Library / Laws / 113th / hr / H.R. 1367 / Introduced in House
I
113th CONGRESS
1st Session
H. R. 1367
IN THE HOUSE OF REPRESENTATIVES
March 21, 2013
Mr. Lynch (for
himself, Mr. Cummings,
Mr. Moran, and
Ms. Norton) introduced the following
bill; which was referred to the Committee
on Oversight and Government Reform
A BILL
To amend chapter 89 of title 5, United States Code, to
ensure program integrity, transparency, and cost savings in the pricing and
contracting of prescription drug benefits under the Federal Employees Health
Benefits Program.
1.
Short title
This Act may be cited as the
FEHBP Prescription Drug Integrity,
Transparency, and Cost Savings Act.
2.
Improved program
integrity, transparency, and cost savings for prescription drug benefits in the
Federal Employees Health Benefits Program
(a)
Change in
contracting requirements
Section 8902 of title 5, United States
Code, is amended by adding at the end the following:
(p) A contract may not be made or a plan
approved under this chapter, with respect to a carrier that is a party to a PBM
carrier arrangement, unless the PBM and such carrier comply with the
requirements of section 8915. The Office shall terminate such contract or
discontinue such plan for failure to comply with such
requirements.
.
(b)
Requirements for
PBMs and related requirements for carriers
Chapter 89 of title 5, United States Code,
is amended by adding at the end the following:
8915.
Requirements
for PBM arrangements
(a)
Limitations on
Cross-Ownership
(1)
In
general
Under a PBM carrier
arrangement a PBM may not be under common corporate control with—
(A) a prescription
drug manufacturer; or
(B) a retail
pharmacy.
(2)
Profit
restriction on corporately affiliated carriers and PBMs
With respect to a PBM carrier arrangement
related to a contract under this chapter, the Office may not permit a carrier
under common corporate control with a PBM to earn a profit resulting from such
control.
(3)
Certification
Each carrier shall certify annually to the
Office of Personnel Management that any PBM with which it has a PBM carrier
arrangement meets the requirements of this subsection.
(4)
Definitions
For
purposes of this subsection—
(A)
Common corporate
control
The term common corporate control means that
2 entities are part of a controlled group of corporations (as such term is
defined in section 1563 of the Internal Revenue Code of 1986).
(B)
Retail
pharmacy
The term
retail pharmacy excludes any mail order pharmacy.
(b)
Restrictions on
brand name prescription drug substitutions
(1)
In
general
Under a PBM carrier arrangement, and with respect to a
prescription drug prescribed to an enrollee covered under such arrangement, a
PBM may not request payment from a carrier for a brand name prescription drug
that was dispensed to the enrollee, at the request of the PBM, in substitution
for the drug that was originally prescribed to such enrollee, unless each of
the following requirements is met:
(A)
Lower net
cost
The substitute drug has a lower net cost than the drug
originally prescribed to such enrollee.
(B)
Authorization by
prescriber
The prescriber of the originally prescribed drug
submits an express, verifiable authorization of the substitution to the
pharmacist and such authorization includes a determination by the prescriber
that the drug substitution will not endanger the health of the enrollee for
whom the drug is prescribed.
(C)
Additional
requirements
Each of the requirements described in
paragraph (2) are met.
(2)
Additional
requirements
The requirements
described in this paragraph are, with respect to a brand name prescription drug
that was dispensed to an enrollee, at the request of the PBM, in substitution
for the drug that was originally prescribed to such enrollee, the
following:
(A) To the extent
appropriate, the PBM consults the enrollee concerning such drug
substitution.
(B) The PBM discloses
to the prescriber of the originally prescribed drug, the carrier, and the
enrollee for whom such drug was prescribed—
(i) the reason why the
PBM proposed a drug substitution for such drug; and
(ii) the financial
impact of the drug substitution on the PBM, the carrier, and the
enrollee.
