Notice Regarding 340B Drug Pricing Program-Children's Hospitals, 45206-45211 [E9-21109]
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Federal Register / Vol. 74, No. 168 / Tuesday, September 1, 2009 / Notices
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[FR Doc. E9–20976 Filed 8–31–09: 2:25 pm]
BILLING CODE 6750–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Notice Regarding 340B Drug Pricing
Program—Children’s Hospitals
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AGENCY: Health Resources and Services
Administration, HHS.
ACTION: Final notice.
SUMMARY: Section 340B of the Public
Health Service Act (section 340B) and
section 1927(a) of the Social Security
Act (section 1927(a)) implement a drug
pricing program in which manufacturers
who sell covered outpatient drugs to
covered entities must agree to charge a
price that will not exceed an amount
determined under a statutory formula.
Section 6004 of the Deficit Reduction
Act of 2005 (Pub. L. 109–171) (section
6004) added certain qualifying
children’s hospitals to the list of
covered entities eligible to access 340B
discounted drugs. The purpose of this
notice is to inform interested parties of
final guidelines regarding the addition
of children’s hospitals that meet certain
requirements, specifically: (1) The
process for the registration of children’s
hospitals to the 340B Program; and (2)
the obligation of manufacturers to
provide the statutorily mandated
discount to those children’s hospitals.
FOR FURTHER INFORMATION CONTACT: Mr.
Jimmy Mitchell, Director, Office of
Pharmacy Affairs (OPA), Healthcare
Systems Bureau (HSB), Health
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Resources and Services Administration
(HRSA), 5600 Fishers Lane, Parklawn
Building, Room 10C–03, Rockville, MD
20857, or by telephone through the
Pharmacy Services Support Center at
1–800–628–6297.
DATES: Effective Date: September 1,
2009.
SUPPLEMENTARY INFORMATION:
(A) Background
Proposed guidelines for children’s
hospitals were announced in the
Federal Register at 72 FR 37250 on July
9, 2007. A comment period of 60 days
was established to allow interested
parties to submit comments. HRSA,
HSB, acting through the OPA, received
20 comments concerning the proposal.
Section 602 of Public Law 102–585,
the Veterans Health Care Act of 1992,
established section 340B of the Public
Health Service Act and added certain
implementation provisions for the 340B
Program to section 1927(a) of the Social
Security Act. Section 340B contains the
majority of the requirements for covered
entities participating in the 340B
Program, while the relevant provisions
of section 1927(a) of the Social Security
Act provide primarily for the
requirement that manufacturers provide
the statutorily mandated discount to
covered entities.
Section 340B contains a list of
covered entities that are eligible to
receive discounts through the 340B
Program. The list includes entities such
as Federally Qualified Health Centers,
State-operated AIDS drug purchasing
assistance programs, and certain
disproportionate share hospitals.
Children’s hospitals were not included
as covered entities under section 340B
in the Veterans Health Care Act of 1992
as enacted.
Section 6004 of the Deficit Reduction
Act (DRA), Pub. L. 109–171, added
certain qualifying children’s hospitals as
covered entities eligible to access 340B
discounted drugs. Section 6004 did not
amend section 340B (which contains
many of the requirements for covered
entities), however, the DRA provision
amended section 1927(a) of the Social
Security Act (which primarily contains
requirements for manufacturers’
participation) to add children’s
hospitals to the 340B Program.
To be eligible for the 340B Drug
Pricing Program, section 1927(a), as
amended by section 6004 of the DRA,
requires children’s hospitals to meet the
requirements of clauses (i) and (iii) of
section 340B(a)(4)(L) of the Public
Health Service Act, which contain
provisions for State or local government
affiliations and non-participation in
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group purchasing organizations. In
addition, children’s hospitals must meet
the requirements of clause (ii) of such
section, which contains requirements
for the provision of indigent care, if
such section ‘‘were applied by taking
into account the percentage of care
provided by the hospital to patients
eligible for medical assistance’’ under
Medicaid.
We received several comments in
support of the proposal. Supporting
comments agreed with the proposed
guidelines and that section 6004 of the
DRA brings eligible children’s hospitals
into the 340B program. Several
commenters agreed with requiring
children’s hospitals to demonstrate their
status as defined by the Social Security
Act section 1886(d)(1)(B)(iii) and to
obtain a Medicare provider number in
the 3300 series. Many comments
supported obtaining an independent
audit to certify eligibility requirements
and to help ensure program integrity.
Comments supported HRSA’s position
that current Pharmaceutical Pricing
Agreements (PPAs) are already broad
enough to include children’s hospitals
as covered entities.
Additional comments challenged
HRSA’s legal authority and compliance
with the Administrative Procedure Act
as well as contractual authority with
existing PPAs. Other comments raised
issues of retroactive discounts,
prevention of duplicate discounts, and
alternative eligibility criteria such as
using disproportionate patient
percentages and independent audits. All
comments discussed the potential
impacts on covered entities, patients,
and manufacturers.
The following section presents a
summary of all major comments,
grouped by subject, and a response to
each comment. All comments were
considered in developing this final
notice and changes were made to
content when appropriate.
(B) Comments and Responses
(1) HRSA’s Legal Authority
Comment: HRSA lacks authority to
add children’s hospitals to the 340B
program through guidelines.
Response: HRSA disagrees. The
Department publishes guidelines in the
Federal Register providing a public
comment period to obtain input into
guidance development. Congress did
not prescribe the process by which
children’s hospitals would be added
into the 340B program. HRSA has
authority to provide guidelines
interpreting the statute and its intended
administration of the 340B program.
The guidelines are not subject to the
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Administrative Procedure Act’s notice
and comment requirements; however,
the Department chose to solicit and
respond to public comments. These
guidelines help to fulfill the Secretary’s
obligation to provide for the operation
of the program under section 340B.
Comment: It is unclear that Congress
has authorized the Secretary to enter
into PPAs that include children’s
hospitals. Contractual obligations of the
PPA are directly tied to section 340B,
which has not been amended to include
children’s hospitals as covered entities.
Response: HRSA acknowledges that
section 6004 of the DRA did not amend
section 340B to include children’s
hospitals as covered entities. However,
Congress did add children’s hospitals to
the 340B program by amending section
1927(a) of the Social Security Act which
requires that manufacturers provide the
statutorily mandated discount to
covered entities. Congress specifically
defined the term covered entity as
including certain qualifying children’s
hospitals. Considering the statutory
scheme as a whole, it is clear that the
Secretary has been authorized to
include children’s hospitals within the
program.
Comment: Since the appropriate
legislative changes were not made, it is
out of the scope of authority of the
Secretary and HRSA to read the current
PPA as including children’s hospitals.
Response: The existing PPAs do not
need to be amended to include
children’s hospitals. The PPAs require
manufacturers to extend 340B pricing to
all covered entities listed by HRSA in its
database. The PPA also requires that it
be interpreted in a manner that best
effectuates the underlying statutory
scheme. As previously discussed,
including children’s hospitals as
covered entities for purposes of the PPA
best effectuates the statutory scheme
and therefore children’s hospitals are
covered entities for purposes of the
PPA.
(2) Certification of Eligibility
Comment: Clarify the Social Security
Act definition of children’s hospitals to
mean that in any fiscal year or calendar
year, no less than 80 percent of patient
days involve patients under 18 years of
age.
Response: We disagree with a
suggestion that HRSA utilize an 80
percent figure. It is unclear on what
basis such a figure would be
determined. The statute indicates that
section 1886(d)(1)(B)(iii) of the Social
Security Act defines the term children’s
hospital for purposes of 340B eligibility.
This section defines a children’s
hospital as ‘‘a hospital whose inpatients
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are predominantly individuals under 18
years of age.’’ In using the statutory
definition, HRSA has taken into account
the CMS interpretation of this provision
and the context of the 340B Drug Pricing
Program.
Comment: The guidelines should
require participating children’s
hospitals to demonstrate that the entity
is a children’s hospital as defined by the
Social Security Act and obtain a
Medicare provider number in the 3300
series identifying it as a children’s
hospital.
Response: We agree. The statute
defines ‘‘children’s hospitals’’ by
reference to section 1886(d)(1)(B)(iii) of
the Social Security Act. CMS has
reserved the 3300 series of Medicare
Provider Numbers for children’s
hospitals that meet the statutory
definition. The guidelines have been
changed accordingly to make this
clearer.
Comment: Clarify how the
disproportionate share adjustment
percentage eligibility criteria can be
applied to children’s hospitals since
children’s hospitals do not receive
Medicare disproportionate share
hospital (DSH) payment adjustments.
