U.S. Department of Justice
Drug Enforcement Administration
Office of the Deputy Administrator
Washington, D.C. 20537
December 19, 2008
Mr. Carl Olsen
130 E Aurora Avenue
Des Moines, Iowa 50313-3654
Dear Mr. Olsen:
On May 12,2008, you petitioned the Drug Enforcement Administration (DEA) to initiate
rulemaking proceedings under the rescheduling provisions ofthe Controlled Substances
Act (CSA). You requested that DEA remove marijuana from schedule I of the CSA based
on your assertion that the federal definition for a schedule I controlled substance
no longer applies to it. You contend that federal drug law gives states the authority
to determine accepted medical use and that marijuana, therefore, has a "currently
accepted medical use in treatment in the United States" because 12 states have
passed laws relating to the use of marijuana for medical purposes. Based on these
same assertions, on August 5, 2008, you filed a "Notice and Deadline to Cease
and Desist Illegal Enforcement of Fraudulant [sic] Marijuana Regulation." The
notice states that the DEA must "cease and desist enforcement of the illegal
regulation of marijuana" within 30 days or you will file a federal civil injunction.
The Deputy Administrator finds, for the reasons stated herein, that the grounds
upon which you rely are not sufficient to justify the initiation of proceedings
for the removal of marijuana from schedule I ofthe CSA. Accordingly, your petition
is hereby denied. For the same reasons, the Deputy Administrator finds that the
notice to cease and desist also lacks merit. Accordingly, to the extent you seek
action based on this filing, this request also is hereby denied.
Legal Background
When the CSA was created, Congress specified the initial scheduling of controlled
substances and the criteria by which controlled substances could be rescheduled.
21 U.S.C. §§ 811-812 (2008). Congress placed marijuana into schedule I. See
Comprehensive Drug Abuse Prevention and Control Act of 1970, Pub. L. 91-513, § 202(c),
schedule I (c)(10), 84 Stat. 1247.
The Attorney General "may by rule" transfer a drug or other substance
between schedules if he finds that such drug or other substance has a potential
for abuse and makes with respect to such drug or other substance the findings prescribed
by subsection (b) of Section 812 for the schedule in which such drug is to be placed.
21 U.S.C. § 811(a)(I). In order for a substance to be placed in schedule I, the
Attorney General must find that:
(A) The drug or other substance has a high potential for abuse;
(B) The drug or other substance has no currently accepted medical use in treatment
in the United States; and
(C) There is a lack of accepted safety for use of the drug or other substance under
medical supervision.
21 U.S.C. § 812(b)(1)(A)-(C). To be classified in one of the other schedules (II
through V), a drug of abuse must have a "currently accepted medical use in
treatment in the United States." [Footnote 1]
The CSA provides that, in making any rescheduling determination, the Attorney General
shall consider the following eight factors:
(1) The drug's actual or relative potential for abuse;
(2) Scientific evidence of its pharmacological effect, if known;
(3) The state of current scientific knowledge regarding the drug;
(4) Its history and current pattern of abuse;
(5) The scope, duration, and significance of abuse;
(6) What, if any, risk there is to the public health;
(7) The drug's psychic or physiological dependence liability; and
(8) Whether the substance is an immediate precursor of a substance already controlled
under the CSA.
21 U.S.C. § 811(c). The Attorney General has delegated this authority to the Administrator
of DEA, who has redelegated it to the Deputy Administrator. See 28 C.F.R.
§§ 0.100(b) & 0.104, Appendix to Subpart R, sec. 12 (2008).
The CSA further provides that, before initiating proceedings to reschedule a drug,
the Administrator must gather the necessary data and request from the Secretary
of Health and Human Services (HHS) a scientific and medical evaluation and recommendations
as to whether the controlled substance should be rescheduled as the petitioner proposes.
21 U.S.C. § 811(b); 21 C.F.R. § 130S.43(d); Gettman v. DEA, 290 F.3d 430,
432 (D.C. Cir. 2002). In making such evaluation and recommendations, the Secretary
must consider the factors listed in paragraphs (2), (3), (6), (7), and (8) above,
and any scientific or medical considerations involved in paragraphs (1), (4), and
(5) above. 21 U.S.C. § 811(b). The Secretary has delegated this function to the
Assistant Secretary for Health. [Footnote 2] If the Administrator determines that
the evaluations and recommendations of the Assistant Secretary and "all other
relevant data" constitute substantial evidence that the drug that is the subject
of the petition should be subjected to lesser control or removed entirely from the
schedules, he shall initiate proceedings to reschedule the drug or remove it from
the schedules as the evidence dictates. 21 U.S.C. § 811(b); 21 C.F.R. § 1308.43(e).
