Privacy Act of 1974; Report of New System of Records, 73095-73101 [2010-29952]
Download as PDF
Federal Register / Vol. 75, No. 228 / Monday, November 29, 2010 / Notices
We encourage the participation of
appropriate organizations with expertise
in the use of ESAs for treatment of
anemia in adults with CKD including
patients on dialysis and patients not on
dialysis.
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II. Meeting Format
This meeting is open to the public.
The Committee will hear oral
presentations from the public for
approximately 45 minutes. The
Committee may limit the number and
duration of oral presentations to the
time available. Your comments should
focus on issues specific to the list of
topics that we have proposed to the
Committee. The list of research topics to
be discussed at the meeting will be
available on the following Web site
prior to the meeting: https://
www.cms.hhs.gov/mcd/index_list.asp?
list_type=mcac. We require that you
declare at the meeting whether you have
any financial involvement with
manufacturers (or their competitors) of
any items or services being discussed.
The Committee will deliberate openly
on the topics under consideration.
Interested persons may observe the
deliberations, but the Committee will
not hear further comments during this
time except at the request of the
chairperson. The Committee will also
allow a 15-minute unscheduled open
public session for any attendee to
address issues specific to the topics
under consideration. At the conclusion
of the day, the members will vote and
the Committee will make its
recommendation(s) to CMS.
III. Registration Instructions
CMS’ Coverage and Analysis Group is
coordinating the meetings registration
process. While there is no registration
fee, individuals must register to attend.
You may register online at https://
www.cms.gov/apps/events/
upcomingevents.asp?
strOrderBy=1&type=3 or by phone by
contacting the person listed in the FOR
FURTHER INFORMATION CONTACT section of
this notice by the deadline listed in the
DATES section of this notice. Please
provide your full name (as it appears on
your government—issued photographic
identification), address, organization,
telephone, fax number(s), and e-mail
address. You will receive a registration
confirmation with instructions for your
arrival at the CMS complex or you will
be notified the seating capacity has been
reached.
You must register for the Webinar
portion of the meeting at https://
webinar.cms.hhs.gov/esamedcac119/
event/registration.html by the deadline
listed in the DATES section of this notice.
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IV. Security, Building, and Parking
Guidelines
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
This meeting will be held in a Federal
government building; therefore, Federal
security measures are applicable. We
recommend that confirmed registrants
arrive reasonably early, but no earlier
than 45 minutes prior to the start of the
meeting, to allow additional time to
clear security. Security measures
include the following:
• Presentation of government-issued
photographic identification to the
Federal Protective Service or Guard
Service personnel.
• Inspection of vehicle’s interior and
exterior (this includes engine and trunk
inspection) at the entrance to the
grounds. Parking permits and
instructions will be issued after the
vehicle inspection.
• Inspection, via metal detector or
other applicable means of all persons
brought entering the building. We note
that all items brought into CMS,
whether personal or for the purpose of
presentation or to support a
presentation, are subject to inspection.
We cannot assume responsibility for
coordinating the receipt, transfer,
transport, storage, set-up, safety, or
timely arrival of any personal
belongings or items used for
presentation or to support a
presentation.
Centers for Medicare & Medicaid
Services
Note: Individuals who are not registered in
advance will not be permitted to enter the
building and will be unable to attend the
meeting. The public may not enter the
building earlier than 45 minutes prior to the
convening of the meeting. All visitors must
be escorted in areas other than the lower and
first floor levels in the Central Building.
Authority: 5 U.S.C. App. 2, section 10(a).
(Catalog of Federal Domestic Assistance
Program No. 93.773, Medicare—Hospital
Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: November 16, 2010.
Barry M. Straube,
CMS Chief Medical Officer and Director,
Office of Clinical Standards and Quality,
Centers for Medicare & Medicaid Services.
[FR Doc. 2010–29964 Filed 11–26–10; 8:45 am]
BILLING CODE 4120–01–P
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Privacy Act of 1974; Report of New
System of Records
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (HHS).
ACTION: Notice of a New System of
Records.
AGENCY:
In accordance with the
requirements of the Privacy Act of 1974,
CMS is establishing a new system of
records (SOR) titled, ‘‘Medicare and
Medicaid Electronic Health Record
(EHR) Incentive Program National Level
Repository’’ System No. 09–70–0587.
The final rule for the Medicare and
Medicaid EHR Incentive Program
implements the provisions of the
American Recovery and Reinvestment
Act of 2009 (the Recovery Act) (Pub. L.
111–5). Specifically, Title IV of Division
B of the Recovery Act amends Titles
XVIII and XIX of the Social Security Act
(the Act) by establishing incentive
payments to eligible professionals (EPs),
eligible hospitals and critical access
hospitals (CAHs) and Medicare
Advantage (MA) Organizations
participating in Medicare and Medicaid
programs that adopt and successfully
demonstrate meaningful use of certified
electronic health record (EHR)
technology. These Recovery Act
provisions, together with Title XIII of
Division A of the Recovery Act, may be
cited as the ‘‘Health Information
Technology for Economic and Clinical
Health Act,’’ or the ‘‘HITECH Act.’’
The final rule specified the initial
criteria EPs, eligible hospitals and
CAHs, and MA Organizations must meet
in order to qualify for an incentive
payment; calculation of the incentive
payment amounts; payment adjustments
under Medicare for covered professional
services and inpatient hospital services
provided by EPs, eligible hospitals and
CAHs failing to demonstrate meaningful
use of certified EHR technology
beginning in 2015; and other program
participation requirements. Also, the
Office of the National Coordinator for
Health Information Technology (ONC)
issued a closely related final rule that
specified the initial set of standards,
implementation specifications, and
certification criteria for certified EHR
technology. ONC has also issued a
separate final rule on the establishment
of certification programs for health
information technology (HIT).
To register for the Medicare and
Medicaid EHR Incentive Program, EPs,
SUMMARY:
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eligible hospitals and CAHs, and MA
Organizations will be required to
provide the following information:
Name, National Provider Identifier
(NPI), business address and business
phone for each EP, eligible hospital or
CAH; Taxpayer Identification Number
(TIN) to which the EP, eligible hospital
or CAH wants the incentive payment to
be made; For EPs, whether they choose
to participate in the Medicare EHR
Incentive Program or the Medicaid EHR
Incentive Program; For eligible hospitals
and CAHs, their CMS Certification
Number (CCN); and other information as
specified by CMS. EPs, eligible hospitals
and CAHs will also have the option to
provide their e-mail address at the time
of registration. MA Organizations will
be required to provide their contract
number on behalf of their MA-affiliated
EPs and hospitals. At this time,
participation in the Medicare and
Medicaid EHR Incentive Programs is
voluntary for EPs, eligible hospitals and
CAHs.
Per section 1886(n)(4)(B) of the Act, as
added by section 4102(c) of the HITECH
Act, the Secretary will post on the
Internet Web site of the Centers for
Medicare & Medicaid Services, in an
easily understandable format, a list of
the names, business addresses, and
business phone numbers of the
Medicare EPs, eligible hospitals and
CAHs who are meaningful EHR users in
the Medicare EHR Incentive Program.
Sections 1853(m)(5) and 1853(l)(7) of
the Act, as added by sections 4101(c)
and 4102(c) of the HITECH Recovery
Act, require the Secretary to post the
same information for EPs and eligible
hospitals participating in the MA
program as would be required if they
were in the Medicare FFS program.
Additionally, the Secretary must post
the names of the qualifying MA
Organizations receiving the incentive
payment or payments. The routine uses
established with this system contain a
proper explanation as to the need for the
disclosure provisions and provide
clarity to CMS’ intention to disclose
provider-specific information contained
in this system.
