Federal
Prescription Pricing for the People Act of 2021
Source: Congress.gov ·
1,025 words in original text
Plain English summary not yet available
The full original text is available below. Check back soon as we process this bill.
II
117TH CONGRESS
1ST SESSION
S. 1388
To require the Federal Trade Commission to study the role of intermediaries
in the pharmaceutical supply chain and provide Congress with appro-
priate policy recommendations, and for other purposes.
IN THE SENATE OF THE UNITED STATES
APRIL 27, 2021
Mr. GRASSLEY
(for himself, Ms. CANTWELL, Mrs. BLACKBURN, Mr.
BLUMENTHAL, Ms. ERNST, and Mr. TILLIS) introduced the following bill;
which was read twice and referred to the Committee on the Judiciary
A BILL
To require the Federal Trade Commission to study the role
of intermediaries in the pharmaceutical supply chain and
provide Congress with appropriate policy recommenda-
tions, and for other purposes.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. SHORT TITLE.
3
This Act may be cited as the ‘‘Prescription Pricing
4
for the People Act of 2021’’.
5
SEC. 2. DEFINITIONS.
6
In this Act:
7
VerDate Sep 11 2014
03:29 May 22, 2021
Jkt 019200
PO 00000
Frm 00001
Fmt 6652
Sfmt 6201
E:\BILLS\S1388.IS
S1388
kjohnson on DSK79L0C42PROD with BILLS
2
•S 1388 IS
(1)
APPROPRIATE
COMMITTEES
OF
CON-
1
GRESS.—The term ‘‘appropriate committees of Con-
2
gress’’ means—
3
(A) the Committee on the Judiciary of the
4
Senate; and
5
(B) the Committee on the Judiciary of the
6
House of Representatives.
7
(2) COMMISSION.—The term ‘‘Commission’’
8
means the Federal Trade Commission.
9
SEC. 3. STUDY OF PHARMACEUTICAL SUPPLY CHAIN
10
INTERMEDIARIES AND MERGER ACTIVITY.
11
(a) REPORT.—Not later than 1 year after the date
12
of enactment of this Act, the Commission shall submit to
13
the appropriate committees of Congress a report that—
14
(1) addresses at minimum—
15
(A) whether pharmacy benefit managers—
16
(i) charge payers a higher price than
17
the reimbursement rate at which the phar-
18
macy benefit managers reimburse phar-
19
macies owned by the pharmacy benefit
20
manager and pharmacies not owned by the
21
pharmacy benefit manager;
22
(ii) steer patients for competitive ad-
23
vantage to any pharmacy, including a re-
24
tail, mail-order, or any other type of phar-
25
VerDate Sep 11 2014
03:29 May 22, 2021
Jkt 019200
PO 00000
Frm 00002
Fmt 6652
Sfmt 6201
E:\BILLS\S1388.IS
S1388
kjohnson on DSK79L0C42PROD with BILLS
3
•S 1388 IS
macy, in which the pharmacy benefit man-
1
agers have an ownership interest;
2
(iii) audit or review proprietary data,
3
including acquisition costs, patient infor-
4
mation, or dispensing information, of phar-
5
macies not owned by the pharmacy benefit
6
manager and use such proprietary data to
7
increase revenue or market share for com-
8
petitive advantage; or
9
(iv) use formulary designs to increase
10
the market share of higher cost prescrip-
11
tion drugs or depress the market share of
12
lower cost prescription drugs (each net of
13
rebates and discounts);
14
(B) trends or observations on the state of
15
competition in the healthcare supply chain, par-
16
ticularly with regard to intermediaries and their
17
integration with other intermediaries, suppliers,
18
or payers of prescription drug benefits;
19
(C) how companies and payers assess the
20
benefits, costs, and risks of contracting with
21
intermediaries, including pharmacy services ad-
22
ministrative organizations, and whether more
23
information about the roles of intermediaries
24
VerDate Sep 11 2014
03:29 May 22, 2021
Jkt 019200
PO 00000
Frm 00003
Fmt 6652
Sfmt 6201
E:\BILLS\S1388.IS
S1388
kjohnson on DSK79L0C42PROD with BILLS
4
•S 1388 IS
should be available to consumers and payers;
1
and
2
(D) whether there are any specific legal or
3
regulatory obstacles the Commission currently
4
faces in enforcing the antitrust and consumer
5
protection laws in the pharmaceutical supply
6
chain, including the pharmacy benefit manager
7
marketplace and pharmacy services administra-
8
tive organizations; and
9
(2) provides—
10
(A) observations or conclusions drawn
11
from the November 2017 roundtable entitled
12
‘‘Understanding Competition in Prescription
13
Drug Markets: Entry and Supply Chain Dy-
14
namics,’’ and any similar efforts;
15
(B) specific actions the Commission in-
16
tends to take as a result of the November 2017
17
roundtable, and any similar efforts, including a
18
detailed description of relevant forthcoming ac-
19
tions, additional research or roundtable discus-
20
sions, consumer education efforts, or enforce-
21
ment actions; and
22
(C) policy or legislative recommendations
23
to—
24
VerDate Sep 11 2014
03:29 May 22, 2021
Jkt 019200
PO 00000
Frm 00004
Fmt 6652
Sfmt 6201
E:\BILLS\S1388.IS
S1388
kjohnson on DSK79L0C42PROD with BILLS
5
•S 1388 IS
(i) improve transparency and competi-
1
tion in the pharmaceutical supply chain;
2
(ii) prevent and deter anticompetitive
3
behavior in the pharmaceutical supply
4
chain; and
5
(iii) best ensure that consumers ben-
6
efit from any cost savings or efficiencies
7
that may result from mergers and consoli-
8
dations.
9
(b) INTERIM REPORT.—Not later than 180 days
10
after the date of enactment of this Act, the Commission
11
shall submit to the appropriate committees of Congress
12
an interim report on the progress of the report required
13
by subsection (a), along with preliminary findings and
14
conclusions based on information collected to that date.
15
SEC. 4. REPORT.
16
The Commission shall submit to the appropriate com-
17
mittees of Congress a report that includes—
18
(1) the number and nature of complaints re-
19
ceived by the Commission relating to an allegation
20
of anticompetitive conduct by a manufacturer of a
21
sole-source drug;
22
(2) the ability of the Commission to bring an
23
enforcement action against a manufacturer of a sole-
24
source drug; and
25
VerDate Sep 11 2014
03:29 May 22, 2021
Jkt 019200
PO 00000
Frm 00005
Fmt 6652
Sfmt 6201
E:\BILLS\S1388.IS
S1388
kjohnson on DSK79L0C42PROD with BILLS
6
•S 1388 IS
(3) policy or legislative recommendations to
1
strengthen enforcement actions relating to anti-
2
competitive behavior.
3
Æ
VerDate Sep 11 2014
03:29 May 22, 2021
Jkt 019200
PO 00000
Frm 00006
Fmt 6652
Sfmt 6301
E:\BILLS\S1388.IS
S1388
kjohnson on DSK79L0C42PROD with BILLS
Important: This plain English summary was generated by AI and is provided for informational purposes only.
It is not legal advice. Always consult the official bill text on Congress.gov
or a qualified attorney for legal matters.