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II
116TH CONGRESS
1ST SESSION
S. 2764
To amend the Controlled Substances Act to clarify how controlled substance
analogues that are imported or offered for import are to be regulated,
and for other purposes.
IN THE SENATE OF THE UNITED STATES
OCTOBER 31, 2019
Mr. GRASSLEY (for himself, Ms. ERNST, and Mrs. FEINSTEIN) introduced the
following bill; which was read twice and referred to the Committee on the
Judiciary
A BILL
To amend the Controlled Substances Act to clarify how con-
trolled substance analogues that are imported or offered
for import are to be regulated, 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; TABLE OF CONTENTS.
3
(a) SHORT TITLE.βThis Act may be cited as the
4
ββStop the Importation and Manufacturing of Synthetic
5
Analogues Act of 2019ββ or ββSIMSAββ.
6
(b) TABLE OF CONTENTS.βThe table of contents of
7
this Act is as follows:
8
Sec. 1. Short title; table of contents.
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Sec. 2. Establishment of Schedule A.
Sec. 3. Temporary and permanent scheduling of schedule A substances.
Sec. 4. Penalties.
Sec. 5. False labeling of schedule A controlled substances.
Sec. 6. Registration requirements for importers and exporters of schedule A
substances.
Sec. 7. Additional conforming amendments.
Sec. 8. Sentencing review.
Sec. 9. Rules of construction.
SEC. 2. ESTABLISHMENT OF SCHEDULE A.
1
Section 202 of the Controlled Substances Act (21
2
U.S.C. 812) is amendedβ
3
(1) in subsection (a), by striking ββfive schedules
4
of controlled substances, to be known as schedules I,
5
II, III, IV, and Vββ and inserting ββsix schedules of
6
controlled substances, to be known as schedules I,
7
II, III, IV, V, and Aββ;
8
(2) in subsection (b), by adding at the end the
9
following:
10
ββ(6) SCHEDULE A.β
11
ββ(A) IN GENERAL.βThe drug or substanceβ
12
ββ(i) is or has been imported, or is offered
13
for import, into the United States;
14
ββ(ii) hasβ
15
ββ(I) a chemical structure that is sub-
16
stantially similar to the chemical structure
17
of a controlled substance in schedule I, II,
18
III, IV, or V; and
19
ββ(II) an actual or predicted stimulant,
20
depressant, or hallucinogenic effect on the
21
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central nervous system that is substantially
1
similar to or greater than the stimulant,
2
depressant, or hallucinogenic effect on the
3
central nervous system of a controlled sub-
4
stance in schedule I, II, III, IV, or V; and
5
ββ(iii) is notβ
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ββ(I) listed or otherwise included in
7
any other schedule in this section or by
8
regulation of the Attorney General; and
9
ββ(II) with respect to a particular per-
10
son, subject to an exemption that is in ef-
11
fect for investigational use, for that person,
12
under section 505 of the Federal Food,
13
Drug, and Cosmetic Act (21 U.S.C. 355)
14
to the extent conduct with respect to such
15
substance is pursuant to such exemption.
16
ββ(B) PREDICTED STIMULANT, DEPRESSANT, OR
17
HALLUCINOGENIC
EFFECT.βFor purpose of this
18
paragraph, a predicted stimulant, depressant, or hal-
19
lucinogenic effect on the central nervous system may
20
be based onβ
21
ββ(i)(I) the chemical structure; and
22
ββ(II)(aa) the structure activity relation-
23
ships; or
24
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ββ(bb) binding receptor assays and other
1
relevant scientific information about the sub-
2
stance;
3
ββ(ii)(I) the current or relative potential for
4
abuse of the substance; and
5
ββ(II) the clandestine importation, manu-
6
facture, or distribution, or diversion from legiti-
7
mate channels, of the substance; or
8
ββ(iii) the capacity of the substance to
9
cause a state of dependence, including physical
10
or psychological dependence that is similar to or
11
greater than that of a controlled substance in
12
schedule I, II, III, IV, or V.ββ; and
13
(3) in subsection (c)β
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(A) in the matter preceding schedule I, by
15
striking ββIV, and Vββ and inserting ββIV, V, and
16
Aββ; and
17
(B) by adding at the end the following:
18
ββSCHEDULE A
19
ββAny substance temporarily or permanently sched-
20
uled by the Attorney General in accordance with section
21
201(k).ββ.
22
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SEC. 3. TEMPORARY AND PERMANENT SCHEDULING OF
1
SCHEDULE A SUBSTANCES.