Children’s hospitals should be
permitted to rely on its disproportionate
patient percentage (DPP) as defined by
CMS for purposes of Medicaid. The DPP
formula demonstrating a percentage of
greater than 27.32 percent is just as
reliable as the required greater than
11.75 percent disproportionate share
adjustment percentage.
Response: HRSA agrees with the
comment that children’s hospitals that
do not receive Medicare DSH payment
adjustments may have difficulty in
showing their disproportionate share
adjustment percentage. As an
alternative, children’s hospitals can
show compliance with this requirement
if they provide independent verification
that if the disproportionate share
adjustment percentage were calculated,
it would be greater than 11.75 percent.
Under current law, one method for
reaching such a conclusion would be to
have a DPP greater than a threshold
amount that equates to a
disproportionate share adjustment
percentage greater than 11.75 percent.
DPP for this purpose is defined at 42
CFR 412.106 and is used in the current
applicable statutory formula to calculate
the disproportionate share adjustment
percentage for DSHs.
Comment: Many children’s hospitals
do not file any or full Medicare cost
reports. If no cost report exists,
children’s hospitals should be permitted
to rely on their own independent
auditors to confirm their DPP.
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Response: If a children’s hospital does
not file a Medicare cost report, HRSA
agrees that children’s hospitals can
confirm eligibility through the findings
of an independent auditor and
certification by the covered entity as to
the appropriate value of the hospital’s
disproportionate share adjustment
percentage, as based upon the DPP.
Comment: In addition to requiring
verification from independent auditors
from children’s hospitals that the entity
meets 340B eligibility requirements, a
comment was made to require this
verification to OPA annually because
the data used in the calculation to meet
the requirements of section
340B(a)(4)(L)(ii) are subject to change.
Response: HRSA agrees that there is a
need for ongoing verification as to
whether this eligibility requirement
continues to be met over time. After
enrollment, children’s hospitals, as do
all covered entities, have an ongoing
responsibility to immediately notify the
OPA in the event of any change in
eligibility for the 340B Drug Pricing
Program. No less than on an annual
basis, children’s hospitals will need to
demonstrate that the children’s hospital
continues to have the required
disproportionate share adjustment
percentage or DPP. The OPA will
provide additional guidance as it
develops its plans to annually certify
covered entities. To the extent that the
OPA is able to obtain periodic
documentation of data similar to that
provided by CMS with respect to DSHs,
it may notify the covered entity that
information need not be provided.
(3) Eligibility for Rebates Back to
February 8, 2006
Comment: The eligibility criteria for
receiving retroactive discounts are
overwhelming and confusing to both
manufacturers and covered entities.
HRSA should remove the ability to
receive retroactive discounts from the
final rule or, at a minimum, clearly
define these criteria.
Response: Although the statute can be
complex, we disagree that it is
overwhelming or that unilaterally
disallowing any ‘‘retroactive’’ discounts
is appropriate. The parties are in the
best position to understand and resolve
claims over these issues. In this
guidance, HRSA believes it has
provided an appropriate level of detail
as to its view on how covered entities
can qualify for rebates on purchase back
to February 8, 2006, the date of
enactment of the DRA.
Comment: HRSA should post on its
on-line database the date when a
children’s hospital satisfied the 340B
eligibility criteria for manufacturers to
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verify if and when the children’s
hospital was entitled to receive
retroactive discounts.
Response: HRSA does not currently
plan to provide the eligibility date on its
Web site for purposes of retroactive
rebates. HRSA intends to follow the
current practice of listing the date of
eligibility for direct purchase under the
340B Drug Pricing Program as is
consistent with the purpose of that
database. The addition of retroactivity
dates would be outside the established
purpose of the database and lead to
potential confusion. If a covered entity
and manufacturer are unable to agree on
the date that the covered entity
complied with program requirements or
otherwise disagree, HRSA believes that
it is most appropriate to follow its
published dispute procedures that
require the parties to resolve any
disputes in good faith. HRSA’s first
priority is to have eligible children’s
hospitals register for the 340B Drug
Pricing Program. HRSA has concluded
that this approach is the most efficient
and that HRSA will assist parties to
resolve disputes through the published
dispute resolution process to the extent
resources permit.
Comment: HRSA should clarify
‘‘appropriate’’ documentation to
demonstrate that drugs did not generate
Medicaid rebates.
Response: This is a fact-specific
inquiry that may vary from case to case
and State to State. The children’s
hospital should demonstrate that the
covered outpatient drugs for which it
seeks retroactive discounts were not
subject to Medicaid rebates because they
were not billed to Medicaid or it can
otherwise show the State did not seek
a rebate on the drugs for which a
retroactive claim is sought.
Comment: Children’s hospitals lack
access to Medicaid drug rebate invoices/
claims data needed to establish the
requirement that covered outpatient
drugs did not generate Medicaid rebates
during retroactive periods.
Response: HRSA believes it
appropriate to require that children’s
hospitals seeking refunds provide
sufficient factual evidence to
demonstrate compliance with statutory
requirements. Children’s hospitals
seeking retroactive discounts should
have access to records of which drugs
were billed to Medicaid and which
drugs were not billed to Medicaid.
HRSA suggests that children’s hospitals
consider contacting State Medicaid
agencies for supporting documentation
as is appropriate.
Comment: HRSA should coordinate
with CMS to provide guidance regarding
monthly Average Manufacturer Price
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(AMP) and quarterly Average Sales
Price (ASP) calculations already
submitted, if retroactive discounts are
given.
Response: HRSA will do what it
reasonably can to assist in the process;
however, the issue of resolving whether
retroactive discounts are appropriate
should be resolved to the full extent
possible by the covered entities and
manufacturers. Manufacturers will need
to consult with CMS with respect to the
separate issue on how to handle
calculations reported to CMS.
Comment: Children’s hospitals should
not be penalized for use of Group
Purchasing Organizations (GPOs) during
the long interval that has elapsed since
enactment of section 6004. Initially,
HRSA allowed DSHs to use GPOs and
to receive 340B retroactive discounts as
long as discounts were not for drugs
obtained through the GPO. Similarly,
children’s hospitals should be eligible to
receive retroactive discounts for covered
outpatient drugs that were not
purchased through a GPO.
Response: HRSA disagrees and finds
the proposed treatment of retroactive
rebates to be inconsistent with the
applicable standards for DSHs. The
statute makes clear that children’s
hospitals must meet the same criteria
applicable to DSHs. In 1994, final
guidance was published on the GPO
exclusion that expressly provides that
any participation in a GPO or other
group purchasing arrangement for
covered outpatient drugs by a DSH
results in loss of eligibility as a covered
entity. HRSA believes that under the
statute and under current guidance it
should exclude from eligibility for
retroactive rebates any purchases while
the children’s hospital purchased
covered outpatient drugs through a GPO
or other purchasing arrangement.
The guideline for retroactive rebates
published in 1994 (59 FR 25110) was
consistent with the GPO exclusion
guideline in place for the period of
retroactivity. Likewise, this guideline
for retroactive rebates is consistent with
the GPO exclusion guideline in place for
the period of retroactivity.
Comment: Retroactive discounts
should only apply to children’s
hospitals that comply with statutory
prohibition against use of a GPO.
Furthermore, a comment was received
stating that children’s hospital should
not be able to request retroactive rebates
on a covered outpatient drug that was
not purchased under a GPO contract if
the entity used a GPO contract for other
covered outpatient drugs during that
same time period.
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Response: HRSA agrees and has
changed the guidelines to make this
issue clear.
Comment: HRSA should be required
to establish a process to document the
eligibility and compliance of these new
entities for any time period of eligibility,
including retroactive periods. HRSA
should create an audit or certification
process to determine the actual date that
the facility met all requirements.
Manufacturers should be allowed to
audit the processes and documentation
before they are obligated to provide the
retroactive discounts.
Response: HRSA believes that the
process outlined in the guidelines
provides enough safeguards to ensure
program integrity. To the extent that a
manufacturer has a specific concern
about a covered entity’s status, the
manufacturer should bring those
concerns to HRSA’s attention.
Manufacturers also have the option of
bringing a dispute through the dispute
resolution process as addressed in
previous guidance (61 FR 65406). The
issue of manufacturer audits has also
been previously addressed in finalized
guidance (61 FR 65406).
Comment: HRSA should shorten the
proposed 120-day period allowed to
submit requests for retroactive discounts
to 30 days, similar to its Federal
Register notice dated May 13, 1994,
following the enactment of section 340B
in 1992, where HRSA permitted eligible
covered entities to request retroactive
discounts within 30 days of publication
of guidelines.
