[Federal Register Volume 72, Number 192 (Thursday, October 4, 2007)]
[Rules and Regulations]
[Pages 56632-56644]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E7-19636]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Office of the Secretary

Office of Inspector General

42 CFR Part 1001


Medicare and State Health Care Programs: Fraud and Abuse; Safe 
Harbor for Federally Qualified Health Centers Arrangements Under the 
Anti-Kickback Statute

AGENCY: Office of Inspector General (OIG), HHS.

ACTION: Final rule.

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SUMMARY: In accordance with section 431 of the Medicare Prescription 
Drug, Improvement, and Modernization Act of 2003 (MMA), this final rule 
sets forth a safe harbor under the anti-kickback statute to protect 
certain arrangements involving goods, items, services, donations, and 
loans provided by individuals and entities to certain health centers 
funded under section 330 of the Public Health Service Act. The goods, 
items, services, donations, or loans must contribute to the health 
center's ability to maintain or increase the availability, or enhance 
the quality, of services available to a medically underserved 
population.

DATES: Effective Date: These regulations are effective on December 3, 
2007.

FOR FURTHER INFORMATION CONTACT: Spencer Turnbull, Office of Counsel to 
the Inspector General, (202) 619-0335.

SUPPLEMENTARY INFORMATION:

I. Background

Overview--Establishing New Safe Harbor for Arrangements Involving 
Federally Qualified Health Centers

    This final regulation establishes safe harbor protection under the 
anti-kickback statute for certain arrangements involving Federally 
qualified health centers. Section I of this preamble contains a brief 
background discussion addressing the anti-kickback statute and safe 
harbors; a discussion of section 330-funded health centers; a summary 
of the relevant MMA provisions; a summary of the proposed safe harbor; 
and a summary of the final safe harbor. Section II of this preamble 
sets forth a summary of the public comments and our responses to those 
comments.
A. The Anti-Kickback Statute and Safe Harbors
    The anti-kickback statute provides criminal penalties for 
individuals or entities that knowingly and willfully offer, pay, 
solicit, or receive remuneration in order to induce or reward the 
referral of business reimbursable under any of the Federal health care 
programs, as defined in section 1128B(f) of the Act. The offense is 
classified as a felony and is punishable by fines of up to $25,000 and 
imprisonment for up to five years. Violations of the anti-kickback 
statute may also result in the imposition of civil money penalties 
(CMPs) under section 1128A(a)(7) of the Act (42 U.S.C. 1320a-7a(a)(7)), 
program exclusion under section 1128(b)(7) of the Act (42 U.S.C. 1320a-
7(b)(7)), and liability under the False Claims Act, (31 U.S.C. 3729-
33).
    The types of remuneration prohibited specifically include, without 
limitation, kickbacks, bribes, and rebates, whether made directly or 
indirectly, overtly or covertly, in cash or in kind. Prohibited conduct 
includes not only the payment of remuneration intended to induce or 
reward referrals of patients, but also the payment of remuneration 
intended to induce or reward the purchasing, leasing, or ordering of, 
or arranging for or recommending the purchasing, leasing, or ordering 
of, any good, facility, service, or item reimbursable by any Federal 
health care program.
    Because of the broad reach of the statute, concern was expressed 
that some relatively innocuous commercial arrangements were covered by 
the statute and, therefore, potentially subject to criminal 
prosecution. In response, Congress enacted section 14 of the Medicare 
and Medicaid Patient and Program Protection Act of 1987, Public Law 
100-93 (section 1128B(b)(3)(E) of the Act), which specifically required 
the development and promulgation of regulations, the so-called ``safe 
harbor'' provisions, which would specify various payment and business 
practices that would not be treated as criminal offenses under the 
anti-kickback statute, even though they may potentially be

[[Page 56633]]

capable of inducing referrals of business under the Federal health care 
programs. Since July 29, 1991, OIG has published in the Federal 
Register a series of final regulations establishing ``safe harbors'' in 
various areas.\1\ These OIG safe harbor provisions have been developed 
``to limit the reach of the statute somewhat by permitting certain non-
abusive arrangements, while encouraging beneficial or innocuous 
arrangements.'' (56 FR 35952, 35958; July 21, 1991).
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    \1\ 56 FR 35952 (July 29, 1991); 61 FR 2122 (January 25, 1996); 
64 FR 63518 (November 19, 1999); 64 FR 63504 (November 19, 1999); 66 
FR 62979 (December 4, 2001); and 71 FR 45110 (August 8, 2006).
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    Health care providers and others may voluntarily seek to comply 
with safe harbors so that they have the assurance that their business 
practices will not be subject to liability under the anti-kickback 
statute, the CMP provision for anti-kickback violations, or the program 
exclusion authority related to kickbacks. In giving the Department the 
authority to protect certain arrangements and payment practices from 
penalties under the anti-kickback statute, Congress intended the safe 
harbor regulations to be evolving rules that would be updated 
periodically to reflect changing business practices and technologies in 
the health care industry.
B. Section 330--Funded Health Centers
    Beginning in the 1960s, Congress enacted various health center 
programs to assist the large number of individuals living in medically 
underserved areas, as well as the growing number of special populations 
with limited access to preventive and primary health care services. In 
the Health Centers Consolidation Act of 1996, Public Law 104-299, 
Congress consolidated the four then-existing Federal health center 
grant programs (the Migrant Health Center Program, the Community Health 
Center Program, the Health Care for the Homeless Program, and the 
Health Services for Residents of Public Housing Program) into a single 
program under section 330 of the Public Health Service (PHS) Act. See 
S. Rep. 104-186 (December 15, 1995). In the Health Care Safety Net 
Amendments of 2002, Public Law 107-251, Congress reauthorized and 
strengthened the health centers program. In 2005, the Federal health 
center programs supported 954 organizations that provided care to over 
14 million patients at 3,745 health care service delivery sites.\2\
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    \2\ HRSA Bureau of Primary Health Care, Uniform Data System: 
Calendar Year 2005 Data (available upon request at http://www.bphc.hrsa.gov/uds/default.htm).
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    Section 330 grant recipients play a vital role in the health care 
safety net, providing cost effective care for communities with limited 
access to health care resources. All recipients of grants under section 
330 are public, nonprofit, or tax-exempt entities. The health centers 
must serve ``a population that is medically underserved, or a special 
medically underserved population comprised of migratory and seasonal 
agricultural workers, the homeless, and residents of public housing.'' 
42 U.S.C. 254b(a)(1). Health centers must be community based; to this 
end, a majority of a health center's governing board must be users of 
the center and must, as a group, represent the individuals being served 
by the center.\3\ 42 U.S.C. 254b(k)(3)(H)(i). Health centers receiving 
section 330 grant funding must provide, either directly or through 
contracts or cooperative arrangements, a broad range of required 
primary health care services, including clinical services by 
physicians, and, where appropriate, physician assistants, nurse 
practitioners, and nurse midwives; diagnostic laboratory and 
radiological services; preventive health services; emergency medical 
services; certain pharmaceutical services; referrals to other providers 
(including substance abuse and mental health services); patient case 
management; services that enable individuals to use the services of the 
health center (e.g., outreach, transportation, and translation 
services); and patient and community education services. 42 U.S.C. 
254b(b)(1). They may also provide certain additional health services 
that are appropriate to serve the health needs of the population served 
by the health center. 42 U.S.C. 254b(b)(2). These additional health 
services may include mental health and substance abuse services; 
recuperative care services; environmental health services; special 
occupation-related health services for migratory and seasonal 
agricultural workers; programs to control infectious disease; and 
injury prevention programs.
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    \3\ Health centers receiving grant funding to serve migratory 
and seasonal agricultural workers, homeless people, or residents of 
public housing may, upon a showing of good cause, obtain a waiver of 
this requirement. 42 U.S.C. 254b(k)(3)(H).
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    Consistent with their mission and the terms of their PHS grants, 
section 330 grant recipients serve predominantly low-income 
individuals, including some beneficiaries of the Medicare and Medicaid 
programs. In 2005, 36 percent of patients treated by section 330 grant 
recipients were beneficiaries of a Medicaid program, 7.5 percent were 
beneficiaries of the Medicare program, and 2.3 percent were 
beneficiaries of another public insurance program.\4\ Section 330 grant 
recipients also treat a substantial and growing number of uninsured 
patients. In 1996, section 330 grant recipients provided services to 
3.2 million uninsured patients, and by 2005, this number had increased 
to 5.6 million, representing nearly 40 percent of patients treated at 
those centers during that year.\5\
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    \4\ HRSA Bureau of Primary Health Care, Uniform Data System: 
Calendar Year 2005 Data--Table 4: Users by Socioeconomic 
Characteristics (available upon request at http://www.bphc.hrsa.gov/uds/default.htm).
    \5\ HRSA Bureau of Primary Health Care, Uniform Data System: 
Calendar Year 2005 Data--UDS Trend Data for Years 1996 through 2005 
(available upon request at http://www.bphc.hrsa.gov/uds/default.htm).
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    Section 330 grant recipients must serve all residents of their 
``catchment'' area regardless of the patient's ability to pay and must 
establish a fee schedule with discounts to adjust fees on the basis of 
ability to pay. 42 U.S.C. 254b(a)(1)(B) and 254b(k)(3)(G)(i). Section 
330 grant recipients must also make and continue ``every reasonable 
effort to establish and maintain collaborative relationships with other 
health care providers in the catchment area of the center'' (42 U.S.C. 
254b(k)(3)(B)), and must ``develop an ongoing referral relationship'' 
with at least one hospital in the area. 42 U.S.C. 254b(k)(3)(L).
    Section 330 grant funds are intended to defray the costs of serving 
uninsured patients. Grant recipients are required to seek reimbursement 
from those patients who are able to pay all or a portion of the charges 
for their care (applying a schedule of fees and a corresponding 
schedule of discounts adjusted on the basis of the patient's ability to 
pay) or who have private insurance or public coverage, such as Medicare 
or Medicaid. The amount of a section 330 grant may not exceed the 
amount by which the costs of operation of the health center in such 
fiscal year exceed the total of: (i) State, local, and other 
operational funding provided to the health center; and (ii) the fees, 
premiums, and third-party reimbursements that the center may reasonably 
be expected to receive for its operations in such fiscal year. By 
statute, nongrant funds must be used to further the objectives of the 
recipient's section 330 grant.
    Section 330 grant funding accounts for approximately 20 percent of 
revenue for health centers receiving such grants. The majority of 
health center funding derives from charges for patient services. On 
average, the largest source

