Exemption of Certain Systems of Records Under the Privacy Act, 29289-29292 [E7-10143]
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29289
Federal Register / Vol. 72, No. 101 / Friday, May 25, 2007 / Proposed Rules
TABLE 1.—MACT STANDARDS, SOURCE CATEGORIES, AND CORRESPONDING NAICS AND MACT CODES ADDRESSED BY
THIS ANPRM—Continued
NAICS
code
MACT standard/source category name
Group I Polymers and Resins:
Epichlorohydrin Elastomers Production ...........................................................................................................................
HypalonTM Production ......................................................................................................................................................
Nitrile Butadiene Rubber Production ................................................................................................................................
Polybutadiene Rubber Production ....................................................................................................................................
Styrene-Butadiene Rubber and Latex Production ...........................................................................................................
Group IV Polymers and Resins:
Acrylic-Butadiene-Styrene Production ..............................................................................................................................
Methyl Methacrylate-Acrylonitrile-Butadiene-Styrene Production ....................................................................................
Methyl Methacrylate-Butadiene-Styrene Production ........................................................................................................
Nitrile Resins Production ..................................................................................................................................................
Polyethylene Terephthalate Production ...........................................................................................................................
Polystyrene Production .....................................................................................................................................................
Styrene-Acrylonitrile Production .......................................................................................................................................
Primary Aluminum Reduction Plants .......................................................................................................................................
Printing and Publishing Industry ..............................................................................................................................................
Shipbuilding and Ship Repair Operations ...............................................................................................................................
HQ–OAR–2006–0859. Information on
how to access the docket is presented
above in the ADDRESSES section. In
addition, information may be obtained
from the Web page for the proposed
rulemaking at: https://www.epa.gov/ttn/
atw/rrisk/rtrpg.html.
Comment Period
cprice-sewell on PROD1PC71 with PROPOSALS
Worldwide Web (WWW). In addition
to being available in the docket, an
electronic copy of today’s notice will be
available on the WWW through the
Technology Transfer Network (TTN).
Following the Assistant Administrator’s
signature, a copy of this notice will be
posted on TTN’s policy and guidance
page for newly proposed or promulgated
rules at https://www.epa.gov/ttn/oarpg.
The TTN provides information and
technology exchange in various areas of
air pollution control. Additional
information is available on the Risk and
Technology Review Phase II webpage at
https://www.epa.gov/ttn/atw/rrisk/
rtrpg.html. This information includes
source category descriptions and
detailed emissions and other data that
will be used as model inputs.
45 CFR Part 5b
We received 15 requests to extend the
public comment period on the advance
notice of proposed rulemaking for the
Risk and Technology Review, Phase II,
Group 2 (72 FR 14734, March 29, 2007).
We are extending the comment period
to June 29, 2007, for all source
categories except Petroleum Refineries.
EPA is under a court-ordered deadline
to propose action on the technology
review for this source category by
August 22, 2007. All comments for
Petroleum Refineries must be received
by May 29, 2007. Public comments must
be received on or before June 29, 2007
for all other source categories.
[CMS–0029–P]
How can I get copies of the proposed
amendments and other related
information?
EPA has established the official
public docket for the proposed
rulemaking under Docket ID No. EPA–
VerDate Aug<31>2005
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Dated: May 18, 2007.
William L. Wehrum,
Acting Assistant Administrator for Air and
Radiation.
[FR Doc. E7–10128 Filed 5–24–07; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
RIN 0938–A069
Exemption of Certain Systems of
Records Under the Privacy Act
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
AGENCY:
SUMMARY: This proposed rule would
exempt the four system of records from
subsections (c)(3), (d)(1) through (d)(4),
(e)(4)(G) and (H), and (f) of the Privacy
Act pursuant to 5 U.S.C. 552a(k)(2): The
Automated Survey Processing
Environment (ASPEN) Complaint/
Incidents Tracking System (‘‘ACTS’’),
HHS/CMS, System No. 09–70–0565; the
Health Insurance Portability and
Accountability Act (HIPAA) Information
Tracking System (‘‘HITS’’), HHS/CMS,
System No. 09–70–0544; the Organ
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MACT
code
325212
325212
325212
325212
325212
1311
1315
1321
1325
1339
325211
325211
325211
325211
325211
325211
325211
331312
32311
336611
1302
1317
1318
1342
1328
1331
1338
0201
0714
0715
Procurement Organizations System
(‘‘OPOS’’), HHS/CMS, System No. 09–
70–0575; and the Fraud Investigation
Database (‘‘FID’’), HHS/CMS, System
No. 09–70–0527.
DATES: To be assured consideration,
comments must be received at one of
the addresses provided below, no later
than 5 p.m. on July 24, 2007.
ADDRESSES: In commenting, please refer
to file code CMS–0029–P. Because of
staff and resource limitations, we cannot
accept comments by facsimile (Fax)
transmission.