The primary purpose of this system,
called the National Level Repository or
NLR, is to collect, maintain, and process
information that is required for the
Medicare and Medicaid EHR Incentive
Program. Information in this system will
also be disclosed to: (1) Support
regulatory, incentive payments and
policy functions such as evaluation and
reporting, whether performed by the
Agency or by an Agency contractor or
consultant; (2) assist another Federal
and/or state agency, agency of a state
government, or an agency established by
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state law; (3) assist in making the
individual physician-level participation
data available through an Agency
website and by various other means of
data dissemination; (4) assist the
Department’s Office of the National
Coordinator of Health Information
Technology’s (ONC’s) grantees for the
purpose of supporting ‘‘eligible
professional’’ (EP) adoption and
meaningful use of certified EHR
technology; (5) support litigation
involving the Agency; (6) combat fraud,
waste, and abuse in certain health
benefits programs, and (7) assist in a
response to a suspected or confirmed
breach of the security or confidentiality
of information. We have provided
background information about this new
system in the ‘‘Supplementary
Information’’ section below. Although
the Privacy Act requires only that CMS
provide an opportunity for interested
persons to comment on the proposed
routine uses, CMS invites comments on
all portions of this notice. See ‘‘Effective
Dates’’ section for information about the
comment period.
DATES: Effective Dates: CMS filed a new
system report with the Chair of the
House Committee on Government
Reform and Oversight, the Chair of the
Senate Committee on Homeland
Security & Governmental Affairs, and
the Administrator, Office of Information
and Regulatory Affairs, Office of
Management and Budget (OMB) on
November 29, 2010. To ensure that all
parties have adequate time in which to
comment, the new system, including
routine uses, will become effective 30
days from the publication of the notice,
or 40 days from the date it was
submitted to OMB and Congress,
whichever is later, unless CMS receives
comments that require alterations to this
notice.
ADDRESSES: The public should address
comments to: CMS Privacy Officer,
Division of Information Security and
Privacy Management, Enterprise
Architecture and Strategy Group, Office
of Information Services, CMS, Room
N1–24–08, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
Comments received will be available for
review at this location, by appointment,
during regular business hours, Monday
through Friday from 9 a.m.—3 p.m.,
eastern time zone.
FOR FURTHER INFORMATION CONTACT:
Rachel Maisler, Health Insurance
Specialist, Office of E–Health Standards
and Services, CMS, 7500 Security
Boulevard, Mail-stop: S2–26–17,
Baltimore, MD 21244–1850. Office: 410–
786–5754, Facsimile: 410–786–1347, Email address: rachel.maisler@cms.gov.
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Sections
4101(a), 4102(a) and 4102(a)(2) of the
HITECH Act respectively add sections
1848(o), 1886(n) and 1814(l)(A)(3) to the
Act to limit incentive payments in the
Medicare Fee-for-service (FSS) EHR
incentive program to an EP, eligible
hospital or CAH that is a ‘‘meaningful
EHR user.’’ Sections 4101(c) and 4102(c)
of the HITECH Act respectively adds
sections 1853(l) and 1853(m) which
outline the application of incentive
payments for certain MA-affiliated EPs
and MA-affiliated hospitals. Section
4201(a)(2) of the HITECH Act added
section 1903(t) to the Act to limit
incentive payments in the Medicaid
context to EPs, as defined at section
1903(t)(2)(A), who meet the
requirements of 1903(t). As described in
our final rule discussed below, these
eligible professionals can receive an
incentive payment for adoption or
utilization of, or upgrade to, certified
EHR technology in 2011, and can
receive incentive payments in certain
subsequent years if they demonstrate
meaningful use of certified EHR
technology.
In sections 1848(o)(2)(A) and
1886(n)(3) of the Act, the Congress
specified three types of requirements for
meaningful use in the Medicare context:
(1) Use of certified EHR technology in
a meaningful manner; (2) that the
certified EHR technology is connected
in a manner that provides for the
electronic exchange of health
information to improve the quality of
care; and (3) that, in using certified EHR
technology, the provider submits to the
Secretary information on clinical quality
measures and such other measures
selected by the Secretary.
In our final rule on the EHR incentive
program, we stated that we are not
limited to collecting only information
pertaining to Medicare and Medicaid
beneficiaries. Therefore, in our final
rule, we require that, in order to
demonstrate meaningful use, an EP,
eligible hospital or CAH, or MA
Organization must report aggregate
information on clinical quality measures
for all patients to whom clinical quality
measures apply. As explained in the
final rule for EHR incentive payments,
for the 2011 payment year, we use an
attestation methodology for the
submission of summary information on
clinical quality measures as a condition
of demonstrating meaningful use of
certified EHR technology.
For the Medicaid incentive program,
as stated in our final rule, for their first
year of payment, providers are not
required to demonstrate meaningful use,
and may receive an incentive payment
by demonstrating adoption,
SUPPLEMENTARY INFORMATION:
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implementation, or upgrade to certified
EHR technology. We expect that, for
2011, the majority of Medicaid
providers will receive an incentive
payment through this pathway. In their
second, third, fourth, fifth and sixth
payment year, Medicaid EPs and
hospitals will be required to
demonstrate meaningful use of certified
EHR technology to qualify for an
incentive payment.
As stated in our final rule, we will use
a phased approach for meaningful use
criteria, based on currently available
technology capabilities and provider
practice experience. We refer to the
initial meaningful use criteria as ‘‘Stage
1.’’ In the final rule, we require that EPs,
eligible hospitals and CAHs, including
MA-affiliated EPs and hospitals,
demonstrate that they satisfy all the
required meaningful use objectives and
associated measures of the Stage 1
criteria during the reporting period for
2011 through attestation in order to
receive incentive payments. In addition,
we require that EPs, eligible hospitals
and CAHs, and MA Organizations attest
to the accuracy and completeness of the
numerators and denominators for each
of the applicable measures, and that the
information submitted includes
information on all patients to whom the
measure applies.
To qualify as a meaningful EHR user
for 2011, we require that EPs, eligible
hospitals, or CAHs demonstrate that
they meet all of the required meaningful
use objectives and the associated
measures using certified EHR
technology. In order to receive an
incentive payment, all EPs, eligible
hospitals and CAHs must register for the
program in the NLR and then attest that
they have successfully demonstrated
meaningful use of certified EHR
technology after the completion of their
EHR reporting period, which is defined
at 75 FR 44566.
Section 1848(o)(3)(D) of the Act
requires the Secretary to list, in an
easily understandable format, the
names, business addresses, and business
phone numbers of the Medicare EPs for
being meaningful EHR users under the
Medicare FFS program on the Internet
web site of CMS. Section 1886(n)(4)(B)
of the Act requires the Secretary to list,
in an easily understandable format, the
names and other relevant data as
determined appropriate, of eligible
hospitals and CAHs who are meaningful
EHR users under the Medicare FFS
program, on the CMS Internet web site.
Sections 1853(m)(5) and 1853(I)(7) of
the Act require the Secretary to post the
same information for EPs and eligible
hospitals in the MA program as would
be required if they were in the Medicare
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FFS program. Therefore, we collect the
information necessary to post the name,
business address and business phone
numbers of all EPs, eligible hospitals
and CAHs participating in the Medicare
FFS and MA EHR Incentive Program,,
and post this information on our
Internet web site. The routine uses
established with this system contain a
proper explanation as to the need for the
disclosure provisions and provide
clarity to CMS’ intention to disclose
provider-specific information contained
in this system.
