Samirkumar Shah, M.D.; Decision and Order, 71931-71934 [2024-19731]
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71931
Federal Register / Vol. 89, No. 171 / Wednesday, September 4, 2024 / Notices
The Drug Enforcement
Administration requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
ADDRESSES:
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment.
In
accordance with 21 CFR 1301.33(a), this
is notice that on July 24, 2024,
Cambridge Isotope Laboratories, Inc., 50
Frontage Road, Andover, Massachusetts
01810–5413, applied to be registered as
a bulk manufacturer of the following
basic class(es) of controlled
substance(s):
SUPPLEMENTARY INFORMATION:
Controlled substance
Drug code
Tetrahydrocannabinols ..................................................................................................................................................
The company plans to synthetically
bulk manufacture the controlled
substance Tetrahydrocannabinols to
produce analytical standards for
distribution to its customers. No other
activity for this drug code is authorized
for this registration.
Marsha L. Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024–19788 Filed 9–3–24; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
importer of basic class(es) of controlled
substance(s). Refer to Supplementary
Information listed below for further
drug information.
Registered bulk manufacturers of
the affected basic class(es), and
applicants, therefore, may submit
electronic comments on or objections to
the issuance of the proposed registration
on or before October 4, 2024. Such
persons may also file a written request
for a hearing on the application on or
before October 4, 2024.
DATES:
The Drug Enforcement
Administration requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
ADDRESSES:
Drug Enforcement Administration
[Docket No. DEA–1422]
Importer of Controlled Substances
Application: Fisher Clinical Services,
Inc.
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Fisher Clinical Services, Inc.
has applied to be registered as an
SUMMARY:
In
accordance with 21 CFR 1301.34(a), this
is notice that on July 10, 2024, Fisher
Clinical Services, Inc., 700A–C Nestle
Way, Breinigsville, Pennsylvania
18031–1522, applied to be registered as
an importer of the following basic
class(es) of controlled substance(s):
Drug code
ddrumheller on DSK120RN23PROD with NOTICES1
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approved finished dosage forms for
commercial sale.
Marsha L. Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024–19791 Filed 9–3–24; 8:45 am]
BILLING CODE P
PO 00000
I
SUPPLEMENTARY INFORMATION:
Marihuana Extract ..........................................................................................................................................................
Dimethyltryptamine ........................................................................................................................................................
Psilocybin .......................................................................................................................................................................
Methylphenidate .............................................................................................................................................................
Levorphanol ...................................................................................................................................................................
Noroxymorphone ...........................................................................................................................................................
Tapentadol .....................................................................................................................................................................
VerDate Sep<11>2014
7370
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment. All
requests for a hearing must be sent to:
(1) Drug Enforcement Administration,
Attn: Hearing Clerk/OALJ, 8701
Morrissette Drive, Springfield, Virginia
22152; and (2) Drug Enforcement
Administration, Attn: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for a hearing should
also be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152.
Controlled substance
The company plans to import the
listed controlled substances for use in
clinical trials only. No other activities
for these drug codes are authorized for
this registration.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of Food and Drug
Administration-approved or non-
Schedule
Schedule
7350
7435
7437
1724
9220
9668
9780
I
I
I
II
II
II
II
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 23–15]
Samirkumar Shah, M.D.; Decision and
Order
On November 28, 2022, the Drug
Enforcement Administration (DEA or
Government) issued an Order to Show
Cause (OSC) to Samirkumar Shah, M.D.,
(Applicant) of Pittsburgh, Pennsylvania.
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OSC, at 1, 3. The OSC proposed the
denial of Applicant’s application for a
DEA Certificate of Registration, Control
No. W21057811C, alleging that
Applicant has been excluded from
participation in Medicare, Medicaid,
and all federal health care programs
pursuant to 42 U.S.C. 1320a–7(a). Id. at
1 (citing 21 U.S.C. 824(a)(5)).1
A hearing was held before DEA Chief
Administrative Law Judge John J.