You may submit comments in one of
four ways (no duplicates, please):
1. Electronically. You may submit
electronic comments on specific issues
in this regulation to https://
www.cms.hhs.gov/eRulemaking. Click
on the link ‘‘Submit electronic
comments on CMS regulations with an
open comment period.’’ (Attachments
should be in Microsoft Word,
WordPerfect, or Excel; however, we
prefer Microsoft Word.)
2. By regular mail. You may mail
written comments (one original and two
copies) to the following address Only:
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Attention: CMS–0029–
P, P.O. Box 8017, Baltimore, MD 21244–
8017.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments (one
original and two copies) to the following
address Only: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–0029–P, Mail Stop C4–26–05,
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7500 Security Boulevard, Baltimore, MD
21244–1850.
4. By hand or courier. If you prefer,
you may deliver (by hand or courier)
your written comments (one original
and two copies) before the close of the
comment period to one of the following
addresses. If you intend to deliver your
comments to the Baltimore address,
please call telephone number (410) 786–
7195 in advance to schedule your
arrival with one of our staff members.
Room 445–G, Hubert H. Humphrey
Building, 200 Independence Avenue,
SW., Washington, DC 20201; or 7500
Security Boulevard, Baltimore, MD
21244–1850.
(Because access to the interior of the
HHH Building is not readily available to
persons without Federal Government
identification, commenters are
encouraged to leave their comments in
the CMS drop slots located in the main
lobby of the building. A stamp-in clock
is available for persons wishing to retain
a proof of filing by stamping in and
retaining an extra copy of the comments
being filed.)
Comments mailed to the addresses
indicated as appropriate for hand or
courier delivery may be delayed and
received after the comment period.
FOR FURTHER INFORMATION CONTACT:
Katherine Brewer, (410) 786–7235.
SUPPLEMENTARY INFORMATION:
Submitting Comments: We welcome
comments from the public on all issues
set forth in this rule to assist us in fully
considering issues and developing
policies. You can assist us by
referencing the file code CMS–0029–P
and the specific ‘‘issue identifier’’ that
precedes the section on which you
choose to comment.
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following Web
site as soon as possible after they have
been received: https://www.cms.hhs.gov/
eRulemaking. Click on the link
‘‘Electronic Comments on CMS
Regulations’’ on that Web site to view
public comments.
Comments received timely will also
be available for public inspection as
they are received, generally beginning
approximately 3 weeks after publication
of a document, at the headquarters of
the Centers for Medicare & Medicaid
Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday
through Friday of each week from 8:30
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a.m. to 4 p.m. To schedule an
appointment to view public comments,
phone 1–800–743–3951.
I. Background
The four SORs that are the subject of
this proposed rule are as follows:
A. The Automated Survey Processing
Environment Complaints/Incidents
Tracking System (‘‘ACTS’’), HHS/CMS,
System No. 09–70–0565.
In the May 23, 2006 Federal Register
(71 FR 29643), we published a notice of
a modified or altered SOR titled
Automated Survey Processing
Environment (ASPEN) Complaint/
Incidents Tracking System (‘‘ACTS’’),
HHS/CMS, System No. 09–70–0565.
ACTS is a Windows-based program
whose primary purpose is to track and
process complaints and incidents
reported against health care facilities
regulated by CMS and State agencies.
These facilities include Clinical
Laboratory Improvement Amendment
(CLIA)-certified laboratories, skilled
nursing facilities (SNFs), nursing
facilities, hospitals, home health
agencies, end stage renal disease (ESRD)
facilities, hospices, rural health clinics,
comprehensive outpatient rehabilitation
facilities (CORFs), outpatient physical
therapy services, community mental
health centers, ambulatory surgical
centers, suppliers of portable x-ray
services, and intermediate care facilities
for persons with mental retardation.
ACTS is designed to manage all
operations associated with complaint
and incident tracking and processing,
from initial intake and investigation
through the final disposition.
B. The Health Insurance Portability and
Accountability Act (HIPAA) Information
Tracking System (‘‘HITS’’), HHS/CMS,
System No. 09–70–0544.
In the July 6, 2005 issue of the
Federal Register (70 FR 38944), we
published a notice of a new SOR titled
Health Insurance Portability and
Accountability Act (HIPAA) Information
Tracking System (‘‘HITS’’), HHS/CMS,
System No. 09–70–0544. In general,
HITS consists of an electronic repository
of information, documents, and
supplementary paper document files.
HITS’ purpose is to store the results of
all of our investigations, to determine if
there were violations as charged in the
original complaint, to investigate
complaints that appear to be in violation
of the Transactions and Code Sets,
Security, and Unique Identifier
provisions of HIPAA, to refer violations
to law enforcement entities as
necessary, and to maintain and retrieve
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records of the results of the complaint
investigations.
Investigative files maintained in HITS
are received either as electronic
documents or as paper records that are
compiled for law enforcement purposes.
C. The Organ Procurement
Organizations System (‘‘OPOS’’), HHS/
CMS, System No. 09–70–0575.