I. Description of the Proposed System of
Records
A. Statutory and Regulatory Basis for
System
Authority for the collection,
maintenance, and disclosures from this
system is provided under §§ 1848(o),
1886(m), 1848(l), and 1853(m) of the
Social Security Act which were added
by the HITECH Act, respectively
authorize incentive payments for EPs,
eligible hospitals, CAHs and MA
Organizations that successfully
demonstrate meaningful use of certified
EHR technology. Sections 1903(a)(3)
and 1903(t) of the Social Security Act
provides authority for the Medicaid
EHR Incentive Program. These
provisions are implemented by 75 FR
44314 and 42 CFR parts 412, 413, 422,
collectively known as the Medicare and
Medicaid Programs; Electronic Health
Record Incentive Program; Final Rule.
B. Collection and Maintenance of Data
in the System
The National Level Repository (NLR)
contains information on eligible
professionals who receive Medicare
incentives as meaningful users of
certified EHR technology. Information
in the NLR will be populated from other
CMS systems, including the Provider
Enrollment, Chain, and Ownership
System (PECOS) and the National Plan
& Provider Enumeration System
(NPPES). The NLR will contain provider
name, National Provider Identifier
(NPI), business address and phone
number, Taxpayer Identification
Number (TIN) to which the EP, eligible
hospital or CAH, or MA Organization
wants the incentive payment to be
made, and, for EPs, whether they choose
to participate in the Medicare EHR
Incentive Program or the Medicaid EHR
Incentive Program. For eligible hospitals
and CAHs, their CCN will also be
included. For MA Organizations, their
CMS contract number will be included.
For providers participating in the
Medicaid EHR Incentive Program, it will
include the State in which they choose
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to participate. Additionally, EPs,
eligible hospitals and CAHs will have
the option to provide an e-mail address
for inclusion in the system. At this time,
participation in the Medicare and
Medicaid EHR Incentive Program is
voluntary for EPs, eligible hospitals and
CAHs.
II. Agency Policies, Procedures, and
Restrictions On Routine Uses
A. 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 information collected in the
NLR that can be associated with an
individual EP as provided for under
‘‘Section III. Proposed Routine Use
Disclosures of Data in the System.’’
Identifiable data may be disclosed under
a routine use.
We will only disclose the minimum
provider-level data necessary to achieve
the purpose of the Medicare and
Medicaid EHR Incentive Program. CMS
has the following policies and
procedures concerning disclosures of
information that will be maintained in
the system. These policies do not apply
to Routine Use No. 3 for this system. In
general, disclosure of information from
the system will be approved only for the
minimum information 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, maintain, and process
information promoting the nationwide
health information technology
infrastructure that allows for the
electronic use and exchange of
information.
2. Determines that:
a. The purpose of the disclosure can
only be accomplished if the record is
provided in an 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
provider 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;
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b. Remove or destroy at the earliest
time all individually-identifiable
information; and
c. Agree to not use or disclose the
information for any purpose other than
the stated purpose under which the
information was disclosed.
4. Determines that the data are valid
and reliable.
III. Proposed Routine Use Disclosures
of Data In the System
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A. Entities Who May Receive
Disclosures under Routine Use
These routine uses specify
circumstances, in addition to those
provided by statute in the Privacy Act
of 1974, under which CMS may release
information from the Medicare and
Medicaid EHR Incentive Program
without the consent of the individual to
whom such information pertains. 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. We propose to establish the
following routine use disclosures of
information maintained in the system:
1. To support Agency contractors or
consultants who have been engaged by
the Agency to assist in accomplishment
of a CMS function relating to the
purposes for this SOR and who need to
have access to the records in order to
assist CMS.
We contemplate disclosing
information under this routine use only
in situations in which CMS may enter
into a contractual or similar agreement
with a third party to assist in
accomplishing a CMS function relating
to purposes for this SOR.
CMS occasionally contracts out
certain of its functions when doing so
would contribute to effective and
efficient operations. CMS must be able
to give a contractor or consultant
whatever information is necessary for
the contractor or consultant to fulfill its
duties. In these situations, safeguards
are provided in the contract prohibiting
the contractor or consultant from using
or disclosing the information for any
purpose other than that described in the
contract and requires the contractor or
consultant to return or destroy all
information at the completion of the
contract.
2. To assist another Federal or state
agency, agency of a state government, or
an agency established by state law
pursuant to agreements with CMS to:
a. Contribute to the accuracy of CMS’s
proper incentive payment to Medicare
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and Medicaid EHR Incentive Program
participants, and
b. Assist Federal/state Medicaid
programs which may require Medicare
and Medicaid EHR Incentive Program
information for purposes related to this
system.
c. Assist other Federal agencies that
have the authority to perform collection
of debts owed to the Federal
government.
Other Federal or state agencies in
their administration of a Federal health
program may require EHR Incentive
Program information in order to support
evaluations and monitoring of various
aspects of the Medicare and Medicaid
EHR Incentive payments.
2. To assist in making the information
for EPs, eligible hospitals and CAHs,
and MA Organizations that receive
Medicare EHR incentive payments
through the new payment contractor,
available through a public web site. If
local websites are used by a local or
regional collaborative, CMS would have
links to these Web sites on its main Web
site.
This information would be posted for
the purpose of, and in a manner that
would promote the use of EHRs by EPs,
eligible hospitals and CAHs, and MA
Organizations to Medicare and
Medicaid beneficiaries.
3. To assist the Department’s Office of
the National Coordinator of Health
Information Technology’s (ONC’s)
grantees for the purpose of supporting
‘‘eligible professional’’ (EP) adoption and
meaningful use of certified EHR
technology.
We contemplate disclosing
information under this routine use only
in situations in which CMS may be
asked to provide necessary information
to ONC grantees, also referred to as
Health Information Technology
Regional Extension Centers (RECs) to
assist in accomplishing an ONC
function relating to support for ‘‘eligible
professional’’ (EP) adoption of,
meaningful use of certified EHR
technology, and provider support.
4. 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
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
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litigation and that the use of such
records by the DOJ, court or
adjudicatory body is compatible with
the purpose for which the agency
collected the records.
Whenever CMS is involved in
litigation, or occasionally when another
party is involved in litigation and CMS’s
policies or operations could be affected
by the outcome of the litigation, CMS
would be able to disclose information to
the DOJ, court, or adjudicatory body
involved.
5. To assist a CMS contractor
(including, but not limited to Medicare
Administrative Contractors, fiscal
intermediaries, and carriers) that assists
in the administration of a CMSadministered health benefits program,
or to a grantee of a CMS-administered
grant program, when disclosure is
deemed reasonably necessary by CMS to
prevent, deter, discover, detect,
investigate, examine, prosecute, sue
with respect to, defend against, correct,
remedy, or otherwise combat fraud,
waste or abuse in such program.
We contemplate disclosing
information under this routine use only
in situations in which CMS may enter
into a contract or grant with a third
party to assist in accomplishing CMS
functions relating to the purpose of
combating fraud, waste or abuse.
CMS occasionally contracts out
certain of its functions when doing so
would contribute to effective and
efficient operations. CMS must be able
to give a contractor or 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 or grant and requiring the
contractor or grantee to return or destroy
all information.
6. 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 Medicare
and Medicaid EHR Incentive Program
information for the purpose of
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combating fraud, waste or abuse in such
Federally-funded programs.
7. To assist 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 unnecessary
for the assistance.
Other Federal agencies and
contractors may require EHR Incentive
Program information for the purpose of
assisting in a respond to a suspected or
confirmed breach of the security or
confidentiality of information.
