S. Department of Health and Human
Services, 200 Independence Ave, SW.,
Room Number 436E.2, Washington, DC
20201. 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. Call
202–205–8999 for appointment.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Hunter McKay, Office of the Assistant
Secretary for Planning and Evaluation,
U.S. Department of Health and Human
Services, 200 Independence Ave, SW.,
Room Number 424E, Washington, DC
20201. The telephone number is (202)
205–8999 and the e-mail address is
hunter.mckay@hhs.gov.
SUPPLEMENTARY INFORMATION:
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Frm 00028
Fmt 4703
Sfmt 4703
SYSTEM NO.
09–90–0085
Partnership for Long Term Care Data
Set.
SECURITY CLASSIFICATION:
None.
SYSTEM LOCATION:
Thomson Reuters, 610 Opperman
Drive, Eagan, Minnesota 55123.
CATEGORIES OF INDIVIDUALS COVERED BY THE
SYSTEM:
Purchasers of long term care
insurance policies certified by a selected
state (Medicaid state plan amendment
approved after May 14, 1993) insurance
commissioner as meeting the state’s
Partnership’s requirements for
certification.
CATEGORIES OF RECORDS IN THE SYSTEM:
◊ Name
◊ Address
◊ Social Security Number
◊ Date of Birth
◊ Long Term Care Insurance Policy
Information
Æ Long Term Care Insurance
Company
Æ Long Term Care Insurance Policy
Number
Æ Type of Policy (Group, Individual
and Comprehensive, Nursing Home
Only)
Æ Policy Issue State
Æ Lifetime Maximum Benefit
Æ Duration of Insurance Benefits
(dollars or days)
Æ Daily Benefit Amount
Æ Inflation Protection Feature
(required by DRA for select ages)
◊ Claims Information
Æ Qualifying Condition for Claim
(ADL, Cognitive Impairment, Other)
Æ Benefits Payment by Type of
Service (institutional or home)
Æ Remaining Lifetime Maximum
Benefits (by service type when multiple
pools)
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
The authority for this system of
records is contained in Section 6021 of
the Deficit Reduction Act of 2005,
Public Law 109–171, 42 U.S.C. 1396p
note.
PURPOSE(S) OF THE SYSTEM:
The purpose of the system of records
is to support Medicaid eligibility
determinations for persons participating
in a Partnership for long term care
program.
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77028
Federal Register / Vol. 73, No. 244 / Thursday, December 18, 2008 / Notices
mstockstill on PROD1PC66 with NOTICES
ROUTINE USES OF RECORDS MAINTAINED IN THE
SYSTEM, INCLUDING CATEGORIES OF USERS AND
THE PURPOSE OF SUCH USES:
Section 552a(b)(3) of the Privacy Act
permits an agency to establish
disclosures not anticipated by the
statute itself, compatible with the
purpose for which the information was
collected, under which the information
may be released without the consent of
the individual to whom the information
pertains. ASPE is identifying the
following routine disclosures for
information held in the Partnership for
Long Term Care Data Set. Each
proposed disclosure of information
under these routine uses will be
evaluated to ensure that the disclosure
is legally permissible, including, but not
limited to, ensuring that the purpose of
the disclosure is compatible with the
purpose for which the information was
collected. Disclosure may be made
under the following circumstances.
1. Disclosure may be made to a State,
local, tribal or other public authority for
the purpose of verifying Partnership
program participation and calculation of
the amount of the Medicaid Partnership
asset disregard.
2. Disclosure may be made to the
Department of Justice when: (a) The
agency or any component thereof; or (b)
any employee of the agency in his or her
official capacity; (c) any employee of the
agency in his or her individual capacity
where agency or the Department of
Justice 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, the agency determines
that the records are both relevant and
necessary to the litigation and the use of
such records by the Department of
Justice is therefore deemed by the
agency to be for a purpose that is
compatible with the purpose for which
the agency collected the records.
3. Disclosure may be made to a court
or adjudicative body in a proceeding
when: (a) The agency or any component
thereof; or (b) any employee of the
agency in his or her official capacity; (c)
any employee of the agency in his or her
individual capacity where agency or the
Department of Justice 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, the
agency determines that the records are
both relevant and necessary to the
litigation and the use of such records is
therefore deemed by the agency to be for
a purpose that is compatible with the
purpose for which the agency collected
the records.