(C) In the case of a
mail order pharmacy, the PBM ensures that, at the time the drug is dispensed,
the enrollee receives a written notice that such drug substitution occurred and
that such substitution occurred with the approval of the prescriber.
(3)
Definitions
For
purposes of this subsection—
(A)
Brand name
prescription drug
The term
brand name prescription drug means a drug approved pursuant to an
application submitted under section 505(b) of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 355(b)).
(B)
Net
cost
The term net cost means, with respect to a
drug, a carrier, and an enrollee, the sum of—
(i) the final cost of
the drug to the carrier after all adjustments (including discounts, rebates,
associated dispensing fees and administrative fees, and enrollee cost sharing);
and
(ii) the final cost of the drug to the enrollee
(including cost-sharing).
(C)
Prescriber
The
term prescriber means an individual who is authorized under State
and Federal law to prescribe drugs and who prescribes a drug to an enrollee of
a health benefits plan under this chapter.
(c)
Reimbursement of
carriers
Under a PBM carrier
arrangement, not later than the last day of each quarter of the contract
year—
(1) the PBM shall pay
to a carrier an amount that is at least 99 percent of the sum of—
(A) all compensation that the PBM received
during the previous quarter from a prescription drug manufacturer under a PBM
manufacturer contract (to the extent such arrangement relates to the PBM
carrier arrangement) including compensation (but excluding rebates) that the
Office of Personnel Management categorizes (regardless of how such compensation
is categorized by the PBM) as—
(i) market share
incentives;
(ii) prescription drug
substitution programs;
(iii) educational
support;
(iv) commissions;
(v) mail service
purchase discounts;
(vi) administrative or
management fees; or
(vii) any other form
of compensation;
(B) all compensation received by the PBM during
the previous quarter for sales of utilization or claims data that the PBM
possesses as a result of the PBM carrier arrangement; and
(C) all rebates paid to the PBM during the
previous quarter by a prescription drug manufacturer to the extent that such
rebates are based on prescription drugs dispensed under the PBM carrier
arrangement; and
(2) the PBM shall disclose to the carrier and
the Office, in a form and manner specified by the Office—
(A) the compensation
described in
paragraph (1)(A), by the amount of
compensation for each category under such paragraph;
(B) the compensation
described in
paragraph (1)(B); and
(C) the rebates
described in
paragraph (1)(C), on a drug-by-drug
basis.
(d)
Sale of
utilization and claims data
Under a PBM carrier arrangement, if the PBM
intends to sell utilization or claims data that the PBM possesses as a result
of such arrangement—
(1) the PBM shall notify the Office of
Personnel Management before selling such data and shall provide the Office with
the name of the potential purchaser of such data and the expected use of such
data by such purchaser; and
(2) the PBM may not
sell such data unless the sale complies with all Federal and State laws and the
PBM has received approval for such sale from the Office.
(e)
Pricing
(1)
Spread
pricing
(A)
Limitation on
charges to a carrier
A PBM under a PBM carrier arrangement shall
not charge a carrier an amount for a prescription drug that is covered under
such arrangement (and is dispensed by a pharmacy) that is more than the amount
(including the ingredient cost and the dispensing fee) that the PBM reimburses
the pharmacy for the drug.
(B)
Disclosures
(i)
Initial
disclosure
Before entering into a PBM carrier arrangement, the
PBM shall disclose to the carrier and the Office of Personnel Management the
reimbursement basis (including the type of benchmark price and the source of
the data for determining such price) and methodology that the PBM uses to
compute reimbursement amounts for retail and mail order pharmacies.
(ii)
Updates
Not later than 30 days after making a
change to the reimbursement basis or methodology under
clause (i), the PBM shall
disclose such change to the carrier and the Office.
(iii)
Transition
rule
In the case of a PBM
carrier arrangement that is in effect on the effective date of the FEHBP
Prescription Drug Integrity, Transparency, and Cost Savings Act, the PBM shall
disclose the information under
clause (i) not later than 1 year
after such date.