In the May 22, 2006 issue of the
Federal Register (71 FR 29336), we
published a notice of a new SOR titled
Organ Procurement Organizations
System (‘‘OPOS’’), HHS/CMS, System
No. 09–70–0575. OPOS is a Windowsbased program whose purpose is to
track and process complaints and
incidents reported against Organ
Procurement Organizations. Section 701
of the Organ Procurement Organization
System Certification Act of 2000 (Pub.
L. 106–505) gave us the authority to
collect and maintain individually
identifiable information pertaining to
complaint allegations filed by a
complainant, beneficiary, or provider of
services against Organ Procurement
Organizations; this information includes
information gathered during all aspects
of an investigation, including initial
complaints, findings, results,
disposition, and relevant
correspondence.
D. The Fraud Investigation Database
(‘‘FID’’), HHS/CMS, System No. 09–70–
0527
In the October 28, 2002 Federal
Register (70 FR 65795), we published a
notice of a modified or altered system of
records (SOR) that changed the name of
a SOR entitled ‘‘CMS Utilization Review
Investigatory Files, System No. 09–70–
0527’’ to be the ‘‘CMS Fraud
Investigation Database (FID).’’ The FID
system contains the name, work
address, work phone number, social
security number, Unique Provider
Identification Number (UPIN), and other
identifying demographics of individuals
alleged to have violated provisions of
the Social Security Act (‘‘the Act’’)
related to Medicare, Medicaid, HMO/
Managed Care, and the Children’s
Health Insurance Program. The FID
system also contains the contact
information and other identifying
demographics of individuals alleged to
have violated other criminal or civil
statutes connected with the Act and the
Act’s programs. Here, individuals are
persons alleged to have abused the Act’s
programs. (For example, an individual
could be a person alleged to have
rendered unnecessary services to
Medicare beneficiaries or Medicaid
recipients, over-used services, or
engaged in improper billing.) They are
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persons whose activities have provided
a substantial basis for criminal or civil
prosecution, or who are identified as
defendants in criminal prosecution
cases.
II. Provisions of the Proposed Rule
We propose to exempt the ACTS,
HITS, OPOS, and FIS systems of records
from subsection (c)(3), (d)(1) through
(d)(4), (e)(4)(G) and (H), and (f) of the
Privacy Act pursuant to 5 U.S.C.
552a(k)(2). These exemptions apply
only to the extent that information in a
record is subject to exemption pursuant
to 5 U.S.C. 552a(k)(2). The ACTS, HITS,
OPOS, and FIS systems of records are
exempted from the following
subsections for the reasons set forth
below:
• Subsection (c)(3). CMS investigative
files are records that we compile for law
enforcement purposes. In the course of
investigations, we often have a need to
obtain confidential information
involving individuals other than the
individual who is the subject of the file.
In these cases, it is necessary for us to
preserve the confidentiality of the
information to avoid unwarranted
invasions of personal privacy and to
assure recipients of Federal financial
assistance that this information will be
kept confidential. This assurance is
often central to resolving disputes
concerning access by CMS to the
recipient’s records, and is necessary to
facilitate prompt and effective
completion of investigations. Disclosure
of confidential information to the
subject individual could impede
ongoing investigations, invade the
personal privacy of individuals, reveal
the identities of confidential sources, or
otherwise impair our ability to conduct
investigations.
• Subsections (d)(1) through (d)(4).
CMS investigative files are records that
we compile for law enforcement
purposes. In the course of
investigations, we often have a need to
obtain confidential information
involving individuals other than the
individual who is the subject of the file.
In these cases, it is necessary for us to
preserve the confidentiality of the
information to avoid unwarranted
invasions of personal privacy and to
assure recipients of Federal financial
assistance that this information will be
kept confidential. This assurance is
often central to resolving disputes
concerning access by CMS to the
recipient’s records, and is necessary to
facilitate prompt and effective
completion of investigations.
Unrestricted disclosure of confidential
information in CMS files could impede
ongoing investigations, invade the
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personal privacy of individuals, reveal
the identities of confidential sources, or
otherwise impair our ability to conduct
investigations.
• Subsection (e)(4)(G). CMS
investigative files are records that we
compile for law enforcement purposes.
In the course of investigations, we often
have a need to obtain confidential
information involving individuals other
than the individual who is the subject
of the file. In these cases, it is necessary
for us to preserve the confidentiality of
the information to avoid unwarranted
invasions of personal privacy and to
assure recipients of Federal financial
assistance that this information will be
kept confidential. This assurance is
often central to resolving disputes
concerning access by CMS to the
recipient’s records, and is necessary to
facilitate prompt and effective
completion of investigations.
Notification of existence of CMS
investigative files could impede ongoing
investigations, invade the personal
privacy of individuals, reveal the
identities of confidential sources, or
otherwise impair our ability to conduct
investigations.
• From subsection (e)(4)(H). CMS
investigative files are records that we
compile for law enforcement purposes.