IV. Safeguards
CMS has safeguards in place for
authorized users and monitors such
users to ensure against 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 include 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 E–
Government Act of 2002, the ClingerCohen Act of 1996; the Medicare
Modernization Act of 2003, and the
corresponding implementing
regulations. OMB Circular A–130,
Management of Federal Resources,
Appendix III, Security of Federal
Automated Information Resources also
applies. Federal, HHS, and CMS
policies and standards include but are
not limited to: All pertinent National
Institute of Standards and Technology
publications; the HHS Information
Systems Program Handbook and the
CMS Information Security Handbook.
V. Effects of the New System On the
Rights of Individuals
CMS proposes to establish this system
in accordance with the principles and
requirements of the Privacy Act and will
collect, use, and disseminate
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information only as prescribed therein.
We will only disclose the minimum
personal data necessary to achieve the
purpose of the data collection and the
routine uses contained in this notice.
Disclosure of information from the
system will be approved only to the
extent necessary to accomplish the
purpose of the disclosure. CMS has
assigned a higher level of security
clearance for the information
maintained in this system in an effort to
provide added security and protection
of data in this system.
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.
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 the
disclosure of information relating to
individuals.
Dated: November 16, 2010.
Michelle Snyder,
Deputy Chief Operating Officer, Centers for
Medicare & Medicaid Services.
SYSTEM No. 09–70–0587
SYSTEM NAME:
‘‘Medicare and Medicaid Electronic
Health Record (EHR) Incentive Program
National Level Repository’’ HHS/CMS/
OESS.
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive.
SYSTEM LOCATION:
CMS Data Center, 7500 Security
Boulevard, North Building, First Floor,
Baltimore, Maryland 21244–1850 and at
various contractor sites.
CATEGORIES OF INDIVIDUALS COVERED BY THE
SYSTEM:
The National Level Repository (NLR)
contains information on eligible
professionals who receive Medicare
incentives as meaningful users of
certified EHR technology.
CATEGORIES OF RECORDS IN THE SYSTEM:
The NLR will contain provider name,
National Provider Identifier (NPI),
business address and phone number,
Taxpayer Identification Number (TIN) to
which the EP, eligible hospital or CAH,
or MA Organization wants the incentive
payment to be made, and, for EPs,
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Sfmt 4703
73099
whether they choose to participate in
the Medicare EHR Incentive Program or
the Medicaid EHR Incentive Program.
For eligible hospitals and CAHs, their
CCN will also be included. For MA
Organizations, their CMS contract
number will be included. For providers
participating in the Medicaid EHR
Incentive Program, it will include the
State in which they choose to
participate. Additionally, EPs, eligible
hospitals and CAHs will have the option
to provide an e-mail address for
inclusion in the system. At this time,
participation in the Medicare and
Medicaid EHR Incentive Program is
voluntary for EPs, eligible hospitals and
CAHs.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for the collection,
maintenance, and disclosures from this
system is provided under §§ 1848(o),
1886(m), 1848(l), and 1853(m) of the
Social Security Act which were added
by the HITECH Act, respectively
authorize incentive payments for EPs,
eligible hospitals, CAHs and MA
Organizations that successfully
demonstrate meaningful use of certified
EHR technology. Sections 1903(a)(3)
and 1903(t) of the Social Security Act
provides authority for the Medicaid
EHR Incentive Program. These
provisions are implemented by 75 FR
44314 and 42 CFR parts 412, 413, 422,
collectively known as the Medicare and
Medicaid Programs; Electronic Health
Record Incentive Program; Final Rule.
PURPOSE(S) OF THE SYSTEM:
The primary purpose of this system,
called the National Level Repository or
NLR, is to collect, maintain, and process
information that is required for the
Medicare and Medicaid EHR Incentive
Program. Information in this system will
also be disclosed to: (1) Support
regulatory, incentive payments and
policy functions such as evaluation and
reporting, whether performed by the
Agency or by an Agency contractor or
consultant; (2) assist another Federal
and/or state agency, agency of a state
government, or an agency established by
state law; (3) assist in making the
individual physician-level participation
data available through an Agency
website and by various other means of
data dissemination; (4) assist the
Department’s Office of the National
Coordinator of Health Information
Technology’s (ONC’s) grantees for the
purpose of supporting ‘‘eligible
professional’’ (EP) adoption and
meaningful use of certified EHR
technology; (5) support litigation
involving the Agency; (6) combat fraud,
waste, and abuse in certain health
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benefits programs, and (7) assist in a
response to a suspected or confirmed
breach of the security or confidentiality
of information.
ROUTINE USES OF RECORDS MAINTAINED IN THE
SYSTEM, INCLUDING CATEGORIES OR USERS AND
THE PURPOSES OF SUCH USES:
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A. ENTITIES WHO MAY RECEIVE DISCLOSURES
UNDER ROUTINE USE
These routine uses specify
circumstances, in addition to those
provided by statute in the Privacy Act
of 1974, under which CMS may release
information from the EHRI without the
consent of the individual to whom such
information pertains. 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. We propose to establish the
following routine use disclosures of
information maintained in the system:
1. To support Agency contractors,
consultants, or CMS grantees who have
been engaged by the Agency to assist in
accomplishment of a CMS function
relating to the purposes for this SOR
and who need to have access to the
records in order to assist CMS.
2. To assist another Federal or state
agency, agency of a state government, or
an agency established by state law
pursuant to agreements with CMS to:
a. Contribute to the accuracy of CMS’s
proper incentive payment to Medicare
and Medicaid EHR Incentive Program
participants, and
b. Assist Federal/state Medicaid
programs which may require Medicare
and Medicaid EHR Incentive Program
information for purposes related to this
system.
c. Assist other Federal agencies that
have the authority to perform collection
of debts owed to the Federal
government.
3. To assist in making the information
for EPs, eligible hospitals and critical
access hospitals (CAHs), who receive
EHR incentive payments through the
new payment contractor, available
through a public website. If local Web
sites are used by a local or regional
collaborative, CMS would have links to
these websites on its main website.
4. To assist the Department’s Office of
the National Coordinator of Health
Information Technology’s (ONC’s)
grantees for the purpose of supporting
‘‘eligible professional’’ (EP) adoption and
meaningful use of certified EHR
technology.
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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
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 limited to fiscal
intermediaries and carriers) that assists
in the administration of a CMSadministered health benefits program,
or to a grantee of a CMS-administered
grant program, when disclosure is
deemed reasonably necessary by CMS to
prevent, deter, discover, detect,
investigate, examine, prosecute, sue
with respect to, defend against, correct,
remedy, or otherwise combat fraud,
waste or abuse in such program.
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.
8. To assist 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
the assistance.
POLICIES AND PRACTICES FOR STORING,
RETRIEVING, ACCESSING, RETAINING, AND
DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
Records are stored on both tape
cartridges (magnetic storage media) and
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in a DB2 relational database
management environment (DASD data
storage media).
RETRIEVABILITY:
Information is most frequently
retrieved by provider number (facility,
physician, IDs), service dates, and
prescriber identification number.
SAFEGUARDS:
CMS has safeguards in place for
authorized users and monitors such
users to ensure against 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 include 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
E–Government Act of 2002, the ClingerCohen Act of 1996; the Medicare
Modernization Act of 2003, and the
corresponding implementing
regulations. OMB Circular A–130,
Management of Federal Resources,
Appendix III, Security of Federal
Automated Information Resources also
applies. Federal, HHS, and CMS
policies and standards include but are
not limited to: All pertinent National
Institute of Standards and Technology
publications; the HHS Information
Systems Program Handbook and the
CMS Information Security Handbook.
RETENTION AND DISPOSAL:
Records are maintained with
identifiers for all transactions after they
are entered into the system for a period
of 10 years. Records are housed in both
active and archival files. All claimsrelated records are encompassed by the
document preservation order and will
be retained until notification is received
from the Department of Justice.