Mulrooney, II (the Chief ALJ), who, on
November 16, 2023, issued his
Recommended Rulings, Findings of
Fact, Conclusions of Law, and Decision
(Recommended Decision or RD), which
recommended denial of Applicant’s
application. RD, at 19. Following the
issuance of the RD, Applicant filed
Exceptions.2 Having reviewed the entire
record, the Agency adopts and hereby
incorporates by reference the entirety of
the Chief ALJ’s rulings, credibility
findings,3 findings of fact, conclusions
of law, sanctions analysis, and
recommended sanction as found in the
RD.
1 In its OSC, the Government relies upon 21
U.S.C. 824(a), grounds which Congress provided to
support revocation or suspension, not denial of an
application. Prior Agency decisions have repeatedly
determined that it is appropriate to consider a
provision of 21 U.S.C. 824(a) when determining
whether to grant a practitioner registration
application. Robert Wayne Locklear, M.D., 86 FR
33,738, 33,744–33,745 (2021) (collecting cases); see
also Dinorah Drug Store, Inc., 61 FR 15,972,
15,973–15,974 (1996).
2 In Applicant’s Exceptions document, dated
November 22, 2023, Applicant does not put forward
any particular arguments contesting the Chief ALJ’s
Recommended Decision, but simply requests an
appeal of the Decision. Applicant’s Exceptions, at
1–2.
3 The Agency adopts the Chief ALJ’s summary of
each of the witnesses’ testimonies as well as the
Chief ALJ’s assessment of each of the witnesses’
credibility. See RD, at 3–10. The Agency agrees
with the Chief ALJ that the testimony from the DEA
Diversion Investigator (DI), which was primarily
focused on the non-controversial introduction of
documentary evidence and the DI’s contact with the
case, was sufficiently detailed, plausible, and
internally consistent without indication of any
motive to fabricate or exaggerate and thus
warranted full credibility. Id. at 4. The Agency also
agrees with the Chief ALJ that the testimony from
Applicant, which was focused on Applicant’s
criminal conviction, the underlying facts of
Applicant’s criminal conviction, and the mandatory
exclusion resulting from Applicant’s criminal
conviction, was ‘‘ubiquitously inconsistent,
frequently lacking in detail, and commonly bereft
of even a modest level of basic plausibility.’’ Id. at
9. The Chief ALJ also noted, and the Agency agrees,
that Applicant was ‘‘unwilling to acknowledge his
own misconduct on any level.’’ Id. Based on these
factors, the Chief ALJ found, and the Agency agrees,
that Applicant’s testimony was lacking in
credibility and warranted reduced weight. Id. at 9–
10.
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I. Findings of Fact
1. Applicant’s Criminal Conviction and
Exclusion
In 2021, Applicant was convicted of
two felony counts of healthcare fraud in
violation of 18 U.S.C. 1347. RD, at 4;
Government Exhibit (GX) 3. As a result
of Applicant’s conviction, the U.S.
Department of Health and Human
Services, Office of Inspector General
(HHS/OIG) excluded Applicant,
effective July 20, 2022, from
participation in Medicare, Medicaid,
and all federal health care programs
pursuant to 42 U.S.C. 1320a–7(a) for a
period of twenty-seven years. RD, at 4;
GX 4; Tr. 26–28.
2. Applicant’s Argument
Regarding the allegations underlying
his criminal conviction, Applicant
testified that he started implementing in
his practice a cardiovascular therapy
called ‘‘external counter pulsation
therapy’’ (ECP) designed to help
patients with heart failure. Tr. 59.
Applicant testified that he offered this
therapy with 25 certified physicians in
Pennsylvania. Id. According to
Applicant, ‘‘[t]he mistake was the
billing of this therapy.’’ RD; at 7; Tr. 59–
60. Applicant testified that he is ‘‘not
trained as a biller’’ and he ‘‘had a
private company who prepared all the
codes and billing forms.’’ RD, at 7; Tr.
at 60. Applicant asserted that he ‘‘did
not realize that the billing was not done
correctly,’’ but also that he ‘‘did
everything by the book and the law.’’
RD, at 7; Tr. 60, 90. Nonetheless,
Applicant stated, ‘‘the biller is
responsible for what happened . . . my
name was used, but he’s liable.’’ RD, at
7; Tr. 104.