In the course of investigations, we often
have a need to obtain confidential
information involving individuals other
than the individual who is the subject
of the file. In these cases, it is necessary
for us to preserve the confidentiality of
the information to avoid unwarranted
invasions of personal privacy and to
assure recipients of Federal financial
assistance that this information will be
kept confidential. This assurance is
often central to resolving disputes
concerning access by CMS to the
recipient’s records, and is necessary to
facilitate prompt and effective
completion of investigations. Access
and correction by subject individuals to
CMS files could impede ongoing
investigations, invade the personal
privacy of individuals, reveal the
identities of confidential sources, or
otherwise impair our ability to conduct
investigations.
• Subsection (f). CMS investigative
files are records that we compile for law
enforcement purposes. In the course of
investigations, we often have a need to
obtain confidential information
involving individuals other than the
individual who is the subject of the file.
In these cases, it is necessary for us to
preserve the confidentiality of the
information to avoid unwarranted
invasions of personal privacy and to
assure recipients of Federal financial
assistance that this information will be
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29291
kept confidential. This assurance is
often central to resolving disputes
concerning access by CMS to the
recipient’s records, and is necessary to
facilitate prompt and effective
completion of investigations.
Unrestricted disclosure of confidential
information in CMS files to subject
individuals could impede ongoing
investigations, invade the personal
privacy of individuals, reveal the
identities of confidential sources, or
otherwise impair our ability to conduct
investigations.
Accordingly, this proposed rule
would amend 45 CFR 5b.11(b)(2)(ii) of
the Privacy Act regulations by—
• Adding a new paragraph (H) that
exempts investigative materials
compiled for law enforcement purposes
from ACTS;
• Adding a new paragraph (I) that
exempts investigative materials
compiled for law enforcement purposes
from HITS;
• Adding a new paragraph (J) that
exempts investigative materials
compiled for law enforcement purposes
from OPOS; and
• Adding a new paragraph (K) that
exempts investigative materials
compiled for law enforcement purposes
from FID.
We request public comment on these
proposed exemptions.
III. Collection of Information
Requirements
This proposed rule does not impose
any information collection or
recordkeeping requirements.
Consequently, it need not be reviewed
by the Office of Management and
Budget under the authority of the
Paperwork Reduction Act of 1995.
IV. Response to Comments
Because of the large number of public
comments we normally receive on
Federal Register documents, we are not
able to acknowledge or respond to them
individually. We will consider all
comments we receive by the date and
time specified in the DATES section of
this preamble, and, when we proceed
with a subsequent document, we will
respond to the comments in the
preamble to that document.
V. Regulatory Impact Statement
We have examined the impact of this
rule as required by Executive Order
12866 (September 1993, Regulatory
Planning and Review), the Regulatory
Flexibility Act (RFA) (September 19,
1980, Pub. L. 96–354), section 1102(b) of
the Social Security Act, the Unfunded
Mandates Reform Act of 1995 (Pub. L.
104–4), and Executive Order 13132.
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Executive Order 12866 directs
agencies to assess all costs and benefits
of available regulatory alternatives and,
if regulation is necessary, to select
regulatory approaches that maximize
net benefits (including potential
economic, environmental, public health
and safety effects, distributive impacts,
and equity). A regulatory impact
analysis (RIA) must be prepared for
major rules with economically
significant effects ($100 million or more
in any 1 year). This rule does not reach
the economic threshold and thus is not
considered a major rule.
The RFA requires agencies to analyze
options for regulatory relief of small
businesses. For purposes of the RFA,
small entities include small businesses,
nonprofit organizations, and small
governmental jurisdictions. Most
hospitals and most other providers and
suppliers are small entities, either by
nonprofit status or by having revenues
of $6 million to $29 million in any 1
year. Individuals and States are not
included in the definition of a small
entity. We are not preparing an analysis
for the RFA because we have
determined that this rule will not have
a significant economic impact on a
substantial number of small entities.
In addition, section 1102(b) of the Act
requires us to prepare a regulatory
impact analysis if a rule may have a
significant impact on the operations of
a substantial number of small rural
hospitals. This analysis must conform to
the provisions of section 603 of the
RFA. For purposes of section 1102(b) of
the Act, we define a small rural hospital
as a hospital that is located outside of
a Metropolitan Statistical Area and has
fewer than 100 beds. We are not
preparing an analysis for section 1102(b)
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15:35 May 24, 2007
Jkt 211001
of the Act because we have determined
that this rule will not have a significant
impact on the operations of a substantial
number of small rural hospitals.
Section 202 of the Unfunded
Mandates Reform Act of 1995 also
requires that agencies assess anticipated
costs and benefits before issuing any
rule whose mandates require spending
in any 1 year of $100 million in 1995
dollars, updated annually for inflation.
That threshold level is currently
approximately $120 million. This rule
will have no consequential effect on
State, local, or tribal governments or on
the private sector.
Executive Order 13132 establishes
certain requirements that an agency
must meet when it promulgates a
proposed rule (and subsequent final
rule) that imposes substantial direct
requirement costs on State and local
governments, preempts State law, or
otherwise has Federalism implications.
Since this regulation does not impose
any costs on State or local governments,
the requirements of E.O. 13132 are not
applicable.
