HHS Acquisition Regulation: Acquisition of Information Technology; Standards for Health Information Technology (HHSAR Case 2023-001), 65303-65311 [2024-17096]
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Federal Register / Vol. 89, No. 154 / Friday, August 9, 2024 / Proposed Rules
model approved in Order No. 7049 for
estimating the volume variability of box
time because it ‘‘adds precision to the
estimating by ferreting out the different
effects by using groupings of mail
products that have similar coveragecausing characteristics.’’ Id. at 17.
Regarding the second research topic,
the Postal Service proposes the
following volume variabilities for the
nine sequences ordered by the
Commission in Order No. 7049 for it to
research:
Sequence
026
037
038
049
051
052
053
063
083
Proposed volume
variability
(%)
..................................
..................................
..................................
..................................
..................................
..................................
..................................
..................................
..................................
29.48
84.32
84.66
29.48
84.32
84.66
84.66
5.96
46.05
Source: Response at 33, Table 15; see generally, id. at 18–32.
Chairman’s Information Request No. 4
(CHIR No. 4) is issued today, July 30,
2024, concerning the Postal Service’s
Response and the Postal Service’s
response to CHIR No. 4 is due August
13, 2024.3
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III. Notice of Filing and Related
Proceeding
The Commission hereby informs the
public of the Postal Service’s Response
and of the reopening of Docket No.
RM2024–2 for the limited purpose of
considering issues raised by the
Response. More information on the
Response and additional filings in this
proceeding may be accessed via the
Commission’s website at https://
www.prc.gov. Any material filed in this
proceeding that is subject to an
application for non-public treatment
(filed under seal) may be accessed via
the Commission’s website only by
account holders granted access by an
order or in accordance with 39 CFR
3011.300(a). The Commission’s rules on
non-public materials (including access
to material filed under seal) appear in
39 CFR part 3011.
Interested persons may submit
comments on the Response no later than
August 27, 2024. Pursuant to 39 U.S.C.
505, Nikki Brendemuehl continues to
serve as an officer of the Commission
(Public Representative) to represent the
interests of the general public in this
proceeding.
3 Chairman’s Information Request No. 4, July 30,
2024.
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IV. Ordering Paragraphs
It is ordered:
1. The Commission reopens Docket
No. RM2024–2 for the limited purpose
of considering issues raised by the
Response of the United States Postal
Service to Order No. 7049 Regarding
Rural Carrier Costing, filed July 1, 2024.
2. Comments by interested persons in
this proceeding are due no later than
August 27, 2024.
3. Pursuant to 39 U.S.C. 505, the
Commission appoints Nikki
Brendemuehl to continue to serve as an
officer of the Commission (Public
Representative) to represent the
interests of the general public in this
docket.
4. The Secretary shall arrange for
publication of this order in the Federal
Register.
By the Commission.
Jennie L. Jbara,
Primary Certifying Official.
[FR Doc. 2024–17156 Filed 8–8–24; 8:45 am]
BILLING CODE 7710–FW–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
48 CFR Parts 339 and 352
RIN 0991–AC35
HHS Acquisition Regulation:
Acquisition of Information Technology;
Standards for Health Information
Technology (HHSAR Case 2023–001)
Department of Health and
Human Services.
ACTION: Proposed rule.
AGENCY:
The Department of Health and
Human Services (HHS) is proposing to
amend and update its Health and
Human Services Acquisition Regulation
(HHSAR) to implement requirements to
procure health information technology
(health IT) that meets standards and
implementation specifications
(standards) adopted by the Office of the
National Coordinator for Health
Information Technology (ONC) in the
following parts: Acquisition of
Information Technology and
Solicitation Provisions and Contract
Clauses.
SUMMARY:
Comments must be received on
or before October 8, 2024, to be
considered in the formulation of the
final rule.
ADDRESSES: Submit written comments
in response to HHSAR Case 2023–001
through the Federal eRulemaking Portal
at: https://www.regulations.gov by
searching for ‘‘HHSAR Case 2023–001’’.
DATES:
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Select the link ‘‘Comment Now’’ and
follow the ‘‘Submit a comment’’
instructions. Please include your name,
company name (if any), and indicate
they are submitted in response to ‘‘RIN
0991–AC35—HHS Acquisition
Regulation: Acquisition of Information
Technology; Standards for Health
Information Technology (HHSAR Case
2023–001).’’
Warning: Do not include any
personally identifiable information or
confidential business information that
you do not want publicly disclosed. All
comments may be posted on the internet
and can be retrieved by most internet
search engines. No deletions,
modifications, or redactions will be
made to comments received.
Inspection of Public Comments: All
comments received before the close of
the comment period will be available for
viewing by the public, including
personally identifiable or confidential
business information that is included in
a comment. You may wish to consider
limiting the amount of personal
information that you provide in any
voluntary public comment submission
you make. HHS reserves the right to
withhold information provided in
comments from public viewing that it
determines may have an adverse impact
on an individual(s). For additional
information, please read the Privacy Act
notice that is available via the link in
the footer of https://
www.regulations.gov. Follow the search
instructions on that website to view the
public comments.
FOR FURTHER INFORMATION CONTACT: Mr.
Jarreau Vieira, Chief, Acquisition RuleMaking Branch, U.S. Department of
Health and Human Services, Office of
the Assistant Secretary for Financial
Resources, Office of Acquisition Policy,
200 Independence Avenue SW,
Washington, DC 20201. Email:
acquisition_policy@hhs.gov, Telephone:
(202) 731–4625. This is not a toll-free
telephone number.
SUPPLEMENTARY INFORMATION:
I. Background
A. Authority
This rulemaking is being taken under
the authority of the Office of Federal
Procurement Policy (OFPP) Act which
provides the authority for an agency
head to authorize the issuance of agency
acquisition regulations that implement
or supplement the Federal Acquisition
Regulation (FAR). The OFPP Act, as
codified in 41 U.S.C. 1702, provides the
authority for the FAR and for the
issuance of agency acquisition
regulations consistent with the FAR.
This authority ensures that Government
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procurements are handled fairly and
consistently, that the Government
receives overall best value, and that the
Government and contractors both
operate under a known set of rules. The
Health and Human Services Acquisition
Regulation (HHSAR) is set forth at Title
48 CFR, chapter 3, parts 301 through
370.
Under this authority, we are seeking
to implement a department-wide
management policy issued by the
Secretary of the Department of Health
and Human Services (Secretary) in July
2022 (hereafter the ‘‘Secretary’s July
2022 Memorandum’’), that directed
HHS agencies to align and coordinate
health IT-related activities in support of
HHS health IT and interoperability
goals. This policy was supported by
requirements in sections 13111 and
13112 of the Health Information
Technology for Economic and Clinical
Health Act (HITECH Act) (Pub. L. 111–
5).
B. Genesis of Standards for Health
Information Technology in the HHSAR
The Secretary’s July 2022
Memorandum recognized that HHS
spending on health IT-related activities
has grown dramatically in recent years,
as various agencies have begun to
leverage the large foundation of
electronic health records put in place by
the $40 billion invested as a result of the
HITECH Act, as part of the American
Recovery and Reinvestment Act of 2009
(Pub. L. 111–5, Feb. 17, 2009), and the
related clinical data and interoperability
standards that HHS continues to
promote. Advancing interoperability
and the effective and appropriate use of
health IT systems is a key HHS
objective, and COVID–19 has further
demonstrated the importance of
interoperable data to improve the
quality, safety, affordability, and
efficiency of health care delivery;
inform pandemic response; and identify
and address disparities in care. As
health IT-related activities begin to play
an increasingly prominent role in
programs across the Department, the
Secretary’s July 2022 Memorandum
states that it is critical to ensure
alignment of such activities to avoid the
proliferation of ad-hoc health IT and
data silos. These silos undercut the
effectiveness and efficiency of the
Department’s policies and programs, are
costly for Federal and state agencies and
private sector partners to create and
maintain, have no synergies across
programs, and—due to lack of alignment
across and within HHS agencies—
impose significant burden on health
care providers, technology developers,
and other health care stakeholders.
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As part of the Secretary’s July 2022
Memorandum, the Secretary directed
HHS agencies, working with the
Assistant Secretary for Financial
Resources (ASFR), to develop standard
language for use in grants, cooperative
agreements, or contracts. The
Secretary’s July 2022 Memorandum
further identified the general elements
of this standard language, including
that: recipients are expected to utilize
health IT that meets standards adopted
under Section 3004 of the Public Health
Service Act (PHSA), if applicable, when
the funding mechanism includes
provisions requiring recipients to
implement, acquire, or upgrade health
IT; health care providers who have been
eligible to participate in Center for
Medicare & Medicaid Services’s (CMS’s)
health IT-focused incentive programs
can meet alignment requirements under
this policy by using certified health IT
which incorporates standards adopted
under PHSA Section 3004; and, where
there are no applicable standards
adopted under PHSA Section 3004,
recipients are encouraged to use other
HHS-identified standards or nonproprietary, consensus-based standards
developed by a national standard setting
organization, such as those referenced
in the Interoperability Standards
Advisory, are recommended.
We note that this regulation does not
impact existing HHS authorities for
standards adoption and note that HHS
agencies are committed to working
together to ensure that standards under
such authorities are aligned to advance
interoperability for a nationwide health
IT infrastructure.
Section 13111 of the HITECH Act
requires agencies identified by the
Director of the Office of Management
and Budget (OMB), in consultation with
the Secretary, when implementing,
acquiring, or upgrading health IT
systems used for the direct exchange of
individually identifiable health
information between agencies and with
non-Federal entities, to utilize, where
available, health IT systems and
products that meet standards and
implementation specifications adopted
by ONC on behalf of the Secretary under
section 3004 of the Public Health
Service Act (PHSA).
Section 13112 of the HITECH Act
specifies that agencies, as defined in
Executive Order 13410, shall require in
contracts or agreements with health care
providers, health plans, or health
insurance issuers that as each provider,
plan, or issuer implements, acquires, or
upgrades health IT systems, it shall
utilize, where available, health IT
systems and products that meet
standards and implementation
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specifications adopted under Section
3004 of the PHSA.
On behalf of HHS, ONC adopts
standards and implementation
specifications under section 3004 of the
PHSA in 45 CFR part 170, subpart B.
Standards adopted under section 3004
are included in certification criteria for
health IT in the ONC Health Information
Technology Certification Program in 45
CFR part 170, subpart C. For more
information on the ONC Certification
Program, see https://www.healthit.gov/
topic/certification-ehrs/certificationhealth-it. Health care providers who
have been eligible to participate in
CMS’s health IT-focused incentive
programs under sections 4101, 4102,
and 4201 of the HITECH Act have been
incentivized to adopt health IT that
meets certification criteria which
incorporate standards in 45 CFR part
170, subpart B. Consistent with HHS
policy, the proposals address use of
certified health IT by these providers,
where applicable.