[[Page 56634]]

of revenue, 37 percent comes from Medicaid payments, 6.5 percent of 
health center revenues come from private third-party reimbursement, 6 
percent from Medicare payments, and 6.5 percent from self-payments from 
patients. Remaining revenue comes from a mix of other Federal, State, 
local, and philanthropic sources.\6\
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    \6\ HRSA Bureau of Primary Health Care, Uniform Data System: 
Calendar Year 2005 Data--Exhibit A: Total Revenue Received by BPHC 
Grantees (available upon request at http://www.bphc.hrsa.gov/uds/default.htm).
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    Frequently, health centers are provided with, or seek out, 
opportunities to enter into arrangements with hospitals or other 
providers or suppliers to further the health centers' patient care 
mission.\7\ For example, providers or suppliers may agree to provide 
health centers with capital development grants, low cost (or no cost) 
loans, reduced price services, or in-kind donations of supplies, 
equipment, or space.
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    \7\ Congress has previously recognized the importance of health 
center affiliations with hospitals and other health care service 
providers in promoting efficiency and quality of care. The Health 
Centers Consolidation Act expressly requires health centers to 
maintain collaborative relationships with other providers. With 
respect to integrated delivery systems, the Report states:
    ``The committee believes, based on expert testimony given at the 
May 14, 1995, hearing, that the development of integrated health 
care provider networks is key to preserving and strengthening access 
to community-based health care services in rural areas. Provider 
networks offer a number of advantages: They can work to ensure that 
a continuum of health care services is available, reduce the 
duplication of services, produce savings in administrative and other 
costs through shared services and an enhanced ability to negotiate 
in the health care market place, and recruit and utilize health 
professionals more effectively and efficiently.''
    S. Rep. 104-186 at p. 11.
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    Some providers and suppliers expressed concern that remuneration 
offered to health centers might be viewed as suspect under the anti-
kickback statute, because the health centers are frequently in a 
position to refer Federal health care program beneficiaries to the 
provider or supplier. Accordingly, Congress enacted section 431 of MMA 
to enable some health centers to conserve section 330 and other monies 
by accepting needed goods, items, services, donations, or loans for 
free or at reduced rates from willing providers and suppliers.
C. Section 431 of MMA
    Section 431 of MMA amended the anti-kickback statute to create a 
new safe harbor for certain agreements involving health centers. 
Specifically, section 431(a) of MMA excludes from the reach of the 
anti-kickback statute any remuneration between: (i) A health center 
described under section 1905(l)(2)(B)(i) or 1905(l)(2)(B)(ii) of the 
Act; and (ii) an individual or entity providing goods, items, services, 
donations, loans, or a combination of these to the health center 
pursuant to a contract, lease, grant, loan, or other agreement, 
provided that such agreement contributes to the health center's ability 
to maintain or increase the availability, or enhance the quality, of 
services provided to a medically underserved population served by the 
health center.
    In other words, Congress intended to permit health centers to 
accept certain remuneration that would otherwise implicate the anti-
kickback statute when the remuneration furthers a core purpose of the 
Federal health centers program: ensuring the availability and quality 
of safety net health care services to otherwise underserved 
populations. As discussed in greater detail below, Congress limited the 
scope of the safe harbor to certain health centers engaged in 
arrangements involving specific types of identifiable remuneration.
    In establishing regulatory standards relating to the safe harbor, 
Congress directed the Department to consider the following factors:
     Whether the arrangement results in savings of Federal 
grant funds or increased revenues to the health center. We believe this 
factor evidences Congress' intent that a protected arrangement directly 
benefit the health center economically and that the benefits of the 
arrangement primarily inure to the health center, rather than the 
individual or entity providing the remuneration.
     Whether the arrangement restricts or limits patient 
freedom of choice. We believe this factor evidences Congress' intent 
that protected arrangements not result in inappropriate steering of 
patients. Under the safe harbor, patients remain free to obtain 
services from any provider or supplier willing to furnish them.
     Whether the arrangement protects the independent medical 
judgment of health care professionals regarding medically appropriate 
treatment for patients. We believe this factor evidences Congress' 
intent to safeguard the integrity of medical decision-making and ensure 
it is untainted by direct or indirect financial interests. In all 
cases, the best interests of the patient should guide the medical 
decision-making of health centers and their affiliated health care 
professionals.
    Section 431(b)(1)(B) of MMA provides that these three factors are 
``among'' the factors the Department may consider in establishing the 
safe harbor standards. The statute authorizes the Department to include 
``other standards and criteria that are consistent with the intent of 
Congress in enacting'' the health center safe harbor. Accordingly, we 
interpret the statute to permit us to consider other relevant factors 
and to establish other relevant safe harbor standards consistent with 
the anti-kickback statute and the health center safe harbor. Among the 
factors we have considered is whether arrangements would pose a risk of 
fraud or abuse to any Federal health care programs or their 
beneficiaries. We believe Congress intended to protect arrangements 
that foster an important goal of the section 330 grant program--
assuring the availability and quality of needed health care services 
for medically underserved populations--without adversely impacting 
other Federal programs or their beneficiaries.
D. Summary of Proposed Safe Harbor
    On July 1, 2005, we issued a notice of proposed rulemaking (70 FR 
38081) to set forth standards related to the safe harbor described in 
section 431 of MMA, in which we proposed: (1) To protect remuneration 
in the form of goods, items, services, donations, loans, or a 
combination thereof provided by an individual or entity (hereinafter in 
this preamble ``Donor'') to a qualifying health center; (2) that 
remuneration must be medical or clinical in nature or relate directly 
to patient services provided by the health center as part of the scope 
of the health center's section 330 grant; and (3) importantly, that a 
protected arrangement must contribute to the ability of the health 
center to maintain or increase the availability, or enhance the 
quality, of services provided to a medically underserved population.
    The proposed regulation proposed that protected arrangements must 
be pursuant to a comprehensive contract, lease, grant, loan, or other 
agreement that is written and signed by the parties, and the amount of 
the protected remuneration must not be conditioned on the volume or 
value of Federal health care program business generated between the 
parties. As we said in the notice of proposed rulemaking:

    ``In the unique and limited context of arrangements described in 
the proposed safe harbor, we would extend safe harbor protection to 
arrangements where only the methodology, and not the absolute value 
of the remuneration, is predetermined. For example, a health center 
might agree to pay a supplier a set hourly or per visit fee that is 
below fair market value for services furnished by the supplier to 
the health center, provided that the formula for

[[Page 56635]]

calculating the compensation (e.g., $ x per hour or $ x per service) 
is fixed in advance and not conditioned on referrals to the 
supplier.'' 70 FR 38084.