VerDate Aug<31>2005
17:51 Dec 17, 2008
Jkt 217001
4. When a record on its face, or in
conjunction with other records,
indicates a violation or potential
violation of law, whether civil, criminal,
or regulatory in nature, and whether
arising by general statute or particular
program statute, or by regulation, rule,
or order issued pursuant thereto,
disclosure may be made to the
appropriate public authority, whether
Federal, foreign, state, local, tribal, or
otherwise responsible for enforcing,
investigating, or prosecuting such
violation or charged with enforcing, or
implementing the statute, rule,
regulation, or order issued pursuant
hereto, if the information disclosed is
relevant to any enforcement, regulatory,
investigative or prosecutorial
responsibility of the receiving entity.
5. Disclosure may be made to a
Member of Congress or to a
congressional staff member in response
to an inquiry of the congressional office
made at the written request of the
constituent about whom the record is
maintained. The Member of Congress
does not have any greater authority to
obtain records than the individual
would have if requesting the record
directly.
6. Disclosure may be made to agency
contractors, grantees, or volunteers who
have been engaged to assist the agency
in the performance of a contract service,
grant, cooperative agreement or other
activity related to this system of records
and who need to have access to the
records in order to perform the activity.
Recipients shall be required to comply
with the requirements of the Privacy Act
of 1974, as amended 5 U.S.C. 552a.
7. Disclosure may be made to an
individual or organization conducting a
research, demonstration, or evaluation
project related to long term care
financing generally, the performance of
long term care insurance or Partnership
programs, or for the purposes of
determining, evaluating, assessing cost
effectiveness, or quality of the long term
care services provided through a
Partnership program.
8. To another Federal or state agency
for the purpose of operating the
Medicaid program or otherwise assisting
states in the administration of those
portions of the Medicaid program with
direct connection to state Partnership
programs.
9. To appropriate federal agencies and
Department contractors that have a need
to know the information for the purpose
of assisting the Department’s efforts to
respond to a suspected or confirmed
breach of the security or confidentiality
of information maintained in this
system of records, and the information
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Fmt 4703
Sfmt 4703
disclosed is relevant and necessary for
that assistance.
POLICIES AND PRACTICES FOR STORING,
RETRIEVING, ACCESSING, RETAINING, AND
DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
All records are stored on paper or
magnetic media.
RETRIEVABILITY:
The records are retrieved by the long
term care insurance policy number,
name, social security number, or a
combination of these.
SAFEGUARDS:
For computerized records, safeguards
established in accordance with
Department standards and National
Institute of Standards and Technology
guidelines (e.g., security codes) will be
used, limiting access to authorized
personnel. System security policy and
practices are established in accordance
with HHS, Information Resources
Management (IRM) Circular #10,
Automated Information Systems
Security Program; HCFA Automated
Information System (AIS) Guide,
Systems Security Policies; and OMB
Circular No. A–130 (revised), Appendix
III.
RETENTION AND DISPOSAL:
We are working with the National
Archives and Records Administration
(NARA) to determine the appropriate
retention schedule. Due to the nature of
these records, we expect them to be
preserved for at least 20 years after the
death of the policyholder. When the
retention period has been approved by
NARA, we will amend this notice.
SYSTEM MANAGER(S) AND ADDRESS:
Hunter McKay, Office of the Assistant
Secretary for Planning and Evaluation,
U.S. Department of Health and Human
Services, 200 Independence Ave, SW.,
Room Number 424E, Washington, DC
20201.
NOTIFICATION PROCEDURE:
For purpose of notification,
individuals may write the system
manager, who will require the insured’s
name, insurance company name,
insurance policy number, and, for
verification purposes, date of birth, to
ascertain whether or not the
individual’s record is in the system.
(These notification procedures are in
accordance with Department regulation
45 CFR part 5b.)
RECORD ACCESS PROCEDURE:
Same as notification procedures.