C. Implementation Via Class Deviation
(2023–01)
On December 20, 2022, the HHS
Senior Procurement Executive issued
HHSAR Class Deviation (2023–01) from
part 339, Acquisition of Information
Technology; Standards for Health
Information Technology, in advance of
this proposed rule to implement in the
HHSAR the requirements of the HITECH
Act and HHS’ implementation
standards.
D. Purpose of Rule
This proposed rule is issued to
comply with the requirements of 41
U.S.C. 1707 and FAR subpart 1.5 that
require publication of a proposed rule
for public comment.
Consistent with HHS policy,
including the Secretary’s July 2022
Memorandum, and with sections 13111
and 13112 of the HITECH Act (Pub. L.
111–5), HHS is proposing to amend the
HHSAR to implement and align
requirements related to the procurement
of health IT with standards and
implementation specifications adopted
by ONC under section 3004 of the
PHSA.
This proposed rule would add a new
HHSAR subpart 339.70, Standards for
Health Information Technology, which
provides definitions, policy, and a
prescription for a new HHSAR clause to
implement requirements of the HITECH
Act, to include: (1) when contracting
officers must procure health IT
consistent with requirements in the
HITECH Act; and (2) when to require
use of health IT in a manner consistent
with requirements in the HITECH Act,
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in contracts and agreements with health
care providers, health plans, or health
insurance issuers.
This proposed rule would implement
requirements in the HHSAR that would
apply to all solicitations and contracts,
issued by or on behalf of HHS entities,
that involve implementing, acquiring, or
upgrading health IT used (1) for the
direct exchange of individually
identifiable health information between
agencies and non-Federal entities, or (2)
by health care providers, health plans,
or health insurance issuers.
II. Discussion and Analysis
A. HITECH Act Discussion
In this section, we provide discussion
of several issues in connection to our
proposals in this proposed rule.
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1. Acquiring, Implementing, or
Upgrading Health IT
We believe additional discussion of
terms used in sections 13111 and 13112
of the HITECH Act will help the public
to understand how these proposals will
be implemented. Specifically, we note
that both sections refer to implementing,
acquiring, or upgrading of health IT
systems as activities to which the
statutory provisions apply. We believe
the terms acquiring and upgrading
health IT are clear for the purpose of
this policy. However, we believe
additional explanation of the term
‘‘implementing’’ as it is used in this
policy is warranted. ‘‘Implementing’’
health IT may include a variety of
activities that are distinct from
acquiring or upgrading health IT. For
instance, ‘‘implementing’’ health IT may
include investments in health IT for its
maintenance and upkeep, the use of
health IT to collect, store, and share
health information, and activities
supporting the piloting, but not the
acquisition, of health IT tools.
We note that the proposals in HHSAR
parts 339 and 352 in this proposed rule
pertain to ‘‘work performed under the
contract that involves implementing,
acquiring, or upgrading health IT.’’ For
example, a contracted party performing
research may obtain data from health IT
systems. Unless the contract defines
specific health IT activities and/or
investments related to these data, such
activities would be considered
incidental to the work performed under
the contract and would not be subject to
our proposed requirements. We seek
comment on additional details that
would help with clarifying when a
contract activity would be considered
‘‘implementing’’ health IT.
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B. Authorities and Summary of
Proposed Changes
We propose to revise the following
parts of the HHSAR, 48 CFR chapter 3:
parts 339 and 352.
We propose to revise the authority
citations cited in each HHSAR part to
reflect as follows: 5 U.S.C. 301; 40
U.S.C. 121(c); 41 U.S.C. 1121(c)(3); 41
U.S.C. 1702; and 48 CFR 1.301 through
1.304. Where additional authorities for
a specific part are applicable, we
identify them under that discussion of
each HHSAR part later in this preamble.
We propose to retain the authority of
5 U.S.C. 301. This authority provides
that the head of an Executive
department or military department may
prescribe regulations for the government
of his department, the conduct of its
employees, the distribution and
performance of its business, and the
custody, use, and preservation of its
records, papers, and property.
We propose to retain the authority of
40 U.S.C. 121(c) and slightly revise the
reference. This authorizes the head of
each executive agency to issue orders
and directives that the agency head
considers necessary to carry out the
regulations. The Federal Acquisition
Regulation System and the publication
of the FAR is issued pursuant to this
authority as are agency supplements to
the FAR such as the HHSAR.
We propose to include a reference to
41 U.S.C. 1121(c)(3). This provision
states that the authority of an executive
agency under another law to prescribe
policies, regulations, procedures, and
forms for procurement is subject to the
authority conferred in section 1121, as
well as other sections of title 41.
We propose to add an authority
citation for 41 U.S.C. 1702 which
addresses the acquisition planning and
management responsibilities that are
carried out by the HHS Senior
Procurement Executive.
And we propose to add the citation of
48 CFR 1.301 through 1.304 to reflect
the authority and responsibility set forth
in the FAR and delegated to Federal
agencies to issue agency regulations that
supplement and implement the FAR.
Any other proposed changes to
authorities are shown under the
individual parts below.
1. HHSAR Part 339—Acquisition of
Information Technology
We propose to revise the authority
citations for part 339, for the reasons set
forth in the discussion and analysis
section, to read as follows: 5 U.S.C. 301;
40 U.S.C. 121(c); 41 U.S.C. 1121(c)(3);
41 U.S.C. 1702; and 48 CFR 1.301
through 1.304.
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We propose to add subpart 339.70,
Standards for Health Information
Technology, to include underlying
sections 339.7000, 339.7001, 339.7002,
and 339.7003. This subpart is added to
implement standards under the
authority of the HITECH Act, Public
Law 111–5, title XIII, sections 13111
and 13112 that are applicable for HHS
contracts, as well as HHS policy.
We propose to add section 339.7000,
Scope of subpart, to provide general
scope and purpose of the subpart and its
underlying sections, which implements
and aligns requirements related to the
procurement of health IT with standards
and implementation specifications
adopted by ONC, under section 3004 of
the PHSA, consistent with sections
13111 and 13112 of the HITECH Act
(Pub. L. 111–5) and HHS policy to
advance health IT alignment. The
subpart describes the policies and
procedures for solicitations and
contracts that involve implementing,
acquiring, or upgrading health IT that is
used for the direct exchange of
individually identifiable health
information between agencies and with
non-Federal entities; or by health care
providers, health plans, or health
insurance issuers.
We propose to add section 339.7001,
Definitions. This section is added to
include three definitions applicable to
the new subpart: Health information
technology (health IT), individually
identifiable health information, and the
ONC Health Information Technology
Certification Program.
We propose to add section 339.7002,
Policy—standards for health
information technology. This section is
added to implement standards for
health IT in HHS contracts. This section
would require, pursuant to the HITECH
Act, Public Law 111–5, title XIII,
sections 13111 and 13112, and HHS
policy, that health IT shall meet
standards and implementation
specifications adopted in 45 CFR part
170, subpart B, if applicable. This
includes health IT that is—
• Procured by or on behalf of HHS
entities, or
• Procured through HHS contracts
with health care providers, health plans,
or health insurance issuers that involve
implementing, acquiring, or upgrading
health IT.
Section 339.7002 would prohibit
contracting officers from awarding a
contract involving health IT as
described in this preamble, unless
certain conditions are met. First, this
section would prohibit contracting
officers from awarding a contract that
includes implementing, acquiring, or
upgrading health IT used for the direct
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exchange of individually identifiable
health information between agencies
and with non-Federal entities unless an
offeror/quoter/contractor shall utilize
health IT that—
• Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support work
performed under the contract; or
• Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support work performed under the
contract (see certification criteria in 45
CFR part 170, subpart C), when the
contractor is—
Æ an eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102, and
4201 of the HITECH Act; or
Æ implementing, acquiring, or
upgrading technology to be used by an
eligible professional in an ambulatory
setting, or hospital, eligible under
sections 4101, 4102, and 4201 of the
HITECH Act.
Further, this section would also
prohibit contracting officers from
awarding a contract if a contractor is a
health care provider, health plan, or
health insurance issuer, or, to perform
the contract, is establishing an
agreement with a health care provider,
health plan, or health insurance issuer,
for any work performed under the
contract that involves implementing,
acquiring, or upgrading health IT,
unless the offeror/quoter/contractor
agrees that it shall utilize health IT
that—
• Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support work
performed under the contract; or
• Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support work performed under the
contract (see certification criteria in 45
CFR part 170, subpart C), when the
contractor is—
Æ an eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102, and
4201 of the HITECH Act; or
Æ implementing, acquiring, or
upgrading technology to be used by an
eligible professional in an ambulatory
setting, or hospital, eligible under
sections 4101, 4102, and 4201 of the
HITECH Act.
Finally, this section would also
encourage offerors/quoters/contractors,
if standards and implementation
specifications adopted in 45 CFR part
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170, subpart B, cannot support the work
as specified in the contract, to use
health IT that meets non-proprietary
standards and implementation
specifications developed by consensusbased standards development
organizations. This may include
standards identified in the ONC
Interoperability Standards Advisory,
available at https://www.healthit.gov/
isa/.
We propose to add section 339.7003,
Contract clause, to prescribe a new
clause at 352.239–70, Standards for
Health Information Technology, in
solicitations and contracts, issued by or
on behalf of HHS entities, that involve
implementing, acquiring, or upgrading
health IT used—
(a) for the direct exchange of
individually identifiable health
information between agencies and with
non-Federal entities; or
(b) by health care providers, health
plans, or health insurance issuers.
2. HHSAR Part 352—Solicitation
Provisions and Contract Clauses
We propose to revise the authority
citations for part 352, for the reasons set
forth in the discussion and analysis
section, to read as follows: 5 U.S.C. 301;
40 U.S.C. 121(c); 41 U.S.C. 1121(c)(3);
41 U.S.C. 1702; and 48 CFR 1.301
through 1.304.
We propose to add clause 352.239–70,
Standards for Health Information
Technology, to set forth requirements
for the standards for health IT provided
or utilized on a contract. The clause
would include three definitions: Health
information technology (health IT),
individually identifiable health
information, and the ONC Health
Information Technology Certification
Program.
The clause would provide that by
submission of an offer or a quote, and
execution of a contract, the offeror/
quoter/contractor agrees that—
• For any work performed under the
contract that involves implementing,
acquiring, or upgrading health IT
procured by or on behalf of HHS entities
used for the direct exchange of
individually identifiable health
information between agencies and with
non-Federal entities, the offeror/quoter/
contractor shall utilize health IT that—
(1) Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support the work
performed under the contract; or
(2) Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support the work performed under the
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contract (see certification criteria in 45
CFR part 170, subpart C), when the
Contractor is—
(i) an eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102 and
4201 of the HITECH Act; or
(ii) is implementing, acquiring or
upgrading technology to be used by an
eligible professional in an ambulatory
setting, or a hospital, eligible under
sections 4101, 4102 and 4201 of the
HITECH Act.