2
Section 201 of the Controlled Substances Act (21
3
U.S.C. 811) is amended by adding at the end the fol-
4
lowing:
5
ββ(k) TEMPORARY AND PERMANENT SCHEDULING OF
6
SCHEDULE A SUBSTANCES.β
7
ββ(1) IN GENERAL.βThe Attorney General may
8
issue a temporary order adding a drug or substance
9
to schedule A if the Attorney General finds thatβ
10
ββ(A) the drug or other substance satisfies
11
the criteria for being considered a schedule A
12
substance; and
13
ββ(B) adding such drug or substance to
14
schedule A will assist in preventing abuse of the
15
drug or other substance.
16
ββ(2) DURATION OF TEMPORARY SCHEDULING
17
ORDER.βA temporary scheduling order issued under
18
paragraph (1) shallβ
19
ββ(A) not take effect until 30 days after the
20
date of the publication by the Attorney General
21
of a notice in the Federal Register of the inten-
22
tion to issue such order and the grounds upon
23
which such order is to be issued; and
24
ββ(B) expire not later than 5 years after
25
the date on which the order becomes effective,
26
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except that the Attorney General may, during
1
the pendency of proceedings under paragraph
2
(5), extend the temporary scheduling order for
3
up to 180 days.
4
ββ(3) EFFECT
OF
ISSUANCE
OF
PERMANENT
5
SCHEDULING
ORDER.βA
temporary
scheduling
6
order issued under paragraph (1) shall be vacated
7
upon the issuance of a permanent order issued
8
under paragraph (5) with regard to the same sub-
9
stance, or upon the subsequent issuance of any
10
scheduling order under this section.
11
ββ(4) LIMITATION
ON
JUDICIAL
REVIEW.βA
12
temporary scheduling order issued under paragraph
13
(1) shall not be subject to judicial review.
14
ββ(5) PERMANENT SCHEDULING ORDER.β
15
ββ(A) IN GENERAL.βExcept as provided in
16
subparagraph (B), not earlier than 3 years
17
after the date on which the Attorney General
18
issues an order temporarily scheduling a drug
19
or substance under this subsection, the Attor-
20
ney General may, by rule, issue a permanent
21
order adding the drug or other substance to
22
schedule A if such drug or substance satisfies
23
the criteria for being considered a schedule A
24
substance.
25
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ββ(B) LIMITATION.βIf the Secretary of
1
Health and Human Services has determined,
2
based on relevant scientific studies and nec-
3
essary data requested by the Secretary of
4
Health and Human Services and gathered by
5
the Attorney General, that a drug or other sub-
6
stance that has been temporarily placed in
7
schedule A does not have sufficient potential for
8
abuse to warrant control in any schedule, and
9
provides written notice of such determination to
10
the Attorney General, the Attorney Generalβ
11
ββ(i) may not issue a permanent sched-
12
uling order under subparagraph (A); and
13
ββ(ii) not later than 30 days after the
14
date on which the Attorney General re-
15
ceives such notice, shall issue an order im-
16
mediately
terminating
the
temporary
17
scheduling order for the drug or other sub-
18
stance.
19
ββ(6) NOTICE TO HHS.βBefore initiating pro-
20
ceedings under paragraph (1), the Attorney General
21
shall transmit notice of a temporary order proposed
22
to be issued to the Secretary of Health and Human
23
Services. In issuing an order under paragraph (1),
24
the Attorney General shall take into consideration
25
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any comments submitted by the Secretary of Health
1
and Human Services in response to a notice trans-
2
mitted pursuant to this paragraph.ββ.
3
SEC. 4. PENALTIES.