    We proposed that health centers must reasonably determine before 
entering into an agreement that the arrangement is likely to contribute 
to the health center's ability to maintain or increase the 
availability, or enhance the quality, of services provided to a 
medically underserved population. We also proposed that health centers 
would have to periodically re-evaluate agreements to ensure ongoing 
compliance with this benefit standard and terminate as expeditiously as 
possible any arrangements that are not reasonably expected to continue 
to meet the standard. We proposed that the initial determination and 
any re-evaluations should be contemporaneously documented.
    Our proposed rule stated that health centers must not be required 
to refer patients to a particular provider or supplier. In addition, we 
proposed that Donors that offer to provide goods, items, or services 
must accept all referrals of patients from the health center who 
clinically qualify for the goods, items, or services, regardless of 
payor status or ability to pay. We proposed that protected arrangements 
could not be exclusive. The proposed rule also required health centers 
to provide effective notification to patients of their freedom to 
choose any willing provider or supplier and to disclose the existence 
and nature of protected arrangements.
    We proposed to give health centers the option of requiring that a 
Donor that enters into a protected arrangement charge a referred health 
center patient the same rate it charges other similarly situated 
persons not referred by the health center or that the items or services 
be furnished to health center patients at a reduced rate or free of 
charge.
    Finally, we proposed that an arrangement could not be protected 
under the safe harbor unless it complied with the requirements of the 
health center's section 330 grant funding.
E. Summary of Final Safe Harbor
1. Major Changes
    We have modified the proposed rule in a number of areas in response 
to public comments. The substantial changes and clarifications being 
made in the final regulations include:
     Clarifying the definition of the term ``remuneration'' for 
purposes of the safe harbor;
     Eliminating the requirement that arrangements that do not 
comply with the safe harbor be terminated;
     Eliminating the requirement that arrangements must comply 
with all relevant requirements of the health center's section 330 grant 
funding;
     Consolidating and clarifying the documentation 
requirements;
     Clarifying that health centers do not need to develop set 
standards for determining whether an arrangement is expected to 
contribute meaningfully to services for underserved patients;
     Simplifying the safe harbor requirement pertaining to 
disclosures to patients;
     Clarifying health centers' freedom to refer patients; and
     Clarifying the conditions under which individuals and 
entities furnish separately billable goods, items, or services to 
health centers.
2. Final Safe Harbor Conditions
    As discussed more fully in this preamble and regulations, the 
health center safe harbor protects remuneration in the form of goods, 
items, services, donations or loans (whether the donation or loan is in 
cash or in-kind), or a combination thereof provided by a Donor to a 
qualifying health center. Qualifying health centers are health centers 
described under section 1905(l)(2)(B)(i) or 1905(l)(2)(B)(ii) of the 
Act. Remuneration must be medical or clinical in nature or relate 
directly to services provided by the health center as part of the scope 
of the health center's section 330 grant. A protected arrangement must 
contribute to the ability of the health center to maintain or increase 
the availability of, or enhance the quality of, services provided to a 
medically underserved population.
    Protected arrangements must be pursuant to a contract, lease, 
grant, loan, or other agreement that is written, signed by the parties, 
and covers all of the remuneration to be provided. The amount of the 
remuneration must be specified and not be conditioned on the volume or 
value of Federal health care program business generated between the 
parties.
    Health centers must reasonably expect before entering into an 
agreement that the arrangement is likely to contribute to the health 
center's ability to maintain or increase the availability, or enhance 
the quality, of services provided to a medically underserved population 
as defined at 42 U.S.C. 254b(b)(3). Health centers must document the 
basis for their determination that the arrangement will yield such a 
benefit. Health centers must periodically re-evaluate agreements to 
ensure ongoing compliance with the benefit standard. These 
determinations must be contemporaneously documented.
    Health centers must not be required to refer patients to a 
particular provider or supplier under the arrangement, and must be free 
to refer patients to any provider or supplier. In addition, Donors that 
offer to furnish goods, items, or services for health center patients 
must furnish those goods, items, or services to all health center 
patients who clinically qualify for them, regardless of payor status or 
ability to pay.
    Health centers are required to provide effective notification to 
patients of their freedom to choose any willing provider or supplier 
and to disclose to patients, upon request, the existence and nature of 
the arrangement with the Donor.
    The safe harbor makes clear that a health center may, at its 
option, require a Donor that enters into a protected arrangement to 
charge a referred health center patient the same rate it charges other 
similarly situated persons not referred by the health center or furnish 
items or services to health center patients at a reduced rate (where 
the discount applies to the total charge and not just the cost-sharing 
portion owed by an insured patient).

II. Summary of Public Comments and OIG Responses

    In response to our proposed rulemaking, OIG received a total of 
nine timely filed comments from trade associations, hospitals, health 
centers, and other interested parties. We have divided the summaries of 
the public comments and our responses into three parts: general 
comments; comments on statutory elements; and comments on additional 
regulatory standards.

A. General Comments

    All the commenters supported the establishment of a safe harbor for 
arrangements involving Federally Qualified Health Centers. While some 
commenters expressed their support for all of the regulatory standards 
in the proposed rule, other commenters took issue with one or more 
specific aspects of the proposal.
    Comment: A trade association objected to the number of standards in 
the proposed regulation. The commenter suggested that the number of 
standards is too high and might dissuade parties from participating in 
safe harbored arrangements.
    Response: As discussed in detail elsewhere in this preamble, we 
have reduced the number of standards from eleven in the proposed rule 
to nine in

[[Page 56636]]

the final rule. We do not believe that the regulatory standards should 
create an undue burden or otherwise chill participation in arrangements 
under the safe harbor.
    Comment: Several commenters responded to the statement in the 
preamble to the proposed rule that OIG intended to monitor participants 
in safe harbored arrangements for compliance with billing rules, in 
order to guard against improper billing of Federal health care programs 
or inappropriate transfers of governmental funds. See 70 FR 38086. Two 
trade associations requested that we remove any mention of such 
monitoring, lest it discourage parties from participating in 
arrangements under this safe harbor. Another trade association 
suggested that, in return for safe harbor protection, it would be 
appropriate that health centers be monitored closely for compliance 
with the requirements of section 330 funding to determine whether the 
funding is used for its intended purpose. In particular, the commenter 
stated that it is important to ensure that any government benefits 
provided to health centers to serve uninsured patients are used to 
provide services to those patients and not diverted to subsidizing 
unrelated service lines.
    Response: Our use of the term ``monitor'' may have inadvertently 
created the misimpression that parties to arrangements under this safe 
harbor would be subject to a higher level of scrutiny than parties to 
other arrangements. We clarify that we were referring simply to our 
usual and customary oversight authorities and practices. Participation 
in a safe harbored arrangement would not necessarily make parties a 
target of OIG attention or subject parties to heightened scrutiny; 
however, as providers who receive funding from Federal health care 
programs, health centers remain subject to our general oversight tools, 
including monitoring for proper billing and appropriate transfers of 
governmental funds. With that clarification, we do not believe that 
referencing our longstanding oversight authority should discourage 
participation in safe harbored arrangements. We agree with the last 
commenter and affirm our continued commitment to ensuring that 
Government funding is used for its intended purposes.
    Comment: A trade association requested that we remove the proposed 
requirement at Sec.  1001.952(w)(11), which would have required any 
safe harbored agreement to comply with all relevant requirements of the 
health center's section 330 grant funding. The commenter suggested that 
the requirement is unnecessary, because health centers already operate 
under an obligation to comply with all requirements of their section 
330 grant funding. Moreover, the commenter observed that including this 
provision in the safe harbor regulations might chill a Donor's 
willingness to participate in safe harbored arrangements, if that Donor 
also becomes obligated to ensure that the arrangements comply with the 
terms of a health center's section 330 grant funding.
    Response: We agree with this commenter and are eliminating the 
standard in the final rule. The remaining safe harbor conditions, in 
combination with health centers' existing obligations to comply with 
the requirements of their section 330 grant funding, should be 
sufficient to minimize any risk of fraud and abuse.
    Comment: We received a comment from a health center network noting 
that the safe harbor only offers protection under the anti-kickback 
statute and does not offer protection under the physician self-referral 
law, section 1877 of the Act (commonly known as the ``physician self-
referral law'' or ``Stark'' law). The commenter expressed concern that 
the need to comply with both statutes may prove burdensome for health 
centers, and suggested that the requirements of the two laws be 
consolidated.
    Response: The commenter correctly notes that the safe harbor only 
protects arrangements under the anti-kickback statute, and, where 
applicable, parties would also need to comply with the physician self-
referral law. An exception under the physician self-referral law is 
beyond the scope of this rulemaking. The anti-kickback statute and the 
physician self-referral law, while similar in that they both address 
abuses of the Medicare and Medicaid programs, are different in scope 
and application. Congress has made clear that the physician self-
referral law and the anti-kickback statute are separate legal 
authorities, and compliance with one does not necessarily ensure 
compliance with the other. See, e.g., H.R. Conf. Rep. No. 386, 101st 
Cong., 1st session 856 (1989).

B. Comments on Statutory Elements

1. Protected Health Centers
    Comment: A trade association suggested we broaden the scope of the 
safe harbor to apply to arrangements involving other types of health 
centers that are similar to the health centers described in sections 
1905(l)(2)(B)(i) and 1905(l)(2)(B)(ii) of the Act, except for the fact 
that they lack section 330 funding. These other facilities are often 
called ``look-alike'' facilities.
    Response: We decline to adopt this suggestion. Congress 
specifically provided that the safe harbor should apply to the 
facilities described in sections 1905(l)(2)(B)(i) and 1905(l)(2)(B)(ii) 
of the Act and not to other types of facilities. Moreover, we believe 
the lack of section 330 funding, which entails a higher level of 
Government oversight, constitutes a significant distinction between 
section 330-funded health centers and look-alike facilities. Extending 
safe harbor protection to entities without such Government funding and 
such a level of oversight would pose a greater risk of fraud and abuse. 
We recognize that many look-alike facilities play important roles in 
the health care safety net, and we note that just because arrangements 
with look-alike facilities do not fall within the safe harbor does not 
mean they are necessarily illegal. The fact that the safe harbor does 
not apply simply means that such arrangements must be analyzed on a 
case-by-case basis to determine whether they violate the anti-kickback 
statute.
    Comment: A trade association asked us to commit to considering the 
issuance of a regulatory safe harbor protecting arrangements involving 
look-alike facilities.
    Response: We may consider this option in the future, depending on 
our experience with this safe harbor in practice.
2. Protected Remuneration
    Comment: Several commenters sought clarification as to whether 
community benefit grants and other types of cash donations qualify as 
protected remuneration under this safe harbor. A trade association 
asked that we add language in Sec.  1001.952(w)(2) that clarifies that 
donations and loans could include cash donations, such as community 
benefit grants, and are not limited to in-kind donations and loans. One 
commenter noted that some community benefit grants entail 
reconciliation provisions, which allow the donor (i) to augment the 
grant if grant funds fall short of actual health center expenditures or 
(ii) to determine the use of excess funds where grant funds exceed 
actual health center spending. Two trade associations requested 
clarification of the definition of ``remuneration'' and assurance that 
the definition includes community benefit grants or similar payments to 
health centers by public hospitals and health systems, even if the 
amount of