(2)
Maximum for mail
order prescription drugs prices and dispensing fees
(A)
In
general
If a prescription drug is supplied by a mail order
pharmacy to an enrollee, under a PBM carrier arrangement, a PBM may not charge
a carrier an amount for the ingredient cost for such prescription drug that is
greater than an amount that is equal to the actual acquisition cost for the
drug minus any cost sharing for such drug that is the responsibility of the
enrollee.
(B)
Dispensing
fee
Under a PBM carrier
arrangement, a PBM may not charge a carrier an amount for a dispensing fee
related to a prescription drug dispensed by a mail order pharmacy to an
enrollee that is greater than the amount that the PBM charges health plans for
similar services that are not covered under a PBM carrier arrangement.
(C)
Transparency
Under
a PBM carrier arrangement, a PBM shall provide the carrier and the Office of
Personnel Management, at the request of such carrier or Office, information on
the method used to determine the amount of—
(i) the ingredient
cost under
subparagraph (A); and
(ii) the dispensing
fee under
subparagraph (B).
(D)
Actual
acquisition cost defined
For purposes of this paragraph, the term
actual acquisition cost means the amount a pharmacy pays for a
prescription drug, net of discounts, rebates, charge backs, and other
adjustments to the price of the drug.
(f)
Right to
explanation of benefits
Under a PBM carrier arrangement, not
later than 90 days after the date on which a pharmacy dispenses a prescription
drug covered under the arrangement, the PBM shall provide (by mail or
electronically) to the enrollee to whom such drug was dispensed an explanation
of benefits statement that contains the following information:
(1) The date the claim
for such drug was made by the pharmacy.
(2) The name of such
drug and the strength and quantity dispensed to the enrollee.
(3) The amount paid by
the enrollee for such drug.
(4) The total amount paid to the pharmacy by
the PBM for such drug. Such amount shall include all amounts paid to the
pharmacy with respect to dispensing such drug, including fees.
(5) The amount paid by
the carrier to the PBM for such drug.
(g)
Nondiscriminatory
contract
(1)
In
general
Under a PBM carrier arrangement, a PBM may not require
that a pharmacy participate in a pharmacy network managed by such PBM as a
condition of the pharmacy participating in another network managed by such
PBM.
(2)
Pharmacy network
defined
For purposes of this subsection, the term pharmacy
network means a group of pharmacies that have agreed, through a contract
with a PBM or carrier, to provide prescription medications to enrollees at
rates and with discounts that are specified in such contract.
(h)
Access to PBM
contract information
(1)
In
general
Under a PBM carrier arrangement, at the request of the
Office of Personnel Management, a PBM shall provide to the Office and to the
Inspector General of the Office of Personnel Management full access to
information relating to contracts entered into by such PBM under such
arrangement (such as PBM manufacturer contracts and PBM contracts with
pharmacies). Such information shall include—
(A) companywide rebate
receipt aging reports that cover all of the PBM’s lines of business;
(B) information and
methodology used to calculate and allocate rebates between the PBM’s lines of
business;
(C) information on
average wholesale prices, wholesale acquisition costs, and maximum allowable
costs;
(D) information on
dispensing fees paid; and
(E) information and
methodologies used to calculate additional administrative and service fees
charged to the carrier.
(2)
Confidentiality
Information provided by a PBM under this
subsection is confidential and shall not be disclosed by the Office, except
that nothing in this paragraph shall prevent—
(A) a disclosure
required under the Inspector General Act of 1978; or
(B) any disclosure
which the Office, in its sole discretion, considers necessary in order to carry
out this section, if such disclosure is made in a form which does not disclose
the identity of a specific PBM or carrier or the price charged for a particular
prescription drug.
(3)
Exemption from
FOIA
Any information obtained under this subsection shall be
exempt from disclosure under section 552.