• When the contractor is a health care
provider, health plan, or health
insurance issuer, or, to perform the
contract, is establishing an agreement
with a health care provider, health plan,
or health insurance issuer, for work
performed under the contract that
involves implementing, acquiring, or
upgrading health IT, the offeror/quoter/
contractor shall utilize heath IT that—
(1) Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support the work
performed under the contract; or
(2) Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support the work performed under the
contract (see certification criteria in 45
CFR part 170, subpart C), when the
Contractor is—
(i) an eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102 and
4201 of the HITECH Act; or
(ii) implementing, acquiring or
upgrading technology to be used by an
eligible professional in an ambulatory
setting, or a hospital, eligible under
sections 4101, 4102 and 4201 of the
HITECH Act.
Additionally, this section would also
encourage contractors, if such standards
and implementation specifications
adopted in 45 CFR part 170, subpart B,
cannot support the work as specified in
the contract, to use health IT that meets
non-proprietary standards and
implementation specifications
developed by consensus-based
standards development organizations.
This may include standards identified
in the ONC Interoperability Standards
Advisory, available at https://
www.healthit.gov/isa/.
III. Executive Order 12866 and 13563
Executive Orders (E.O.) 12866 and
13563 direct agencies to assess all costs
and benefits of available regulatory
alternatives and, when regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
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environmental, public health and safety,
and other advantages; distributive
impacts; and equity). E.O. 13563
(Improving Regulation and Regulatory
Review) emphasizes the importance of
quantifying both costs and benefits,
reducing costs, harmonizing rules, and
promoting flexibility.
The Office of Information and
Regulatory Affairs has examined the
economic, interagency, budgetary, legal,
and policy implications of this
regulatory action, and has determined
that this proposed rule is not a
significant regulatory action under E.O.
12866.
HHS’s impact analysis can be found
as a supporting document at https://
www.regulations.gov, usually within 48
hours after the rulemaking document is
published.
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IV. Paperwork Reduction Act
This proposed rule contains no
provisions constituting a collection of
information under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3521).
V. Regulatory Flexibility Act
The Secretary hereby certifies that
this proposed rule would not have a
significant economic impact on a
substantial number of small entities as
they are defined in the Regulatory
Flexibility Act (5 U.S.C. 601–612).
Therefore, pursuant to 5 U.S.C. 605(b),
the initial and final regulatory flexibility
analysis requirements of 5 U.S.C. 603
and 604 do not apply.
HHS expects that the overall impact
of the proposed rule would benefit
small businesses because the HHSAR is
being updated to provide needed
guidance to ensure HHS’s contractors
properly understand and can propose
and provide health IT that meets
standards and implementation
specifications adopted by the ONC,
consistent with sections 13111 and
13112 of the HITECH Act (Pub. L. 111–
5, title XIII, sections 13111 and 13112)
and HHS policy.
Any additional costs associated with
the proposed rule, such as costs to
implement the substantive new and
revised requirements concerning the
HITECH Act, can be factored into the
contract price. There are no alternatives
that would permit treating small
businesses providing services and
equipment to HHS differently than other
firms. However, with clear guidance and
an understanding of the requirement,
small businesses will be better postured
to provide offers and quotes with fully
compliant equipment and thus be able
to effectively participate in HHS
acquisitions. The use of consensus-
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based standards presents a potential
benefit to small businesses as it
provides clear technical guidelines for
health IT requirements. This can help to
reduce development burden by offering
open technical guidelines for
implementation, rather than
necessitating resource allocation to
standards development. In addition, the
use of non-proprietary standards allows
greater flexibility for customers and
mitigates the risk of being ‘‘locked in’’
to any one product or vendor. Overall,
the use of open, consensus-based
standards increases small businesses’
ability to compete in the health IT
landscape. On this basis, the Secretary
hereby certifies that this proposed rule
will not have a significant economic
impact on a substantial number of small
entities as they are defined in the
Regulatory Flexibility Act, 5 U.S.C. 601–
612. Therefore, pursuant to 5 U.S.C.
605(b), the initial regulatory flexibility
analysis requirements of section 603
does not apply.
While on the basis of the foregoing,
HHS has determined that the agency is
not required to prepare an Initial
Regulatory Flexibility Analysis (IRFA),
HHS has prepared an IRFA that is
summarized here. Comments are
solicited from small businesses and
other interested parties and will be
considered in the development of the
final rule.
VI. Initial Regulatory Flexibility
Analysis
This Initial Regulatory Flexibility
Analysis (IRFA) has been prepared
consistent with 5 U.S.C. 603.
1. Description of the reasons why the
action is being taken.
This proposed rule would amend the
Health and Human Services Acquisition
Regulation (HHSAR) to implement
updates to the HHSAR to add
substantive new language to align
requirements related to the procurement
of health information technology (health
IT) with standards and implementation
specifications (standards) adopted by
the Office of the National Coordinator
for Health Information Technology
(ONC), consistent with sections 13111
and 13112 of the Health Information
Technology for Economic and Clinical
Health Act (‘‘HITECH Act’’) (Pub. L.
111–5, title XIII, sections 13111 and
13112) and HHS policy.
Section 13111 of the HITECH Act
requires agencies identified by the
Director of the Office of Management
and Budget (OMB), in consultation with
the Secretary, when implementing,
acquiring, or upgrading health IT
systems used for the direct exchange of
individually identifiable health
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65307
information between agencies and with
non-Federal entities, to utilize, where
available, health IT systems and
products that meet standards and
implementation specifications adopted
by ONC on behalf of the Secretary under
section 3004 of the Public Health
Service Act (PHSA).
Section 13112 of the HITECH Act
specifies that agencies, as defined in
Executive Order 13410, shall require in
contracts or agreements with health care
providers, health plans, or health
insurance issuers that as each provider,
plan, or issuer implements, acquires, or
upgrades health IT systems, it shall
utilize, where available, health IT
systems and products that meet
standards and implementation
specifications adopted under section
3004 of the PHSA.
On behalf of HHS, ONC adopts
standards and implementation
specifications under section 3004 of the
PHSA in 45 CFR part 170, subpart B.
Standards adopted under section 3004
are included in certification criteria for
health IT in the ONC Health Information
Technology Certification Program at 45
CFR part 170, subpart C. For more
information on the ONC Certification
Program, see https://www.healthit.gov/
topic/certification-ehrs/certificationhealth-it.
This proposed rule would implement
requirements in the HHSAR that would
apply to all solicitations and contracts,
issued by or on behalf of HHS entities,
that involve implementing, acquiring, or
upgrading health IT used (1) for the
direct exchange of individually
identifiable health information between
agencies and non-Federal entities, or (2)
by health care providers, health plans,
or health insurance issuers under HHS
contracts. Based on a review of the
potential impact on small business
entities, HHS has determined that the
requirements specified in the proposed
rule are inherent to successful
performance on any relevant Federal
contract.
This proposed rule would provide
definitions, policy, and a prescription
for a new HHSAR clause to implement
requirements of the HITECH Act, to
include: (1) when contracting officers
must procure health IT that complies
with the HITECH Act; and (2) when to
require health IT that complies with the
HITECH Act in contracts and
agreements with health care providers,
health plans, or health insurance
issuers.
2. Succinct statement of the objectives
of, and legal basis for, the rule.
The proposed rule implements the
HITECH Act, sections 13111 and 13112,
and HHS policy. This must be
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implemented in the HHSAR in
accordance with 41 U.S.C. 1707, and
FAR subpart 1.5 that require publication
of a proposed rule for public comment.
3. Description of and, where feasible,
estimate of the number of small entities
to which the rule will apply.
To estimate the number of small
businesses that could potentially be
impacted by the proposed rule, HHS
identified contract award actions across
key North American Industry
Classification System (NAICS) codes, as
well as Product Service Codes (PSC)
that could be affected for five fiscal
years—FY 2018, 2019, 2020, 2021 and
2022 as set forth in the table below.
HHS focused on businesses that
potentially could be impacted by the
proposed revisions to parts 339 and 352
involving health IT, because of the
potential costs resulting from the
utilization of health information
technology that meets standards and
implementation specifications adopted
under section 3004 of the PHSA,
consistent with the HITECH Act, in
HHS acquisitions containing such
requirements.
Number of contract actions
NAICS
NAICS description
FY 2018
518210
524292
541511
541512
541513
541519
541715
541990
611310
Computing Infrastructure Providers, Data Processing, Web
Hosting, and Related Services.
Pharmacy Benefit Management
and Other Third Party Administration of Insurance and Pension Funds.
Custom Computer Programming
Services.
Computer Systems Design Services.
Computer Facilities Management
Services.
Other Computer Related Services.
Research and Development in
the Physical, Engineering, and
Life Sciences (except Nanotechnology and Biotechnology).
All Other Professional, Scientific,
and Tech. Svcs.
Colleges, Universities, and Professional Schools.
NAICS
Total
.....................................................
PSC
Product service code description
7010 .....
Information Technology Equipment System Configuration.
Information Technology Central
Processing Unit (CPU, Computer), Analog.
Information Technology Central
Processing Unit (CPU, Computer), Digital.
Information Technology Central
Processing Unit (CPU, Computer), Hybrid.
Information Technology Input/
Output and Storage Devices.
Information Technology Software
Information Technology Support
Equipment.
7020 .....
7021 .....
7022 .....
7025 .....
7030 .....
7035 .....
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PSC Total ................................
Total .....................................
As shown, HHS awarded over 84,838
contract actions for nine NAICS
(products or services) and seven Product
Service Codes for IT or IT-related
services during the period FY 2018
through FY 2022. To estimate the
number of small businesses potentially
impacted by this proposed rule
involving the much narrower health IT
certification standards and
requirements, HHS notes that in FY
2022, the total number of contract
actions awarded to small business
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FY 2019
FY 2020
FY 2021
FY 2022
Total
Average
772
799
797
754
909
4,031
806.2
29
29
32
29
44
163
32.6
1,327
1,288
1,343
1,332
1,668
6,958
1,391.6
2,838
3,095
2,891
3,103
4,497
16,424
3,284.8
125
130
155
121
161
692
138.4
4,857
4,264
4,813
4,141
4,610
22,685
4,537
322
644
1,074
1,498
2,227
5,765
1,153
3,356
2,943
3,216
3,305
4,271
17,091
3,418.2
336
265
228
222
265
1,316
263.2
13,962
13,457
14,549
14,505
18,652
75,125
15,025
94
94
94
94
94
94
94
47
41
79
19
5
191
38.2
231
116
207
23
14
591
118.2
18
18
14
6
0
56
11.2
149
105
136
40
23
453
90.6
1,934
501
1,524
353
1,971
426
674
106
514
79
6,617
1,465
1,323.4
293
2,974
16,936
2,253
15,710
2,931
17,480
898
15,403
657
19,309
9,713
84,838
1,942.6
16,967.6
concerns across the nine NAICS and all
operating administrations was around
55%. Using this figure to project the
potential impact to small business
entities that may be affected by the
proposed rule, the Department estimates
that up to 8,484 contract actions could
be awarded to small businesses.