[[Page 56637]]

the payments are subject to reconciliation.
    Response: The definition of ``remuneration'' at Sec.  1001.952(w) 
would generally extend to community benefit grants or similar payments, 
even where such grants or payments are subject to a reconciliation 
provision. So long as the reconciliation methodology is fixed in 
advance and does not hinge on the volume or value of referrals from the 
health center to the Donor, funding subject to reconciliation could 
comply with the condition at Sec.  1001.952(w)(1) and be protected 
remuneration under this safe harbor (provided all other safe harbor 
conditions are satisfied). Donations and loans need not be limited to 
in-kind goods or services, and indeed may be in monetary form. We have 
clarified the scope of Sec.  1001.952(w) to make this point more 
explicit: ``As used in section 1128B of the Act, 'remuneration' does 
not include the transfer of any goods, items, services, donations or 
loans (whether the donation or loan is in cash or in-kind), or 
combination thereof from an individual or entity to a health center * * 
*'' (emphasis added).
    Comment: A trade association suggested we expand the scope of the 
safe harbor to cover arrangements whereby the remuneration is provided 
not to the health center, but from the health center to an individual 
or entity related to the health center. The commenter said there are 
arrangements not covered by other safe harbors where a health center 
could provide payments or other forms of support to a provider that 
would result in improving the overall health outcomes of patients.
    Response: Section 431 of MMA does not protect remuneration from a 
health center to an individual or entity. We believe it is clear that 
Congress intended the safe harbor to enhance the resources available to 
health centers in order to help them achieve their community benefit 
mission, and we decline to adopt the commenter's recommendation. We 
recognize that there may be beneficial arrangements where remuneration 
flows away from the health center that may not fit within a safe 
harbor; such arrangements would be evaluated on a case-by-case basis to 
ensure compliance with the anti-kickback statute. We note that some 
arrangements pursuant to which a health center provides remuneration to 
an individual or entity may qualify for other safe harbors, including, 
for example, the safe harbors for personal services, employees, 
practitioner recruitment, and electronic health records items a nd 
services. See Sec. Sec.  1001.952(d), (i), (n), and (y).
    Comment: A trade association noted that our proposed rule stated 
that section 431 ``only protects remuneration provided to a health 
center and does not protect remuneration provided to individuals 
affiliated with a health center * * *.'' 70 FR 38084. The commenter 
asked whether, for purposes of this safe harbor, remuneration to the 
health center could include funds provided by a hospital, if such funds 
were used to help recruit a physician to the health center.
    Response: The donation described by the commenter raises the 
possibility of two scenarios: one in which the donation could be used 
to recruit a physician to the health center primarily for the benefit 
of health center patients, and one where it could be used to recruit a 
physician primarily for the benefit of the donor hospital. If the 
hospital made the donation of funds to the health center primarily for 
the benefit of health center patients, then its donation of funds for 
the purpose of supporting general physician recruitment by the health 
center could qualify for protection under this safe harbor, if all safe 
harbor conditions are satisfied. Conversely, we believe Congress did 
not intend the safe harbor to protect arrangements where the donation 
primarily creates a benefit to the Donor instead of to the health 
center. Likewise, this safe harbor would not protect an arrangement 
where a Donor used the health center as a conduit to transfer 
remuneration to a particular recruited physician; to transfer 
remuneration specifically for the purpose of recruiting a physician to 
join the Donor's medical staff, or to practice in the Donor's service 
area; or to transfer remuneration to existing group practices. The safe 
harbor does not protect remuneration provided by Donors to individuals 
affiliated with the health center. Section 431 evidences Congress' 
intent to protect the provision of certain remuneration ``to'' a health 
center. It does not protect remuneration transferred to an individual 
affiliated with a health center, nor does it protect remuneration 
transferred from a health center to an individual or entity. We note 
that, depending on the circumstances, such a recruitment arrangement 
between a health center and a physician may be eligible for protection 
under another safe harbor, such as the safe harbor for practitioner 
recruitment at Sec.  1001.952(n). When evaluating arrangements with 
potential Donors for funds to support physician recruitment, health 
centers should consider whether the remuneration would be used for 
expenses commonly or typically borne by the health center, such that 
the arrangement results in measurable savings that will benefit a 
medically underserved population, or would be used to recruit a health 
care professional needed by the health center to serve a medically 
underserved population. If a recruited physician were to join the 
health center's medical staff, it would be some evidence that the 
benefit primarily runs to medically underserved populations served by 
the health center as opposed to the Donor.
    Comment: We received several comments regarding the proposed 
regulatory text for Sec.  1001.952(w)(2), which provides examples of 
``patient services furnished by the health center as part of its 
section 330 grant'' in the parenthetical portion of the text, but does 
not similarly list examples of ``goods, items, donations, or loans.'' 
The commenters expressed concern that this suggested that only services 
could constitute protected remuneration. These commenters requested 
that the regulatory text also supply examples of protected goods, 
items, donations, and loans.
    Response: The commenters misread proposed Sec.  1001.952(w)(2). 
Goods, items, donations, and loans--and services--can indeed constitute 
protected remuneration under this safe harbor. In the interest of 
clarifying Sec.  1001.952(w)(2) so that health centers and Donors do 
not interpret the scope of protected remuneration to be narrower than 
it actually is, we have deleted the term ``patient services furnished'' 
and replaced it with the term ``services provided.'' Section 
1001.952(w)(2) now requires that goods, items, services, donations, or 
loans (or combination thereof) must either (i) Be medical or clinical 
in nature or (ii) relate directly to services provided by the health 
center in furtherance of its section 330 grant. The parenthetical list 
offers illustrative examples of the kind of services that meet the 
latter test and makes clear that such services need not be medical or 
clinical in nature. For example, goods, items, services, donations, or 
loans directly related to a health center's billing, administrative, 
social services, and health information functions can qualify. We note 
that the term ``medical or clinical in nature'' broadly covers all 
medical or clinical services (e.g., physician services, nurse 
practitioner and physician assistant services, diagnostic services, 
therapeutic services, etc.); medical or clinical goods and items (e.g., 
pharmaceuticals, knee braces, stethoscopes, x-ray machines, etc.); 
donations of money or other forms of remuneration that the health 
center can use to furnish medical or clinical

[[Page 56638]]

services or to acquire goods, items, or services that are medical or 
clinical in nature; and loans of money or other forms of remuneration 
that the health center can use to furnish medical or clinical services 
or to acquire goods, items, or services that are medical or clinical in 
nature.
    Comment: A non-profit organization and several health centers 
submitted comments seeking clarification that the definition of 
remuneration at Sec.  1001.952(w) would include pharmaceutical 
manufacturers' donations of pharmaceutical products to health centers 
with the intent that these products be used to treat patients of the 
health center. They requested that we amend Sec.  1001.952(w) 
specifically to include donations of pharmaceutical products from 
pharmaceutical manufacturers, citing concerns that absent such an 
explicit acknowledgement, pharmaceutical manufacturers would refuse to 
donate to health centers.
    Response: Nothing in Sec.  1001.952(w) excludes donations of 
pharmaceuticals by pharmaceutical companies from protection by the safe 
harbor. To the contrary, as discussed in the preceding response, such 
donations are clearly within the meaning of the language ``goods * * * 
[that] are medical or clinical in nature'' in Sec.  1001.952(w)(2). 
Pharmaceutical donations can play an important role in ensuring a 
health center safety net for vulnerable patients, and many arrangements 
between health centers and pharmaceutical companies may be eligible for 
protection. That said, we are not enumerating in the regulatory text 
any particular types of Donors. Whether something fits in the 
definition of protected ``remuneration'' at Sec.  1001.952(w) turns on 
the nature of the remuneration, not on its source. By listing some 
Donors and not others, we might create a misimpression regarding the 
scope of the safe harbor.
    Comment: A non-profit organization sought clarification that a 
health center's practice of purchasing discounted drugs by means of 
participation in the 340B Drug Pricing Program would not preclude that 
health center from receiving free drugs pursuant to a donation 
protected under this safe harbor.
    Response: We confirm that this safe harbor could protect 
arrangements involving the donation of pharmaceuticals to health 
centers, including to health centers that participate in the 340B Drug 
Pricing Program.
3. Documentation Requirements
    Comment: Several commenters supported our documentation 
requirements at proposed Sec. Sec.  1001.952(w)(1) and (3) 
(consolidated at Sec.  1001.952(w)(1) of the final rule). A trade 
association commented that the documentation requirements at proposed 
Sec. Sec.  1001.952(w)(1) and (3) are inconsistent with statements in 
the preamble. According to the commenter, the use of the term ``written 
agreement'' in the proposed regulatory language implies that all 
arrangements between a health center and a Donor must be included in a 
single writing, while the preamble says that all such arrangements 
should be memorialized ``by one comprehensive writing or by means of 
multiple writings that cross-reference and otherwise incorporate the 
agreements between the parties.''
    Response: For clarity and ease of application, we have combined the 
documentation requirements at proposed Sec. Sec.  1001.952(w)(1) and 
(3) of the proposed rule into one requirement at Sec.  1001.952(w)(1) 
in the final rule. We confirm that it may be satisfied by one 
comprehensive writing or by multiple writings that cross-reference and 
otherwise incorporate the agreements between the parties. We have 
revised the safe harbor to reflect this. We have also revised the safe 
harbor to provide the option of using a centralized master list in lieu 
of cross-referencing and incorporation of multiple agreements. The 
master list must be maintained centrally and in a manner that preserves 
the historical record of arrangements, kept up to date, and made 
available for review by the Secretary upon request. This flexibility 
should enhance the ability of Donors and health centers to use the safe 
harbor. The safe harbor does not require that all arrangements between 
a health center and a Donor be included in a single agreement that 
would qualify under the safe harbor.
    Comment: A trade association sought clarification that the 
documentation requirements at proposed Sec. Sec.  1001.952(w)(1) and 
(3) (Sec.  1001.952(w)(1) of the final rule) apply only to arrangements 
related to a safe harbored arrangement, and not to other interactions 
between the health center and the Donor that truly are unrelated to a 
safe harbored arrangement. The commenter believed that the 
documentation requirements imply that all arrangements between a health 
center and a Donor must be included in a single arrangement that would 
qualify under the safe harbor. The commenter suggested that only 
arrangements that ``require safe harbor protection'' should require 
documentation.
    Response: The safe harbor does not require that all arrangements 
between a health center and a Donor be included in a single arrangement 
that would qualify under the safe harbor. The documentation standards 
at Sec.  1001.952(w)(1) (Sec. Sec.  1001.952(w)(1) and (3) in our 
proposed rule) require that the written documentation ``cover all 
goods, items, services, donations, or loans to be provided to the 
health center.'' In the interest of providing bright-line guidance with 
respect to what must be documented under Sec.  1001.952(w)(1), we 
clarify that this paragraph requires the documentation of all 
arrangements for the transfer of goods, items, services, donations, or 
loans from a Donor to a health center. With respect to the commenter's 
assertion that certain arrangements ``require safe harbor protection,'' 
we note that, like all safe harbors, compliance with this safe harbor 
is voluntary and no arrangement requires safe harbor protection. 
Rather, arrangements must comply with the anti-kickback statute. 
Compliance with a safe harbor is one option for ensuring compliance 
with the anti-kickback statute.
4. Benefit to a Medically Underserved Population
    Comment: A trade association asked us to clarify Sec.  
1001.952(w)(4) of the proposed rule (Sec.  1001.952(w)(3) of the final 
rule), which requires that arrangements protected under the safe harbor 
be reasonably expected to contribute meaningfully to the health 
center's ability to maintain or increase the availability, or enhance 
the quality of, services provided to a medically underserved 
population. Specifically, the commenter sought confirmation that, in 
order to contribute meaningfully, the arrangement need not result in a 
financial gain for the health center. The commenter asked us to 
consider the case of a health center that does not offer a particular 
service for its patients, but enters into an arrangement with a Donor 
for that service for free. The commenter observed that since the health 
center had not previously incurred expenses for the service, the new 
arrangement would not offer a financial gain to the health center. 
Another trade association requested confirmation that proposed Sec.  
1001.952(w)(4) would not necessarily require direct savings of section 
330 funding and could be satisfied without a monetary benefit to the 
health center.
    Response: We confirm that proposed Sec.  1001.952(w)(4) (Sec.  
1001.952(w)(3) of the final rule) does not require a