Requestors should also reasonably
specify the record contents being
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Federal Register / Vol. 73, No. 244 / Thursday, December 18, 2008 / Notices
sought. (These access procedures are in
accordance with the Department
regulation 45 CFR 5b.5(a)(2).)
CONTESTING RECORD PROCEDURES:
Contact the system 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:
Information is reported by private
long term care insurance companies
selling policies that have been certified
by a state insurance commissioner as
Partnership qualified in a state that had
obtained a Medicaid state plan
amendment approved after of May 14,
1993.
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS
OF THE ACT:
None.
[FR Doc. E8–28345 Filed 12–17–08; 8:45 am]
BILLING CODE 4154–05–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0613]
Clinical Studies of Safety and
Effectiveness of Orphan Products
AGENCY:
Food and Drug Administration,
HHS.
mstockstill on PROD1PC66 with NOTICES
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration’s (FDA) Office of
Orphan Product Development (OPD) is
providing notice of a funding
opportunity announcement for Federal
assistance. The goal of the OPD grant
program is to support the clinical
development of products for use in rare
diseases or conditions where no current
therapy exists or where the proposed
product will be superior to the existing
therapy. FDA provides grants for
clinical studies on safety and/or
effectiveness that will either result in, or
substantially contribute to, market
approval of these products.
DATES: See section IV.E of the
SUPPLEMENTARY INFORMATION section for
application submission dates.
FOR FURTHER INFORMATION CONTACT:
Scientific/Research Contact:
Katherine Needleman, Office of
Orphan Products Development,
Food and Drug Administration
VerDate Aug<31>2005
17:51 Dec 17, 2008
Jkt 217001
(HF–35), rm. 6A–55, 5600 Fishers
Lane, Rockville, MD 20857, 301–
827–3666, e-mail:
katherine.needleman@fda.hhs.gov.
Financial/Grants Management
Contact: Vieda Hubbard, Office of
Acquisitions & Grant Services, 5630
Fishers Lane (HFA–500), rm. 2104,
Rockville, MD 20857, 301–827–
7177, e-mail:
vieda.hubbard@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Funding Opportunity Description
Research Project Grants (R01)
Request for Application (RFA) Number:
RFA–FD–09–001
Catalog of Federal Domestic Assistance
Number(s): 93.103
A. Research Objectives
1. Background
OPD was created to identify and
promote the development of orphan
products. Orphan products are drugs,
biologics, medical devices, and foods for
medical purposes that are indicated for
a rare disease or condition (that is, one
with prevalence, not incidence, of fewer
than 200,000 people in the United
States). Diagnostics and vaccines will
qualify for orphan status only if the U.S.
population to whom they will be
administered is fewer than 200,000
people per year.
2. Research Objectives
The goal of FDA’s OPD grant program
is to support the clinical development of
products for use in rare diseases or
conditions where no current therapy
exists or where the proposed product
will be superior to the existing therapy.
FDA provides grants for clinical studies
on safety and/or effectiveness that will
either result in, or substantially
contribute to, market approval of these
products. Applicants must include, in
the application’s ‘‘Background and
Significance’’ section, documentation to
support the estimated prevalence of the
orphan disease or condition (or in the
case of a vaccine or diagnostic,
information to support the estimates of
how many people will be administered
the diagnostic or vaccine annually) and
an explanation of how the proposed
study will either help gain product
approval or provide essential data
needed for product development.
See section VII.A of this document for
policies related to this announcement.
II. Award Information
A. Mechanism of Support
Support will be in the form of a
research project (R01) grant. The R01
grant is an award made to support a
PO 00000
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Fmt 4703
Sfmt 4703
77029
discrete, specified, circumscribed
project to be performed by the named
investigator(s) in an area representing
the investigator’s specific interest and
competencies, based on the mission of
FDA. The Project Director/Principal
Investigator (PD/PI) will be solely
responsible for planning, directing, and
executing the proposed project.