SYSTEM MANAGER AND ADDRESS:
Director, Office of E–Health Standards
and Services, Centers for Medicare &
Medicaid Services, 7500 Security Blvd,
Mail-stop: S2–26–17, Baltimore, MD
21244–1850.
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NOTIFICATION PROCEDURE:
For purpose of notification, the
subject individual should write to the
system manager who will require the
system name, and the retrieval selection
criteria (e.g., Provider number, SSN,
etc.).
Provider Enrollment, Chain, and
Ownership System (PECOS) and the
National Plan & Provider Enumeration
System (NPPES).
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS
OF THE ACT:
None.
RECORD ACCESS PROCEDURE:
[FR Doc. 2010–29952 Filed 11–26–10; 8:45 am]
For purpose of access, use the same
procedures outlined in Notification
Procedures above. Requestors should
also reasonably specify the record
contents being sought. (These
procedures are in accordance with
Department regulation 45 CFR
5b.5(a)(2)).
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
CONTESTING RECORD PROCEDURES:
The subject individual should 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 in the National Level
Repository will be populated from other
CMS systems of records, including the
Proposed Information Collection
Activity; Comment Request
Title: Evaluation of Pregnancy
Prevention Approaches and Teen
Pregnancy Prevention Evaluation.
OMB No.: 0970–0360.
Description: The Administration for
Children and Families (ACF), the Office
of the Assistant Secretary for Planning
and Evaluation (ASPE), and the Office
of the Assistant Secretary for Health
(ASH), 13.5. Department of Health and
Human Services (HHS), are proposing a
data collection activity to be undettaken
by two related studies—the Evaluation
of Pregnancy Prevention Approaches
study and the Teen Pregnancy
Prevention Evaluation. Both studies are
sponsored by ASH and will use the
same data collection instruments; ACF
is facilitating the Evaluation of
Pregnancy Prevention Approaches,
while ASPE is facilitating the Teen
Pregnancy Prevention Evaluation.
These two studies will assess the
effectiveness of a range of programs
designed to prevent or reduce sexual
risk behavior and pregnancy among
older adolescents. Knowing what types
of programs are effective will enhance
programmatic decisions by
policymakers and practitioners.
The proposed activity involves the
collection of information from
observations of program activities and
interviews with a range of experts and
persons involved with programs about
various aspects of existing prevention
programs and topics the experts view as
important to address through
evaluation. These data will be used to
help enhance decisions about the types
of programs to be evaluated in the
studies.
Respondents: Researchers and policy
experts, program directors, program
staff, or school administrators.
ANNUAL BURDEN ESTIMATES
Annual number of respondents
Instrument
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Discussion Guide for Use with Researchers and Policy Experts ...................
Discussion Guide for Use with Program Directors ..........................................
Discussion Guide for Use with Program Staff .................................................
Focus Group Discussion Guide for Use with Program Participants ...............
Discussion Guide for Use with School Administrators ....................................
Estimated Total Annual Burden
Hours: 920.
In compliance with the requirements
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade, SW., Washington, DC
20447, Attn: OPRE Reports Clearance
Officer. E-mail address:
OPREinfocollection@acf.hhs.gov. All
requests should be identified by the title
of the information collection.
The Department specifically requests
comments on (a) Whether the proposed
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Dated: November 22, 2010.
Steven Hanmer,
OPRE Reports Clearance Officer.
[FR Doc. 2010–29917 Filed 11–26–10; 8:45 am]
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Average burden hours per
response
Estimated annual burden
hours
1
2
1
1
1
1
2
2
1.5
1
30
120
120
450
200
30
30
60
300
200
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
BILLING CODE 4184–01–M
Number of responses per
respondent
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0601]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Current Good
Manufacturing Practice Regulations for
Medicated Feeds
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal Agencies are required to
SUMMARY:
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Agencies
[Federal Register Volume 75, Number 228 (Monday, November 29, 2010)]
[Notices]
[Pages 73095-73101]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-29952]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
Privacy Act of 1974; Report of New System of Records
AGENCY: Centers for Medicare & Medicaid Services (CMS), Department of
Health and Human Services (HHS).
ACTION: Notice of a New System of Records.
-----------------------------------------------------------------------
SUMMARY: In accordance with the requirements of the Privacy Act of
1974, CMS is establishing a new system of records (SOR) titled,
``Medicare and Medicaid Electronic Health Record (EHR) Incentive
Program National Level Repository'' System No. 09-70-0587. The final
rule for the Medicare and Medicaid EHR Incentive Program implements the
provisions of the American Recovery and Reinvestment Act of 2009 (the
Recovery Act) (Pub. L. 111-5). Specifically, Title IV of Division B of
the Recovery Act amends Titles XVIII and XIX of the Social Security Act
(the Act) by establishing incentive payments to eligible professionals
(EPs), eligible hospitals and critical access hospitals (CAHs) and
Medicare Advantage (MA) Organizations participating in Medicare and
Medicaid programs that adopt and successfully demonstrate meaningful
use of certified electronic health record (EHR) technology. These
Recovery Act provisions, together with Title XIII of Division A of the
Recovery Act, may be cited as the ``Health Information Technology for
Economic and Clinical Health Act,'' or the ``HITECH Act.''
The final rule specified the initial criteria EPs, eligible
hospitals and CAHs, and MA Organizations must meet in order to qualify
for an incentive payment; calculation of the incentive payment amounts;
payment adjustments under Medicare for covered professional services
and inpatient hospital services provided by EPs, eligible hospitals and
CAHs failing to demonstrate meaningful use of certified EHR technology
beginning in 2015; and other program participation requirements. Also,
the Office of the National Coordinator for Health Information
Technology (ONC) issued a closely related final rule that specified the
initial set of standards, implementation specifications, and
certification criteria for certified EHR technology. ONC has also
issued a separate final rule on the establishment of certification
programs for health information technology (HIT).
To register for the Medicare and Medicaid EHR Incentive Program,
EPs,
[[Page 73096]]
eligible hospitals and CAHs, and MA Organizations will be required to
provide the following information: Name, National Provider Identifier
(NPI), business address and business phone for each EP, eligible
hospital or CAH; Taxpayer Identification Number (TIN) to which the EP,
eligible hospital or CAH wants the incentive payment to be made; For
EPs, whether they choose to participate in the Medicare EHR Incentive
Program or the Medicaid EHR Incentive Program; For eligible hospitals
and CAHs, their CMS Certification Number (CCN); and other information
as specified by CMS. EPs, eligible hospitals and CAHs will also have
the option to provide their e-mail address at the time of registration.
MA Organizations will be required to provide their contract number on
behalf of their MA-affiliated EPs and hospitals. At this time,
participation in the Medicare and Medicaid EHR Incentive Programs is
voluntary for EPs, eligible hospitals and CAHs.
Per section 1886(n)(4)(B) of the Act, as added by section 4102(c)
of the HITECH Act, the Secretary will post on the Internet Web site of
the Centers for Medicare & Medicaid Services, in an easily
understandable format, a list of the names, business addresses, and
business phone numbers of the Medicare EPs, eligible hospitals and CAHs
who are meaningful EHR users in the Medicare EHR Incentive Program.
Sections 1853(m)(5) and 1853(l)(7) of the Act, as added by sections
4101(c) and 4102(c) of the HITECH Recovery Act, require the Secretary
to post the same information for EPs and eligible hospitals
participating in the MA program as would be required if they were in
the Medicare FFS program. Additionally, the Secretary must post the
names of the qualifying MA Organizations receiving the incentive
payment or payments. The routine uses established with this system
contain a proper explanation as to the need for the disclosure
provisions and provide clarity to CMS' intention to disclose provider-
specific information contained in this system.