[[Page 56639]]

financial gain to the health center and does not require the direct 
savings of section 330 funding. Whether the condition is satisfied will 
depend on the specific facts and circumstances. As noted in the 
preamble to the proposed rule at 70 FR 38085, we believe health centers 
are well-situated in the first instance to make a reasonable 
determination whether an arrangement contributes meaningfully to the 
health center's ability to maintain or increase the availability, or 
enhance the quality of, services provided to a medically underserved 
population, and we believe health centers should have flexibility in 
making these determinations. In the preamble to the proposed rule at 70 
FR 38085, we listed factors that are exemplars of the type that should 
be considered in making these determinations:
     Does the arrangement directly benefit a medically 
underserved population?
     Does the arrangement involve goods, items, or services of 
a type that are commonly or typically purchased by the health center, 
such that the arrangement results in measurable savings that will 
benefit a medically underserved population?
     If the arrangement involves a donation to the health 
center, would the donation result in the increased availability of an 
item, good, device, service, technology, or treatment needed by a 
medically underserved population but not previously available in 
sufficient quantities due to financial limitations?
     Does the health center need the donated items, goods, or 
services, or the loaned funds to satisfy the scope of its section 330 
grant?
    The arrangement described in the first commenter's example could 
contribute meaningfully, if it increased the availability of the 
service for the health center's medically underserved population. With 
respect to the second commenter, we observe that while an arrangement 
that conserves a health center's section 330 funding means the health 
center has more money available to provide or enhance services for a 
medically underserved population, there are many other ways that 
remuneration could maintain, increase, or enhance services for a 
medically underserved population without the direct savings of section 
330 funding. For example, if an arrangement allowed a health center to 
begin delivering an important new clinical service, which the health 
center was not previously able to provide, a meaningful benefit to a 
medically underserved population would likely be achieved without a 
direct monetary gain to the health center.
    Comment: A trade association had a concern regarding the 
significance of the list of factors in the preamble that we wrote 
``should be considered'' in determining whether an arrangement would 
result in a meaningful benefit to a medically underserved population. 
See 70 FR 38085. The commenter asked for confirmation that the factors 
in the list are only examples, and that it is not necessary to satisfy 
all of the factors to demonstrate a meaningful benefit under proposed 
Sec.  1001.952(w)(4) (Sec.  1001.952(w)(3) of the final rule).
    Response: The factors listed in the proposed rule and noted in the 
preceding response are examples of ways to analyze the existence of a 
meaningful benefit, and the commenter correctly understood that it is 
not necessary to satisfy each exemplary factor to establish the 
existence of a meaningful benefit to a medically underserved population 
under Sec.  1001.952(w)(3) of the final rule.
    Comment: A trade association commented that our requirement at 
proposed Sec.  1001.952(w)(4) that health centers apply ``reasonable, 
consistent, and uniform standards'' when determining whether an 
arrangement bestows a meaningful benefit for services provided to a 
medically underserved population provides insufficient guidance to 
health centers for structuring arrangements. The commenter also 
objected to the proposed requirement that health centers document 
evaluation of such standards. It expressed concern that these 
requirements would have a chilling effect on parties' participation in 
safe harbored arrangements, as parties would be unsure whether their 
standards would satisfy the requirements of the safe harbor. The 
commenter requested that we provide examples of acceptable standards 
and how to document them, or eliminate the requirement all together.
    Response: We intended the language ``reasonable, consistent and 
uniform standards'' to give health centers flexibility in assessing 
benefits to a medically underserved population, while at the same time 
requiring accountability and providing safeguards against abuse. Upon 
further consideration and consistent with our original intent, we have 
determined that proposed Sec.  1001.952(w)(4) (now Sec.  
1001.952(w)(3)) can be simplified. Under Sec.  1001.952(w)(3) of the 
final rule, parties need not develop or apply any separate 
``standards,'' nor document that they have applied them. They must, 
however, document the basis for the reasonable expectation of benefits 
to a medically underserved population prior to entering the 
arrangement. Parties may, as a matter of prudent business practice, 
develop standards that are reasonable, uniform, and consistently 
applied as part of the methodology they use in assessing the expected 
benefit to a medically underserved population. We have similarly 
changed the corresponding language in Sec.  1001.952(w)(4) of the final 
rule, which concerns the reevaluation of arrangements. With respect to 
the commenter's concern that proposed Sec.  1001.952(w)(4) (Sec.  
1001.952(w)(3) in the final rule) will chill participation in the safe 
harbor, we note that our approach here is consistent with several 
existing safe harbors that provide parties with flexibility to 
determine how to satisfy key conditions (e.g., how to determine fair 
market value). A health center can document its determination of a 
meaningful benefit to a medically underserved population, for example, 
by maintaining written or electronic records of the data and 
methodology used to assess the expected maintenance of, increase in, or 
enhanced quality of services to a medically underserved population and 
the outcome of such assessment. We believe that the documentation 
necessary to satisfy this requirement is consistent with that generally 
kept in the usual and customary course of a health center's business. 
For example, in many cases a health center's section 330 grant 
documents, in combination with the agreement required under Sec.  
1001.952(w)(1), may serve as the documentation of a sufficient benefit 
to a medically underserved population, to the extent they transparently 
document that a volume of items or services specified by the section 
330 grant requirements will be provided under the agreement. Parties 
with concerns about their specific practices can avail themselves of 
OIG's advisory opinion process.
5. Periodic Re-Evaluation of Arrangements
    Comment: A health network supported the requirement at proposed 
Sec.  1001.952(w)(5) (Sec.  1001.952(w)(4) of the final rule) that 
parties periodically re-evaluate arrangements. The commenter stated 
that it seems reasonable and useful for health centers participating in 
these arrangements to re-evaluate agreements periodically and document 
such factors as fair market value of equipment or costs of providing 
services. A trade association requested that we eliminate the 
requirement that an arrangement that, upon reevaluation,

[[Page 56640]]

fails to meet the benefit standard be terminated. This commenter also 
asked us to clarify that continuation of such an arrangement would not 
automatically constitute a violation of the anti-kickback statute.
    Response: We agree with these commenters. We have adopted the trade 
association's recommendation to eliminate the language in Sec.  
1001.952(w)(5) of the proposed rule that required noncompliant 
arrangements to be promptly terminated. We also confirm that a decision 
by a health center to continue participating in an arrangement that no 
longer satisfies the requirements of Sec.  1001.952(w)(3) of the final 
rule will not necessarily give rise to a violation of the anti-kickback 
statute. Rather, the continuation of such an arrangement would fall 
outside of the safe harbor, and its legality under the anti-kickback 
statute would be determined on a case-by-case basis, based on all the 
facts and circumstances, including the intent of the parties. Finally, 
we agree with the commenter that, depending on the arrangement, it 
would be reasonable and useful for health centers participating in 
these arrangements to re-evaluate agreements periodically and document 
such factors as fair market value of equipment or costs of providing 
services.