In accordance with the provisions of
Executive Order 12866, this regulation
was reviewed by the Office of
Management and Budget.
List of Subjects for 45 CFR Part 5b
Privacy.
For the reasons set forth in the
preamble, the Department of Health and
Human Services would amend 45 CFR
part 5b as set forth below:
PART 5b—PRIVACY ACT
REGULATIONS
1. The authority citation for part 5b
continues to read as follows:
Authority: 5 U.S.C. 301, 5 U.S.C. 552a.
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2. Section 5b.11 is revised by adding
paragraphs (b)(2)(ii)(H), (I), (J), and (K)
to read as follows:
§ 5b.11
Exempt Systems
*
*
*
*
*
(b) * * *
(2) * * *
(ii) * * *
(H) Investigative materials compiled
for law enforcement purposes from the
Automated Survey Processing
Environment (ASPEN) Complaints/
Incidents Tracking System (‘‘ACTS’’),
HHS/CMS.
(I) Investigative materials compiled
for law enforcement purposes from the
Health Insurance Portability and
Accountability Act (HIPAA) Information
Tracking System (‘‘HITS’’), HHS/CMS.
(J) Investigative materials compiled
for law enforcement purposes from the
Organ Procurement Organizations
System (‘‘OPOS’’), HHS/CMS.
(K) Investigative materials compiled
for law enforcement purposes from the
CMS Fraud Investigation Database
(‘‘FID’’), HHS/CMS.
*
*
*
*
*
Authority: 5 U.S.C. 552a.
Dated: September 29, 2006.
Mark B. McClellan,
Administrator, Centers for Medicare &
Medicaid Services.
Approved: January 26, 2007.
Michael O. Leavitt,
Secretary.
Editorial Note: This document was
received at the Office of the Federal Register
on Tuesday, May 22, 2007.
[FR Doc. E7–10143 Filed 5–24–07; 8:45 am]
BILLING CODE 4120–01–P
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Agencies
[Federal Register Volume 72, Number 101 (Friday, May 25, 2007)]
[Proposed Rules]
[Pages 29289-29292]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-10143]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
45 CFR Part 5b
[CMS-0029-P]
RIN 0938-A069
Exemption of Certain Systems of Records Under the Privacy Act
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: This proposed rule would exempt the four system of records
from subsections (c)(3), (d)(1) through (d)(4), (e)(4)(G) and (H), and
(f) of the Privacy Act pursuant to 5 U.S.C. 552a(k)(2): The Automated
Survey Processing Environment (ASPEN) Complaint/Incidents Tracking
System (``ACTS''), HHS/CMS, System No. 09-70-0565; the Health Insurance
Portability and Accountability Act (HIPAA) Information Tracking System
(``HITS''), HHS/CMS, System No. 09-70-0544; the Organ Procurement
Organizations System (``OPOS''), HHS/CMS, System No. 09-70-0575; and
the Fraud Investigation Database (``FID''), HHS/CMS, System No. 09-70-
0527.
DATES: To be assured consideration, comments must be received at one of
the addresses provided below, no later than 5 p.m. on July 24, 2007.
ADDRESSES: In commenting, please refer to file code CMS-0029-P. Because
of staff and resource limitations, we cannot accept comments by
facsimile (Fax) transmission.
You may submit comments in one of four ways (no duplicates,
please):
1. Electronically. You may submit electronic comments on specific
issues in this regulation to https://www.cms.hhs.gov/eRulemaking. Click
on the link ``Submit electronic comments on CMS regulations with an
open comment period.'' (Attachments should be in Microsoft Word,
WordPerfect, or Excel; however, we prefer Microsoft Word.)
2. By regular mail. You may mail written comments (one original and
two copies) to the following address Only: Centers for Medicare &
Medicaid Services, Department of Health and Human Services, Attention:
CMS-0029-P, P.O. Box 8017, Baltimore, MD 21244-8017.
Please allow sufficient time for mailed comments to be received
before the close of the comment period.
3. By express or overnight mail. You may send written comments (one
original and two copies) to the following address Only: Centers for
Medicare & Medicaid Services, Department of Health and Human Services,
Attention: CMS-0029-P, Mail Stop C4-26-05,
[[Page 29290]]
7500 Security Boulevard, Baltimore, MD 21244-1850.
4. By hand or courier. If you prefer, you may deliver (by hand or
courier) your written comments (one original and two copies) before the
close of the comment period to one of the following addresses. If you
intend to deliver your comments to the Baltimore address, please call
telephone number (410) 786-7195 in advance to schedule your arrival
with one of our staff members. Room 445-G, Hubert H. Humphrey Building,
200 Independence Avenue, SW., Washington, DC 20201; or 7500 Security
Boulevard, Baltimore, MD 21244-1850.
(Because access to the interior of the HHH Building is not readily
available to persons without Federal Government identification,
commenters are encouraged to leave their comments in the CMS drop slots
located in the main lobby of the building. A stamp-in clock is
available for persons wishing to retain a proof of filing by stamping
in and retaining an extra copy of the comments being filed.)