The primary purpose of this system, called the National Level
Repository or NLR, is to collect, maintain, and process information
that is required for the Medicare and Medicaid EHR Incentive Program.
Information in this system will also be disclosed to: (1) Support
regulatory, incentive payments and policy functions such as evaluation
and reporting, whether performed by the Agency or by an Agency
contractor or consultant; (2) assist another Federal and/or state
agency, agency of a state government, or an agency established by state
law; (3) assist in making the individual physician-level participation
data available through an Agency website and by various other means of
data dissemination; (4) assist the Department's Office of the National
Coordinator of Health Information Technology's (ONC's) grantees for the
purpose of supporting ``eligible professional'' (EP) adoption and
meaningful use of certified EHR technology; (5) support litigation
involving the Agency; (6) combat fraud, waste, and abuse in certain
health benefits programs, and (7) assist in a response to a suspected
or confirmed breach of the security or confidentiality of information.
We have provided background information about this new system in the
``Supplementary Information'' section below. Although the Privacy Act
requires only that CMS provide an opportunity for interested persons to
comment on the proposed routine uses, CMS invites comments on all
portions of this notice. See ``Effective Dates'' section for
information about the comment period.
DATES: Effective Dates: CMS filed a new system report with the Chair of
the House Committee on Government Reform and Oversight, the Chair of
the Senate Committee on Homeland Security & Governmental Affairs, and
the Administrator, Office of Information and Regulatory Affairs, Office
of Management and Budget (OMB) on November 29, 2010. To ensure that all
parties have adequate time in which to comment, the new system,
including routine uses, will become effective 30 days from the
publication of the notice, or 40 days from the date it was submitted to
OMB and Congress, whichever is later, unless CMS receives comments that
require alterations to this notice.
ADDRESSES: The public should address comments to: CMS Privacy Officer,
Division of Information Security and Privacy Management, Enterprise
Architecture and Strategy Group, Office of Information Services, CMS,
Room N1-24-08, 7500 Security Boulevard, Baltimore, Maryland 21244-1850.
Comments received will be available for review at this location, by
appointment, during regular business hours, Monday through Friday from
9 a.m.--3 p.m., eastern time zone.
FOR FURTHER INFORMATION CONTACT: Rachel Maisler, Health Insurance
Specialist, Office of E-Health Standards and Services, CMS, 7500
Security Boulevard, Mail-stop: S2-26-17, Baltimore, MD 21244-1850.
Office: 410-786-5754, Facsimile: 410-786-1347, E-mail address:
rachel.maisler@cms.gov.
SUPPLEMENTARY INFORMATION: Sections 4101(a), 4102(a) and 4102(a)(2) of
the HITECH Act respectively add sections 1848(o), 1886(n) and
1814(l)(A)(3) to the Act to limit incentive payments in the Medicare
Fee-for-service (FSS) EHR incentive program to an EP, eligible hospital
or CAH that is a ``meaningful EHR user.'' Sections 4101(c) and 4102(c)
of the HITECH Act respectively adds sections 1853(l) and 1853(m) which
outline the application of incentive payments for certain MA-affiliated
EPs and MA-affiliated hospitals. Section 4201(a)(2) of the HITECH Act
added section 1903(t) to the Act to limit incentive payments in the
Medicaid context to EPs, as defined at section 1903(t)(2)(A), who meet
the requirements of 1903(t). As described in our final rule discussed
below, these eligible professionals can receive an incentive payment
for adoption or utilization of, or upgrade to, certified EHR technology
in 2011, and can receive incentive payments in certain subsequent years
if they demonstrate meaningful use of certified EHR technology.
In sections 1848(o)(2)(A) and 1886(n)(3) of the Act, the Congress
specified three types of requirements for meaningful use in the
Medicare context: (1) Use of certified EHR technology in a meaningful
manner; (2) that the certified EHR technology is connected in a manner
that provides for the electronic exchange of health information to
improve the quality of care; and (3) that, in using certified EHR
technology, the provider submits to the Secretary information on
clinical quality measures and such other measures selected by the
Secretary.
In our final rule on the EHR incentive program, we stated that we
are not limited to collecting only information pertaining to Medicare
and Medicaid beneficiaries. Therefore, in our final rule, we require
that, in order to demonstrate meaningful use, an EP, eligible hospital
or CAH, or MA Organization must report aggregate information on
clinical quality measures for all patients to whom clinical quality
measures apply. As explained in the final rule for EHR incentive
payments, for the 2011 payment year, we use an attestation methodology
for the submission of summary information on clinical quality measures
as a condition of demonstrating meaningful use of certified EHR
technology.
For the Medicaid incentive program, as stated in our final rule,
for their first year of payment, providers are not required to
demonstrate meaningful use, and may receive an incentive payment by
demonstrating adoption,
[[Page 73097]]
implementation, or upgrade to certified EHR technology. We expect that,
for 2011, the majority of Medicaid providers will receive an incentive
payment through this pathway. In their second, third, fourth, fifth and
sixth payment year, Medicaid EPs and hospitals will be required to
demonstrate meaningful use of certified EHR technology to qualify for
an incentive payment.
As stated in our final rule, we will use a phased approach for
meaningful use criteria, based on currently available technology
capabilities and provider practice experience. We refer to the initial
meaningful use criteria as ``Stage 1.'' In the final rule, we require
that EPs, eligible hospitals and CAHs, including MA-affiliated EPs and
hospitals, demonstrate that they satisfy all the required meaningful
use objectives and associated measures of the Stage 1 criteria during
the reporting period for 2011 through attestation in order to receive
incentive payments. In addition, we require that EPs, eligible
hospitals and CAHs, and MA Organizations attest to the accuracy and
completeness of the numerators and denominators for each of the
applicable measures, and that the information submitted includes
information on all patients to whom the measure applies.
To qualify as a meaningful EHR user for 2011, we require that EPs,
eligible hospitals, or CAHs demonstrate that they meet all of the
required meaningful use objectives and the associated measures using
certified EHR technology. In order to receive an incentive payment, all
EPs, eligible hospitals and CAHs must register for the program in the
NLR and then attest that they have successfully demonstrated meaningful
use of certified EHR technology after the completion of their EHR
reporting period, which is defined at 75 FR 44566.
Section 1848(o)(3)(D) of the Act requires the Secretary to list, in
an easily understandable format, the names, business addresses, and
business phone numbers of the Medicare EPs for being meaningful EHR
users under the Medicare FFS program on the Internet web site of CMS.
Section 1886(n)(4)(B) of the Act requires the Secretary to list, in an
easily understandable format, the names and other relevant data as
determined appropriate, of eligible hospitals and CAHs who are
meaningful EHR users under the Medicare FFS program, on the CMS
Internet web site. Sections 1853(m)(5) and 1853(I)(7) of the Act
require the Secretary to post the same information for EPs and eligible
hospitals in the MA program as would be required if they were in the
Medicare FFS program. Therefore, we collect the information necessary
to post the name, business address and business phone numbers of all
EPs, eligible hospitals and CAHs participating in the Medicare FFS and
MA EHR Incentive Program,, and post this information on our Internet
web site. The routine uses established with this system contain a
proper explanation as to the need for the disclosure provisions and
provide clarity to CMS' intention to disclose provider-specific
information contained in this system.