Response: While HRSA understands
that after enactment of the 340B statute
and the implementation of the initial
guidances, there was only a 30-day
retroactivity period, there are materially
different circumstances between the
situations in 1994 and today. HRSA
must take into account the potential
time necessary to obtain sufficient
evidence to demonstrate eligibility
(requirements which did not exist in
1994) as well as the delay between the
time of application to the 340B Drug
Pricing Program and listing in the
Covered Entity Database at the
beginning of the quarter. Upon further
review, taking into account changes to
this final guidance, HRSA has
determined that in order to ensure that
all eligible hospitals have reasonable
time they should have three full
calendar quarters after publication
during which they must get registered
and officially listed on the 340B
Covered Entity Database. To be eligible
a children’s hospital must register and
be listed on 340B Covered Entity
Database within one year of publication
of this notice. This amount of time will
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ensure that all eligible children’s
hospitals will have reasonable time to
obtain the necessary documentation,
enroll, and be listed on the 340B Drug
Pricing Program Database as eligible to
purchase under 340B. Children’s
hospitals will need to abide by all
applicable deadlines for registration and
will only be added to the list at the time
of standard quarterly updates. Once
listed on the 340B Drug Pricing Program
Database, a children’s hospital will have
30 days to notify manufacturers in
writing to preserve their claims.
(4) Eligibility of Off-site Facilities of
Children’s Hospitals
Comment: HRSA did not address how
off-site locations of children’s hospitals
may participate in 340B. The DSH
requirement states that the off-site
location be an ‘‘integral’’ part of the
hospital and be reimbursable on the
Medicare cost report. HRSA should be
partially guided by Medicare providerbased standards to establish an
alternative to the cost report for off-site
facilities of children’s hospitals to be
eligible for 340B.
Response: To the extent possible,
eligibility for off-site locations will be
determined through the same method
applied for DSHs in the 340B Program.
Additional clarification on this issue
has been provided in the final guidance.
(5) Hemophilia Treatment Centers
Comment: Several commenters asked
that HRSA require, as prerequisite, that
children’s hospitals agree to maintain
Hemophilia Treatment Centers as
independent purchasers under 340B.
Response: HRSA does not find that
such a requirement is necessary to
ensure against duplicate discounts or
diversion, and does not find sufficient
basis to issue such a requirement in this
guidance.
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(6) Miscellaneous Comments
Comment: There should be a dispute
resolution process if a manufacturer has
reason to believe that HRSA’s
determination of eligibility period for a
children’s hospital is incorrect.
Response: HRSA is not initially
making such a determination. HRSA
does have guidance on its dispute
resolution process.
Comment: HRSA should require
explicitly that children’s hospitals abide
by program guidance relating to the
patient definition.
Response: HRSA agrees and finds that
the guidance as proposed already makes
that explicit.
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(C) Obligation of Manufacturers To
Provide 340B Discounts to Children’s
Hospitals
(2) Certification by Children’s Hospitals
Prior to 340B Drug Pricing Program
Entry
Section 1927(a)(5)(A) of the Social
Security Act requires manufacturers to
enter into agreements with the Secretary
that meet the requirements of section
340B with respect to covered outpatient
drugs purchased by a covered entity.
Section 1927(a)(5)(B), as amended by
section 6004, defines covered entities
for purposes of section 1927(a)(5) as
those covered entities listed in the
Public Health Service Act and certain
children’s hospitals. As section
1927(a)(5)(A) requires manufacturers to
enter into agreements ‘‘with respect to
covered outpatient drugs purchased by
a covered entity,’’ and covered entity is
defined as including children’s
hospitals for purposes of section 1927,
manufacturers are required to extend
340B pricing to eligible children’s
hospitals.
The PPAs between the Secretary and
each manufacturer require
manufacturers to provide 340B
discounted covered outpatient drugs to
covered entities. Given the clear
congressional intent in section 6004 to
expand the category of covered entities,
the PPAs currently in place effectively
require manufacturers to provide 340B
discounts to children’s hospitals
without need for further amendment to
currently existing PPAs.
As with other covered entities, prior
to entry into the 340B Drug Pricing
Program, children’s hospitals will be
required to provide OPA with a
certification regarding several different
program requirements. As a threshold
matter, a hospital wishing to qualify for
the 340B Program as a children’s
hospital must demonstrate that the
hospital is a ‘‘children’s hospital’’ as
defined by section 6004. Section 6004
requires that a hospital wishing to
qualify as a children’s hospital covered
entity must satisfy the definition of
‘‘children’s hospital’’ contained in
section 1886(d)(1)(B)(iii) of the Social
Security Act; and meet minimum
requirements for the receipt of an
additional payment under Medicare
pursuant to section 1886(d)(5)(F)(i) of
the Social Security Act (if such clause
were applied to the children’s hospital
while taking into account the percentage
of care provided by the hospital to
Medicaid patients).
(D) Process for Admission of Children’s
Hospitals to the 340B Program
(1) Children’s Hospitals Participation
Children’s hospitals participation in
the 340B Drug Pricing Program is
voluntary. Consistent with the
participation of other covered entities,
once a children’s hospital has elected to
participate in the program, it must wait
to enter or withdraw from the program
until the next official update of the 340B
covered entity database. Participating
children’s hospitals must comply with
all program guidelines for covered
entities until the date they are removed
from the 340B covered entity database.
The OPA will accept applications from
children’s hospitals for entry into the
340B Program as of the date of
publication of the final notice of these
guidelines. Hospitals that submitted
documentation seeking recognition as a
children’s hospital eligible for the 340B
Drug Pricing Program prior to the
publication of the guidance should
apply again in accordance with the
procedures described in this guidance.
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(i) Certify That the Hospital Is a
Children’s Hospital as Defined by
Statute
Given the reliance of section 6004 on
Medicare payment provisions for the
definition of ‘‘children’s hospital’’ and
the requirement that a children’s
hospital must demonstrate that they
would meet the same requirements as a
DSH, if they were eligible for DSH
payments, a hospital will need to
demonstrate that it has been assigned a
Medicare provider number identifying
the hospital as a ‘‘children’s hospital’’
(i.e., a hospital with a 3300 series
Medicare provider number).
(ii) Certify That the Hospital Will Abide
by All Requirements of Section 340B of
the Public Health Service Act
Prior to entry into the 340B Program,
a children’s hospital must certify that it
will abide by all the requirements of
section 340B that all other covered
entities abide by (e.g., prohibition on
resale of covered outpatient drugs;
prohibition on duplicate discounts or
rebates). While children’s hospitals are
not explicitly mentioned in section
340B, it is implicit in section 1927(a) of
the Social Security Act that children’s
hospitals abide by the requirements of
section 340B. Section 1927(a) provides
that manufacturers must have entered
into agreements with the Secretary that
meet the requirements of section 340B
and several of the provisions contained
in these agreements concern covered
entities’ compliance with provisions of
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section 340B. Furthermore, it is within
the Secretary’s authority under section
340B to create guidelines necessary for
the implementation of the program.
Unless children’s hospitals are subject
to all of the same rules as other covered
entities, the inclusion of children’s
hospitals in the 340B Program would be
difficult, if not impossible.
(iii) Certify Compliance With
340B(a)(4)(L) as Modified by Section
6004 of the DRA
Prior to entry into the 340B Program,
a children’s hospital must certify
compliance (along with the date of
compliance) with clauses (i), (ii), and
(iii) of section 340B(a)(4)(L) (in
accordance with section 1927(a)(5)(B) of
the Social Security Act) in the following
manner:
(A) Meets the requirements of section
340B(a)(4)(L)(i).
To comply with the requirements of
section 340B(a)(4)(L)(i), a children’s
hospital will have to certify (and
include such supporting documentation
as requested by OPA) that the hospital
is (1) owned or operated by a unit of
State or local government; (2) is a public
or private non-profit corporation which
is formally granted governmental
powers by a unit of State or local
government; or (3) is a private nonprofit hospital under contract with State
or local government to provide health
care services to low income individuals
who are not eligible for Medicare or
Medicaid.
(B) Meets the requirements of section
340B(a)(4)(L)(ii).
To comply with section
340B(a)(4)(L)(ii), as modified by section
6004, a children’s hospital will have to
certify (and include such supporting
documentation as requested by OPA)
that the children’s hospital (1) is located
in an urban area, has 100 or more beds,
and can demonstrate that its net
inpatient care revenues (excluding any
of such revenues attributable to
Medicare), during the cost reporting
period in which the discharges occur,
for indigent care from State and local
government sources and Medicaid
exceed 30 percent of its total of such net
inpatient care revenues during the
period; or (2) for the most recent cost
reporting period that ended before the
calendar quarter involved, had a
disproportionate share adjustment
percentage (as determined under section
1886(d)(5)(F) of the Social Security Act)
greater than 11.75 percent.