4. Description of projected reporting,
recordkeeping, and other compliance
requirements of the rule, including an
estimate of the classes of small entities
which will be subject to the requirement
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and the type of professional skills
necessary for preparation of the report
or record.
This proposed rule contains no
provisions constituting a collection of
information under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3521).
5. Identification, to the extent
practicable, of all relevant Federal rules
which may duplicate, overlap, or
conflict with the rule.
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The proposed rule does not duplicate,
overlap, or conflict with any other
Federal rules.
6. Description of any significant
alternatives to the rule which
accomplish the stated objectives of
applicable statutes and which minimize
any significant economic impact of the
rule on small entities.
HHS considered whether any other
alternatives would reduce the impact on
small businesses but concluded that the
proposed rule was necessary for
consistency with the FAR, for
compliance with the HITECH Act and
HHS policy, and to ensure the
information security and integrity of
HHS information and information
systems.
IV. Comments on the Economic Impacts
of the Rule
HHS has submitted a copy of the
IRFA to the Chief Counsel for Advocacy
of the Small Business Administration.
HHS will consider comments from
small entities concerning the affected
HHSAR parts, to include 339 and 352
that pertains to IT. Interested parties
should cite 5 U.S.C. 601, et seq. and
reference 0991–AC35—HHS Acquisition
Regulation: Acquisition of Information
Technology; Standards for Health
Information Technology (HHSAR Case
2023–001), in comments on the
certification or the IRFA presented in
this proposed rule.
A. Unfunded Mandates
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The Unfunded Mandates Reform Act
of 1995 (URMA) requires, at 2 U.S.C.
1532, that agencies prepare an
assessment of anticipated costs and
benefits before issuing any rule that may
result in the expenditure by State, local,
and tribal governments, in the aggregate,
or by the private sector, of $100 million
or more (adjusted annually for inflation)
in any one year. In 2023, that threshold
is approximately $177 million. HHS has
determined that this proposed rule
would have no such effect on State,
local, and tribal governments or on the
private sector. Therefore, the analytical
requirements of UMRA do not apply.
List of Subjects in 48 CFR Parts 339 and
352
Government procurement.
Xavier Becerra,
Secretary, Department of Health and Human
Services.
For the reasons set out in the
preamble, HHS proposes to amend 48
CFR parts 339 and 352 as follows:
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PART 339—ACQUISITION OF
INFORMATION TECHNOLOGY
1. The authority citation for part 339
is revised to read as follows:
■
Authority: 5 U.S.C. 301; 40 U.S.C. 121(c);
41 U.S.C. 1121(c)(3); 41 U.S.C. 1702; and 48
CFR 1.301 through 1.304.
2. Subpart 339.70 is added to read as
follows:
■
Subpart 339.70—Standards for Health
Information Technology
339.7000
Scope of subpart.
339.7001
Definitions.
339.7002 Policy—standards for health
information technology.
339.7003
339.7000
Contract clause.
Scope of Subpart
(a) This subpart implements and
aligns requirements related to the
procurement of health information
technology (health IT) with standards
and implementation specifications
(standards) adopted by the Office of the
National Coordinator for Health
Information Technology (ONC) under
section 3004 of the Public Health
Service Act (PHSA), consistent with
sections 13111 and 13112 of the
HITECH Act (Pub. L. 111–5) and HHS
policy to advance health IT alignment.
(b) This subpart provides policies and
procedures for solicitations and
contracts that involve implementing,
acquiring, or upgrading health IT used—
(1) For the direct exchange of
individually identifiable health
information between agencies and with
non-Federal entities; or
(2) By health care providers, health
plans, or health insurance issuers.
339.7001
Definitions
As used in this subpart—
Health information technology (health
IT) means hardware, software,
integrated technologies or related
licenses, intellectual property, upgrades,
or packaged solutions sold as services
that are designed for or support the use
by health care entities or patients for the
electronic creation, maintenance,
access, or exchange of health
information. (42 U.S.C. 300jj(5))
Individually identifiable health
information means any information,
including demographic information
collected from an individual, that—
(1) Is created or received by a health
care provider, health plan, employer, or
health care clearinghouse; and
(2) Relates to the past, present, or
future physical or mental health
condition of an individual; the
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65309
provision of health care to an
individual; or the past, present, or
future payment for the provision of
health care to an individual; and
(i) Identifies the individual; or
(ii) With respect to which there is a
reasonable basis to believe the
information can be used to identify the
individual. (42 U.S.C. 300jj(8), 1320d(6))
ONC Health Information Technology
Certification Program means the
voluntary certification program
administered by ONC using a thirdparty conformity assessment program
for health IT. Certification criteria for
the Program are found in 45 CFR part
170, subpart C, and incorporate
standards and implementation
specifications in 45 CFR part 170
subpart B.
339.7002 Policy—Standards for
Health Information Technology
(a) Pursuant to the HITECH Act,
Public Law 111–5, title XIII, sections
13111 and 13112, and HHS policy,
health IT procured by or on behalf of
HHS entities, or procured through HHS
contracts with health care providers,
health plans, or health insurance issuers
that involve implementing, acquiring, or
upgrading health IT, shall meet
standards and implementation
specifications adopted in 45 CFR part
170, subpart B, if applicable.
(b) Contracting officers shall not
award a contract unless the offeror/
quoter/contractor agrees, by submission
of an offer (or a quote) and execution of
the contract, that—
(1) For any work performed under the
contract that involves implementing,
acquiring, or upgrading health IT
procured by or on behalf of HHS entities
used for the direct exchange of
individually identifiable health
information between agencies and with
non-Federal entities unless the offeror/
quoter/contractor shall utilize health IT
that—
(i) Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support work
performed under the contract; or
(ii) Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support work performed under the
contract (see certification criteria in 45
CFR part 170, subpart C), when the
contractor is—
(A) An eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102, and
4201 of the HITECH Act; or
(B) Implementing, acquiring, or
upgrading technology to be used by an
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eligible professional in an ambulatory
setting, or hospital, eligible under
sections 4101, 4102, and 4201 of the
HITECH Act.
(2) If the contractor is a health care
provider, health plan, or health
insurance issuer, or, to perform the
contract, is establishing an agreement
with a health care provider, health plan,
or health insurance issuer, for any work
performed under the contract that
involves implementing, acquiring, or
upgrading health IT, the offeror/quoter/
contractor shall utilize health IT that—
(i) Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support work
performed under the contract; or
(ii) Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support work performed under the
contract (see certification criteria in 45
CFR part 170, subpart C), when the
contractor is—
(A) An eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102, and
4201 of the HITECH Act; or
(B) Implementing, acquiring, or
upgrading technology to be used by an
eligible professional in an ambulatory
setting, or hospital, eligible under
sections 4101, 4102, and 4201 of the
HITECH Act.
(c) If standards and implementation
specifications adopted in 45 CFR part
170, subpart B, cannot support the work
as specified in the contract, the offeror/
quoter/contractor is encouraged to use
health IT that meets non-proprietary
standards and implementation
specifications developed by consensusbased standards development
organizations. This may include
standards identified in the ONC
Interoperability Standards Advisory,
available at https://www.healthit.gov/
isa/.
339.7003 Contract Clause
The contracting officer shall insert the
clause at 352.239–70, Standards for
Health Information Technology, in
solicitations and contracts issued by or
on behalf of HHS entities that—
(a) Involve implementing, acquiring,
or upgrading health IT used for the
direct exchange of individually
identifiable health information between
agencies and with non-Federal entities;
or
(b) Are with health care providers,
health plans, or health insurance issuers
that, under the solicitation or contract,
would be implementing, acquiring, or
upgrading health IT.
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PART 352—SOLICITATION
PROVISIONS AND CONTRACT
CLAUSES
3. The authority for part 352 is revised
to read as follows:
■
Authority: 5 U.S.C. 301; 40 U.S.C. 121(c);
41 U.S.C. 1121(c)(3); 41 U.S.C. 1702; 42
U.S.C. 2003; and 48 CFR 1.301 through 1.304.
Subpart 352.2—Text of Provisions and
Clauses
4. The heading for subpart 352.2 is
revised to read as set forth above.
■ 5. Section 352.239–70 is added to read
as follows:
■
352.239–70 Standards for Health
Information Technology
As prescribed in 339.7003, insert the
following clause:
Standards for Health Information
Technology
(Date)
(a) Definitions. As used in this
clause—
Health information technology (health
IT) means hardware, software,
integrated technologies or related
licenses, intellectual property, upgrades,
or packaged solutions sold as services
that are designed for or support the use
by health care entities or patients for the
electronic creation, maintenance,
access, or exchange of health
information. (42 U.S.C. 300jj(5))
Individually identifiable health
information means any information,
including demographic information
collected from an individual, that—
(1) Is created or received by a health
care provider, health plan, employer, or
health care clearinghouse; and
(2) Relates to the past, present, or
future physical or mental health
condition of an individual; the
provision of health care to an
individual; or the past, present, or
future payment for the provision of
health care to an individual; and
(i) Identifies the individual; or
(ii) With respect to which there is a
reasonable basis to believe the
information can be used to identify the
individual. (42 U.S.C. 300jj(8), 1320d(6))
ONC Health Information Technology
Certification Program means the
voluntary certification program
administered by the HHS Office of the
National Coordinator for Health
Information Technology (ONC) using a
third-party conformity assessment
program for health IT. Certification
criteria for the Program are found in 45
CFR part 170, subpart C, and
incorporate standards and
implementation specifications in 45
CFR part 170, subpart B.
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(b) Pursuant to the Health Information
Technology for Economic and Clinical
Health Act (HITECH Act), Public Law
111–5, title XIII, sections 13111 and
13112, and HHS policy, by submission
of an offer (or a quote) and execution of
a contract, the offeror/quoter/Contractor
agrees that—
(1) For any work performed under the
contract that involves implementing,
acquiring, or upgrading health IT
procured by or on behalf of HHS entities
used for the direct exchange of
individually identifiable health
information between agencies and with
non-Federal entities, the offeror/quoter/
Contractor shall utilize health IT that—
(i) Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support the work
performed under the contract; or
(ii) Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support the work performed under the
contract (see certification criteria in 45
CFR part 170, subpart C), when the
Contractor is—
(A) An eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102 and
4201 of the HITECH Act; or
(B) Implementing, acquiring, or
upgrading technology to be used by an
eligible professional in an ambulatory
setting, or a hospital, eligible under
sections 4101, 4102 and 4201 of the
HITECH Act.