Basis for Denial of Your Petition and Notice
Your petition and notice rest on your contention that federal drug law gives states
the authority to determine, for purposes of the CSA, whether a drug has a "currently
accepted medical use in treatment in the United States," and that marijuana
has such a currently accepted medical use because 12 states have passed laws relating
to the use of marijuana for medical purposes. See Carl Olsen Petition for
Marijuana Rescheduling (May 12, 200S) ("Pet."); Carl Olsen Memorandum
of Law in Support ofPetition for Marijuana Rescheduling (May 25, 200S) ("Mem.");
Notice and Deadline to Cease and Desist Illegal Enforcement of Fraudulant [sic]
Marijuana Regulation (Aug. 5, 200S) ("Notice"). [Footnote 3] For the following
reasons, your contention is not in accordance with law.
A. The CSA's Statutory Scheme
The CSA's statutory scheme disproves your contention that federal drug law gives
states the authority to determine whether a drug has a "currently accepted
medical use" within the meaning ofthe CSA. You rely on Section 903 ofthe CSA,
see Pet. at 2; Mem. at 16; Notice at 1, which provides that: "No provision
ofthis subchapter shall be construed as indicating an intent on the part ofthe Congress
to occupy the field in which that provision operates, including criminal penalties,
to the exclusion of any state law on the same subject matter which would otherwise
be within the authority of the State, unless there is a positive conflict between
that provision of this subchapter and that State law so that the two cannot consistently
stand together." 21 U.S.C. § 903 (2008).
As a threshold matter, 21 U.S.C. § 903 merely reaffirms, for purposes of the CSA,
what is inherent in the supremacy clause of the United States Constitution: that
any state law that actually conflicts with federal law is preempted by federal law
and therefore invalid under the supremacy clause. [Footnote 4] Section 903 also
provides that, so long as the states do not enact a law relating to controlled substances
that creates a positive conflict with the CSA, the states are free to enact laws
regulating controlled substances which would otherwise be within their authority
that will operate alongside the CSA. Thus, it would be antithetical to the text
of section 903 to cite it for the proposition that state controlled substance laws
that conflict with the CSA can override or frustrate the purposes of the CSA. As
the Supreme Court stated in the context of marijuana possession and cultivation
taking place in purported compliance with California law: "The Supremacy Clause
unambiguously provides that if there is any conflict between federal and state law,
federal law shall prevail." [Footnote 5]
Furthermore, the CSA plainly does not assign to the states the authority to make
findings relevant to CSA scheduling determinations. Rather, the CSA expressly delegates
the task of making such findings - including whether a substance has any currently
accepted medical use - to the Attorney General. 21 U.S.C. § 811(a). The CSA also
expressly tasks the Secretary of HHS to provide a scientific and medical evaluation
and scheduling recommendations to inform the Attorney General's findings. 21 U.S.C.
§ 811 (b). [Footnote 6] That Congress explicitly provided scheduling authority to
these two federal entities further precludes your argument that Section 903 reserves
this authority to the states.
In addition, the CSA explicitly provides that in making a scheduling determination,
the Attorney General shall consider the following eight factors:
(1) The drug's actual or relative potential for abuse;
(2) Scientific evidence of its pharmacological effect, if known;
(3) The state ofcurrent scientific knowledge regarding the drug;
(4) Its history and current pattern of abuse;
(5) The scope, duration, and significance of abuse;
(6) What, if any, risk there is to the public health;
(7) The drug's psychic or physiological dependence liability; and
(8) Whether the substance is an immediate precursor of a substance already controlled
under the CSA.
21 U.S.C. § 811(c). These factors do not include state law. The CSA's statutory
text evidences that Congress did not envision such a role for state law in establishing
the schedules of controlled substances under the CSA. [Footnote 7]
B. Gonzales v. Oregon and Other Recent Supreme Court Cases
You further rely on Gonzales v. Oregon, 546 U.S. 243 (2006). See
Pet. at 2-3; Mem. at 13; Notice at 4. This reliance also is misplaced. You argue
that Oregon supports your petition by requiring federal authorities to
defer to states' determinations on issues of medical practice. To the contrary,
Oregon affirms the core federal authority of the Attorney General, in consultation
with the Secretary of HHS, as to drug scheduling.
In Oregon, the United States Supreme Court considered the Attorney General's Interpretive
Rule prohibiting doctors from prescribing controlled substances for use in physician-assisted
suicide under an Oregon state law that permitted the procedure. Id. at
248. The Court held that the Rule was not entitled to deference because it was not
issued pursuant to an explicit delegation of rule making authority. Id.
at 258-69. The Court did not find the Attorney General's interpretation persuasive
and invalidated the Rule because the CSA "manifests no intent to regulate the
practice of medicine generally." Id. at 270.