(4)
Definitions
For
purposes of this subsection—
(A)
Generic
drug
The term generic
drug means a drug approved pursuant to an abbreviated application
submitted under section 505(j) of the Federal Food, Drug, and Cosmetic Act (21
U.S.C. 355(j)).
(B)
Maximum
allowable cost
The term maximum allowable cost means
a cost that is set by a PBM as the upper payment limit on the ingredient costs
for a generic drug.
(C)
Wholesale
acquisition cost
The term wholesale acquisition cost
means a publicly available list price for sales of a drug by a manufacturer to
a wholesaler.
(i)
Treatment of
non-Compliance
(1)
In
general
Under a PBM carrier arrangement, a PBM that knowingly
provides false information to a carrier related to a claim made to such carrier
by the PBM under such arrangement shall be treated, for purposes of chapter 37
of title 31, in the same manner as a person that makes a false claim to the
United States Government under section 3729 of such chapter.
(2)
Use of
collections
Any monetary penalty collected under
paragraph (1) shall be deposited into
the Employees Health Benefits Fund under section 8909.
(3)
Additional
penalties
Any penalties resulting from the application of
paragraph (1) shall be in addition to
any other penalties available to the Office of Personnel Management under law
or regulation.
(j)
No application
to community-Rated carriers
The provisions of this section and section
8902(p) of this title—
(1) shall apply to
experience-rated carriers; and
(2) shall not apply to
carriers that use rates based on a per member per month capitation
amount.
(k)
Limitation of
application to prescription drugs
The provisions of this section and section
8902(p) of this title shall not be construed to apply to drugs that are not
prescription drugs.
(l)
General
definitions
For purposes of this section and section 8902(p) of
this title:
(1)
Dispensing
fee
The term dispensing fee means a fee paid to a
pharmacy for the service of filling or dispensing prescriptions and excludes
any payment for the cost of the drug dispensed.
(2)
Drug
substitution
The term drug substitution means any
change from one prescription drug to another prescription drug that is intended
to address or treat the same illness or condition.
(3)
PBM carrier
arrangement
The term PBM carrier arrangement means a
contract between a PBM and a carrier for the provision or administration of a
program of prescription drug coverage under a health benefits plan under this
chapter. Such a contract may provide, among other duties, for the PBM
to—
(A) process and pay
prescription drug claims;
(B) provide programs
and services designed to—
(i) maximize the
effectiveness of prescription drugs dispensed under such plan; or
(ii) contain
prescription drug expenditures under such plan; and
(C) engage in other
activities related to the administration of such prescription drug
coverage.
(4)
PBM manufacturer
contract
The term PBM manufacturer contract means a
contract between a PBM and a prescription drug manufacturer for the provision
of prescription drugs to enrollees of health benefits plans with prescription
drug coverage that is administered or provided by the PBM.
(5)
Pharmacy benefit
manager; PBM
The terms pharmacy benefit manager and
PBM mean an entity that contracts with a carrier to provide or
administer prescription drug coverage under a health benefits plan under this
chapter.
.
(c)
Clerical
amendment
The table of sections for chapter 89 of title 5, United
States Code, is amended by adding at the end the following:
8915. Requirements for PBM
arrangements.
.
(d)
Effective Date;
waiver; regulations
(1)
Effective
date
The amendments made by this section shall apply to contract
years beginning on or after January 1, 2014.
(2)
Waiver
The Office of Personnel Management may
waive the application of 1 or more of the requirements of section 8915 of title
5, United States Code, but only for contract year 2014.
(3)
Expediting
implementation of regulations
Not later than 6 months after the date of
the enactment of this Act, the Office of Personnel Management shall issue
interim final regulations to carry out this section which may be effective and
final immediately on an interim basis as of the date of publication of such
regulations. If the Office provides for an interim final regulation, the Office
shall provide for a period of public comment on such regulation after the date
of publication. The Office may change or revise such regulation after
completion of the period of public comment.