(2) If the Contractor is a health care
provider, health plan, or health
insurance issuer, or, to perform the
contract, is establishing an agreement
with a health care provider, health plan,
or health insurance issuer, for any work
performed under the contract that
involves implementing, acquiring, or
upgrading health IT, the offeror/quoter/
Contractor shall utilize health IT that—
(i) Meets standards and
implementation specifications adopted
in 45 CFR part 170, subpart B, if such
standards and implementation
specifications can support the work
performed under the contract; or
(ii) Is certified under the ONC Health
Information Technology Certification
Program, if certified technology can
support the work performed under the
contract (see certification criteria in 45
CFR part 170, subpart C), when the
Contractor is—
(A) An eligible professional in an
ambulatory setting, or a hospital,
eligible under sections 4101, 4102 and
4201 of the HITECH Act; or
(B) Implementing, acquiring, or
upgrading technology to be used by an
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eligible professional in an ambulatory
setting, or a hospital, eligible under
sections 4101, 4102 and 4201 of the
HITECH Act.
(c) If standards and implementation
specifications adopted in 45 CFR part
170, subpart B, cannot support the work
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as specified in the contract, the
Contractor is encouraged to use health
IT that meets non-proprietary standards
and implementation specifications
developed by consensus-based
standards development organizations.
This may include standards identified
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65311
in the ONC Interoperability Standards
Advisory, available at https://
www.healthit.gov/isa/.
(End of clause)
[FR Doc. 2024–17096 Filed 8–8–24; 8:45 am]
BILLING CODE 4151–19–P
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Agencies
[Federal Register Volume 89, Number 154 (Friday, August 9, 2024)]
[Proposed Rules]
[Pages 65303-65311]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-17096]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
48 CFR Parts 339 and 352
RIN 0991-AC35
HHS Acquisition Regulation: Acquisition of Information
Technology; Standards for Health Information Technology (HHSAR Case
2023-001)
AGENCY: Department of Health and Human Services.
ACTION: Proposed rule.
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SUMMARY: The Department of Health and Human Services (HHS) is proposing
to amend and update its Health and Human Services Acquisition
Regulation (HHSAR) to implement requirements to procure health
information technology (health IT) that meets standards and
implementation specifications (standards) adopted by the Office of the
National Coordinator for Health Information Technology (ONC) in the
following parts: Acquisition of Information Technology and Solicitation
Provisions and Contract Clauses.
DATES: Comments must be received on or before October 8, 2024, to be
considered in the formulation of the final rule.
ADDRESSES: Submit written comments in response to HHSAR Case 2023-001
through the Federal eRulemaking Portal at: https://www.regulations.gov
by searching for ``HHSAR Case 2023-001''. Select the link ``Comment
Now'' and follow the ``Submit a comment'' instructions. Please include
your name, company name (if any), and indicate they are submitted in
response to ``RIN 0991-AC35--HHS Acquisition Regulation: Acquisition of
Information Technology; Standards for Health Information Technology
(HHSAR Case 2023-001).''
Warning: Do not include any personally identifiable information or
confidential business information that you do not want publicly
disclosed. All comments may be posted on the internet and can be
retrieved by most internet search engines. No deletions, modifications,
or redactions will be made to comments received.
Inspection of Public Comments: All comments received before the
close of the comment period will be available for viewing by the
public, including personally identifiable or confidential business
information that is included in a comment. You may wish to consider
limiting the amount of personal information that you provide in any
voluntary public comment submission you make. HHS reserves the right to
withhold information provided in comments from public viewing that it
determines may have an adverse impact on an individual(s). For
additional information, please read the Privacy Act notice that is
available via the link in the footer of https://www.regulations.gov.
Follow the search instructions on that website to view the public
comments.
FOR FURTHER INFORMATION CONTACT: Mr. Jarreau Vieira, Chief, Acquisition
Rule-Making Branch, U.S. Department of Health and Human Services,
Office of the Assistant Secretary for Financial Resources, Office of
Acquisition Policy, 200 Independence Avenue SW, Washington, DC 20201.
Email: [email protected], Telephone: (202) 731-4625. This is
not a toll-free telephone number.
SUPPLEMENTARY INFORMATION:
I. Background
A. Authority
This rulemaking is being taken under the authority of the Office of
Federal Procurement Policy (OFPP) Act which provides the authority for
an agency head to authorize the issuance of agency acquisition
regulations that implement or supplement the Federal Acquisition
Regulation (FAR). The OFPP Act, as codified in 41 U.S.C. 1702, provides
the authority for the FAR and for the issuance of agency acquisition
regulations consistent with the FAR. This authority ensures that
Government
[[Page 65304]]
procurements are handled fairly and consistently, that the Government
receives overall best value, and that the Government and contractors
both operate under a known set of rules. The Health and Human Services
Acquisition Regulation (HHSAR) is set forth at Title 48 CFR, chapter 3,
parts 301 through 370.
Under this authority, we are seeking to implement a department-wide
management policy issued by the Secretary of the Department of Health
and Human Services (Secretary) in July 2022 (hereafter the
``Secretary's July 2022 Memorandum''), that directed HHS agencies to
align and coordinate health IT-related activities in support of HHS
health IT and interoperability goals. This policy was supported by
requirements in sections 13111 and 13112 of the Health Information
Technology for Economic and Clinical Health Act (HITECH Act) (Pub. L.
111-5).
B. Genesis of Standards for Health Information Technology in the HHSAR
The Secretary's July 2022 Memorandum recognized that HHS spending
on health IT-related activities has grown dramatically in recent years,
as various agencies have begun to leverage the large foundation of
electronic health records put in place by the $40 billion invested as a
result of the HITECH Act, as part of the American Recovery and
Reinvestment Act of 2009 (Pub. L. 111-5, Feb. 17, 2009), and the
related clinical data and interoperability standards that HHS continues
to promote. Advancing interoperability and the effective and
appropriate use of health IT systems is a key HHS objective, and COVID-
19 has further demonstrated the importance of interoperable data to
improve the quality, safety, affordability, and efficiency of health
care delivery; inform pandemic response; and identify and address
disparities in care. As health IT-related activities begin to play an
increasingly prominent role in programs across the Department, the
Secretary's July 2022 Memorandum states that it is critical to ensure
alignment of such activities to avoid the proliferation of ad-hoc
health IT and data silos. These silos undercut the effectiveness and
efficiency of the Department's policies and programs, are costly for
Federal and state agencies and private sector partners to create and
maintain, have no synergies across programs, and--due to lack of
alignment across and within HHS agencies--impose significant burden on
health care providers, technology developers, and other health care
stakeholders.
As part of the Secretary's July 2022 Memorandum, the Secretary
directed HHS agencies, working with the Assistant Secretary for
Financial Resources (ASFR), to develop standard language for use in
grants, cooperative agreements, or contracts. The Secretary's July 2022
Memorandum further identified the general elements of this standard
language, including that: recipients are expected to utilize health IT
that meets standards adopted under Section 3004 of the Public Health
Service Act (PHSA), if applicable, when the funding mechanism includes
provisions requiring recipients to implement, acquire, or upgrade
health IT; health care providers who have been eligible to participate
in Center for Medicare & Medicaid Services's (CMS's) health IT-focused
incentive programs can meet alignment requirements under this policy by
using certified health IT which incorporates standards adopted under
PHSA Section 3004; and, where there are no applicable standards adopted
under PHSA Section 3004, recipients are encouraged to use other HHS-
identified standards or non-proprietary, consensus-based standards
developed by a national standard setting organization, such as those
referenced in the Interoperability Standards Advisory, are recommended.
We note that this regulation does not impact existing HHS
authorities for standards adoption and note that HHS agencies are
committed to working together to ensure that standards under such
authorities are aligned to advance interoperability for a nationwide
health IT infrastructure.
Section 13111 of the HITECH Act requires agencies identified by the
Director of the Office of Management and Budget (OMB), in consultation
with the Secretary, when implementing, acquiring, or upgrading health
IT systems used for the direct exchange of individually identifiable
health information between agencies and with non-Federal entities, to
utilize, where available, health IT systems and products that meet
standards and implementation specifications adopted by ONC on behalf of
the Secretary under section 3004 of the Public Health Service Act
(PHSA).
Section 13112 of the HITECH Act specifies that agencies, as defined
in Executive Order 13410, shall require in contracts or agreements with
health care providers, health plans, or health insurance issuers that
as each provider, plan, or issuer implements, acquires, or upgrades
health IT systems, it shall utilize, where available, health IT systems
and products that meet standards and implementation specifications
adopted under Section 3004 of the PHSA.
On behalf of HHS, ONC adopts standards and implementation
specifications under section 3004 of the PHSA in 45 CFR part 170,
subpart B. Standards adopted under section 3004 are included in
certification criteria for health IT in the ONC Health Information
Technology Certification Program in 45 CFR part 170, subpart C. For
more information on the ONC Certification Program, see https://www.healthit.gov/topic/certification-ehrs/certification-health-it.
Health care providers who have been eligible to participate in CMS's
health IT-focused incentive programs under sections 4101, 4102, and
4201 of the HITECH Act have been incentivized to adopt health IT that
meets certification criteria which incorporate standards in 45 CFR part
170, subpart B. Consistent with HHS policy, the proposals address use
of certified health IT by these providers, where applicable.
C. Implementation Via Class Deviation (2023-01)
On December 20, 2022, the HHS Senior Procurement Executive issued
HHSAR Class Deviation (2023-01) from part 339, Acquisition of
Information Technology; Standards for Health Information Technology, in
advance of this proposed rule to implement in the HHSAR the
requirements of the HITECH Act and HHS' implementation standards.
D. Purpose of Rule
This proposed rule is issued to comply with the requirements of 41
U.S.C. 1707 and FAR subpart 1.5 that require publication of a proposed
rule for public comment.
Consistent with HHS policy, including the Secretary's July 2022
Memorandum, and with sections 13111 and 13112 of the HITECH Act (Pub.
L. 111-5), HHS is proposing to amend the HHSAR to implement and align
requirements related to the procurement of health IT with standards and
implementation specifications adopted by ONC under section 3004 of the
PHSA.
This proposed rule would add a new HHSAR subpart 339.70, Standards
for Health Information Technology, which provides definitions, policy,
and a prescription for a new HHSAR clause to implement requirements of
the HITECH Act, to include: (1) when contracting officers must procure
health IT consistent with requirements in the HITECH Act; and (2) when
to require use of health IT in a manner consistent with requirements in
the HITECH Act,
[[Page 65305]]
in contracts and agreements with health care providers, health plans,
or health insurance issuers.