Comments mailed to the addresses indicated as appropriate for hand
or courier delivery may be delayed and received after the comment
period.
FOR FURTHER INFORMATION CONTACT: Katherine Brewer, (410) 786-7235.
SUPPLEMENTARY INFORMATION:
Submitting Comments: We welcome comments from the public on all
issues set forth in this rule to assist us in fully considering issues
and developing policies. You can assist us by referencing the file code
CMS-0029-P and the specific ``issue identifier'' that precedes the
section on which you choose to comment.
Inspection of Public Comments: All comments received before the
close of the comment period are available for viewing by the public,
including any personally identifiable or confidential business
information that is included in a comment. We post all comments
received before the close of the comment period on the following Web
site as soon as possible after they have been received: https://
www.cms.hhs.gov/eRulemaking. Click on the link ``Electronic Comments on
CMS Regulations'' on that Web site to view public comments.
Comments received timely will also be available for public
inspection as they are received, generally beginning approximately 3
weeks after publication of a document, at the headquarters of the
Centers for Medicare & Medicaid Services, 7500 Security Boulevard,
Baltimore, Maryland 21244, Monday through Friday of each week from 8:30
a.m. to 4 p.m. To schedule an appointment to view public comments,
phone 1-800-743-3951.
I. Background
The four SORs that are the subject of this proposed rule are as
follows:
A. The Automated Survey Processing Environment Complaints/Incidents
Tracking System (``ACTS''), HHS/CMS, System No. 09-70-0565.
In the May 23, 2006 Federal Register (71 FR 29643), we published a
notice of a modified or altered SOR titled Automated Survey Processing
Environment (ASPEN) Complaint/Incidents Tracking System (``ACTS''),
HHS/CMS, System No. 09-70-0565. ACTS is a Windows-based program whose
primary purpose is to track and process complaints and incidents
reported against health care facilities regulated by CMS and State
agencies. These facilities include Clinical Laboratory Improvement
Amendment (CLIA)-certified laboratories, skilled nursing facilities
(SNFs), nursing facilities, hospitals, home health agencies, end stage
renal disease (ESRD) facilities, hospices, rural health clinics,
comprehensive outpatient rehabilitation facilities (CORFs), outpatient
physical therapy services, community mental health centers, ambulatory
surgical centers, suppliers of portable x-ray services, and
intermediate care facilities for persons with mental retardation. ACTS
is designed to manage all operations associated with complaint and
incident tracking and processing, from initial intake and investigation
through the final disposition.
B. The Health Insurance Portability and Accountability Act (HIPAA)
Information Tracking System (``HITS''), HHS/CMS, System No. 09-70-0544.
In the July 6, 2005 issue of the Federal Register (70 FR 38944), we
published a notice of a new SOR titled Health Insurance Portability and
Accountability Act (HIPAA) Information Tracking System (``HITS''), HHS/
CMS, System No. 09-70-0544. In general, HITS consists of an electronic
repository of information, documents, and supplementary paper document
files. HITS' purpose is to store the results of all of our
investigations, to determine if there were violations as charged in the
original complaint, to investigate complaints that appear to be in
violation of the Transactions and Code Sets, Security, and Unique
Identifier provisions of HIPAA, to refer violations to law enforcement
entities as necessary, and to maintain and retrieve records of the
results of the complaint investigations.
Investigative files maintained in HITS are received either as
electronic documents or as paper records that are compiled for law
enforcement purposes.
C. The Organ Procurement Organizations System (``OPOS''), HHS/CMS,
System No. 09-70-0575.
In the May 22, 2006 issue of the Federal Register (71 FR 29336), we
published a notice of a new SOR titled Organ Procurement Organizations
System (``OPOS''), HHS/CMS, System No. 09-70-0575. OPOS is a Windows-
based program whose purpose is to track and process complaints and
incidents reported against Organ Procurement Organizations. Section 701
of the Organ Procurement Organization System Certification Act of 2000
(Pub. L. 106-505) gave us the authority to collect and maintain
individually identifiable information pertaining to complaint
allegations filed by a complainant, beneficiary, or provider of
services against Organ Procurement Organizations; this information
includes information gathered during all aspects of an investigation,
including initial complaints, findings, results, disposition, and
relevant correspondence.
D. The Fraud Investigation Database (``FID''), HHS/CMS, System No. 09-
70-0527
In the October 28, 2002 Federal Register (70 FR 65795), we
published a notice of a modified or altered system of records (SOR)
that changed the name of a SOR entitled ``CMS Utilization Review
Investigatory Files, System No. 09-70-0527'' to be the ``CMS Fraud
Investigation Database (FID).'' The FID system contains the name, work
address, work phone number, social security number, Unique Provider
Identification Number (UPIN), and other identifying demographics of
individuals alleged to have violated provisions of the Social Security
Act (``the Act'') related to Medicare, Medicaid, HMO/Managed Care, and
the Children's Health Insurance Program. The FID system also contains
the contact information and other identifying demographics of
individuals alleged to have violated other criminal or civil statutes
connected with the Act and the Act's programs. Here, individuals are
persons alleged to have abused the Act's programs. (For example, an
individual could be a person alleged to have rendered unnecessary
services to Medicare beneficiaries or Medicaid recipients, over-used
services, or engaged in improper billing.) They are
[[Page 29291]]
persons whose activities have provided a substantial basis for criminal
or civil prosecution, or who are identified as defendants in criminal
prosecution cases.