C. Comments on Additional Regulatory Standards

1. General Comments
    Comment: A trade association asserted that the regulatory standards 
OIG proposed in accordance with section 431 of MMA should be limited to 
the factors set forth in section 431 and should not include additional 
requirements. As discussed in our preamble to the proposed rule at 70 
FR 38083, in addition to the standards established by Congress, section 
431 of MMA authorizes OIG to add other standards or criteria consistent 
with Congress' intent in creating this safe harbor. The commenter 
stated that establishing additional safe harbor standards consistent 
with the anti-kickback statute contravenes the plain language of the 
statute and Congress' intent. The commenter asked that the regulatory 
standards created in accordance with section 431 not include additional 
requirements that health centers and their partners would have to meet 
to be consistent with the anti-kickback statute. Finally, the commenter 
contended that these standards wrongly ``reconsider'' whether the 
arrangements pose a risk of fraud and abuse. According to the 
commenter, by definition, all the arrangements described in the safe 
harbor pose a risk of fraud and abuse, which is why they require safe 
harbor protection in the first place.
    Response: We agree with the commenter's view that the regulatory 
standards we create in accordance with section 431 must be consistent 
with the language of section 431, and we believe that our regulations 
meet that test. Section 431 explicitly requires us to consider health 
center resources, patient freedom of choice, and independent medical 
judgment; however, it further states that these factors are ``among'' 
those to be considered and that ``the Secretary may also include other 
standards and criteria that are consistent with the intent of Congress 
in enacting the exception established under this section.'' Every safe 
harbor is established to protect arrangements that otherwise implicate 
the anti-kickback statute. Therefore, we believe Congress charged the 
Secretary with promulgating regulations implementing the health center 
safe harbor in a manner that furthers beneficial health center 
arrangements without posing an undue risk of fraud and abuse under the 
anti-kickback statute. This approach is consistent with our 
longstanding approach to safe harbor rulemaking. For instance, in our 
preamble to the proposed rule for the first ten safe harbors we stated 
that: ``[w]e have attempted in these proposed regulations to permit 
physicians to freely engage in business practices and arrangements that 
encourage competition, innovation and economy. However, we have added 
criteria to each `safe harbor' in order to reduce the potential for 
abuse.'' (50 FR 3088; January 23, 1989) Congress enacted section 431 in 
the context of this regulatory history. Moreover, we do not believe 
Congress intended to protect arrangements that pose significant risk to 
Federal health care programs or their beneficiaries. We believe our 
regulations directly and reasonably derive from the guidelines 
specifically enacted in section 431 and Congress' invitation to include 
other standards consistent with the establishment of the safe harbor. 
With respect to the commenter's final comment, historically, regulatory 
safe harbors were initiated in response to concerns that the anti-
kickback statute covered some relatively innocuous commercial 
arrangements. (See 50 FR 3088; January 23, 1989 and 56 FR 35952; July 
29, 1991) These safe harbors are meant to protect arrangements that do 
not pose undue risk for Federal health care programs or beneficiaries; 
they are not meant to protect arrangements that pose high risks to 
Federal health care programs.
2. Patient Freedom of Choice and Independent Medical Judgment
    Comment: A trade association sought clarification that proposed 
Sec. Sec.  1001.952(w)(6) and (8) (Sec. Sec.  1001.952(w)(5) and (7) of 
the final rule) would permit a health center to select a single 
supplier of particular goods or services if the health center followed 
the procurement rules applicable to health centers set forth at 45 CFR 
74.40 through 74.48. The commenter presented the scenario of a health 
center purchasing laboratory services where the health center has a 
choice of suppliers, which are equal in all respects except that one 
prospective supplier will offer free laboratory services for uninsured 
patients while the other will not. The commenter suggested that it may 
be appropriate for the health center to enter into an exclusive 
contract with the supplier that offers free services.
    Response: Where a health center purchases or receives a particular 
good or service from a supplier, the health center may limit the number 
of suppliers with which it contracts, in keeping with health center 
procurement rules. Nothing in this safe harbor is to the contrary. We 
agree that in some circumstances it would be appropriate for a health 
center to contract with one supplier (e.g., a single supplier of 
laboratory services), and that such an arrangement would not be likely 
to impinge unduly or significantly on the freedom of choice of patients 
seeking care at a section 330 health center. We have made clarifying 
revisions to Sec.  1001.952(w)(5) of the final rule to reflect that a 
Donor may not require a health center to refer patients to a particular 
individual or entity. Nothing in this provision limits a health 
center's ability to contract with one supplier consistent with the 
procurement rules.
    Similarly, proposed Sec.  1001.952(w)(8) (Sec.  1001.952(w)(7) of 
the final rule) prohibits a Donor from requiring the health center to 
forego arrangements with other prospective Donors, but does not 
prohibit the health center from entering into an exclusive arrangement 
with a provider or supplier when the health center so chooses, and when 
it can do so in compliance with relevant procurement rules. In the 
commenter's example, a health center can accept the offer of free 
laboratory services for uninsured patients under the safe harbor, 
provided all other safe harbor conditions are met. We emphasize that 
this safe harbor is unique to Federally Qualified Health Centers. In 
general,

[[Page 56641]]

arrangements where a provider or supplier offers free or discounted 
items or services to a potential referral source that would otherwise 
incur out-of-pocket costs for such items or services pose a substantial 
risk of fraud under the anti-kickback statute. Nevertheless, Congress 
enacted a law that protects such arrangements in the health center 
context, where the remuneration inures to the benefit of a section 330 
health center and its medically underserved patients, and where other 
appropriate safeguards are in place. Other similar arrangements outside 
the health center context are fundamentally different and pose 
substantial risk under the anti-kickback statute.
    Comment: A trade association offered mixed reactions to proposed 
Sec.  1001.952(w)(7) (Sec.  1001.952(w)(6) in the final rule), which 
provides that Donors who offer to provide goods, items, or services to 
health center patients cannot limit their acceptance of health center 
patient referrals based on a patient's insurance status. The commenter 
stated that asking Donors to accept all health center patients without 
regard to insurance status is a laudable goal, but expressed concern 
that this requirement would put prospective Donors at significant 
financial risk and could have a chilling effect on parties' willingness 
to participate in safe harbored arrangements. The commenter also stated 
that allowing Donors to ``impose reasonable limits on the aggregate 
volume or value of referrals it will accept'' might cause risk averse 
Donors to commit to serving a smaller number of health center patients 
than they otherwise would.
    Response: We are mindful of the commenter's concerns and we believe 
that the regulations strike an appropriate balance between preserving 
health center patients' access to care, allowing prospective Donors to 
limit their risk, and reducing the risk of parties abusing the safe 
harbor by ``cherry picking'' lucrative patients from the health 
centers. We believe a requirement that Donors that offer to furnish 
goods, items, or services to health center patients should do so for 
all health center patients without regard to insurance status is 
essential to effectuating Congress' intent that the safe harbor promote 
arrangements that provide a benefit to the health centers and the 
medically underserved populations they serve. We are mindful that this 
requirement could discourage prospective Donors from participating in 
safe harbored arrangements absent a way for them to limit their risk, 
which is why we have provided a mechanism for Donors to set a 
reasonable cap on the volume or value of items or services they will 
provide. Furthermore, nothing in Sec.  1001.952(w)(6) of the final rule 
precludes Donors from billing for such goods, items, or services in 
accordance with the Donor's usual billing practice (absent an agreement 
between the parties as provided for in Sec.  1001.952(w)(9)). The safe 
harbor does not protect arrangements through which Donors limit their 
financial risk by cherry picking which health center patients will 
receive their goods or services based on the patient's insurance 
status. For example, if a physician were to offer physician services to 
a health center, he or she could not condition the offer on treating 
only patients who are Federal healthcare program beneficiaries. 
However, the physician could cap the number of hours he or she would 
work at the health center. Similarly, an end stage renal disease 
facility cannot offer to provide free dialysis for one uninsured health 
center patient for every four insured patients the health center refers 
to the facility. However, the facility could offer to provide a fixed 
number of dialysis treatments to the health center. Finally, we 
clarified that Sec.  1001.952(w)(6) concerns goods, items, or services 
furnished by Donors to the health center, and not donations or loans.
    Comment: A health system commenter asked if the requirements of 
proposed Sec.  1001.952(w)(7) (Sec.  1001.952(w)(6) of the final rule) 
would apply to Donors providing remuneration in the form of loans or 
donations, since a patient cannot ``clinically qualify'' for a loan or 
donation.
    Response: Proposed Sec.  1001.952(w)(7) (Sec.  1001.952(w)(6) of 
the final rule) does not apply to Donors providing donations or loans 
to a health center. For clarity and consistency of meaning, we have 
replaced the term ``provide'' with the term ``furnish'' in Sec.  
1001.952(w)(6) of the final rule. As defined at 42 CFR 1000.10, 
``[f]urnished refers to items or services provided or supplied, 
directly or indirectly, by any individual or entity.'' We have further 
clarified the subsequent language in this paragraph by conforming it to 
reflect that the term ``furnish'' refers to items or services provided 
or supplied, not referrals accepted. We believe these changes better 
distinguish between (i) Donors who furnish items or services for health 
centers patients (and may bill insurers separately for some of these 
items or services), who must comply with Sec.  1001.952(w)(6) of the 
final rule if they want safe harbor protection, and (ii) Donors who 
provide health centers with donations or loans. We note that safe 
harbored donations or loans may not take into account the volume or 
value of Federal health care program referrals, in accordance with 
Sec.  1001.952(w)(1).
3. Patient Notification
    Comment: Two trade associations asked that we eliminate the patient 
notification requirement at proposed Sec.  1001.952(w)(9) (Sec.  
1001.952(w)(8) of the final rule). One commenter suggested that, if the 
requirement is retained, we distinguish providers of health care 
services from suppliers of goods and services since, in the commenter's 
opinion, it is less important to preserve patients' freedom of choice 
to select suppliers of health care goods and services. This commenter 
also questioned why this safe harbor requires patient notification when 
other safe harbors do not. Another trade association asserted that any 
patient notification requirement would be unworkable and would not 
significantly enhance patient freedom of choice.
    Response: We disagree with the commenters and decline to eliminate 
the notification requirement. We will not draw a distinction between 
providers and suppliers for purposes of this subparagraph because 
preserving patient freedom of choice is important for both providers 
and suppliers of health care items and services (we note that 
physicians are ``suppliers'' for Medicare Part B purposes. 42 CFR 
400.202. We believe a patient notification requirement is consistent 
with our specific charge from Congress to protect patient freedom of 
choice. Moreover, this is not the only safe harbor that requires 
patient notification. See, e.g., 42 U.S.C. 1001.952(v). As we noted in 
the preamble to the proposed rule, transparency will help protect the 
informed decision-making of patients, enhancing their ability to act as 
prudent consumers of health care services and preserving freedom of 
choice. (70 FR 38086; July 1, 2005) That said, we have simplified the 
requirements. Under the final rule, health centers must notify patients 
of their freedom of choice and provide information regarding the 
existence and nature of arrangements under this safe harbor to patients 
upon request.
    Comment: A trade association asked that we specify how to satisfy 
the patient notification requirement at proposed Sec.  1001.952(w)(9) 
(Sec.  1001.952(w)(8) of the final rule). The commenter asked us to 
confirm that health centers would be allowed to notify patients 
strictly through broad