This proposed rule would implement requirements in the HHSAR that
would apply to all solicitations and contracts, issued by or on behalf
of HHS entities, that involve implementing, acquiring, or upgrading
health IT used (1) for the direct exchange of individually identifiable
health information between agencies and non-Federal entities, or (2) by
health care providers, health plans, or health insurance issuers.
II. Discussion and Analysis
A. HITECH Act Discussion
In this section, we provide discussion of several issues in
connection to our proposals in this proposed rule.
1. Acquiring, Implementing, or Upgrading Health IT
We believe additional discussion of terms used in sections 13111
and 13112 of the HITECH Act will help the public to understand how
these proposals will be implemented. Specifically, we note that both
sections refer to implementing, acquiring, or upgrading of health IT
systems as activities to which the statutory provisions apply. We
believe the terms acquiring and upgrading health IT are clear for the
purpose of this policy. However, we believe additional explanation of
the term ``implementing'' as it is used in this policy is warranted.
``Implementing'' health IT may include a variety of activities that are
distinct from acquiring or upgrading health IT. For instance,
``implementing'' health IT may include investments in health IT for its
maintenance and upkeep, the use of health IT to collect, store, and
share health information, and activities supporting the piloting, but
not the acquisition, of health IT tools.
We note that the proposals in HHSAR parts 339 and 352 in this
proposed rule pertain to ``work performed under the contract that
involves implementing, acquiring, or upgrading health IT.'' For
example, a contracted party performing research may obtain data from
health IT systems. Unless the contract defines specific health IT
activities and/or investments related to these data, such activities
would be considered incidental to the work performed under the contract
and would not be subject to our proposed requirements. We seek comment
on additional details that would help with clarifying when a contract
activity would be considered ``implementing'' health IT.
B. Authorities and Summary of Proposed Changes
We propose to revise the following parts of the HHSAR, 48 CFR
chapter 3: parts 339 and 352.
We propose to revise the authority citations cited in each HHSAR
part to reflect as follows: 5 U.S.C. 301; 40 U.S.C. 121(c); 41 U.S.C.
1121(c)(3); 41 U.S.C. 1702; and 48 CFR 1.301 through 1.304. Where
additional authorities for a specific part are applicable, we identify
them under that discussion of each HHSAR part later in this preamble.
We propose to retain the authority of 5 U.S.C. 301. This authority
provides that the head of an Executive department or military
department may prescribe regulations for the government of his
department, the conduct of its employees, the distribution and
performance of its business, and the custody, use, and preservation of
its records, papers, and property.
We propose to retain the authority of 40 U.S.C. 121(c) and slightly
revise the reference. This authorizes the head of each executive agency
to issue orders and directives that the agency head considers necessary
to carry out the regulations. The Federal Acquisition Regulation System
and the publication of the FAR is issued pursuant to this authority as
are agency supplements to the FAR such as the HHSAR.
We propose to include a reference to 41 U.S.C. 1121(c)(3). This
provision states that the authority of an executive agency under
another law to prescribe policies, regulations, procedures, and forms
for procurement is subject to the authority conferred in section 1121,
as well as other sections of title 41.
We propose to add an authority citation for 41 U.S.C. 1702 which
addresses the acquisition planning and management responsibilities that
are carried out by the HHS Senior Procurement Executive.
And we propose to add the citation of 48 CFR 1.301 through 1.304 to
reflect the authority and responsibility set forth in the FAR and
delegated to Federal agencies to issue agency regulations that
supplement and implement the FAR.
Any other proposed changes to authorities are shown under the
individual parts below.
1. HHSAR Part 339--Acquisition of Information Technology
We propose to revise the authority citations for part 339, for the
reasons set forth in the discussion and analysis section, to read as
follows: 5 U.S.C. 301; 40 U.S.C. 121(c); 41 U.S.C. 1121(c)(3); 41
U.S.C. 1702; and 48 CFR 1.301 through 1.304.
We propose to add subpart 339.70, Standards for Health Information
Technology, to include underlying sections 339.7000, 339.7001,
339.7002, and 339.7003. This subpart is added to implement standards
under the authority of the HITECH Act, Public Law 111-5, title XIII,
sections 13111 and 13112 that are applicable for HHS contracts, as well
as HHS policy.
We propose to add section 339.7000, Scope of subpart, to provide
general scope and purpose of the subpart and its underlying sections,
which implements and aligns requirements related to the procurement of
health IT with standards and implementation specifications adopted by
ONC, under section 3004 of the PHSA, consistent with sections 13111 and
13112 of the HITECH Act (Pub. L. 111-5) and HHS policy to advance
health IT alignment. The subpart describes the policies and procedures
for solicitations and contracts that involve implementing, acquiring,
or upgrading health IT that is used for the direct exchange of
individually identifiable health information between agencies and with
non-Federal entities; or by health care providers, health plans, or
health insurance issuers.
We propose to add section 339.7001, Definitions. This section is
added to include three definitions applicable to the new subpart:
Health information technology (health IT), individually identifiable
health information, and the ONC Health Information Technology
Certification Program.
We propose to add section 339.7002, Policy--standards for health
information technology. This section is added to implement standards
for health IT in HHS contracts. This section would require, pursuant to
the HITECH Act, Public Law 111-5, title XIII, sections 13111 and 13112,
and HHS policy, that health IT shall meet standards and implementation
specifications adopted in 45 CFR part 170, subpart B, if applicable.
This includes health IT that is--
Procured by or on behalf of HHS entities, or
Procured through HHS contracts with health care providers,
health plans, or health insurance issuers that involve implementing,
acquiring, or upgrading health IT.
Section 339.7002 would prohibit contracting officers from awarding
a contract involving health IT as described in this preamble, unless
certain conditions are met. First, this section would prohibit
contracting officers from awarding a contract that includes
implementing, acquiring, or upgrading health IT used for the direct
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exchange of individually identifiable health information between
agencies and with non-Federal entities unless an offeror/quoter/
contractor shall utilize health IT that--
Meets standards and implementation specifications adopted
in 45 CFR part 170, subpart B, if such standards and implementation
specifications can support work performed under the contract; or
Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the contractor is--
[cir] an eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102, and 4201 of the HITECH
Act; or
[cir] implementing, acquiring, or upgrading technology to be used
by an eligible professional in an ambulatory setting, or hospital,
eligible under sections 4101, 4102, and 4201 of the HITECH Act.
Further, this section would also prohibit contracting officers from
awarding a contract if a contractor is a health care provider, health
plan, or health insurance issuer, or, to perform the contract, is
establishing an agreement with a health care provider, health plan, or
health insurance issuer, for any work performed under the contract that
involves implementing, acquiring, or upgrading health IT, unless the
offeror/quoter/contractor agrees that it shall utilize health IT that--
Meets standards and implementation specifications adopted
in 45 CFR part 170, subpart B, if such standards and implementation
specifications can support work performed under the contract; or
Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the contractor is--
[cir] an eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102, and 4201 of the HITECH
Act; or
[cir] implementing, acquiring, or upgrading technology to be used
by an eligible professional in an ambulatory setting, or hospital,
eligible under sections 4101, 4102, and 4201 of the HITECH Act.
Finally, this section would also encourage offerors/quoters/
contractors, if standards and implementation specifications adopted in
45 CFR part 170, subpart B, cannot support the work as specified in the
contract, to use health IT that meets non-proprietary standards and
implementation specifications developed by consensus-based standards
development organizations. This may include standards identified in the
ONC Interoperability Standards Advisory, available at https://www.healthit.gov/isa/.
We propose to add section 339.7003, Contract clause, to prescribe a
new clause at 352.239-70, Standards for Health Information Technology,
in solicitations and contracts, issued by or on behalf of HHS entities,
that involve implementing, acquiring, or upgrading health IT used--
(a) for the direct exchange of individually identifiable health
information between agencies and with non-Federal entities; or
(b) by health care providers, health plans, or health insurance
issuers.
2. HHSAR Part 352--Solicitation Provisions and Contract Clauses
We propose to revise the authority citations for part 352, for the
reasons set forth in the discussion and analysis section, to read as
follows: 5 U.S.C. 301; 40 U.S.C. 121(c); 41 U.S.C. 1121(c)(3); 41
U.S.C. 1702; and 48 CFR 1.301 through 1.304.
We propose to add clause 352.239-70, Standards for Health
Information Technology, to set forth requirements for the standards for
health IT provided or utilized on a contract. The clause would include
three definitions: Health information technology (health IT),
individually identifiable health information, and the ONC Health
Information Technology Certification Program.
The clause would provide that by submission of an offer or a quote,
and execution of a contract, the offeror/quoter/contractor agrees
that--
For any work performed under the contract that involves
implementing, acquiring, or upgrading health IT procured by or on
behalf of HHS entities used for the direct exchange of individually
identifiable health information between agencies and with non-Federal
entities, the offeror/quoter/contractor shall utilize health IT that--
(1) Meets standards and implementation specifications adopted in 45
CFR part 170, subpart B, if such standards and implementation
specifications can support the work performed under the contract; or
(2) Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support the work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the Contractor is--
(i) an eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102 and 4201 of the HITECH
Act; or
(ii) is implementing, acquiring or upgrading technology to be used
by an eligible professional in an ambulatory setting, or a hospital,
eligible under sections 4101, 4102 and 4201 of the HITECH Act.
When the contractor is a health care provider, health
plan, or health insurance issuer, or, to perform the contract, is
establishing an agreement with a health care provider, health plan, or
health insurance issuer, for work performed under the contract that
involves implementing, acquiring, or upgrading health IT, the offeror/
quoter/contractor shall utilize heath IT that--
(1) Meets standards and implementation specifications adopted in 45
CFR part 170, subpart B, if such standards and implementation
specifications can support the work performed under the contract; or
(2) Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support the work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the Contractor is--
(i) an eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102 and 4201 of the HITECH
Act; or
(ii) implementing, acquiring or upgrading technology to be used by
an eligible professional in an ambulatory setting, or a hospital,
eligible under sections 4101, 4102 and 4201 of the HITECH Act.
Additionally, this section would also encourage contractors, if
such standards and implementation specifications adopted in 45 CFR part
170, subpart B, cannot support the work as specified in the contract,
to use health IT that meets non-proprietary standards and
implementation specifications developed by consensus-based standards
development organizations. This may include standards identified in the
ONC Interoperability Standards Advisory, available at https://www.healthit.gov/isa/.
III. Executive Order 12866 and 13563
Executive Orders (E.O.) 12866 and 13563 direct agencies to assess
all costs and benefits of available regulatory alternatives and, when
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic,
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environmental, public health and safety, and other advantages;
distributive impacts; and equity). E.O. 13563 (Improving Regulation and
Regulatory Review) emphasizes the importance of quantifying both costs
and benefits, reducing costs, harmonizing rules, and promoting
flexibility.