II. Provisions of the Proposed Rule
We propose to exempt the ACTS, HITS, OPOS, and FIS systems of
records from subsection (c)(3), (d)(1) through (d)(4), (e)(4)(G) and
(H), and (f) of the Privacy Act pursuant to 5 U.S.C. 552a(k)(2). These
exemptions apply only to the extent that information in a record is
subject to exemption pursuant to 5 U.S.C. 552a(k)(2). The ACTS, HITS,
OPOS, and FIS systems of records are exempted from the following
subsections for the reasons set forth below:
Subsection (c)(3). CMS investigative files are records
that we compile for law enforcement purposes. In the course of
investigations, we often have a need to obtain confidential information
involving individuals other than the individual who is the subject of
the file. In these cases, it is necessary for us to preserve the
confidentiality of the information to avoid unwarranted invasions of
personal privacy and to assure recipients of Federal financial
assistance that this information will be kept confidential. This
assurance is often central to resolving disputes concerning access by
CMS to the recipient's records, and is necessary to facilitate prompt
and effective completion of investigations. Disclosure of confidential
information to the subject individual could impede ongoing
investigations, invade the personal privacy of individuals, reveal the
identities of confidential sources, or otherwise impair our ability to
conduct investigations.
Subsections (d)(1) through (d)(4). CMS investigative files
are records that we compile for law enforcement purposes. In the course
of investigations, we often have a need to obtain confidential
information involving individuals other than the individual who is the
subject of the file. In these cases, it is necessary for us to preserve
the confidentiality of the information to avoid unwarranted invasions
of personal privacy and to assure recipients of Federal financial
assistance that this information will be kept confidential. This
assurance is often central to resolving disputes concerning access by
CMS to the recipient's records, and is necessary to facilitate prompt
and effective completion of investigations. Unrestricted disclosure of
confidential information in CMS files could impede ongoing
investigations, invade the personal privacy of individuals, reveal the
identities of confidential sources, or otherwise impair our ability to
conduct investigations.
Subsection (e)(4)(G). CMS investigative files are records
that we compile for law enforcement purposes. In the course of
investigations, we often have a need to obtain confidential information
involving individuals other than the individual who is the subject of
the file. In these cases, it is necessary for us to preserve the
confidentiality of the information to avoid unwarranted invasions of
personal privacy and to assure recipients of Federal financial
assistance that this information will be kept confidential. This
assurance is often central to resolving disputes concerning access by
CMS to the recipient's records, and is necessary to facilitate prompt
and effective completion of investigations. Notification of existence
of CMS investigative files could impede ongoing investigations, invade
the personal privacy of individuals, reveal the identities of
confidential sources, or otherwise impair our ability to conduct
investigations.
From subsection (e)(4)(H). CMS investigative files are
records that we compile for law enforcement purposes. In the course of
investigations, we often have a need to obtain confidential information
involving individuals other than the individual who is the subject of
the file. In these cases, it is necessary for us to preserve the
confidentiality of the information to avoid unwarranted invasions of
personal privacy and to assure recipients of Federal financial
assistance that this information will be kept confidential. This
assurance is often central to resolving disputes concerning access by
CMS to the recipient's records, and is necessary to facilitate prompt
and effective completion of investigations. Access and correction by
subject individuals to CMS files could impede ongoing investigations,
invade the personal privacy of individuals, reveal the identities of
confidential sources, or otherwise impair our ability to conduct
investigations.
Subsection (f). CMS investigative files are records that
we compile for law enforcement purposes. In the course of
investigations, we often have a need to obtain confidential information
involving individuals other than the individual who is the subject of
the file. In these cases, it is necessary for us to preserve the
confidentiality of the information to avoid unwarranted invasions of
personal privacy and to assure recipients of Federal financial
assistance that this information will be kept confidential. This
assurance is often central to resolving disputes concerning access by
CMS to the recipient's records, and is necessary to facilitate prompt
and effective completion of investigations. Unrestricted disclosure of
confidential information in CMS files to subject individuals could
impede ongoing investigations, invade the personal privacy of
individuals, reveal the identities of confidential sources, or
otherwise impair our ability to conduct investigations.
Accordingly, this proposed rule would amend 45 CFR 5b.11(b)(2)(ii)
of the Privacy Act regulations by--
Adding a new paragraph (H) that exempts investigative
materials compiled for law enforcement purposes from ACTS;
Adding a new paragraph (I) that exempts investigative
materials compiled for law enforcement purposes from HITS;
Adding a new paragraph (J) that exempts investigative
materials compiled for law enforcement purposes from OPOS; and
Adding a new paragraph (K) that exempts investigative
materials compiled for law enforcement purposes from FID.