[[Page 56642]]

disclosures and that an acceptable notification method would be to 
direct patients to a posted written disclosure notice.
    Response: We confirm that health centers can satisfy the 
notification requirement through broad disclosures. For example, 
directing patients to a written disclosure notice posted in a 
conspicuous place in the health center would be an acceptable 
disclosure method, provided that the written notice is reasonably 
calculated to provide effective notice and to be understood by the 
parties. However, since the most appropriate notification method is 
likely to vary from health center to health center, depending on the 
particular facts and circumstances, we believe it would be 
inappropriate for us to dictate a one-size-fits-all notification method 
to be used by all health centers. Accordingly, we further note that 
broad disclosures are not required. To further improve clarity, we 
replaced the general reference to arrangements under ``this paragraph'' 
with a specific cite to Sec.  1001.952(w)(1).
4. Rates Charged to Health Center Referrals
    Comment: We received several comments concerning proposed Sec.  
1001.952(w)(10) (Sec.  1001.952(w)(9) of the final rule), which gives 
health centers the option of requiring a Donor to charge a patient 
referred from the health center the same rate it charges other patients 
or a reduced rate. A trade association requested that the entire 
proposed provision be deleted from the safe harbor or, if retained, 
clarified as optional. The same trade association sought clarification 
that the provision would not preclude providers or suppliers from 
waiving or reducing cost sharing obligations for health center patients 
under the safe harbor at 42 CFR 1001.952(k).
    Response: We emphasize that proposed Sec.  1001.952(w)(10) (Sec.  
1001.952(w)(9) of the final rule) describes an optional standard. We 
have revised Sec.  1001.952(w)(9) of the final rule to make this 
elective clear. Health centers are not required to exercise this 
option, but they may choose to do so to ensure that Donors giving 
remuneration to a health center do not simply recoup the remuneration 
by overcharging health center patients. Our intent is to allow health 
centers to protect their patients from price gouging. (We note that a 
similar provision is included in the safe harbor for referral services 
at Sec.  1001.952(f).) We added this provision to ensure that health 
centers can protect their patients from being charged prices higher 
than they would be charged in the absence of the health center's 
participation in the safe harbored arrangement. We are concerned, for 
example, that Donors might otherwise seek to recoup part of the cost of 
remuneration offered to a health center by charging health center 
patients inflated rates. We confirm that nothing in the provision would 
preclude hospitals and health centers from offering health center 
patients waivers or reductions of cost sharing obligations, as 
permitted in the safe harbor for waiver of beneficiary coinsurance and 
deductible amounts at Sec.  1001.952(k). Moreover, health centers and 
other providers and suppliers can waive or reduce patients' cost 
sharing amounts based on individualized, good faith assessments of 
financial need. Section 1128A(i)(6)(A)(iii) of the Act.
    Comment: A health system asked whether the regulatory language 
``the same rate it charges other patients'' at proposed Sec.  
1001.952(w)(10) (Sec.  1001.952(w)(9) of the final rule) means the 
entity's customary charges (as defined at 42 CFR 413.13(a)) or the 
discounted rate the provider or supplier actually charges similarly 
situated patients.
    Response: We clarify that ``the same rate it charges other 
patients'' refers to the rate the provider or supplier actually charges 
a patient similarly situated to a patient referred from a health 
center. We have changed the regulatory text at Sec.  1001.952(w)(9) to 
reflect this clarification by inserting the words ``similarly 
situated'' after the word ``other.''

III. Regulatory Impact Statement

A. Regulatory Analysis

    We have examined the impact of this rule as required by Executive 
Order 12866, the Unfunded Mandates Reform Act of 1995, the Regulatory 
Flexibility Act (RFA) of 1980, and Executive Order 13132.
Executive Order 12866
    Executive Order 12866 directs agencies to assess all costs and 
benefits of available regulatory alternatives and, if regulations are 
necessary, to select regulatory approaches that maximize net benefits 
(including potential economic, environmental, public health, and safety 
effects; distributive impacts; and equity). A regulatory impact 
analysis must be prepared for major rules with economically significant 
effects (i.e., $100 million or more in any given year).
    This is not a major rule, as defined at 5 U.S.C. 804(2), and it is 
not economically significant since the overall economic effect of the 
rule is less than $100 million annually. This safe harbor is designed 
to allow health centers to enter into certain beneficial arrangements 
with individuals or entities providing goods, items, services, 
donations, loans, or a combination thereof to the health center. In 
doing so, this regulation would impose no requirements on any party. 
Health centers may voluntarily seek to comply with this provision so 
that they have assurance that participating in covered agreements will 
not subject them to liability under the anti-kickback statute. The safe 
harbor facilitates health centers' ability to provide important health 
care services to communities in need and helps these centers fulfill 
their mission as integral components of the health care safety net. We 
believe that the aggregate economic impact of this rule will be minimal 
and will have no effect on the economy or on Federal or State 
expenditures. To the extent that there is any economic impact, that 
impact will likely result in savings of Federal grant dollars.
Unfunded Mandates Reform Act
    Section 202 of the Unfunded Mandates Reform Act of 1995, Public Law 
104-4, requires that agencies assess anticipated costs and benefits 
before issuing any rule that may result in expenditures in any one year 
by State, local, or tribal governments, in the aggregate, or by the 
private sector, of $110 million. Since compliance with safe harbor 
requirements is voluntary, we believe that there are no significant 
costs associated with this safe harbor that will impose any mandates on 
State, local, or tribal governments or the private sector that would 
result in an expenditure of $110 million or more (adjusted for 
inflation) in any given year, and that a full analysis under the 
Unfunded Mandates Reform Act is not necessary.
Regulatory Flexibility Act
    The Regulatory Flexibility Act (RFA) and the Small Business 
Regulatory Enforcement and Fairness Act of 1996, which amended the RFA, 
require agencies to analyze options for regulatory relief of small 
entities. For purposes of the RFA, small entities include small 
businesses, certain nonprofit organizations, and small governmental 
jurisdictions. Individuals and States are not included in the 
definition of a small entity. In accordance with the RFA, some of the 
health centers that may avail themselves of the protections of the safe 
harbor are considered to be small entities.

[[Page 56643]]

    In addition, section 1102(b) of the Act requires us to prepare a 
regulatory impact analysis if a rule may have a significant impact on 
the operations of a substantial number of small rural hospitals. This 
analysis must conform to the provisions of section 604 of the RFA. 
While this safe harbor may have an impact on small rural hospitals, we 
believe that the aggregate economic impact of this rule will be 
minimal, since it is the nature of the violation and not the size or 
type of the entity that would result in a violation of the anti-
kickback statute. Moreover, the safe harbor should benefit small rural 
hospitals (and their patients) that have relationships with health 
centers by increasing their flexibility to engage in transactions 
involving goods, items, services, donations, and loans that result in 
conservation of Federal grant dollars and other funding without any 
risk under the anti-kickback statute. The safe harbor should 
effectively expand opportunities for health centers to engage in 
arrangements beneficial for fulfilling their mission. For these 
reasons, and because the vast majority of entities potentially affected 
by this rule do not engage in prohibited arrangements, schemes, or 
practices in violation of the law, we have concluded that this rule 
should not have a significant impact on a substantial number of small 
rural hospitals, and that a regulatory flexibility analysis is not 
required for this rulemaking.
Executive Order 13132
    Executive Order 13132, Federalism, establishes certain requirements 
that an agency must meet when it promulgates a rule that imposes 
substantial direct requirements or costs on State and local 
governments, preempts State law, or otherwise has Federalism 
implications. In reviewing this rule under the threshold criteria of 
Executive Order 13132, we have determined that this rule would not 
significantly limit the rights, roles, and responsibilities of State or 
local governments. We have determined, therefore, that a full analysis 
under Executive Order 13132 is not necessary.
    The Office of Management and Budget (OMB) has reviewed this rule in 
accordance with Executive Order 12866.