Supporting documentation must
include a signed statement by an
appropriate official (e.g., Chief Financial
Officer) of the children’s hospital that
he/she is familiar with the requirements
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17:18 Aug 31, 2009
Jkt 217001
under section 340B(a)(4)(L)(ii), has
examined the documentation, and
certifies that to the best of his/her
knowledge that the children’s hospital
satisfies the requirements. In addition,
the documentation must include: (1) An
official document from the Department
of Health and Human Services (HHS) or
a HHS contractor that is authorized to
make official determinations, showing
that the children’s hospital meets one or
both criterion listed above; (2) if the
organization files a Medicare cost
report, the report filed does not contain
a disproportionate share adjustment
percentage, and the report includes
sufficient information to calculate the
disproportionate share adjustment
percentage, include a copy of those
pages of the filed Medicare cost report
with the data necessary to calculate the
disproportionate share adjustment
percentage; or (3) if the organization
does not file a Medicare cost report with
sufficient information to calculate the
disproportionate share adjustment
percentage, a statement from a qualified
independent auditor certifying that the
auditor performed an audit on the
records of the children’s hospital, that
the auditor is familiar with Federal rules
and regulations relevant to its findings,
and found that the hospital would meet
one or both of the criterion in section
340B(a)(4)(L)(ii), as modified by section
6004 (described in the previous
paragraph). The supporting
documentation for (1), (2) or (3) should
identify the basis for that conclusion
including the actual percentage value
upon which the determination is made
(e.g., disproportionate patient
percentage defined at 42 CFR section
412.106), a concise description of any
mathematical calculations, and the
quarter for which the determination was
made. The children’s hospital should
notify OPA if (1), (2) or (3) result in
different conclusions as to eligibility of
the children’s hospital.
(C) Meets the requirements of section
340B(a)(4)(L)(iii).
To comply with section
340B(a)(4)(L)(iii), a children’s hospital
will have to certify that it will not
participate in a group purchasing
organization (GPO) or group purchasing
arrangement for covered outpatient
drugs as of the effective date of
participation as listed in the 340B
covered entity database.
(3) Inclusion of Children’s Hospitals’
Off-Site Outpatient Facilities
Children’s hospitals must meet the
applicable requirements for DSHs as
described in the guidance published in
59 FR 47884 (Sept. 19, 1994).
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(i) Children’s Hospitals That File
Medicare Cost Reports With CMS
Children’s hospitals that file Medicare
cost reports will be required to utilize
the same process to add outpatient
facilities as DSHs (59 FR 47884). A
children’s hospital, eligible for the 340B
Drug Pricing Program, must first request
that the OPA include in its covered
entity database the outpatient facilities
that are included as reimbursable in its
Medicare cost report. A list of these
outpatient facilities along with Medicare
and Medicaid billing status information
must be included with the request.
Second, an appropriate official (e.g.,
Chief Financial Officer) of the children’s
hospital must sign a statement that he/
she is familiar with CMS guidelines
concerning Medicare certification of
hospital components as one cost center,
has examined the list of outpatient
facilities, and certifies that the facilities
are correctly included on the Medicare
cost report of the children’s hospital.
When these outpatient facilities are
added to the master list of eligible and
participating covered entities, the offsite facilities will be able to access 340B
Drug Program pricing. Outpatient
facilities that are not included as
reimbursable on the Medicare cost
report or file independent Medicare cost
reports will not be eligible for 340B
pricing as part of the children’s hospital.
(ii) Children’s Hospitals That Do Not
File Medicare Cost Reports With CMS
Children’s hospitals that do not file a
Medicare cost report with CMS must
first request that the OPA include in its
covered entity database the outpatient
facilities that are integral parts of the
hospital. A list of these outpatient
facilities along with Medicaid billing
status information must be included
with the request. Second, an appropriate
official (e.g., Chief Financial Officer) of
the children’s hospital must sign a
statement that he/she is familiar with
CMS guidelines concerning Medicare
certification of hospitals as a cost center,
has examined the list of outpatient
facilities, and certifies that each facility
is an integral part of the children’s
hospital whose patients are considered
patients of the children’s hospital,
according to the most current published
guidelines on patient definition, and
would have been correctly included on
the Medicare cost report if the hospital
filed such a report and that the
outpatient facility meets the
requirements of a provider-based facility
within a DSH under 42 CFR 413.65.
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mstockstill on DSKH9S0YB1PROD with NOTICES
(E) Annual Re-Certification by
Children’s Hospitals To Maintain
Eligibility Status in 340B Drug Pricing
Program
Children’s hospitals have an ongoing
responsibility to immediately notify
OPA in the event of any change in
eligibility for the 340B Drug Pricing
Program. No less than on an annual
basis, children’s hospitals will need to
demonstrate continued maintenance of
the required disproportionate share
adjustment percentage or
disproportionate patient percentage.
OPA will provide additional guidance
as it gains experience and develops its
plans to annually certify covered
entities. To the extent that OPA is able
to obtain periodic documentation of
such data similar to that provided by
CMS with respect to DSHs, it may notify
the covered entity that such information
need not be provided.
(F) Eligibility for Discounts Back to
February 8, 2006
Section 6004 of the DRA indicates
that the amendment authorizing entry of
children’s hospitals into the 340B
Program ‘‘shall apply to drugs
purchased on or after the date of the
enactment of this Act.’’ The DRA
provision was enacted on February 8,
2006. Therefore, once children’s
hospitals are admitted to the 340B
Program and listed on the Covered
Entity Database, they are eligible for
340B drug pricing back to February 8,
2006. However, a children’s hospital
will be eligible for such retroactive
discounts only to the extent that it has
satisfied all requirements for
participation in the 340B program back
to the date discounts are requested.
Children’s hospitals may request
retroactive discounts (discounts,
rebates, or account credit) directly from
pharmaceutical manufacturers for
covered outpatient drugs when all the
following conditions are satisfied:
(1) The children’s hospital is listed on
the 340B Covered Entity Database as
eligible to purchase under 340B within
one year of publication of this notice.
(2) The children’s hospital sent a
request in writing to each manufacturer
of the drug(s) for which retroactive
discounts are sought within 30 days of
the children’s hospital having been
listed as eligible to purchase under 340B
on the 340B Covered Entity Database;
(3) The covered outpatient drugs must
have been purchased on or after
February 8, 2006;
(4) The covered outpatient drugs must
not have generated Medicaid rebates
(the children’s hospital must have
appropriate documentation to
demonstrate this);
VerDate Nov<24>2008
17:18 Aug 31, 2009
Jkt 217001
(5) The covered outpatient drugs must
not have been sold or transferred to a
person who was not a patient of the
children’s hospital; and
(6) The covered outpatient drugs must
have been purchased on or after the date
on which the children’s hospital
satisfied all requirements for
participation in the 340B Program as
outlined in section (D) of this notice.
In order to satisfy the last condition
listed above, a children’s hospital must
be able to demonstrate, at a minimum,
that as required by section
340B(a)(4)(L)(iii) of the Public Health
Service Act, the children’s hospital did
not have a group purchasing agreement
for covered outpatient drugs and
satisfied the requirements of section
340B(a)(4)(L)(i) and 340B(a)(4)(L)(ii) at
the time the covered outpatient drugs
for which rebates are requested were
purchased. Participation in a GPO for
any covered outpatient drugs would
disqualify a children’s hospital for
retroactive rebates during any quarter
that the children’s hospital purchased
any covered outpatient drug through a
GPO or other group purchasing
arrangement. Consistent with section
340B(a)(5)(C) of the Public Health
Service Act, children’s hospitals must
have auditable records that support
claims for retroactive discounts and
permit the Government or
manufacturers to audit those records (in
accordance with procedures established
by the Secretary relating to the number
scope and duration of such audits (61
FR 65406)).
In fulfilling the conditions listed
above, any children’s hospital that
believes it is entitled to retroactive
discounts may preserve its rights by
sending manufacturers a letter
requesting such refunds, explaining
how they meet the requirements in this
notice, and providing adequate
documentation of purchases within 30
days being listed on the 340B Covered
Entity Database as eligible. Such
children’s hospitals should engage in
good faith efforts to resolve any disputes
with manufacturers. To the extent they
are unable to resolve disputes and wish
to pursue further involvement with the
OPA, they are encouraged to follow the
guidance on the dispute resolution
process as described in the Federal
Register (61 FR 65406).