All awards will be subject to all
policies and requirements that govern
the research grant programs of the
Public Health Service (PHS) as
incorporated in the Department of
Health and Human Services (HHS)
Grants Policy Statement, dated January
1, 2007 (https://www.hhs.gov/grantsnet/
adminis/gpd/index.htm), including the
provisions of 42 CFR part 52 and 45
CFR parts 74 and 92. The regulations
issued under Executive Order 12372 do
not apply to this program. The National
Institutes of Health (NIH) modular grant
program does not apply to this FDA
grant program. All grant awards are
subject to applicable requirements for
clinical investigations imposed by
sections 505, 512, and 515 of the
Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 355, 360b, and 360e), section
351 of the PHS Act, regulations issued
under any of these sections, and other
applicable HHS statutes and regulations
regarding human subject protection.
Except for applications for studies of
medical foods that do not need
premarket approval, FDA will only
award grants to support premarket
clinical studies to determine safety and
effectiveness for approval under section
505 or 515 of the Federal Food, Drug,
and Cosmetic Act or safety, purity, and
potency for licensing under section 351
of the PHS Act. FDA will support the
clinical studies covered by this notice
under the authority of section 301 of the
PHS Act (42 U.S.C. 241). FDA’s research
program is described in the Catalog of
Federal Domestic Assistance (CFDA)
No. 93.103.
B. Funds Available
1. Award Amount
Of the estimated FY 2010 funding
($14.1 million), approximately $10
million will fund noncompeting
continuation awards, and approximately
$4.1 million will fund 10 to 12 new
awards, subject to availability of funds.
It is anticipated that funding for the
number of noncompeting continuation
awards and new awards in FY 2011 will
be similar to FY 2010. Grants will be
awarded up to $200,000 or up to
$400,000 in total (direct plus indirect)
costs per year for up to 4 years. Please
note that the dollar limitation will apply
to total costs, not direct costs, as in
E:\FR\FM\18DEN1.SGM
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Agencies
[Federal Register Volume 73, Number 244 (Thursday, December 18, 2008)]
[Notices]
[Pages 77027-77029]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-28345]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Assistant Secretary for Planning and Evaluation;
Privacy Act of 1974; Report of New System of Records
AGENCY: Office of the Assistant Secretary for Planning and Evaluation
(ASPE).
ACTION: Notice of new System of Records (SOR).
-----------------------------------------------------------------------
SUMMARY: In accordance with the requirements of the Privacy Act of
1974, the Office of Assistant Secretary for Planning and Evaluation
(ASPE) is proposing to establish a new system of records, called the
Partnership for Long Term Care Data Set. The Partnership allows states
to offer special Medicaid asset disregards to persons purchasing
specially certified long term care insurance policies. This program and
the data collection were established by the Deficit Reduction Act of
2005--Section 6021. Although the Privacy Act requires only that the
``routine uses'' portion of the system be published for comment, ASPE
invites comments on all portions of this notice. Elsewhere in today's
Federal Register, a related final rulemaking establishing the State
Long Term Care Partnership: Reporting Requirements for Insurers.
DATES: Effective Date: The new system of records, including routine
uses, will become effective January 27, 2009 unless ASPE receives
comments that require alteration to this notice.
ADDRESSES: Address comments to the Privacy Act Officer, Office of
Assistant Secretary for Planning and Evaluation, U.S. Department of
Health and Human Services, 200 Independence Ave, SW., Room Number
436E.2, Washington, DC 20201. 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. Call 202-
205-8999 for appointment.
FOR FURTHER INFORMATION CONTACT: Hunter McKay, Office of the Assistant
Secretary for Planning and Evaluation, U.S. Department of Health and
Human Services, 200 Independence Ave, SW., Room Number 424E,
Washington, DC 20201. The telephone number is (202) 205-8999 and the e-
mail address is hunter.mckay@hhs.gov.
SUPPLEMENTARY INFORMATION:
The Partnership for Long Term Care initiative was mandated by
Section 6021 of Public Law 109-171, the Deficit Reduction Act of 2005
(DRA). The Partnership allows states to offer special Medicaid asset
disregards to persons purchasing specially certified long term care
insurance policies. The asset disregards allow program participants to
keep additional assets should they need to apply for Medicaid coverage
of long term care. DRA also mandates the use of a standard reporting
system for all insurers participating in a state Partnership for Long
Term Care program through a Medicaid State Plan Amendment approved
after May 14, 1993. Participating insurers are required to report data
on Partnership policy purchasers, features of the policies they
purchase, and, selected claims information.