We request public comment on these proposed exemptions.
III. Collection of Information Requirements
This proposed rule does not impose any information collection or
recordkeeping requirements. Consequently, it need not be reviewed by
the Office of Management and Budget under the authority of the
Paperwork Reduction Act of 1995.
IV. Response to Comments
Because of the large number of public comments we normally receive
on Federal Register documents, we are not able to acknowledge or
respond to them individually. We will consider all comments we receive
by the date and time specified in the DATES section of this preamble,
and, when we proceed with a subsequent document, we will respond to the
comments in the preamble to that document.
V. Regulatory Impact Statement
We have examined the impact of this rule as required by Executive
Order 12866 (September 1993, Regulatory Planning and Review), the
Regulatory Flexibility Act (RFA) (September 19, 1980, Pub. L. 96-354),
section 1102(b) of the Social Security Act, the Unfunded Mandates
Reform Act of 1995 (Pub. L. 104-4), and Executive Order 13132.
[[Page 29292]]
Executive Order 12866 directs agencies to assess all costs and
benefits of available regulatory alternatives and, if regulation is
necessary, to select regulatory approaches that maximize net benefits
(including potential economic, environmental, public health and safety
effects, distributive impacts, and equity). A regulatory impact
analysis (RIA) must be prepared for major rules with economically
significant effects ($100 million or more in any 1 year). This rule
does not reach the economic threshold and thus is not considered a
major rule.
The RFA requires agencies to analyze options for regulatory relief
of small businesses. For purposes of the RFA, small entities include
small businesses, nonprofit organizations, and small governmental
jurisdictions. Most hospitals and most other providers and suppliers
are small entities, either by nonprofit status or by having revenues of
$6 million to $29 million in any 1 year. Individuals and States are not
included in the definition of a small entity. We are not preparing an
analysis for the RFA because we have determined that this rule will not
have a significant economic impact on a substantial number of small
entities.
In addition, section 1102(b) of the Act requires us to prepare a
regulatory impact analysis if a rule may have a significant impact on
the operations of a substantial number of small rural hospitals. This
analysis must conform to the provisions of section 603 of the RFA. For
purposes of section 1102(b) of the Act, we define a small rural
hospital as a hospital that is located outside of a Metropolitan
Statistical Area and has fewer than 100 beds. We are not preparing an
analysis for section 1102(b) of the Act because we have determined that
this rule will not have a significant impact on the operations of a
substantial number of small rural hospitals.
Section 202 of the Unfunded Mandates Reform Act of 1995 also
requires that agencies assess anticipated costs and benefits before
issuing any rule whose mandates require spending in any 1 year of $100
million in 1995 dollars, updated annually for inflation. That threshold
level is currently approximately $120 million. This rule will have no
consequential effect on State, local, or tribal governments or on the
private sector.
Executive Order 13132 establishes certain requirements that an
agency must meet when it promulgates a proposed rule (and subsequent
final rule) that imposes substantial direct requirement costs on State
and local governments, preempts State law, or otherwise has Federalism
implications. Since this regulation does not impose any costs on State
or local governments, the requirements of E.O. 13132 are not
applicable.
In accordance with the provisions of Executive Order 12866, this
regulation was reviewed by the Office of Management and Budget.
List of Subjects for 45 CFR Part 5b
Privacy.
For the reasons set forth in the preamble, the Department of Health
and Human Services would amend 45 CFR part 5b as set forth below:
PART 5b--PRIVACY ACT REGULATIONS
1. The authority citation for part 5b continues to read as follows:
Authority: 5 U.S.C. 301, 5 U.S.C. 552a.
2. Section 5b.11 is revised by adding paragraphs (b)(2)(ii)(H),
(I), (J), and (K) to read as follows:
Sec. 5b.11 Exempt Systems
* * * * *
(b) * * *
(2) * * *
(ii) * * *
(H) Investigative materials compiled for law enforcement purposes
from the Automated Survey Processing Environment (ASPEN) Complaints/
Incidents Tracking System (``ACTS''), HHS/CMS.
(I) Investigative materials compiled for law enforcement purposes
from the Health Insurance Portability and Accountability Act (HIPAA)
Information Tracking System (``HITS''), HHS/CMS.
(J) Investigative materials compiled for law enforcement purposes
from the Organ Procurement Organizations System (``OPOS''), HHS/CMS.
(K) Investigative materials compiled for law enforcement purposes
from the CMS Fraud Investigation Database (``FID''), HHS/CMS.
* * * * *
Authority: 5 U.S.C. 552a.
Dated: September 29, 2006.
Mark B. McClellan,
Administrator, Centers for Medicare & Medicaid Services.
Approved: January 26, 2007.
Michael O. Leavitt,
Secretary.
Editorial Note: This document was received at the Office of the
Federal Register on Tuesday, May 22, 2007.
[FR Doc. E7-10143 Filed 5-24-07; 8:45 am]
BILLING CODE 4120-01-P