Dated: August 26, 2009.
Mary K. Wakefield,
Administrator.
[FR Doc. E9–21109 Filed 8–31–09; 8:45 am]
BILLING CODE 4165–15–P
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45211
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
SUMMARY: This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project: ‘‘Health
IT Community Tracking Study 2009.’’ In
accordance with the Paperwork
Reduction Act of 1995, 44 U.S.C.
3506(c)(2)(A), AHRQ invites the public
to comment on this proposed
information collection.
This proposed information collection
was previously published in the Federal
Register on June 30th, 2009 and allowed
60 days for public comment. No
comments were received. The purpose
of this notice is to allow an additional
30 days for public comment.
DATES: Comments on this notice must be
received by October 1, 2009.
ADDRESSES: Written comments should
be submitted to: AHRQ’s OMB Desk
Officer by fax at (202) 395–6974
(attention: AHRQ’s desk officer) or by email at OIRA_submission@omb.eop.gov
(attention: AHRQ’s desk officer).
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at doris.lefkowitz@ahrg.hhs.gov.
SUPPLEMENTARY INFORMATION:
Proposed Project
Health IT Community Tracking Study
2009
Electronic prescribing (e-prescribing)
is a central focus of efforts to promote
health information technology (IT) and
is of particular interest to AHRQ
because of its potential to improve
patient safety by reducing medication
errors. Despite many public- and
private-sector initiatives to support eprescribing, to date, physician adoption
and use has been limited (Friedman,
Schueth and Bell 2009). Recently,
Section 132 of the Medicare
Improvements for Patients and
E:\FR\FM\01SEN1.SGM
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Agencies
[Federal Register Volume 74, Number 168 (Tuesday, September 1, 2009)]
[Notices]
[Pages 45206-45211]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-21109]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Notice Regarding 340B Drug Pricing Program--Children's Hospitals
AGENCY: Health Resources and Services Administration, HHS.
ACTION: Final notice.
-----------------------------------------------------------------------
SUMMARY: Section 340B of the Public Health Service Act (section 340B)
and section 1927(a) of the Social Security Act (section 1927(a))
implement a drug pricing program in which manufacturers who sell
covered outpatient drugs to covered entities must agree to charge a
price that will not exceed an amount determined under a statutory
formula. Section 6004 of the Deficit Reduction Act of 2005 (Pub. L.
109-171) (section 6004) added certain qualifying children's hospitals
to the list of covered entities eligible to access 340B discounted
drugs. The purpose of this notice is to inform interested parties of
final guidelines regarding the addition of children's hospitals that
meet certain requirements, specifically: (1) The process for the
registration of children's hospitals to the 340B Program; and (2) the
obligation of manufacturers to provide the statutorily mandated
discount to those children's hospitals.
FOR FURTHER INFORMATION CONTACT: Mr. Jimmy Mitchell, Director, Office
of Pharmacy Affairs (OPA), Healthcare Systems Bureau (HSB), Health
Resources and Services Administration (HRSA), 5600 Fishers Lane,
Parklawn Building, Room 10C-03, Rockville, MD 20857, or by telephone
through the Pharmacy Services Support Center at 1-800-628-6297.
DATES: Effective Date: September 1, 2009.
SUPPLEMENTARY INFORMATION:
(A) Background
Proposed guidelines for children's hospitals were announced in the
Federal Register at 72 FR 37250 on July 9, 2007. A comment period of 60
days was established to allow interested parties to submit comments.
HRSA, HSB, acting through the OPA, received 20 comments concerning the
proposal.
Section 602 of Public Law 102-585, the Veterans Health Care Act of
1992, established section 340B of the Public Health Service Act and
added certain implementation provisions for the 340B Program to section
1927(a) of the Social Security Act. Section 340B contains the majority
of the requirements for covered entities participating in the 340B
Program, while the relevant provisions of section 1927(a) of the Social
Security Act provide primarily for the requirement that manufacturers
provide the statutorily mandated discount to covered entities.
Section 340B contains a list of covered entities that are eligible
to receive discounts through the 340B Program. The list includes
entities such as Federally Qualified Health Centers, State-operated
AIDS drug purchasing assistance programs, and certain disproportionate
share hospitals. Children's hospitals were not included as covered
entities under section 340B in the Veterans Health Care Act of 1992 as
enacted.
Section 6004 of the Deficit Reduction Act (DRA), Pub. L. 109-171,
added certain qualifying children's hospitals as covered entities
eligible to access 340B discounted drugs. Section 6004 did not amend
section 340B (which contains many of the requirements for covered
entities), however, the DRA provision amended section 1927(a) of the
Social Security Act (which primarily contains requirements for
manufacturers' participation) to add children's hospitals to the 340B
Program.
To be eligible for the 340B Drug Pricing Program, section 1927(a),
as amended by section 6004 of the DRA, requires children's hospitals to
meet the requirements of clauses (i) and (iii) of section 340B(a)(4)(L)
of the Public Health Service Act, which contain provisions for State or
local government affiliations and non-participation in group purchasing
organizations. In addition, children's hospitals must meet the
requirements of clause (ii) of such section, which contains
requirements for the provision of indigent care, if such section ``were
applied by taking into account the percentage of care provided by the
hospital to patients eligible for medical assistance'' under Medicaid.
We received several comments in support of the proposal. Supporting
comments agreed with the proposed guidelines and that section 6004 of
the DRA brings eligible children's hospitals into the 340B program.
Several commenters agreed with requiring children's hospitals to
demonstrate their status as defined by the Social Security Act section
1886(d)(1)(B)(iii) and to obtain a Medicare provider number in the 3300
series. Many comments supported obtaining an independent audit to
certify eligibility requirements and to help ensure program integrity.
Comments supported HRSA's position that current Pharmaceutical Pricing
Agreements (PPAs) are already broad enough to include children's
hospitals as covered entities.
Additional comments challenged HRSA's legal authority and
compliance with the Administrative Procedure Act as well as contractual
authority with existing PPAs. Other comments raised issues of
retroactive discounts, prevention of duplicate discounts, and
alternative eligibility criteria such as using disproportionate patient
percentages and independent audits. All comments discussed the
potential impacts on covered entities, patients, and manufacturers.
The following section presents a summary of all major comments,
grouped by subject, and a response to each comment. All comments were
considered in developing this final notice and changes were made to
content when appropriate.
(B) Comments and Responses
(1) HRSA's Legal Authority
Comment: HRSA lacks authority to add children's hospitals to the
340B program through guidelines.
Response: HRSA disagrees. The Department publishes guidelines in
the Federal Register providing a public comment period to obtain input
into guidance development. Congress did not prescribe the process by
which children's hospitals would be added into the 340B program. HRSA
has authority to provide guidelines interpreting the statute and its
intended administration of the 340B program. The guidelines are not
subject to the
[[Page 45207]]
Administrative Procedure Act's notice and comment requirements;
however, the Department chose to solicit and respond to public
comments. These guidelines help to fulfill the Secretary's obligation
to provide for the operation of the program under section 340B.
Comment: It is unclear that Congress has authorized the Secretary
to enter into PPAs that include children's hospitals. Contractual
obligations of the PPA are directly tied to section 340B, which has not
been amended to include children's hospitals as covered entities.
Response: HRSA acknowledges that section 6004 of the DRA did not
amend section 340B to include children's hospitals as covered entities.
However, Congress did add children's hospitals to the 340B program by
amending section 1927(a) of the Social Security Act which requires that
manufacturers provide the statutorily mandated discount to covered
entities. Congress specifically defined the term covered entity as
including certain qualifying children's hospitals. Considering the
statutory scheme as a whole, it is clear that the Secretary has been
authorized to include children's hospitals within the program.
Comment: Since the appropriate legislative changes were not made,
it is out of the scope of authority of the Secretary and HRSA to read
the current PPA as including children's hospitals.
Response: The existing PPAs do not need to be amended to include
children's hospitals. The PPAs require manufacturers to extend 340B
pricing to all covered entities listed by HRSA in its database. The PPA
also requires that it be interpreted in a manner that best effectuates
the underlying statutory scheme. As previously discussed, including
children's hospitals as covered entities for purposes of the PPA best
effectuates the statutory scheme and therefore children's hospitals are
covered entities for purposes of the PPA.
(2) Certification of Eligibility
Comment: Clarify the Social Security Act definition of children's
hospitals to mean that in any fiscal year or calendar year, no less
than 80 percent of patient days involve patients under 18 years of age.