Notably, when Applicant appealed
his criminal conviction, the United
States Court of Appeals for the Third
Circuit (Court of Appeals) found that the
ECP therapy that Applicant was
prescribing and billing for was
unnecessary. RD, at 7 (citing United
States v. Shah, 43 F.4th 356, 366–367
(3d Cir. 2022)). Even so, Applicant
testified that every patient to whom he
prescribed ECP therapy needed it. RD, at
7; Tr. 77, 85–86. The Court of Appeals
also found that Applicant had
advertised his ECP therapy to
accomplish unrealistic goals, such as
that it would make patients ‘‘younger
and smarter’’ and could help with a
plethora of conditions including
obesity, erectile disfunction, restless leg
syndrome, and blood pressure issues.
RD, at 7 (citing United States v. Shah,
43 F.4th at 361). According to
Applicant, ‘‘[t]hose comments were
made by a couple of [his] office
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employees without [his] knowledge.’’
RD, at 7; Tr. 89. As for the finding by
the Court of Appeals that Applicant was
often not present to supervise the ECP
treatments, see United States v. Shah,
43 F.4th at 361, Applicant testified that
this finding was ‘‘bogus’’ because other
physicians were present. RD, at 7; Tr.
89–90.
As highlighted by the Chief ALJ,
Applicant also repeatedly emphasized
that he had ‘‘hired a very awful attorney
in Western Pennsylvania as [his]
attorney to defend [his] case.’’ RD, at 7–
8; Tr. 60. Specifically, Applicant took
issue with his attorney’s legal strategy
(which led to the attorney firing
Applicant as a client) as well as the fact
that the attorney went on to accept an
appointment as a federal prosecutor,
which Applicant characterized as
creating a conflict of interest regarding
his case. RD, at 8; Tr. 61. As noted by
the Chief ALJ, Applicant’s latter
complaint was raised with the Court of
Appeals and found to be without merit.
RD, at 8 (citing United States v. Shah,
43 F.4th at 363–365). Furthermore,
Applicant claimed he was forced to go
to trial without access to relevant
medical files and also was unable to
have these files reviewed by a potential
expert witness. RD, at 8; Tr. 77, 81–82,
84. Again, the Court of Appeals found
this contention to be without merit. RD,
at 8 (citing United States v. Shah, 43
F.4th at 364–365). Finally, Applicant
made claims as to the Court of Appeals
itself. Specifically, Applicant claimed
incorrectly that the panel of the Court of
Appeals that affirmed his conviction
was split. RD, at 8 (citing United States
v. Shah, 43 F.4th at 360); Tr. 83.
Applicant also claimed that his request
for an en banc reconsideration of his
case was denied ‘‘because they’re busy,
they’re on vacations and everything,
they denied my ten-judge panel
appeal.’’ RD, at 8; Tr. 83. Overall,
Applicant characterized his conviction
as a ‘‘complete miscarriage of justice.’’
RD, at 8; Tr. 88. Regarding the findings
of HHS/OIG, Applicant testified that
HHS/OIG ‘‘just had a summary
judgment’’ without providing Applicant
with a trial or hearing. RD, at 9; Tr. 93.
Applicant testified that the criminal
court had ordered $1.2 million in
restitution and that he was paying $300
per month. RD, at 9; Tr. 70. As for any
potential remedial measures, Applicant
testified that when he restarts his
practice, he will not need Medicare
patients and he plans to focus on weight
loss and cosmetic procedures for ‘‘cashpaying patients.’’ RD, at 9; Tr. 70–71.
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II. Discussion
1. The Five Public Interest Factors
Pursuant to Section 303(g)(1) of the
Controlled Substances Act (CSA), ‘‘[t]he
Attorney General shall register
practitioners . . . to dispense . . .
controlled substances . . . if the
applicant is authorized to dispense . . .
controlled substances under the laws of
the State in which he practices.’’ 21
U.S.C. 823(g)(1). Section 303(g)(1)
further provides that an application for
a practitioner’s registration may be
denied upon a determination that ‘‘the
issuance of such registration . . . would
be inconsistent with the public
interest.’’ Id. In making the public
interest determination, the CSA requires
consideration of the following factors:
(A) The recommendation of the
appropriate State licensing board or
professional disciplinary authority.