The Privacy Act permits us to disclose information without the
consent of individuals under a ``routine use.'' A routine use is a
disclosure outside of the Department of Health and Human Services that
is compatible with the purpose for which we collected the information.
The proposed routine uses in the new system of records meet the
compatibility criterion of the statute.
Dated: November 21, 2008.
Mary M. McGeein,
Principal Deputy Assistant Secretary for Planning and Evaluation.
SYSTEM NO.
09-90-0085
SYSTEM NAME:
Partnership for Long Term Care Data Set.
SECURITY CLASSIFICATION:
None.
SYSTEM LOCATION:
Thomson Reuters, 610 Opperman Drive, Eagan, Minnesota 55123.
CATEGORIES OF INDIVIDUALS COVERED BY THE SYSTEM:
Purchasers of long term care insurance policies certified by a
selected state (Medicaid state plan amendment approved after May 14,
1993) insurance commissioner as meeting the state's Partnership's
requirements for certification.
CATEGORIES OF RECORDS IN THE SYSTEM:
[diam] Name
[diam] Address
[diam] Social Security Number
[diam] Date of Birth
[diam] Long Term Care Insurance Policy Information
[cir] Long Term Care Insurance Company
[cir] Long Term Care Insurance Policy Number
[cir] Type of Policy (Group, Individual and Comprehensive, Nursing
Home Only)
[cir] Policy Issue State
[cir] Lifetime Maximum Benefit
[cir] Duration of Insurance Benefits (dollars or days)
[cir] Daily Benefit Amount
[cir] Inflation Protection Feature (required by DRA for select
ages)
[diam] Claims Information
[cir] Qualifying Condition for Claim (ADL, Cognitive Impairment,
Other)
[cir] Benefits Payment by Type of Service (institutional or home)
[cir] Remaining Lifetime Maximum Benefits (by service type when
multiple pools)
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
The authority for this system of records is contained in Section
6021 of the Deficit Reduction Act of 2005, Public Law 109-171, 42
U.S.C. 1396p note.
PURPOSE(S) OF THE SYSTEM:
The purpose of the system of records is to support Medicaid
eligibility determinations for persons participating in a Partnership
for long term care program.
[[Page 77028]]
ROUTINE USES OF RECORDS MAINTAINED IN THE SYSTEM, INCLUDING CATEGORIES
OF USERS AND THE PURPOSE OF SUCH USES:
Section 552a(b)(3) of the Privacy Act permits an agency to
establish disclosures not anticipated by the statute itself, compatible
with the purpose for which the information was collected, under which
the information may be released without the consent of the individual
to whom the information pertains. ASPE is identifying the following
routine disclosures for information held in the Partnership for Long
Term Care Data Set. Each proposed disclosure of information under these
routine uses will be evaluated to ensure that the disclosure is legally
permissible, including, but not limited to, ensuring that the purpose
of the disclosure is compatible with the purpose for which the
information was collected. Disclosure may be made under the following
circumstances.
1. Disclosure may be made to a State, local, tribal or other public
authority for the purpose of verifying Partnership program
participation and calculation of the amount of the Medicaid Partnership
asset disregard.
2. Disclosure may be made to the Department of Justice when: (a)
The agency or any component thereof; or (b) any employee of the agency
in his or her official capacity; (c) any employee of the agency in his
or her individual capacity where agency or the Department of Justice
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, the agency determines that the
records are both relevant and necessary to the litigation and the use
of such records by the Department of Justice is therefore deemed by the
agency to be for a purpose that is compatible with the purpose for
which the agency collected the records.
3. Disclosure may be made to a court or adjudicative body in a
proceeding when: (a) The agency or any component thereof; or (b) any
employee of the agency in his or her official capacity; (c) any
employee of the agency in his or her individual capacity where agency
or the Department of Justice 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, the agency
determines that the records are both relevant and necessary to the
litigation and the use of such records is therefore deemed by the
agency to be for a purpose that is compatible with the purpose for
which the agency collected the records.