Response: We disagree with a suggestion that HRSA utilize an 80
percent figure. It is unclear on what basis such a figure would be
determined. The statute indicates that section 1886(d)(1)(B)(iii) of
the Social Security Act defines the term children's hospital for
purposes of 340B eligibility. This section defines a children's
hospital as ``a hospital whose inpatients are predominantly individuals
under 18 years of age.'' In using the statutory definition, HRSA has
taken into account the CMS interpretation of this provision and the
context of the 340B Drug Pricing Program.
Comment: The guidelines should require participating children's
hospitals to demonstrate that the entity is a children's hospital as
defined by the Social Security Act and obtain a Medicare provider
number in the 3300 series identifying it as a children's hospital.
Response: We agree. The statute defines ``children's hospitals'' by
reference to section 1886(d)(1)(B)(iii) of the Social Security Act. CMS
has reserved the 3300 series of Medicare Provider Numbers for
children's hospitals that meet the statutory definition. The guidelines
have been changed accordingly to make this clearer.
Comment: Clarify how the disproportionate share adjustment
percentage eligibility criteria can be applied to children's hospitals
since children's hospitals do not receive Medicare disproportionate
share hospital (DSH) payment adjustments. Children's hospitals should
be permitted to rely on its disproportionate patient percentage (DPP)
as defined by CMS for purposes of Medicaid. The DPP formula
demonstrating a percentage of greater than 27.32 percent is just as
reliable as the required greater than 11.75 percent disproportionate
share adjustment percentage.
Response: HRSA agrees with the comment that children's hospitals
that do not receive Medicare DSH payment adjustments may have
difficulty in showing their disproportionate share adjustment
percentage. As an alternative, children's hospitals can show compliance
with this requirement if they provide independent verification that if
the disproportionate share adjustment percentage were calculated, it
would be greater than 11.75 percent. Under current law, one method for
reaching such a conclusion would be to have a DPP greater than a
threshold amount that equates to a disproportionate share adjustment
percentage greater than 11.75 percent. DPP for this purpose is defined
at 42 CFR 412.106 and is used in the current applicable statutory
formula to calculate the disproportionate share adjustment percentage
for DSHs.
Comment: Many children's hospitals do not file any or full Medicare
cost reports. If no cost report exists, children's hospitals should be
permitted to rely on their own independent auditors to confirm their
DPP.
Response: If a children's hospital does not file a Medicare cost
report, HRSA agrees that children's hospitals can confirm eligibility
through the findings of an independent auditor and certification by the
covered entity as to the appropriate value of the hospital's
disproportionate share adjustment percentage, as based upon the DPP.
Comment: In addition to requiring verification from independent
auditors from children's hospitals that the entity meets 340B
eligibility requirements, a comment was made to require this
verification to OPA annually because the data used in the calculation
to meet the requirements of section 340B(a)(4)(L)(ii) are subject to
change.
Response: HRSA agrees that there is a need for ongoing verification
as to whether this eligibility requirement continues to be met over
time. After enrollment, children's hospitals, as do all covered
entities, have an ongoing responsibility to immediately notify the OPA
in the event of any change in eligibility for the 340B Drug Pricing
Program. No less than on an annual basis, children's hospitals will
need to demonstrate that the children's hospital continues to have the
required disproportionate share adjustment percentage or DPP. The OPA
will provide additional guidance as it develops its plans to annually
certify covered entities. To the extent that the OPA is able to obtain
periodic documentation of data similar to that provided by CMS with
respect to DSHs, it may notify the covered entity that information need
not be provided.
(3) Eligibility for Rebates Back to February 8, 2006
Comment: The eligibility criteria for receiving retroactive
discounts are overwhelming and confusing to both manufacturers and
covered entities. HRSA should remove the ability to receive retroactive
discounts from the final rule or, at a minimum, clearly define these
criteria.
Response: Although the statute can be complex, we disagree that it
is overwhelming or that unilaterally disallowing any ``retroactive''
discounts is appropriate. The parties are in the best position to
understand and resolve claims over these issues. In this guidance, HRSA
believes it has provided an appropriate level of detail as to its view
on how covered entities can qualify for rebates on purchase back to
February 8, 2006, the date of enactment of the DRA.
Comment: HRSA should post on its on-line database the date when a
children's hospital satisfied the 340B eligibility criteria for
manufacturers to
[[Page 45208]]
verify if and when the children's hospital was entitled to receive
retroactive discounts.
Response: HRSA does not currently plan to provide the eligibility
date on its Web site for purposes of retroactive rebates. HRSA intends
to follow the current practice of listing the date of eligibility for
direct purchase under the 340B Drug Pricing Program as is consistent
with the purpose of that database. The addition of retroactivity dates
would be outside the established purpose of the database and lead to
potential confusion. If a covered entity and manufacturer are unable to
agree on the date that the covered entity complied with program
requirements or otherwise disagree, HRSA believes that it is most
appropriate to follow its published dispute procedures that require the
parties to resolve any disputes in good faith. HRSA's first priority is
to have eligible children's hospitals register for the 340B Drug
Pricing Program. HRSA has concluded that this approach is the most
efficient and that HRSA will assist parties to resolve disputes through
the published dispute resolution process to the extent resources
permit.
Comment: HRSA should clarify ``appropriate'' documentation to
demonstrate that drugs did not generate Medicaid rebates.
Response: This is a fact-specific inquiry that may vary from case
to case and State to State. The children's hospital should demonstrate
that the covered outpatient drugs for which it seeks retroactive
discounts were not subject to Medicaid rebates because they were not
billed to Medicaid or it can otherwise show the State did not seek a
rebate on the drugs for which a retroactive claim is sought.
Comment: Children's hospitals lack access to Medicaid drug rebate
invoices/claims data needed to establish the requirement that covered
outpatient drugs did not generate Medicaid rebates during retroactive
periods.
Response: HRSA believes it appropriate to require that children's
hospitals seeking refunds provide sufficient factual evidence to
demonstrate compliance with statutory requirements. Children's
hospitals seeking retroactive discounts should have access to records
of which drugs were billed to Medicaid and which drugs were not billed
to Medicaid. HRSA suggests that children's hospitals consider
contacting State Medicaid agencies for supporting documentation as is
appropriate.
Comment: HRSA should coordinate with CMS to provide guidance
regarding monthly Average Manufacturer Price (AMP) and quarterly
Average Sales Price (ASP) calculations already submitted, if
retroactive discounts are given.
Response: HRSA will do what it reasonably can to assist in the
process; however, the issue of resolving whether retroactive discounts
are appropriate should be resolved to the full extent possible by the
covered entities and manufacturers. Manufacturers will need to consult
with CMS with respect to the separate issue on how to handle
calculations reported to CMS.
Comment: Children's hospitals should not be penalized for use of
Group Purchasing Organizations (GPOs) during the long interval that has
elapsed since enactment of section 6004. Initially, HRSA allowed DSHs
to use GPOs and to receive 340B retroactive discounts as long as
discounts were not for drugs obtained through the GPO. Similarly,
children's hospitals should be eligible to receive retroactive
discounts for covered outpatient drugs that were not purchased through
a GPO.
Response: HRSA disagrees and finds the proposed treatment of
retroactive rebates to be inconsistent with the applicable standards
for DSHs. The statute makes clear that children's hospitals must meet
the same criteria applicable to DSHs. In 1994, final guidance was
published on the GPO exclusion that expressly provides that any
participation in a GPO or other group purchasing arrangement for
covered outpatient drugs by a DSH results in loss of eligibility as a
covered entity. HRSA believes that under the statute and under current
guidance it should exclude from eligibility for retroactive rebates any
purchases while the children's hospital purchased covered outpatient
drugs through a GPO or other purchasing arrangement.
The guideline for retroactive rebates published in 1994 (59 FR
25110) was consistent with the GPO exclusion guideline in place for the
period of retroactivity. Likewise, this guideline for retroactive
rebates is consistent with the GPO exclusion guideline in place for the
period of retroactivity.
Comment: Retroactive discounts should only apply to children's
hospitals that comply with statutory prohibition against use of a GPO.
Furthermore, a comment was received stating that children's hospital
should not be able to request retroactive rebates on a covered
outpatient drug that was not purchased under a GPO contract if the
entity used a GPO contract for other covered outpatient drugs during
that same time period.
Response: HRSA agrees and has changed the guidelines to make this
issue clear.
Comment: HRSA should be required to establish a process to document
the eligibility and compliance of these new entities for any time
period of eligibility, including retroactive periods. HRSA should
create an audit or certification process to determine the actual date
that the facility met all requirements. Manufacturers should be allowed
to audit the processes and documentation before they are obligated to
provide the retroactive discounts.