(B) The applicant’s experience in
dispensing, or conducting research with
respect to controlled substances.
(C) The applicant’s conviction record
under Federal or State laws relating to the
manufacture, distribution, or dispensing of
controlled substances.
(D) Compliance with applicable State,
Federal, or local laws relating to controlled
substances.
(E) Such other conduct which may threaten
the public health and safety.
21 U.S.C. 823(g)(1).
In the current matter, it is undisputed
that Applicant holds a valid state
medical license and is authorized to
dispense controlled substances in the
Commonwealth of Pennsylvania where
he practices. Moreover, because the
Government has not alleged that
Applicant’s registration is inconsistent
with the public interest under section
823, and although the Agency has
considered section 823, the Agency will
not analyze Applicant’s application
under the public interest factors.
Therefore, in accordance with prior
agency decisions, the Agency will move
to assess whether the Government has
proven by substantial evidence that a
ground for suspension exists under 21
U.S.C. 824(a). See supra n.1.
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2. Mandatory Exclusion From Federal
Health Care Programs
Under Section 824(a) of the CSA, a
registration ‘‘may be suspended or
revoked’’ upon a finding of one or more
of five grounds. 21 U.S.C. 824(a). The
ground in 21 U.S.C. 824(a)(5) requires
that the registrant ‘‘has been excluded
(or directed to be excluded) from
participation in a program pursuant to
section 1320a–7(a) of Title 42.’’ Id. at
§ 824(a)(5). Here, there is no dispute in
the record that Applicant is mandatorily
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excluded from federal health care
programs under 42 U.S.C. 1320a–7(a).
The Government has presented
substantial evidence of Applicant’s
exclusion and the underlying criminal
conviction that led to that exclusion,
and Applicant has admitted to the same.
GX 2–8; Applicant’s Post-Hearing Brief,
at 4–5. Accordingly, the Agency will
sustain the Government’s allegation that
Applicant has been excluded from
participation in a program pursuant to
section 1320a–7(a) of Title 42 and find
that the Government has established
that a ground exists upon which a
registration could be revoked pursuant
to 21 U.S.C. 824(a)(5).
Further, although the language of 21
U.S.C. 824(a)(5) discusses suspension
and revocation of a registration, for the
reasons discussed above, see supra n.1,
it may also serve as the basis for the
denial of a DEA registration application.
Dinorah Drug Store, Inc., 61 FR at
15,973. Applicant’s exclusion from
participation in a program under 42
U.S.C. 1320a–7(a), therefore, serves as
an independent basis for denying his
application for DEA registration. 21
U.S.C. 824(a)(5).4
III. Sanction
Where, as here, the Government has
established sufficient grounds for
revocation or denial, the burden shifts
to the registrant to show why he can be
entrusted with the responsibility carried
by a registration. Garret Howard Smith,
M.D., 83 FR 18,882, 18,910 (2018). To
establish that he can be entrusted with
registration, a registrant must both
accept responsibility and demonstrate
that he has undertaken corrective
measures. Holiday CVS, L.L.C., dba CVS
Pharmacy Nos 219 and 5195, 77 FR
62,316, 62,339 (2012) (internal
quotations omitted). Trust is necessarily
a fact-dependent determination based
on individual circumstances; therefore,
the Agency looks at factors such as the
acceptance of responsibility, the
credibility of that acceptance as it
relates to the probability of repeat
violations or behavior, the nature of the
misconduct that forms the basis for
sanction, and the Agency’s interest in
deterring similar acts. See, e.g., Robert
Wayne Locklear, M.D., 86 FR 33,738,
33,746 (2021).