4
Section 1010 of the Controlled Substances Import
5
and Export Act (21 U.S.C. 960) is amendedβ
6
(1) in subsection (a), by inserting ββor a drug or
7
substance in schedule Aββ after ββcontrolled sub-
8
stanceββ each place it appears; and
9
(2) in subsection (b), by adding at the end the
10
following:
11
ββ(8) In the case of a violation under subsection (a)
12
involving a controlled substance in schedule A, the person
13
committing such violation shall be sentenced to a term of
14
imprisonment of not more than 20 years and if death or
15
serious bodily injury results from the use of such sub-
16
stance shall be sentenced to a term of imprisonment for
17
any term of years or for life, a fine not to exceed the great-
18
er of that authorized in accordance with the provisions of
19
title 18, United States Code, or $1,000,000 if the defend-
20
ant is an individual or $5,000,000 if the defendant is other
21
than an individual, or both. If any person commits such
22
a violation after a prior conviction for a felony drug of-
23
fense has become final, such person shall be sentenced to
24
a term of imprisonment of not more than 30 years and
25
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if death or serious bodily injury results from the use of
1
such substance shall be sentenced to a term of imprison-
2
ment for any term of years or for life, a fine not to exceed
3
the greater of twice that authorized in accordance with
4
the provisions of title 18, United States Code, or
5
$2,000,000 if the defendant is an individual or
6
$10,000,000 if the defendant is other than an individual,
7
or both. Notwithstanding section 3583 of title 18, United
8
States Code, any sentence imposing a term of imprison-
9
ment under this paragraph shall, in the absence of such
10
a prior conviction, impose a term of supervised release of
11
not less than 3 years in addition to such term of imprison-
12
ment and shall, if there was such a prior conviction, im-
13
pose a term of supervised release of not less than 6 years
14
in addition to such term of imprisonment. Notwith-
15
standing the prior sentence, and notwithstanding any
16
other provision of law, the court shall not place on proba-
17
tion or suspend the sentence of any person sentenced
18
under the provisions of this paragraph which provide for
19
a mandatory term of imprisonment if death or serious
20
bodily injury results.ββ.
21
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SEC. 5. FALSE LABELING OF SCHEDULE A CONTROLLED
1
SUBSTANCES.
2
(a) IN GENERAL.βSection 305 of the Controlled
3
Substances Act (21 U.S.C. 825) is amended by adding at
4
the end the following:
5
ββ(f) FALSE
LABELING
OF
SCHEDULE
A CON-
6
TROLLED SUBSTANCES.β
7
ββ(1) It shall be unlawful to import or export,
8
with intent to manufacture, distribute, or dispense,
9
a schedule A substance or product containing a
10
schedule A substance, unless the substance or prod-
11
uct bears a label clearly identifying a schedule A
12
substance or product containing a schedule A sub-
13
stance by the nomenclature used by the Inter-
14
national Union of Pure and Applied Chemistry
15
(IUPAC).
16
ββ(2)(A) A product described in subparagraph
17
(B) is exempt from the International Union of Pure
18
and Applied Chemistry nomenclature requirement of
19
this subsection if such product is labeled in the man-
20
ner required under the Federal Food, Drug, and
21
Cosmetic Act.
22
ββ(B) A product is described in this subpara-
23
graph if the productβ
24
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ββ(i) is the subject of an approved applica-
1
tion as described in section 505(b) or (j) of the
2
Federal Food, Drug, and Cosmetic Act; or
3
ββ(ii) is exempt from the provisions of sec-
4
tion 505 of such Act relating to new drugs be-
5
causeβ
6
ββ(I) it is intended solely for investiga-
7
tional use as described in section 505(i) of
8
such Act; and
9
ββ(II) such product is being used ex-
10
clusively for purposes of a clinical trial
11
that is the subject of an effective investiga-
12
tional new drug application.ββ.
13
(b) PENALTIES.βSection 402 of the Controlled Sub-
14
stances Act (21 U.S.C. 842) is amendedβ
15
(1) in subsection (a)β
16
(A) in paragraph (16), by striking ββorββ at
17
the end;
18
(B) by redesignating paragraph (17) as
19
paragraph (18); and
20
(C) by inserting after paragraph (16) the
21
following:
22
ββ(17) to violate section 305(f); orββ; and
23
(2) in subsection (c)β
24
(A) in paragraph (1)β
25
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(i) in subparagraph (B)(i), by striking
1
ββ(17)ββ and inserting ββ(18)ββ; and
2
(ii) in subparagraph (C), by inserting
3
ββor (17)ββ after ββparagraph (16)ββ each
4
place it appears; and
5
(B) in paragraph (2)(D), by striking
6
ββ(17)ββ and inserting ββ(18)ββ.
7
SEC. 6. REGISTRATION REQUIREMENTS FOR IMPORTERS
8
AND
EXPORTERS
OF
SCHEDULE
A
SUB-
9
STANCES.
10
Section 1008 of the Controlled Substances Import
11
and Export Act (21 U.S.C. 958) is amended by adding
12
at the end the following:
13
ββ(j)(1) The Attorney General shall register an appli-
14
cant to import or export a schedule A substance ifβ
15
ββ(A) the applicant demonstrates that the sched-
16
ule A substance will be used for research, analytical,
17
or industrial purposes approved by the Attorney
18
General; and
19
ββ(B) the Attorney General determines that such
20
registration is consistent with the public interest and
21
with the United States obligations under inter-
22
national
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