Response: HRSA believes that the process outlined in the guidelines
provides enough safeguards to ensure program integrity. To the extent
that a manufacturer has a specific concern about a covered entity's
status, the manufacturer should bring those concerns to HRSA's
attention. Manufacturers also have the option of bringing a dispute
through the dispute resolution process as addressed in previous
guidance (61 FR 65406). The issue of manufacturer audits has also been
previously addressed in finalized guidance (61 FR 65406).
Comment: HRSA should shorten the proposed 120-day period allowed to
submit requests for retroactive discounts to 30 days, similar to its
Federal Register notice dated May 13, 1994, following the enactment of
section 340B in 1992, where HRSA permitted eligible covered entities to
request retroactive discounts within 30 days of publication of
guidelines.
Response: While HRSA understands that after enactment of the 340B
statute and the implementation of the initial guidances, there was only
a 30-day retroactivity period, there are materially different
circumstances between the situations in 1994 and today. HRSA must take
into account the potential time necessary to obtain sufficient evidence
to demonstrate eligibility (requirements which did not exist in 1994)
as well as the delay between the time of application to the 340B Drug
Pricing Program and listing in the Covered Entity Database at the
beginning of the quarter. Upon further review, taking into account
changes to this final guidance, HRSA has determined that in order to
ensure that all eligible hospitals have reasonable time they should
have three full calendar quarters after publication during which they
must get registered and officially listed on the 340B Covered Entity
Database. To be eligible a children's hospital must register and be
listed on 340B Covered Entity Database within one year of publication
of this notice. This amount of time will
[[Page 45209]]
ensure that all eligible children's hospitals will have reasonable time
to obtain the necessary documentation, enroll, and be listed on the
340B Drug Pricing Program Database as eligible to purchase under 340B.
Children's hospitals will need to abide by all applicable deadlines for
registration and will only be added to the list at the time of standard
quarterly updates. Once listed on the 340B Drug Pricing Program
Database, a children's hospital will have 30 days to notify
manufacturers in writing to preserve their claims.
(4) Eligibility of Off-site Facilities of Children's Hospitals
Comment: HRSA did not address how off-site locations of children's
hospitals may participate in 340B. The DSH requirement states that the
off-site location be an ``integral'' part of the hospital and be
reimbursable on the Medicare cost report. HRSA should be partially
guided by Medicare provider-based standards to establish an alternative
to the cost report for off-site facilities of children's hospitals to
be eligible for 340B.
Response: To the extent possible, eligibility for off-site
locations will be determined through the same method applied for DSHs
in the 340B Program. Additional clarification on this issue has been
provided in the final guidance.
(5) Hemophilia Treatment Centers
Comment: Several commenters asked that HRSA require, as
prerequisite, that children's hospitals agree to maintain Hemophilia
Treatment Centers as independent purchasers under 340B.
Response: HRSA does not find that such a requirement is necessary
to ensure against duplicate discounts or diversion, and does not find
sufficient basis to issue such a requirement in this guidance.
(6) Miscellaneous Comments
Comment: There should be a dispute resolution process if a
manufacturer has reason to believe that HRSA's determination of
eligibility period for a children's hospital is incorrect.
Response: HRSA is not initially making such a determination. HRSA
does have guidance on its dispute resolution process.
Comment: HRSA should require explicitly that children's hospitals
abide by program guidance relating to the patient definition.
Response: HRSA agrees and finds that the guidance as proposed
already makes that explicit.
(C) Obligation of Manufacturers To Provide 340B Discounts to Children's
Hospitals
Section 1927(a)(5)(A) of the Social Security Act requires
manufacturers to enter into agreements with the Secretary that meet the
requirements of section 340B with respect to covered outpatient drugs
purchased by a covered entity. Section 1927(a)(5)(B), as amended by
section 6004, defines covered entities for purposes of section
1927(a)(5) as those covered entities listed in the Public Health
Service Act and certain children's hospitals. As section 1927(a)(5)(A)
requires manufacturers to enter into agreements ``with respect to
covered outpatient drugs purchased by a covered entity,'' and covered
entity is defined as including children's hospitals for purposes of
section 1927, manufacturers are required to extend 340B pricing to
eligible children's hospitals.
The PPAs between the Secretary and each manufacturer require
manufacturers to provide 340B discounted covered outpatient drugs to
covered entities. Given the clear congressional intent in section 6004
to expand the category of covered entities, the PPAs currently in place
effectively require manufacturers to provide 340B discounts to
children's hospitals without need for further amendment to currently
existing PPAs.
(D) Process for Admission of Children's Hospitals to the 340B Program
(1) Children's Hospitals Participation
Children's hospitals participation in the 340B Drug Pricing Program
is voluntary. Consistent with the participation of other covered
entities, once a children's hospital has elected to participate in the
program, it must wait to enter or withdraw from the program until the
next official update of the 340B covered entity database. Participating
children's hospitals must comply with all program guidelines for
covered entities until the date they are removed from the 340B covered
entity database. The OPA will accept applications from children's
hospitals for entry into the 340B Program as of the date of publication
of the final notice of these guidelines. Hospitals that submitted
documentation seeking recognition as a children's hospital eligible for
the 340B Drug Pricing Program prior to the publication of the guidance
should apply again in accordance with the procedures described in this
guidance.
(2) Certification by Children's Hospitals Prior to 340B Drug Pricing
Program Entry
As with other covered entities, prior to entry into the 340B Drug
Pricing Program, children's hospitals will be required to provide OPA
with a certification regarding several different program requirements.
As a threshold matter, a hospital wishing to qualify for the 340B
Program as a children's hospital must demonstrate that the hospital is
a ``children's hospital'' as defined by section 6004. Section 6004
requires that a hospital wishing to qualify as a children's hospital
covered entity must satisfy the definition of ``children's hospital''
contained in section 1886(d)(1)(B)(iii) of the Social Security Act; and
meet minimum requirements for the receipt of an additional payment
under Medicare pursuant to section 1886(d)(5)(F)(i) of the Social
Security Act (if such clause were applied to the children's hospital
while taking into account the percentage of care provided by the
hospital to Medicaid patients).
(i) Certify That the Hospital Is a Children's Hospital as Defined by
Statute
Given the reliance of section 6004 on Medicare payment provisions
for the definition of ``children's hospital'' and the requirement that
a children's hospital must demonstrate that they would meet the same
requirements as a DSH, if they were eligible for DSH payments, a
hospital will need to demonstrate that it has been assigned a Medicare
provider number identifying the hospital as a ``children's hospital''
(i.e., a hospital with a 3300 series Medicare provider number).
(ii) Certify That the Hospital Will Abide by All Requirements of
Section 340B of the Public Health Service Act
Prior to entry into the 340B Program, a children's hospital must
certify that it will abide by all the requirements of section 340B that
all other covered entities abide by (e.g., prohibition on resale of
covered outpatient drugs; prohibition on duplicate discounts or
rebates). While children's hospitals are not explicitly mentioned in
section 340B, it is implicit in section 1927(a) of the Social Security
Act that children's hospitals abide by the requirements of section
340B. Section 1927(a) provides that manufacturers must have entered
into agreements with the Secretary that meet the requirements of
section 340B and several of the provisions contained in these
agreements concern covered entities' compliance with provisions of
[[Page 45210]]
section 340B. Furthermore, it is within the Secretary's authority under
section 340B to create guidelines necessary for the implementation of
the program. Unless children's hospitals are subject to all of the same
rules as other covered entities, the inclusion of children's hospitals
in the 340B Program would be difficult, if not impossible.
(iii) Certify Compliance With 340B(a)(4)(L) as Modified by Section 6004
of the DRA
Prior to entry into the 340B Program, a children's hospital must
certify compliance (along with the date of compliance) with clauses
(i), (ii), and (iii) of section 340B(a)(4)(L) (in accordance with
section 1927(a)(5)(B) of the Social Security Act) in the following
manner:
(A) Meets the requirements of section 340B(a)(4)(L)(i).
To comply with the requirements of section 340B(a)(4)(L)(i), a
children's hospital will have to certify (and include such supporting
documentation as requested by OPA) that the hospital is (1) owned or
operated by a unit of State or local government; (2) is a public or
private non-profit corporation which is formally granted governmental
powers by a unit of State or local government; or (3) is a private non-
profit hospital under contract with State or local government to
provide health care services to low income individuals who are not
eligible for Medicare or Medicaid.
(B) Meets the requirements of section 340B(a)(4)(L)(ii).