4 The underlying conviction forming the basis for
a registrant’s mandatory exclusion from
participation in federal health care programs need
not involve controlled substances to provide the
grounds for revocation or denial pursuant to section
824(a)(5). Jeffrey Stein, M.D., 84 FR 46,968, 46,971–
46,972 (2019); see also Narciso Reyes, M.D., 83 FR
61,678, 61,681 (2018); KK Pharmacy, 64 FR 49,507,
49,510 (1999) (collecting cases); Melvin N. Seglin,
M.D., 63 FR 70,431, 70,433 (1998); Stanley Dubin,
D.D.S., 61 FR 60,727, 60,728 (1996).
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Here, and as noted by the ALJ,
‘‘[Applicant’s] consistent minimization
and flat out denial of his wrongdoing
supports the proposition that he has not
credibly and unequivocally accepted
responsibility for his actions.’’ RD, at 14.
Further, Applicant repeatedly placed
the blame on others, including his
practice’s third-party billers, his office
employees, his attorney, the Court of
Appeals, and HHS/OIG itself. Id. at 14–
15. Ultimately, the ALJ concluded, and
the Agency agrees, that Applicant has
not demonstrated unequivocal
acceptance of responsibility for his
actions. Id. at 16.5
In addition to acceptance of
responsibility, the Agency considers
both specific and general deterrence
when determining an appropriate
sanction. Daniel A. Glick, D.D.S., 80 FR
at 74,810. In this case, the Agency
agrees with the ALJ that, regarding
specific deterrence, ‘‘[w]ithout
understanding the nature of his
misconduct and his own culpability in
it, there is no rational reason [to] believe
that [Applicant] would make different
choices in the face of the same
circumstances in the future.’’ RD, at 17.
Further, the Agency agrees with the ALJ
that the interests of general deterrence
also support revocation, as a lack of
sanction in the current matter would
send a message to the registrant
community that a registrant can commit
similar misconduct without
consequences. Id. at 18. The Agency
also agrees with the ALJ that
Applicant’s actions were egregious, as
‘‘‘defrauding federal health care
programs is egregious.’’ RD, at 18
(quoting Gilbert Y. Kim, D.D.S., 87 FR
21,139, 21,145 (2022)). As noted by the
ALJ, Applicant was convicted of two
felony counts of healthcare fraud, with
the Court of Appeals itself highlighting
that Applicant ‘‘billed insurers for
millions of dollars in ECP treatments
where they were either not medical
necessary for the patient or delivered
without the required physician
supervision or both.’’ RD, at 18 (quoting
United States v. Shah, 43 F.4th at 367).
In sum, Applicant has not offered any
credible evidence on the record to rebut
the Government’s case for denial of his
5 When a registrant fails to make the threshold
showing of acceptance of responsibility, the Agency
need not address the registrant’s remedial measures.
Ajay S. Ahuja, M.D., 84 FR 5,479, 5,498 n.33 (2019)
(citing Jones Total Health Care Pharmacy, L.L.C. &
SND Health Care, L.L.C., 81 FR 79,188, 79,202–03
(2016)); Daniel A. Glick, D.D.S., 80 FR 74,800,
74,801, 74,810 (2015). Even so, in the current
matter, the Agency has considered Applicant’s
testimony that when he restarts his practice, he
intends to avoid Medicare patients and instead
focus on weight loss and cosmetic procedures for
‘‘cash-paying patients.’’ Tr. 70–71.
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application and Applicant has not
demonstrated that he can be entrusted
with the responsibility of registration.
Id. at 19. Accordingly, the Agency will
order that Applicant’s application be
denied.
Order
document upon publication in the
Federal Register.
Heather Achbach,
Federal Register Liaison Officer, Drug
Enforcement Administration.
[FR Doc. 2024–19731 Filed 9–3–24; 8:45 am]
BILLING CODE 4410–09–P
Pursuant to 28 CFR 0.100(b) and the
authority vested in me by 21 U.S.C. 823,
I hereby deny the pending application
for a DEA Certificate of Registration,
Control No. W21057811C, submitted by
Samirkumar Shah, M.D., as well as any
other pending application of
Samirkumar Shah, M.D., for additional
registration in Pennsylvania. This Order
is effective October 4, 2024.