B. Paperwork Reduction Act

    In accordance with section 3506(c)(2)(A) of the Paperwork Reduction 
Act of 1995 (PRA), we are required to solicit public comments, and 
receive final OMB approval, on any information collection requirements 
set forth in rulemaking.
    In order to fairly evaluate whether an information collection 
should be approved by OMB, section 3506(c)(2)(A) of the PRA requires 
that we solicit comment on the following issues:
     Whether the information collection is necessary and useful 
to carry out the proper functions of the agency;
     The accuracy of the agency's estimate of the information 
collection burden;
     The quality, utility, and clarity of the information to be 
collected;
     Recommendations to minimize the information collection 
burden on the affected public, including automated collection 
techniques.
    On July 1, 2005, we solicited comment under this section upon 
publication of the 60-day notice of proposed rulemaking (70 FR 38081). 
We will publish the 30-day Federal Register notice soliciting public 
comment on each of these issues for the following sections of this 
document that contain information collection requirements following 
publication of this final rule.
    For an arrangement to fall within the safe harbor it will have to 
fulfill the following documentation requirements: (1) It must be set 
out in writing (Sec.  1001.952(w)(1)(i)(A)); (2) the written agreement 
must be signed by the parties (Sec.  1001.952(w)(1)(i)(B)); (3) the 
written agreement must cover, and specify the amount of, all goods, 
items, services, donations, or loans provided by the individual or 
entity to the health center Sec.  1001.952(w)(1)(i)(C)); (4) the health 
center must document its basis for its reasonable expectation that the 
arrangement will benefit a medically underserved population (Sec.  
1001.952(w)(3)); and (5) the health center, at reasonable intervals, 
must re-evaluate the arrangement to ensure that it is expected to 
continue to benefit a medically underserved population, and must 
document the re-evaluation contemporaneously (Sec.  1001.952(w)(4)).
    As required by section 3504(h) of the Paperwork Reduction Act of 
1995, we will submit a copy of this document to OMB for its review and 
approval of these information collection requirements.
    We believe that the documentation requirements necessary to enjoy 
safe harbor protection do not qualify as an added paperwork burden, 
because the requirements deviate minimally, if at all, from the 
information these entities would routinely collect in their normal 
course of business. The statute applies only to the health centers' 
receipt of goods, items, services, donations, or loans pursuant to a 
contract, lease, grant, loan, or other agreement. We believe it is 
usual and customary for health centers to memorialize contracts, 
leases, grants, loans, and other similar agreements in writing. 
Ensuring that such writings are comprehensive and that the actual 
business activities are accurately reflected by documentation are 
standard prudent business practices. The only documentation requirement 
of the safe harbor that potentially imposes an additional recordkeeping 
burden is the requirement that health centers document the statutorily 
mandated expected benefit to a medically underserved population. Since 
serving a medically underserved population is central to the underlying 
mission of the health centers and the section 330 grant program (and 
all health centers serve at least one such population), documentation 
of such benefit would seem to be a prudent business practice to ensure 
continued compliance, not only with the safe harbor, but also with the 
section 330 grant program.
    We note that although we require health centers to provide 
effective notification to patients reminding patients of their freedom 
to choose any willing provider or supplier and to provide information 
about safe harbored arrangements to patients who inquire, these 
disclosures need not be in writing. Instead, we require that health 
centers provide patient disclosures in a manner reasonably calculated 
to provide effective notice and to be understood by the patient. The 
type of notice provided may vary depending on the health center and its 
patients. We believe the notification requirement will achieve the goal 
of protecting patients without imposing an added paperwork burden 
because the notice need not be written. Moreover, we believe the 
notification requirement will be consistent with health centers' 
existing interest in protecting their vulnerable patient populations.
    It should be noted that compliance with a safe harbor under the 
Federal anti-kickback statute is voluntary, and no party is ever 
required to comply with a safe harbor. Instead, safe harbors merely 
offer an optional framework regarding how to structure business 
arrangements to ensure compliance with the anti-kickback statute. All 
parties remain free to enter into arrangements without regard to a safe 
harbor, so long as the arrangements do not involve unlawful payments 
for referrals under the anti-kickback statute.

List of Subjects in 42 CFR Part 1001

    Administrative practice and procedure, Fraud, Grant programs--
health, Health facilities, Health professions, Maternal and child 
health, Medicaid, Medicare.

[[Page 56644]]


0
Accordingly, 42 CFR part 1001 would be amended as set forth below:

PART 1001--[AMENDED]

0
1. The authority citation for part 1001 continues to read as follows:

     Authority: 42 U.S.C. 1302, 1320a-7, 1320a-7b, 1395u(j), 
1395u(k), 1395y(d), 1395y(e), 1395cc(b)(2)(D), (E) and (F), and 
1395hh; and sec. 2455, Pub.L. 103-355, 108 Stat. 3327 (31 U.S.C. 
6101 note).


0
2. Section 1001.952 is amended by republishing the introductory 
paragraph for this section and by adding a new paragraph (w) to read as 
follows:


Sec.  1001.952  Exceptions.

    The following payment practices shall not be treated as a criminal 
offense under section 1128B of the Act and shall not serve as the basis 
for an exclusion:
* * * * *
    (w) Health centers. As used in section 1128B of the Act, 
``remuneration'' does not include the transfer of any goods, items, 
services, donations or loans (whether the donation or loan is in cash 
or in-kind), or combination thereof from an individual or entity to a 
health center (as defined in this paragraph), as long as the following 
nine standards are met--
    (1) (i) The transfer is made pursuant to a contract, lease, grant, 
loan, or other agreement that--
    (A) Is set out in writing;
    (B) Is signed by the parties; and
    (C) Covers, and specifies the amount of, all goods, items, 
services, donations, or loans to be provided by the individual or 
entity to the health center.
    (ii) The amount of goods, items, services, donations, or loans 
specified in the agreement in accordance with paragraph (w)(1)(i)(C) of 
this section may be a fixed sum, fixed percentage, or set forth by a 
fixed methodology. The amount may not be conditioned on the volume or 
value of Federal health care program business generated between the 
parties. The written agreement will be deemed to cover all goods, 
items, services, donations, or loans provided by the individual or 
entity to the health center as required by paragraph (w)(1)(i)(C) of 
this section if all separate agreements between the individual or 
entity and the health center incorporate each other by reference or if 
they cross-reference a master list of agreements that is maintained 
centrally, is kept up to date, and is available for review by the 
Secretary upon request. The master list should be maintained in a 
manner that preserves the historical record of arrangements.
    (2) The goods, items, services, donations, or loans are medical or 
clinical in nature or relate directly to services provided by the 
health center as part of the scope of the health center's section 330 
grant (including, by way of example, billing services, administrative 
support services, technology support, and enabling services, such as 
case management, transportation, and translation services, that are 
within the scope of the grant).
    (3) The health center reasonably expects the arrangement to 
contribute meaningfully to the health center's ability to maintain or 
increase the availability, or enhance the quality, of services provided 
to a medically underserved population served by the health center, and 
the health center documents the basis for the reasonable expectation 
prior to entering the arrangement. The documentation must be made 
available to the Secretary upon request.
    (4) At reasonable intervals, but at least annually, the health 
center must re-evaluate the arrangement to ensure that the arrangement 
is expected to continue to satisfy the standard set forth in paragraph 
(w)(3) of this section, and must document the re-evaluation 
contemporaneously. The documentation must be made available to the 
Secretary upon request. Arrangements must not be renewed or 
renegotiated unless the health center reasonably expects the standard 
set forth in paragraph (w)(3) of this section to be satisfied in the 
next agreement term. Renewed or renegotiated agreements must comply 
with the requirements of paragraph (w)(3) of this section.
    (5) The individual or entity does not (i) Require the health center 
(or its affiliated health care professionals) to refer patients to a 
particular individual or entity, or (ii) restrict the health center (or 
its affiliated health care professionals) from referring patients to 
any individual or entity.
    (6) Individuals and entities that offer to furnish goods, items, or 
services without charge or at a reduced charge to the health center 
must furnish such goods, items, or services to all patients from the 
health center who clinically qualify for the goods, items, or services, 
regardless of the patient's payor status or ability to pay. The 
individual or entity may impose reasonable limits on the aggregate 
volume or value of the goods, items, or services furnished under the 
arrangement with the health center, provided such limits do not take 
into account a patient's payor status or ability to pay.
    (7) The agreement must not restrict the health center's ability, if 
it chooses, to enter into agreements with other providers or suppliers 
of comparable goods, items, or services, or with other lenders or 
donors. Where a health center has multiple individuals or entities 
willing to offer comparable remuneration, the health center must employ 
a reasonable methodology to determine which individuals or entities to 
select and must document its determination. In making these 
determinations, health centers should look to the procurement standards 
for recipients of Federal grants set forth in 45 CFR 74.40 through 
74.48.
    (8) The health center must provide effective notification to 
patients of their freedom to choose any willing provider or supplier. 
In addition, the health center must disclose the existence and nature 
of an agreement under paragraph (w)(1) of this section to any patient 
who inquires. The health center must provide such notification or 
disclosure in a timely fashion and in a manner reasonably calculated to 
be effective and understood by the patient.
    (9) The health center may, at its option, elect to require that an 
individual or entity charge a referred health center patient the same 
rate it charges other similarly situated patients not referred by the 
health center or that the individual or entity charge a referred health 
center patient a reduced rate (where the discount applies to the total 
charge and not just to the cost-sharing portion owed by an insured 
patient).
    For purposes of this paragraph, the term ``health center'' means a 
Federally Qualified Health Center under section 1905(l)(2)(B)(i) or 
1905(l)(2)(B)(ii) of the Act, and ``medically underserved population'' 
means a medically underserved population as defined in regulations at 
42 CFR 51c.102(e).
* * * * *

    Dated: May 8, 2007.
Daniel R. Levinson,
Inspector General.
    Approved: June 27, 2007.
Michael O. Leavitt,
Secretary.
[FR Doc. E7-19636 Filed 10-3-07; 8:45 am]
BILLING CODE 4152-01-P