In so holding, however, the Court repeatedly cited by contrast - as a valid and
explicit delegation of authority - the Attorney General's power as to drug scheduling.
[Footnote 8] The Court observed that, by the text ofthe CSA itself, Congress had
delegated "control" authority to the Attorney General to add, remove,
or reschedule substances. [Footenote 9] The Court further cited the CSA's detailed
scheduling procedures, including the requirement to request a scientific and medical
evaluation by the Secretary of HHS. Id. at 260. Oregon thus confirmed
that, in contrast to the invalidated Rule, drug scheduling authority and the corresponding
scheduling procedures are an appropriate exercise of the federal power granted in
the CSA.
The Court also approvingly cited the CSA's explicit allocation of medical judgments
in the scheduling context - not, as you argue, to states - but rather, to the Secretary:
"The CSA allocates decision making powers among statutory actors so that medical
judgments, if they are to be decided at the federal level and for the limited objects
ofthe statute, are placed in the hands of the Secretary." Id. at 265. Whereas
the invalidated Rule involved an overly broad assertion of authority, the drug scheduling
context exemplified the "CSA's consistent delegation of medical judgments to
the Secretary and its otherwise careful allocation of powers." Id. at 272.
Thus, far from giving authority to the states, Oregon instead confirms the Attorney
General's explicit authority, in conjunction with the Secretary's recommendations
on scientific and medical matters, as to drug scheduling.
The two other recent Supreme Court cases you cite, see Mem. at 15-16; Notice
at 3, likewise affirmed the primacy of federal law over state marijuana laws. In
United States v. Oakland Cannabis Buyers' Cooperative, 532 U.S. 483 (2001)
("OCBC"), the Court held that no medical necessity exception
existed to the CSA's prohibition on manufacturing and distributing marijuana. Notwithstanding
California state law authorizing possession and cultivation of marijuana for claimed
medical purposes, Congress' clear determination that all schedule I controlled substances,
including marijuana, have no currently accepted medical use forecloses any argument
as to whether such drugs can be dispensed and prescribed for medical use. Id.
at 493. The Court in OCBC was explicit in stating that "for purposes
of the [CSA], marijuana has 'no currently accepted medical use' at all. § 812."
Id. at 491. Similarly, in Raich, 545 U.S. 1, the Court held that,
even in a state that had legalized marijuana activity for claimed medical use, Congress'
federal commerce clause power extended to prohibit purportedly intrastate cultivation
and use of marijuana in compliance with the state law. "Limiting the activity
to marijuana possession and cultivation 'in accordance with state law' cannot serve
to place respondents' activities beyond congressional reach." Id.
at 29.
C. Whether A Drug Has A "Currently Accepted Medical Use in Treatment in the
United States"
Your argument that there is no federal definition of"currently accepted medical
use" also fails. In order to determine whether a substance has a "currently
accepted medical use," the Administrator applies a five-part test:
1) The drug's chemistry must be known and reproducible;
2) There must be adequate safety studies;
3) There must be adequate and well-controlled studies proving efficacy;
4) The drug must be accepted by qualified experts; and
5) The scientific evidence must be widely available.
Alliancefor Cannabis Therapeutics v. DEA, 15 F.3d 1131, 1135 (D.C. Cir.
1994) ("ACT II"). This test was approved by the United States
Court of Appeals for the D.C. Circuit as a reasonable interpretation of the statutory
language. See Id. at 1134-5, 1137 (approving the Administrator's
Final Order applying these five criteria); see also Alliance for
Cannabis Therapeutics v. DEA, 930 F.2d 936, 939 (D.C. Cir. 1991) ("ACT
I"). Significantly, with respect to your petition, this test includes
no reference to state law.
D. Other Arguments as to Currently Accepted Medical Use
A substantial portion of the remainder of your memorandum in support of your current
petition and your notice merely rehash arguments as to "currently accepted
medical use" that you unsuccessfully asserted when you petitioned DEA to reschedule
marijuana in 1992 and when you sought review of DEA's denial of that petition by
the United States Court of Appeals for the District of Columbia Circuit. The United
States Court of Appeals, in declining your petition for review in a per curiam order
issued October 3, 1996, stated that the arguments you raised "occasion no need
for an opinion." Olsen v. DEA, No. 94-1605, 1996 WL 590870 (D.C. Cir.
Oct. 3, 1996). It is, therefore, unnecessary for DEA to revisit these same arguments
yet again in 2008.