I. Description of the Proposed System of Records
A. Statutory and Regulatory Basis for System
Authority for the collection, maintenance, and disclosures from
this system is provided under Sec. Sec. 1848(o), 1886(m), 1848(l), and
1853(m) of the Social Security Act which were added by the HITECH Act,
respectively authorize incentive payments for EPs, eligible hospitals,
CAHs and MA Organizations that successfully demonstrate meaningful use
of certified EHR technology. Sections 1903(a)(3) and 1903(t) of the
Social Security Act provides authority for the Medicaid EHR Incentive
Program. These provisions are implemented by 75 FR 44314 and 42 CFR
parts 412, 413, 422, collectively known as the Medicare and Medicaid
Programs; Electronic Health Record Incentive Program; Final Rule.
B. Collection and Maintenance of Data in the System
The National Level Repository (NLR) contains information on
eligible professionals who receive Medicare incentives as meaningful
users of certified EHR technology. Information in the NLR will be
populated from other CMS systems, including the Provider Enrollment,
Chain, and Ownership System (PECOS) and the National Plan & Provider
Enumeration System (NPPES). The NLR will contain provider name,
National Provider Identifier (NPI), business address and phone number,
Taxpayer Identification Number (TIN) to which the EP, eligible hospital
or CAH, or MA Organization wants the incentive payment to be made, and,
for EPs, whether they choose to participate in the Medicare EHR
Incentive Program or the Medicaid EHR Incentive Program. For eligible
hospitals and CAHs, their CCN will also be included. For MA
Organizations, their CMS contract number will be included. For
providers participating in the Medicaid EHR Incentive Program, it will
include the State in which they choose to participate. Additionally,
EPs, eligible hospitals and CAHs will have the option to provide an e-
mail address for inclusion in the system. At this time, participation
in the Medicare and Medicaid EHR Incentive Program is voluntary for
EPs, eligible hospitals and CAHs.
II. Agency Policies, Procedures, and Restrictions On Routine Uses
A. 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 information collected in the NLR that
can be associated with an individual EP as provided for under ``Section
III. Proposed Routine Use Disclosures of Data in the System.''
Identifiable data may be disclosed under a routine use.
We will only disclose the minimum provider-level data necessary to
achieve the purpose of the Medicare and Medicaid EHR Incentive Program.
CMS has the following policies and procedures concerning disclosures of
information that will be maintained in the system. These policies do
not apply to Routine Use No. 3 for this system. In general, disclosure
of information from the system will be approved only for the minimum
information 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, maintain,
and process information promoting the nationwide health information
technology infrastructure that allows for the electronic use and
exchange of information.
2. Determines that:
a. The purpose of the disclosure can only be accomplished if the
record is provided in an 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 provider 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;
[[Page 73098]]
b. Remove or destroy at the earliest time all individually-
identifiable information; and
c. Agree to not use or disclose the information for any purpose
other than the stated purpose under which the information was
disclosed.
4. Determines that the data are valid and reliable.
III. Proposed Routine Use Disclosures of Data In the System
A. Entities Who May Receive Disclosures under Routine Use
These routine uses specify circumstances, in addition to those
provided by statute in the Privacy Act of 1974, under which CMS may
release information from the Medicare and Medicaid EHR Incentive
Program without the consent of the individual to whom such information
pertains. 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. We propose to establish the following routine use
disclosures of information maintained in the system:
1. To support Agency contractors or consultants who have been
engaged by the Agency to assist in accomplishment of a CMS function
relating to the purposes for this SOR and who need to have access to
the records in order to assist CMS.
We contemplate disclosing information under this routine use only
in situations in which CMS may enter into a contractual or similar
agreement with a third party to assist in accomplishing a CMS function
relating to purposes for this SOR.
CMS occasionally contracts out certain of its functions when doing
so would contribute to effective and efficient operations. CMS must be
able to give a contractor or consultant whatever information is
necessary for the contractor or consultant to fulfill its duties. In
these situations, safeguards are provided in the contract prohibiting
the contractor or consultant from using or disclosing the information
for any purpose other than that described in the contract and requires
the contractor or consultant to return or destroy all information at
the completion of the contract.
2. To assist another Federal or state agency, agency of a state
government, or an agency established by state law pursuant to
agreements with CMS to:
a. Contribute to the accuracy of CMS's proper incentive payment to
Medicare and Medicaid EHR Incentive Program participants, and
b. Assist Federal/state Medicaid programs which may require
Medicare and Medicaid EHR Incentive Program information for purposes
related to this system.
c. Assist other Federal agencies that have the authority to perform
collection of debts owed to the Federal government.
Other Federal or state agencies in their administration of a
Federal health program may require EHR Incentive Program information in
order to support evaluations and monitoring of various aspects of the
Medicare and Medicaid EHR Incentive payments.
2. To assist in making the information for EPs, eligible hospitals
and CAHs, and MA Organizations that receive Medicare EHR incentive
payments through the new payment contractor, available through a public
web site. If local websites are used by a local or regional
collaborative, CMS would have links to these Web sites on its main Web
site.
This information would be posted for the purpose of, and in a
manner that would promote the use of EHRs by EPs, eligible hospitals
and CAHs, and MA Organizations to Medicare and Medicaid beneficiaries.
3. To assist the Department's Office of the National Coordinator of
Health Information Technology's (ONC's) grantees for the purpose of
supporting ``eligible professional'' (EP) adoption and meaningful use
of certified EHR technology.
We contemplate disclosing information under this routine use only
in situations in which CMS may be asked to provide necessary
information to ONC grantees, also referred to as Health Information
Technology Regional Extension Centers (RECs) to assist in accomplishing
an ONC function relating to support for ``eligible professional'' (EP)
adoption of, meaningful use of certified EHR technology, and provider
support.
4. 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 DOJ has agreed to represent the employee, or
d. The United States Government, is a party to litigation or has an
interest in such litigation, and by careful review, CMS determines that
the records are both relevant and necessary to the litigation and that
the use of such records by the DOJ, court or adjudicatory body is
compatible with the purpose for which the agency collected the records.
Whenever CMS is involved in litigation, or occasionally when
another party is involved in litigation and CMS's policies or
operations could be affected by the outcome of the litigation, CMS
would be able to disclose information to the DOJ, court, or
adjudicatory body involved.
5. To assist a CMS contractor (including, but not limited to
Medicare Administrative Contractors, 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 contract or grant with a
third party to assist in accomplishing CMS functions relating to the
purpose of combating fraud, waste or abuse.
CMS occasionally contracts out certain of its functions when doing
so would contribute to effective and efficient operations. CMS must be
able to give a contractor or 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 or grant and
requiring the contractor or grantee to return or destroy all
information.
6. 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 Medicare and Medicaid EHR Incentive
Program information for the purpose of
[[Page 73099]]
combating fraud, waste or abuse in such Federally-funded programs.
7. To assist 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 unnecessary for the assistance.
Other Federal agencies and contractors may require EHR Incentive
Program information for the purpose of assisting in a respond to a
suspected or confirmed breach of the security or confidentiality of
information.
IV. Safeguards
CMS has safeguards in place for authorized users and monitors such
users to ensure against 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 include 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 E-Government Act of 2002, the Clinger-
Cohen Act of 1996; the Medicare Modernization Act of 2003, and the
corresponding implementing regulations. OMB Circular A-130, Management
of Federal Resources, Appendix III, Security of Federal Automated
Information Resources also applies. Federal, HHS, and CMS policies and
standards include but are not limited to: All pertinent National
Institute of Standards and Technology publications; the HHS Information
Systems Program Handbook and the CMS Information Security Handbook.
V. Effects of the New System On the Rights of Individuals
CMS proposes to establish this system in accordance with the
principles and requirements of the Privacy Act and will collect, use,
and disseminate information only as prescribed therein. We will only
disclose the minimum personal data necessary to achieve the purpose of
the data collection and the routine uses contained in this notice.