The Office of Information and Regulatory Affairs has examined the
economic, interagency, budgetary, legal, and policy implications of
this regulatory action, and has determined that this proposed rule is
not a significant regulatory action under E.O. 12866.
HHS's impact analysis can be found as a supporting document at
https://www.regulations.gov, usually within 48 hours after the
rulemaking document is published.
IV. Paperwork Reduction Act
This proposed rule contains no provisions constituting a collection
of information under the Paperwork Reduction Act of 1995 (44 U.S.C.
3501-3521).
V. Regulatory Flexibility Act
The Secretary hereby certifies that this proposed rule would not
have a significant economic impact on a substantial number of small
entities as they are defined in the Regulatory Flexibility Act (5
U.S.C. 601-612). Therefore, pursuant to 5 U.S.C. 605(b), the initial
and final regulatory flexibility analysis requirements of 5 U.S.C. 603
and 604 do not apply.
HHS expects that the overall impact of the proposed rule would
benefit small businesses because the HHSAR is being updated to provide
needed guidance to ensure HHS's contractors properly understand and can
propose and provide health IT that meets standards and implementation
specifications adopted by the ONC, consistent with sections 13111 and
13112 of the HITECH Act (Pub. L. 111-5, title XIII, sections 13111 and
13112) and HHS policy.
Any additional costs associated with the proposed rule, such as
costs to implement the substantive new and revised requirements
concerning the HITECH Act, can be factored into the contract price.
There are no alternatives that would permit treating small businesses
providing services and equipment to HHS differently than other firms.
However, with clear guidance and an understanding of the requirement,
small businesses will be better postured to provide offers and quotes
with fully compliant equipment and thus be able to effectively
participate in HHS acquisitions. The use of consensus-based standards
presents a potential benefit to small businesses as it provides clear
technical guidelines for health IT requirements. This can help to
reduce development burden by offering open technical guidelines for
implementation, rather than necessitating resource allocation to
standards development. In addition, the use of non-proprietary
standards allows greater flexibility for customers and mitigates the
risk of being ``locked in'' to any one product or vendor. Overall, the
use of open, consensus-based standards increases small businesses'
ability to compete in the health IT landscape. On this basis, the
Secretary hereby certifies that this proposed rule will not have a
significant economic impact on a substantial number of small entities
as they are defined in the Regulatory Flexibility Act, 5 U.S.C. 601-
612. Therefore, pursuant to 5 U.S.C. 605(b), the initial regulatory
flexibility analysis requirements of section 603 does not apply.
While on the basis of the foregoing, HHS has determined that the
agency is not required to prepare an Initial Regulatory Flexibility
Analysis (IRFA), HHS has prepared an IRFA that is summarized here.
Comments are solicited from small businesses and other interested
parties and will be considered in the development of the final rule.
VI. Initial Regulatory Flexibility Analysis
This Initial Regulatory Flexibility Analysis (IRFA) has been
prepared consistent with 5 U.S.C. 603.
1. Description of the reasons why the action is being taken.
This proposed rule would amend the Health and Human Services
Acquisition Regulation (HHSAR) to implement updates to the HHSAR to add
substantive new language to align requirements related to the
procurement of health information technology (health IT) with standards
and implementation specifications (standards) adopted by the Office of
the National Coordinator for Health Information Technology (ONC),
consistent with sections 13111 and 13112 of the Health Information
Technology for Economic and Clinical Health Act (``HITECH Act'') (Pub.
L. 111-5, title XIII, sections 13111 and 13112) and HHS policy.
Section 13111 of the HITECH Act requires agencies identified by the
Director of the Office of Management and Budget (OMB), in consultation
with the Secretary, when implementing, acquiring, or upgrading health
IT systems used for the direct exchange of individually identifiable
health information between agencies and with non-Federal entities, to
utilize, where available, health IT systems and products that meet
standards and implementation specifications adopted by ONC on behalf of
the Secretary under section 3004 of the Public Health Service Act
(PHSA).
Section 13112 of the HITECH Act specifies that agencies, as defined
in Executive Order 13410, shall require in contracts or agreements with
health care providers, health plans, or health insurance issuers that
as each provider, plan, or issuer implements, acquires, or upgrades
health IT systems, it shall utilize, where available, health IT systems
and products that meet standards and implementation specifications
adopted under section 3004 of the PHSA.
On behalf of HHS, ONC adopts standards and implementation
specifications under section 3004 of the PHSA in 45 CFR part 170,
subpart B. Standards adopted under section 3004 are included in
certification criteria for health IT in the ONC Health Information
Technology Certification Program at 45 CFR part 170, subpart C. For
more information on the ONC Certification Program, see https://www.healthit.gov/topic/certification-ehrs/certification-health-it.
This proposed rule would implement requirements in the HHSAR that
would apply to all solicitations and contracts, issued by or on behalf
of HHS entities, that involve implementing, acquiring, or upgrading
health IT used (1) for the direct exchange of individually identifiable
health information between agencies and non-Federal entities, or (2) by
health care providers, health plans, or health insurance issuers under
HHS contracts. Based on a review of the potential impact on small
business entities, HHS has determined that the requirements specified
in the proposed rule are inherent to successful performance on any
relevant Federal contract.
This proposed rule would provide definitions, policy, and a
prescription for a new HHSAR clause to implement requirements of the
HITECH Act, to include: (1) when contracting officers must procure
health IT that complies with the HITECH Act; and (2) when to require
health IT that complies with the HITECH Act in contracts and agreements
with health care providers, health plans, or health insurance issuers.
2. Succinct statement of the objectives of, and legal basis for,
the rule.
The proposed rule implements the HITECH Act, sections 13111 and
13112, and HHS policy. This must be
[[Page 65308]]
implemented in the HHSAR in accordance with 41 U.S.C. 1707, and FAR
subpart 1.5 that require publication of a proposed rule for public
comment.
3. Description of and, where feasible, estimate of the number of
small entities to which the rule will apply.
To estimate the number of small businesses that could potentially
be impacted by the proposed rule, HHS identified contract award actions
across key North American Industry Classification System (NAICS) codes,
as well as Product Service Codes (PSC) that could be affected for five
fiscal years--FY 2018, 2019, 2020, 2021 and 2022 as set forth in the
table below. HHS focused on businesses that potentially could be
impacted by the proposed revisions to parts 339 and 352 involving
health IT, because of the potential costs resulting from the
utilization of health information technology that meets standards and
implementation specifications adopted under section 3004 of the PHSA,
consistent with the HITECH Act, in HHS acquisitions containing such
requirements.
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Number of contract actions
NAICS NAICS description ---------------------------------------------------------------------------------------------------------------
FY 2018 FY 2019 FY 2020 FY 2021 FY 2022 Total Average
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
518210..................................... Computing Infrastructure Providers, 772 799 797 754 909 4,031 806.2
Data Processing, Web Hosting, and
Related Services.
524292..................................... Pharmacy Benefit Management and 29 29 32 29 44 163 32.6
Other Third Party Administration
of Insurance and Pension Funds.
541511..................................... Custom Computer Programming 1,327 1,288 1,343 1,332 1,668 6,958 1,391.6
Services.
541512..................................... Computer Systems Design Services... 2,838 3,095 2,891 3,103 4,497 16,424 3,284.8
541513..................................... Computer Facilities Management 125 130 155 121 161 692 138.4
Services.
541519..................................... Other Computer Related Services.... 4,857 4,264 4,813 4,141 4,610 22,685 4,537
541715..................................... Research and Development in the 322 644 1,074 1,498 2,227 5,765 1,153
Physical, Engineering, and Life
Sciences (except Nanotechnology
and Biotechnol-ogy).
541990..................................... All Other Professional, Scientific, 3,356 2,943 3,216 3,305 4,271 17,091 3,418.2
and Tech. Svcs.
611310..................................... Colleges, Universities, and 336 265 228 222 265 1,316 263.2
Professional Schools.
----------------------------------------------------------------------------------------------------------------------------------------------------
NAICS Total ................................... 13,962 13,457 14,549 14,505 18,652 75,125 15,025
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
PSC Product service code description...
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
7010....................................... Information Technology Equipment 94 94 94 94 94 94 94
System Configuration.
7020....................................... Information Technology Central 47 41 79 19 5 191 38.2
Processing Unit (CPU, Computer),
Analog.
7021....................................... Information Technology Central 231 116 207 23 14 591 118.2
Processing Unit (CPU, Computer),
Digital.
7022....................................... Information Technology Central 18 18 14 6 0 56 11.2
Processing Unit (CPU, Computer),
Hybrid.
7025....................................... Information Technology Input/Output 149 105 136 40 23 453 90.6
and Storage Devices.
7030....................................... Information Technology Software.... 1,934 1,524 1,971 674 514 6,617 1,323.4
7035....................................... Information Technology Support 501 353 426 106 79 1,465 293
Equipment.
----------------------------------------------------------------------------------------------------------------------------------------------------
PSC Total......................... 2,974 2,253 2,931 898 657 9,713 1,942.6
Total............................. 16,936 15,710 17,480 15,403 19,309 84,838 16,967.6
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
As shown, HHS awarded over 84,838 contract actions for nine NAICS
(products or services) and seven Product Service Codes for IT or IT-
related services during the period FY 2018 through FY 2022. To estimate
the number of small businesses potentially impacted by this proposed
rule involving the much narrower health IT certification standards and
requirements, HHS notes that in FY 2022, the total number of contract
actions awarded to small business concerns across the nine NAICS and
all operating administrations was around 55%. Using this figure to
project the potential impact to small business entities that may be
affected by the proposed rule, the Department estimates that up to
8,484 contract actions could be awarded to small businesses.
4. Description of projected reporting, recordkeeping, and other
compliance requirements of the rule, including an estimate of the
classes of small entities which will be subject to the requirement and
the type of professional skills necessary for preparation of the report
or record.
This proposed rule contains no provisions constituting a collection
of information under the Paperwork Reduction Act of 1995 (44 U.S.C.
3501-3521).
5. Identification, to the extent practicable, of all relevant
Federal rules which may duplicate, overlap, or conflict with the rule.
[[Page 65309]]
The proposed rule does not duplicate, overlap, or conflict with any
other Federal rules.
6. Description of any significant alternatives to the rule which
accomplish the stated objectives of applicable statutes and which
minimize any significant economic impact of the rule on small entities.
HHS considered whether any other alternatives would reduce the
impact on small businesses but concluded that the proposed rule was
necessary for consistency with the FAR, for compliance with the HITECH
Act and HHS policy, and to ensure the information security and
integrity of HHS information and information systems.