Nevertheless, to ensure completeness of the record, we briefly address and dismiss
these contentions. First, you discuss again at length litigation relating to the
1972 petition to reschedule marijuana filed by the National Organization for the
Reform of Marijuana Laws (NORML), see Mem. at 7-9, and the United States
Court of Appeals for the First Circuit's decision in Grinspoon v. DEA,
828 F.2d 881 (1st Cir. 1987). See Mem. at 9-12; Notice at 2. These cases
are inapposite, however, as they were superseded by the subsequent ACT I
and ACT II decisions approving the present five-factor test. See
ACT II, 15 F.3d at 1133 (noting "[t]he petition to reschedule marijuana
was first filed [by NORML] in 1972 and has been before this court on four prior
occasions ...."); ACT I, 930 F.2d at 939-40 (explicitly distinguishing
Grinspoon). [Footnote l0]
Second, you reiterate arguments regarding the Convention on Psychotropic Substances,
contending that it was modified in 1991 to allow for the medical use of the pharmaceutically
pure primary psychoactive ingredient in marijuana, delta-9-THC, and that this ingredient
has been rescheduled twice, from schedule I to schedule III. Mem. at 4. You further
contend that plants are not typically scheduled in schedules more restrictive than
the psychoactive substances that are obtained from them. Mem. at 5. Under the CSA,
however, the regulation of chemicals and the plant material are distinct from each
other: drugs or other substances are treated and classified differently, according
to the enumerated statutory criteria. 21 U.S.C. § 812(b); see also Final Order,
In the Matter of Petition of Carl Eric Olsen (May 16, 1994) (rejecting petition
to reschedule marijuana); Olsen, 1996 WL 590870, at *1 (denying Olsen's
petition for review). Whether marijuana is a source of delta-9-THC is irrelevant
to the status of marijuana under the CSA.
None of your remaining arguments as to whether marijuana has a currently accepted
medical use have merit. [Footnote 11] First, you reference a portion of the 1970
legislative history of the CSA relating to appointment of a commission that issued
a report on marijuana in 1972, citing a portion of the 1972 report itself. See Mem.
at 2-3. In the more than 36 years that have elapsed since these materials were published,
however, numerous individuals and marijuana legalization advocates have pointed
to the 1972 marijuana report to justify CSA violations involving marijuana, to challenge
the constitutionality of the federal marijuana laws, or, as with your latest petition,
to argue that marijuana should be deemed to have medical efficacy for purposes ofthe
CSA. [Footnote 12] None of these efforts have ever succeeded for the simple reason
that Congress took no action to alter the CSA in any respect as a result of the
1972 report. The fact that Congress has not rescheduled marijuana speaks for itself.
You also observe that the federal government has supplied marijuana to medical patients
through a program of compassionate use. Mem. at 5-6 (citing Kuromiya v. United States,
78 F. Supp. 2d 367 (E.D. Pa. 1999)). The existence of this exception is not a ground
for rescheduling. As the federal district court held in Kuromiya, the government's
decision to continue the program at all was a "means of balancing" the
interests of those who had relied on the drug with the government's desire to avoid
distributing marijuana. 78 F. Supp. 2d at 370-71. You further claim that one participant's
primary care doctor has retired, and that she is not able to find another doctor
willing to prescribe marijuana because of the stigma associated with prescribing
a schedule I substance. Mem. at 6. You have not provided any evidence to support
this contention. Even if you had, one individual's potential hardship to participate
in a compassionate use program is not adequate legal grounds for rescheduling. See
21 U.S.C. § 811(c).
Finally, you argue that the "DEA's own Administrative Law Judge [ALJ Young]
has already determined that marijuana is safe for use under medical supervision."
Olsen Petition at 4. As you acknowledge, however, see Pet. at 3, the DEA Administrator
unambiguously rejected ALJ Young's determination in In re Marijuana Rescheduling,
DEA Dkt. No. 86-22 (Sept. 6, 1998) (attached as Ex. 1 to Pet.). The D.C. Circuit
later affirmed the DEA's final order (Mar. 26, 1992) in ACT II, 15 F.3d
at 1135 (denying petition to review DEA's final order declining to reschedule marijuana).
Nor is it accurate that the Administrator's rejection of ALJ Young's determination
depended on the fact that no state had accepted the use of marijuana for medical
purposes. In fact, ALJ Young's opinion had noted the efforts of a number of states
to pass such legislation. See, e.g., In re Marijuana Rescheduling,
DEA Dkt. No. 86-22, 21,22,28. In any case, for the reasons set forth in detail above,
the existence of state legislation is not relevant to a scheduling determination.
Conclusion
Accordingly, there is no statutory basis for DEA to grant your petition to initiate
proceedings to reschedule marijuana. Nor is there any basis to initiate any action
based on your August 5th notice.
The Petitioner's request is denied.
Sincerely,
Michele M. Leonhart
Deputy Administrator