Disclosure of information from the system will be approved only to the
extent necessary to accomplish the purpose of the disclosure. CMS has
assigned a higher level of security clearance for the information
maintained in this system in an effort to provide added security and
protection of data in this system.
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. 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 the disclosure of information
relating to individuals.
Dated: November 16, 2010.
Michelle Snyder,
Deputy Chief Operating Officer, Centers for Medicare & Medicaid
Services.
SYSTEM No. 09-70-0587
SYSTEM NAME:
``Medicare and Medicaid Electronic Health Record (EHR) Incentive
Program National Level Repository'' HHS/CMS/OESS.
SECURITY CLASSIFICATION:
Level Three Privacy Act Sensitive.
SYSTEM LOCATION:
CMS Data Center, 7500 Security Boulevard, North Building, First
Floor, Baltimore, Maryland 21244-1850 and at various contractor sites.
CATEGORIES OF INDIVIDUALS COVERED BY THE SYSTEM:
The National Level Repository (NLR) contains information on
eligible professionals who receive Medicare incentives as meaningful
users of certified EHR technology.
CATEGORIES OF RECORDS IN THE SYSTEM:
The NLR will contain provider name, National Provider Identifier
(NPI), business address and phone number, Taxpayer Identification
Number (TIN) to which the EP, eligible hospital or CAH, or MA
Organization wants the incentive payment to be made, and, for EPs,
whether they choose to participate in the Medicare EHR Incentive
Program or the Medicaid EHR Incentive Program. For eligible hospitals
and CAHs, their CCN will also be included. For MA Organizations, their
CMS contract number will be included. For providers participating in
the Medicaid EHR Incentive Program, it will include the State in which
they choose to participate. Additionally, EPs, eligible hospitals and
CAHs will have the option to provide an e-mail address for inclusion in
the system. At this time, participation in the Medicare and Medicaid
EHR Incentive Program is voluntary for EPs, eligible hospitals and
CAHs.
AUTHORITY FOR MAINTENANCE OF THE SYSTEM:
Authority for the collection, maintenance, and disclosures from
this system is provided under Sec. Sec. 1848(o), 1886(m), 1848(l), and
1853(m) of the Social Security Act which were added by the HITECH Act,
respectively authorize incentive payments for EPs, eligible hospitals,
CAHs and MA Organizations that successfully demonstrate meaningful use
of certified EHR technology. Sections 1903(a)(3) and 1903(t) of the
Social Security Act provides authority for the Medicaid EHR Incentive
Program. These provisions are implemented by 75 FR 44314 and 42 CFR
parts 412, 413, 422, collectively known as the Medicare and Medicaid
Programs; Electronic Health Record Incentive Program; Final Rule.
PURPOSE(S) OF THE SYSTEM:
The primary purpose of this system, called the National Level
Repository or NLR, is to collect, maintain, and process information
that is required for the Medicare and Medicaid EHR Incentive Program.
Information in this system will also be disclosed to: (1) Support
regulatory, incentive payments and policy functions such as evaluation
and reporting, whether performed by the Agency or by an Agency
contractor or consultant; (2) assist another Federal and/or state
agency, agency of a state government, or an agency established by state
law; (3) assist in making the individual physician-level participation
data available through an Agency website and by various other means of
data dissemination; (4) assist the Department's Office of the National
Coordinator of Health Information Technology's (ONC's) grantees for the
purpose of supporting ``eligible professional'' (EP) adoption and
meaningful use of certified EHR technology; (5) support litigation
involving the Agency; (6) combat fraud, waste, and abuse in certain
health
[[Page 73100]]
benefits programs, and (7) assist in a response to a suspected or
confirmed breach of the security or confidentiality of information.
ROUTINE USES OF RECORDS MAINTAINED IN THE SYSTEM, INCLUDING CATEGORIES
OR USERS AND THE PURPOSES OF SUCH USES:
A. Entities Who May Receive Disclosures under Routine Use
These routine uses specify circumstances, in addition to those
provided by statute in the Privacy Act of 1974, under which CMS may
release information from the EHRI without the consent of the individual
to whom such information pertains. 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. We propose to
establish the following routine use disclosures of information
maintained in the system:
1. To support Agency contractors, consultants, or CMS grantees who
have been engaged by the Agency to assist in accomplishment of a CMS
function relating to the purposes for this SOR and who need to have
access to the records in order to assist CMS.
2. To assist another Federal or state agency, agency of a state
government, or an agency established by state law pursuant to
agreements with CMS to:
a. Contribute to the accuracy of CMS's proper incentive payment to
Medicare and Medicaid EHR Incentive Program participants, and
b. Assist Federal/state Medicaid programs which may require
Medicare and Medicaid EHR Incentive Program information for purposes
related to this system.
c. Assist other Federal agencies that have the authority to perform
collection of debts owed to the Federal government.
3. To assist in making the information for EPs, eligible hospitals
and critical access hospitals (CAHs), who receive EHR incentive
payments through the new payment contractor, available through a public
website. If local Web sites are used by a local or regional
collaborative, CMS would have links to these websites on its main
website.
4. To assist the Department's Office of the National Coordinator of
Health Information Technology's (ONC's) grantees for the purpose of
supporting ``eligible professional'' (EP) adoption and meaningful use
of certified EHR technology.
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 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 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 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.
8. To assist 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 the assistance.
POLICIES AND PRACTICES FOR STORING, RETRIEVING, ACCESSING, RETAINING,
AND DISPOSING OF RECORDS IN THE SYSTEM:
STORAGE:
Records are stored on both tape cartridges (magnetic storage media)
and in a DB2 relational database management environment (DASD data
storage media).
RETRIEVABILITY:
Information is most frequently retrieved by provider number
(facility, physician, IDs), service dates, and prescriber
identification number.
SAFEGUARDS:
CMS has safeguards in place for authorized users and monitors such
users to ensure against 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 include 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 E-Government Act of 2002, the Clinger-
Cohen Act of 1996; the Medicare Modernization Act of 2003, and the
corresponding implementing regulations. OMB Circular A-130, Management
of Federal Resources, Appendix III, Security of Federal Automated
Information Resources also applies. Federal, HHS, and CMS policies and
standards include but are not limited to: All pertinent National
Institute of Standards and Technology publications; the HHS Information
Systems Program Handbook and the CMS Information Security Handbook.
RETENTION AND DISPOSAL:
Records are maintained with identifiers for all transactions after
they are entered into the system for a period of 10 years. Records are
housed in both active and archival files. All claims-related records
are encompassed by the document preservation order and will be retained
until notification is received from the Department of Justice.
SYSTEM MANAGER AND ADDRESS:
Director, Office of E-Health Standards and Services, Centers for
Medicare & Medicaid Services, 7500 Security Blvd, Mail-stop: S2-26-17,
Baltimore, MD 21244-1850.
[[Page 73101]]
NOTIFICATION PROCEDURE:
For purpose of notification, the subject individual should write to
the system manager who will require the system name, and the retrieval
selection criteria (e.g., Provider number, SSN, etc.).
RECORD ACCESS PROCEDURE:
For purpose of access, use the same procedures outlined in
Notification Procedures above. Requestors should also reasonably
specify the record contents being sought. (These procedures are in
accordance with Department regulation 45 CFR 5b.5(a)(2)).
CONTESTING RECORD PROCEDURES:
The subject individual should 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 in the National Level Repository will be populated from
other CMS systems of records, including the Provider Enrollment, Chain,
and Ownership System (PECOS) and the National Plan & Provider
Enumeration System (NPPES).
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS OF THE ACT:
None.
[FR Doc. 2010-29952 Filed 11-26-10; 8:45 am]
BILLING CODE 4120-01-P