To comply with section 340B(a)(4)(L)(ii), as modified by section
6004, a children's hospital will have to certify (and include such
supporting documentation as requested by OPA) that the children's
hospital (1) is located in an urban area, has 100 or more beds, and can
demonstrate that its net inpatient care revenues (excluding any of such
revenues attributable to Medicare), during the cost reporting period in
which the discharges occur, for indigent care from State and local
government sources and Medicaid exceed 30 percent of its total of such
net inpatient care revenues during the period; or (2) for the most
recent cost reporting period that ended before the calendar quarter
involved, had a disproportionate share adjustment percentage (as
determined under section 1886(d)(5)(F) of the Social Security Act)
greater than 11.75 percent.
Supporting documentation must include a signed statement by an
appropriate official (e.g., Chief Financial Officer) of the children's
hospital that he/she is familiar with the requirements under section
340B(a)(4)(L)(ii), has examined the documentation, and certifies that
to the best of his/her knowledge that the children's hospital satisfies
the requirements. In addition, the documentation must include: (1) An
official document from the Department of Health and Human Services
(HHS) or a HHS contractor that is authorized to make official
determinations, showing that the children's hospital meets one or both
criterion listed above; (2) if the organization files a Medicare cost
report, the report filed does not contain a disproportionate share
adjustment percentage, and the report includes sufficient information
to calculate the disproportionate share adjustment percentage, include
a copy of those pages of the filed Medicare cost report with the data
necessary to calculate the disproportionate share adjustment
percentage; or (3) if the organization does not file a Medicare cost
report with sufficient information to calculate the disproportionate
share adjustment percentage, a statement from a qualified independent
auditor certifying that the auditor performed an audit on the records
of the children's hospital, that the auditor is familiar with Federal
rules and regulations relevant to its findings, and found that the
hospital would meet one or both of the criterion in section
340B(a)(4)(L)(ii), as modified by section 6004 (described in the
previous paragraph). The supporting documentation for (1), (2) or (3)
should identify the basis for that conclusion including the actual
percentage value upon which the determination is made (e.g.,
disproportionate patient percentage defined at 42 CFR section 412.106),
a concise description of any mathematical calculations, and the quarter
for which the determination was made. The children's hospital should
notify OPA if (1), (2) or (3) result in different conclusions as to
eligibility of the children's hospital.
(C) Meets the requirements of section 340B(a)(4)(L)(iii).
To comply with section 340B(a)(4)(L)(iii), a children's hospital
will have to certify that it will not participate in a group purchasing
organization (GPO) or group purchasing arrangement for covered
outpatient drugs as of the effective date of participation as listed in
the 340B covered entity database.
(3) Inclusion of Children's Hospitals' Off-Site Outpatient Facilities
Children's hospitals must meet the applicable requirements for DSHs
as described in the guidance published in 59 FR 47884 (Sept. 19, 1994).
(i) Children's Hospitals That File Medicare Cost Reports With CMS
Children's hospitals that file Medicare cost reports will be
required to utilize the same process to add outpatient facilities as
DSHs (59 FR 47884). A children's hospital, eligible for the 340B Drug
Pricing Program, must first request that the OPA include in its covered
entity database the outpatient facilities that are included as
reimbursable in its Medicare cost report. A list of these outpatient
facilities along with Medicare and Medicaid billing status information
must be included with the request. Second, an appropriate official
(e.g., Chief Financial Officer) of the children's hospital must sign a
statement that he/she is familiar with CMS guidelines concerning
Medicare certification of hospital components as one cost center, has
examined the list of outpatient facilities, and certifies that the
facilities are correctly included on the Medicare cost report of the
children's hospital. When these outpatient facilities are added to the
master list of eligible and participating covered entities, the off-
site facilities will be able to access 340B Drug Program pricing.
Outpatient facilities that are not included as reimbursable on the
Medicare cost report or file independent Medicare cost reports will not
be eligible for 340B pricing as part of the children's hospital.
(ii) Children's Hospitals That Do Not File Medicare Cost Reports With
CMS
Children's hospitals that do not file a Medicare cost report with
CMS must first request that the OPA include in its covered entity
database the outpatient facilities that are integral parts of the
hospital. A list of these outpatient facilities along with Medicaid
billing status information must be included with the request. Second,
an appropriate official (e.g., Chief Financial Officer) of the
children's hospital must sign a statement that he/she is familiar with
CMS guidelines concerning Medicare certification of hospitals as a cost
center, has examined the list of outpatient facilities, and certifies
that each facility is an integral part of the children's hospital whose
patients are considered patients of the children's hospital, according
to the most current published guidelines on patient definition, and
would have been correctly included on the Medicare cost report if the
hospital filed such a report and that the outpatient facility meets the
requirements of a provider-based facility within a DSH under 42 CFR
413.65.
[[Page 45211]]
(E) Annual Re-Certification by Children's Hospitals To Maintain
Eligibility Status in 340B Drug Pricing Program
Children's hospitals have an ongoing responsibility to immediately
notify OPA in the event of any change in eligibility for the 340B Drug
Pricing Program. No less than on an annual basis, children's hospitals
will need to demonstrate continued maintenance of the required
disproportionate share adjustment percentage or disproportionate
patient percentage. OPA will provide additional guidance as it gains
experience and develops its plans to annually certify covered entities.
To the extent that OPA is able to obtain periodic documentation of such
data similar to that provided by CMS with respect to DSHs, it may
notify the covered entity that such information need not be provided.
(F) Eligibility for Discounts Back to February 8, 2006
Section 6004 of the DRA indicates that the amendment authorizing
entry of children's hospitals into the 340B Program ``shall apply to
drugs purchased on or after the date of the enactment of this Act.''
The DRA provision was enacted on February 8, 2006. Therefore, once
children's hospitals are admitted to the 340B Program and listed on the
Covered Entity Database, they are eligible for 340B drug pricing back
to February 8, 2006. However, a children's hospital will be eligible
for such retroactive discounts only to the extent that it has satisfied
all requirements for participation in the 340B program back to the date
discounts are requested.
Children's hospitals may request retroactive discounts (discounts,
rebates, or account credit) directly from pharmaceutical manufacturers
for covered outpatient drugs when all the following conditions are
satisfied:
(1) The children's hospital is listed on the 340B Covered Entity
Database as eligible to purchase under 340B within one year of
publication of this notice.
(2) The children's hospital sent a request in writing to each
manufacturer of the drug(s) for which retroactive discounts are sought
within 30 days of the children's hospital having been listed as
eligible to purchase under 340B on the 340B Covered Entity Database;
(3) The covered outpatient drugs must have been purchased on or
after February 8, 2006;
(4) The covered outpatient drugs must not have generated Medicaid
rebates (the children's hospital must have appropriate documentation to
demonstrate this);
(5) The covered outpatient drugs must not have been sold or
transferred to a person who was not a patient of the children's
hospital; and
(6) The covered outpatient drugs must have been purchased on or
after the date on which the children's hospital satisfied all
requirements for participation in the 340B Program as outlined in
section (D) of this notice.
In order to satisfy the last condition listed above, a children's
hospital must be able to demonstrate, at a minimum, that as required by
section 340B(a)(4)(L)(iii) of the Public Health Service Act, the
children's hospital did not have a group purchasing agreement for
covered outpatient drugs and satisfied the requirements of section
340B(a)(4)(L)(i) and 340B(a)(4)(L)(ii) at the time the covered
outpatient drugs for which rebates are requested were purchased.
Participation in a GPO for any covered outpatient drugs would
disqualify a children's hospital for retroactive rebates during any
quarter that the children's hospital purchased any covered outpatient
drug through a GPO or other group purchasing arrangement. Consistent
with section 340B(a)(5)(C) of the Public Health Service Act, children's
hospitals must have auditable records that support claims for
retroactive discounts and permit the Government or manufacturers to
audit those records (in accordance with procedures established by the
Secretary relating to the number scope and duration of such audits (61
FR 65406)).
In fulfilling the conditions listed above, any children's hospital
that believes it is entitled to retroactive discounts may preserve its
rights by sending manufacturers a letter requesting such refunds,
explaining how they meet the requirements in this notice, and providing
adequate documentation of purchases within 30 days being listed on the
340B Covered Entity Database as eligible. Such children's hospitals
should engage in good faith efforts to resolve any disputes with
manufacturers. To the extent they are unable to resolve disputes and
wish to pursue further involvement with the OPA, they are encouraged to
follow the guidance on the dispute resolution process as described in
the Federal Register (61 FR 65406).
Dated: August 26, 2009.
Mary K. Wakefield,
Administrator.
[FR Doc. E9-21109 Filed 8-31-09; 8:45 am]
BILLING CODE 4165-15-P