4. When a record on its face, or in conjunction with other records,
indicates a violation or potential violation of law, whether civil,
criminal, or regulatory in nature, and whether arising by general
statute or particular program statute, or by regulation, rule, or order
issued pursuant thereto, disclosure may be made to the appropriate
public authority, whether Federal, foreign, state, local, tribal, or
otherwise responsible for enforcing, investigating, or prosecuting such
violation or charged with enforcing, or implementing the statute, rule,
regulation, or order issued pursuant hereto, if the information
disclosed is relevant to any enforcement, regulatory, investigative or
prosecutorial responsibility of the receiving entity.
5. Disclosure may be made to a Member of Congress or to a
congressional staff member in response to an inquiry of the
congressional office made at the written request of the constituent
about whom the record is maintained. The Member of Congress does not
have any greater authority to obtain records than the individual would
have if requesting the record directly.
6. Disclosure may be made to agency contractors, grantees, or
volunteers who have been engaged to assist the agency in the
performance of a contract service, grant, cooperative agreement or
other activity related to this system of records and who need to have
access to the records in order to perform the activity. Recipients
shall be required to comply with the requirements of the Privacy Act of
1974, as amended 5 U.S.C. 552a.
7. Disclosure may be made to an individual or organization
conducting a research, demonstration, or evaluation project related to
long term care financing generally, the performance of long term care
insurance or Partnership programs, or for the purposes of determining,
evaluating, assessing cost effectiveness, or quality of the long term
care services provided through a Partnership program.
8. To another Federal or state agency for the purpose of operating
the Medicaid program or otherwise assisting states in the
administration of those portions of the Medicaid program with direct
connection to state Partnership programs.
9. To appropriate federal agencies and Department contractors that
have a need to know the information for the purpose of assisting the
Department's efforts to respond to a suspected or confirmed breach of
the security or confidentiality of information maintained in this
system of records, and the information disclosed is relevant and
necessary for that assistance.
POLICIES AND PRACTICES FOR STORING, RETRIEVING, ACCESSING, RETAINING,
AND DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
All records are stored on paper or magnetic media.
RETRIEVABILITY:
The records are retrieved by the long term care insurance policy
number, name, social security number, or a combination of these.
SAFEGUARDS:
For computerized records, safeguards established in accordance with
Department standards and National Institute of Standards and Technology
guidelines (e.g., security codes) will be used, limiting access to
authorized personnel. System security policy and practices are
established in accordance with HHS, Information Resources Management
(IRM) Circular 10, Automated Information Systems Security
Program; HCFA Automated Information System (AIS) Guide, Systems
Security Policies; and OMB Circular No. A-130 (revised), Appendix III.
RETENTION AND DISPOSAL:
We are working with the National Archives and Records
Administration (NARA) to determine the appropriate retention schedule.
Due to the nature of these records, we expect them to be preserved for
at least 20 years after the death of the policyholder. When the
retention period has been approved by NARA, we will amend this notice.
SYSTEM MANAGER(S) AND ADDRESS:
Hunter McKay, Office of the Assistant Secretary for Planning and
Evaluation, U.S. Department of Health and Human Services, 200
Independence Ave, SW., Room Number 424E, Washington, DC 20201.
NOTIFICATION PROCEDURE:
For purpose of notification, individuals may write the system
manager, who will require the insured's name, insurance company name,
insurance policy number, and, for verification purposes, date of birth,
to ascertain whether or not the individual's record is in the system.
(These notification procedures are in accordance with Department
regulation 45 CFR part 5b.)
RECORD ACCESS PROCEDURE:
Same as notification procedures. Requestors should also reasonably
specify the record contents being
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sought. (These access procedures are in accordance with the Department
regulation 45 CFR 5b.5(a)(2).)
CONTESTING RECORD PROCEDURES:
Contact the system 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:
Information is reported by private long term care insurance
companies selling policies that have been certified by a state
insurance commissioner as Partnership qualified in a state that had
obtained a Medicaid state plan amendment approved after of May 14,
1993.
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS OF THE ACT:
None.
[FR Doc. E8-28345 Filed 12-17-08; 8:45 am]
BILLING CODE 4154-05-P