IV. Comments on the Economic Impacts of the Rule
HHS has submitted a copy of the IRFA to the Chief Counsel for
Advocacy of the Small Business Administration. HHS will consider
comments from small entities concerning the affected HHSAR parts, to
include 339 and 352 that pertains to IT. Interested parties should cite
5 U.S.C. 601, et seq. and reference 0991-AC35--HHS Acquisition
Regulation: Acquisition of Information Technology; Standards for Health
Information Technology (HHSAR Case 2023-001), in comments on the
certification or the IRFA presented in this proposed rule.
A. Unfunded Mandates
The Unfunded Mandates Reform Act of 1995 (URMA) requires, at 2
U.S.C. 1532, that agencies prepare an assessment of anticipated costs
and benefits before issuing any rule that may result in the expenditure
by State, local, and tribal governments, in the aggregate, or by the
private sector, of $100 million or more (adjusted annually for
inflation) in any one year. In 2023, that threshold is approximately
$177 million. HHS has determined that this proposed rule would have no
such effect on State, local, and tribal governments or on the private
sector. Therefore, the analytical requirements of UMRA do not apply.
List of Subjects in 48 CFR Parts 339 and 352
Government procurement.
Xavier Becerra,
Secretary, Department of Health and Human Services.
For the reasons set out in the preamble, HHS proposes to amend 48
CFR parts 339 and 352 as follows:
PART 339--ACQUISITION OF INFORMATION TECHNOLOGY
0
1. The authority citation for part 339 is revised to read as follows:
Authority: 5 U.S.C. 301; 40 U.S.C. 121(c); 41 U.S.C. 1121(c)(3);
41 U.S.C. 1702; and 48 CFR 1.301 through 1.304.
0
2. Subpart 339.70 is added to read as follows:
Subpart 339.70--Standards for Health Information Technology
339.7000 Scope of subpart.
339.7001 Definitions.
339.7002 Policy--standards for health information technology.
339.7003 Contract clause.
339.7000 Scope of Subpart
(a) This subpart implements and aligns requirements related to the
procurement of health information technology (health IT) with standards
and implementation specifications (standards) adopted by the Office of
the National Coordinator for Health Information Technology (ONC) under
section 3004 of the Public Health Service Act (PHSA), consistent with
sections 13111 and 13112 of the HITECH Act (Pub. L. 111-5) and HHS
policy to advance health IT alignment.
(b) This subpart provides policies and procedures for solicitations
and contracts that involve implementing, acquiring, or upgrading health
IT used--
(1) For the direct exchange of individually identifiable health
information between agencies and with non-Federal entities; or
(2) By health care providers, health plans, or health insurance
issuers.
339.7001 Definitions
As used in this subpart--
Health information technology (health IT) means hardware, software,
integrated technologies or related licenses, intellectual property,
upgrades, or packaged solutions sold as services that are designed for
or support the use by health care entities or patients for the
electronic creation, maintenance, access, or exchange of health
information. (42 U.S.C. 300jj(5))
Individually identifiable health information means any information,
including demographic information collected from an individual, that--
(1) Is created or received by a health care provider, health plan,
employer, or health care clearinghouse; and
(2) Relates to the past, present, or future physical or mental
health condition of an individual; the provision of health care to an
individual; or the past, present, or future payment for the provision
of health care to an individual; and
(i) Identifies the individual; or
(ii) With respect to which there is a reasonable basis to believe
the information can be used to identify the individual. (42 U.S.C.
300jj(8), 1320d(6))
ONC Health Information Technology Certification Program means the
voluntary certification program administered by ONC using a third-party
conformity assessment program for health IT. Certification criteria for
the Program are found in 45 CFR part 170, subpart C, and incorporate
standards and implementation specifications in 45 CFR part 170 subpart
B.
339.7002 Policy--Standards for Health Information Technology
(a) Pursuant to the HITECH Act, Public Law 111-5, title XIII,
sections 13111 and 13112, and HHS policy, health IT procured by or on
behalf of HHS entities, or procured through HHS contracts with health
care providers, health plans, or health insurance issuers that involve
implementing, acquiring, or upgrading health IT, shall meet standards
and implementation specifications adopted in 45 CFR part 170, subpart
B, if applicable.
(b) Contracting officers shall not award a contract unless the
offeror/quoter/contractor agrees, by submission of an offer (or a
quote) and execution of the contract, that--
(1) For any work performed under the contract that involves
implementing, acquiring, or upgrading health IT procured by or on
behalf of HHS entities used for the direct exchange of individually
identifiable health information between agencies and with non-Federal
entities unless the offeror/quoter/contractor shall utilize health IT
that--
(i) Meets standards and implementation specifications adopted in 45
CFR part 170, subpart B, if such standards and implementation
specifications can support work performed under the contract; or
(ii) Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the contractor is--
(A) An eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102, and 4201 of the HITECH
Act; or
(B) Implementing, acquiring, or upgrading technology to be used by
an
[[Page 65310]]
eligible professional in an ambulatory setting, or hospital, eligible
under sections 4101, 4102, and 4201 of the HITECH Act.
(2) If the contractor is a health care provider, health plan, or
health insurance issuer, or, to perform the contract, is establishing
an agreement with a health care provider, health plan, or health
insurance issuer, for any work performed under the contract that
involves implementing, acquiring, or upgrading health IT, the offeror/
quoter/contractor shall utilize health IT that--
(i) Meets standards and implementation specifications adopted in 45
CFR part 170, subpart B, if such standards and implementation
specifications can support work performed under the contract; or
(ii) Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the contractor is--
(A) An eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102, and 4201 of the HITECH
Act; or
(B) Implementing, acquiring, or upgrading technology to be used by
an eligible professional in an ambulatory setting, or hospital,
eligible under sections 4101, 4102, and 4201 of the HITECH Act.
(c) If standards and implementation specifications adopted in 45
CFR part 170, subpart B, cannot support the work as specified in the
contract, the offeror/quoter/contractor is encouraged to use health IT
that meets non-proprietary standards and implementation specifications
developed by consensus-based standards development organizations. This
may include standards identified in the ONC Interoperability Standards
Advisory, available at https://www.healthit.gov/isa/.
339.7003 Contract Clause
The contracting officer shall insert the clause at 352.239-70,
Standards for Health Information Technology, in solicitations and
contracts issued by or on behalf of HHS entities that--
(a) Involve implementing, acquiring, or upgrading health IT used
for the direct exchange of individually identifiable health information
between agencies and with non-Federal entities; or
(b) Are with health care providers, health plans, or health
insurance issuers that, under the solicitation or contract, would be
implementing, acquiring, or upgrading health IT.
PART 352--SOLICITATION PROVISIONS AND CONTRACT CLAUSES
0
3. The authority for part 352 is revised to read as follows:
Authority: 5 U.S.C. 301; 40 U.S.C. 121(c); 41 U.S.C. 1121(c)(3);
41 U.S.C. 1702; 42 U.S.C. 2003; and 48 CFR 1.301 through 1.304.
Subpart 352.2--Text of Provisions and Clauses
0
4. The heading for subpart 352.2 is revised to read as set forth above.
0
5. Section 352.239-70 is added to read as follows:
352.239-70 Standards for Health Information Technology
As prescribed in 339.7003, insert the following clause:
Standards for Health Information Technology
(Date)
(a) Definitions. As used in this clause--
Health information technology (health IT) means hardware, software,
integrated technologies or related licenses, intellectual property,
upgrades, or packaged solutions sold as services that are designed for
or support the use by health care entities or patients for the
electronic creation, maintenance, access, or exchange of health
information. (42 U.S.C. 300jj(5))
Individually identifiable health information means any information,
including demographic information collected from an individual, that--
(1) Is created or received by a health care provider, health plan,
employer, or health care clearinghouse; and
(2) Relates to the past, present, or future physical or mental
health condition of an individual; the provision of health care to an
individual; or the past, present, or future payment for the provision
of health care to an individual; and
(i) Identifies the individual; or
(ii) With respect to which there is a reasonable basis to believe
the information can be used to identify the individual. (42 U.S.C.
300jj(8), 1320d(6))
ONC Health Information Technology Certification Program means the
voluntary certification program administered by the HHS Office of the
National Coordinator for Health Information Technology (ONC) using a
third-party conformity assessment program for health IT. Certification
criteria for the Program are found in 45 CFR part 170, subpart C, and
incorporate standards and implementation specifications in 45 CFR part
170, subpart B.
(b) Pursuant to the Health Information Technology for Economic and
Clinical Health Act (HITECH Act), Public Law 111-5, title XIII,
sections 13111 and 13112, and HHS policy, by submission of an offer (or
a quote) and execution of a contract, the offeror/quoter/Contractor
agrees that--
(1) For any work performed under the contract that involves
implementing, acquiring, or upgrading health IT procured by or on
behalf of HHS entities used for the direct exchange of individually
identifiable health information between agencies and with non-Federal
entities, the offeror/quoter/Contractor shall utilize health IT that--
(i) Meets standards and implementation specifications adopted in 45
CFR part 170, subpart B, if such standards and implementation
specifications can support the work performed under the contract; or
(ii) Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support the work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the Contractor is--
(A) An eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102 and 4201 of the HITECH
Act; or
(B) Implementing, acquiring, or upgrading technology to be used by
an eligible professional in an ambulatory setting, or a hospital,
eligible under sections 4101, 4102 and 4201 of the HITECH Act.
(2) If the Contractor is a health care provider, health plan, or
health insurance issuer, or, to perform the contract, is establishing
an agreement with a health care provider, health plan, or health
insurance issuer, for any work performed under the contract that
involves implementing, acquiring, or upgrading health IT, the offeror/
quoter/Contractor shall utilize health IT that--
(i) Meets standards and implementation specifications adopted in 45
CFR part 170, subpart B, if such standards and implementation
specifications can support the work performed under the contract; or
(ii) Is certified under the ONC Health Information Technology
Certification Program, if certified technology can support the work
performed under the contract (see certification criteria in 45 CFR part
170, subpart C), when the Contractor is--
(A) An eligible professional in an ambulatory setting, or a
hospital, eligible under sections 4101, 4102 and 4201 of the HITECH
Act; or
(B) Implementing, acquiring, or upgrading technology to be used by
an
[[Page 65311]]
eligible professional in an ambulatory setting, or a hospital, eligible
under sections 4101, 4102 and 4201 of the HITECH Act.
(c) If standards and implementation specifications adopted in 45
CFR part 170, subpart B, cannot support the work as specified in the
contract, the Contractor is encouraged to use health IT that meets non-
proprietary standards and implementation specifications developed by
consensus-based standards development organizations. This may include
standards identified in the ONC Interoperability Standards Advisory,
available at https://www.healthit.gov/isa/.
(End of clause)
[FR Doc. 2024-17096 Filed 8-8-24; 8:45 am]
BILLING CODE 4151-19-P