Signing Authority
This document of the Drug
Enforcement Administration was signed
on August 19, 2024, by Administrator
Anne Milgram. That document with the
original signature and date is
maintained by DEA. For administrative
purposes only, and in compliance with
requirements of the Office of the Federal
Register, the undersigned DEA Federal
Register Liaison Officer has been
authorized to sign and submit the
document in electronic format for
publication, as an official document of
DEA. This administrative process in no
way alters the legal effect of this
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–1419]
Importer of Controlled Substances
Application: Caligor Coghlan Pharma
Services
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Caligor Coghlan Pharma
Services has applied to be registered as
an importer of basic class(es) of
controlled substance(s). Refer to
Supplementary Information listed below
for further drug information.
DATES: Registered bulk manufacturers of
the affected basic class(es), and
applicants, therefore, may submit
electronic comments on or objections to
the issuance of the proposed registration
on or before October 4, 2024. Such
persons may also file a written request
for a hearing on the application on or
before October 4, 2024.
ADDRESSES: The Drug Enforcement
Administration requires that all
SUMMARY:
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment. All
requests for a hearing must be sent to:
(1) Drug Enforcement Administration,
Attn: Hearing Clerk/OALJ, 8701
Morrissette Drive, Springfield, Virginia
22152; and (2) Drug Enforcement
Administration, Attn: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for a hearing should
also be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.34(a), this
is notice that on July 19, 2024, Caligor
Coghlan Pharma Services, 1500
Business Park Drive, Unit B, Bastrop,
Texas 78602, applied to be registered as
an importer of the following basic
class(es) of controlled substance(s):
Controlled substance
Drug code
ddrumheller on DSK120RN23PROD with NOTICES1
Lysergic acid diethylamide ............................................................................................................................................
5-Methoxy-N-N-dimethyltryptamine ...............................................................................................................................
Dimethyltryptamine ........................................................................................................................................................
Psilocyn ..........................................................................................................................................................................
The company plans to import the
listed controlled substances as finished
dosage units for use in clinical trials. No
other activities for these drug codes are
authorized for this registration.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of Food and Drug
Administration-approved or nonapproved finished dosage forms for
commercial sale.
Marsha L. Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024–19785 Filed 9–3–24; 8:45 am]
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Drug Enforcement Administration
[Docket No. DEA–1421]
Bulk Manufacturer of Controlled
Substances Application: Cambrex
High Point, Inc
Notice of application.
Cambrex High Point, Inc has
applied to be registered as a bulk
manufacturer of basic class(es) of
controlled substance(s). Refer to
Supplementary Information listed below
for further drug information.
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Registered bulk manufacturers of
the affected basic class(es), and
applicants, therefore, may submit
electronic comments on or objections to
the issuance of the proposed registration
on or before November 4, 2024. Such
persons may also file a written request
for a hearing on the application on or
before November 4, 2024.
The Drug Enforcement
Administration requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
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ADDRESSES:
Drug Enforcement
Administration, Justice.
AGENCY:
SUMMARY:
I
I
I
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DATES:
DEPARTMENT OF JUSTICE
ACTION:
7315
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Schedule
E:\FR\FM\04SEN1.SGM
04SEN1
Agencies
[Federal Register Volume 89, Number 171 (Wednesday, September 4, 2024)]
[Notices]
[Pages 71931-71934]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-19731]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 23-15]
Samirkumar Shah, M.D.; Decision and Order
On November 28, 2022, the Drug Enforcement Administration (DEA or
Government) issued an Order to Show Cause (OSC) to Samirkumar Shah,
M.D., (Applicant) of Pittsburgh, Pennsylvania.
[[Page 71932]]
OSC, at 1, 3. The OSC proposed the denial of Applicant's application
for a DEA Certificate of Registration, Control No. W21057811C, alleging
that Applicant has been excluded from participation in Medicare,
Medicaid, and all federal health care programs pursuant to 42 U.S.C.
1320a-7(a). Id. at 1 (citing 21 U.S.C. 824(a)(5)).\1\
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\1\ In its OSC, the Government relies upon 21 U.S.C. 824(a),
grounds which Congress provided to support revocation or suspension,
not denial of an application. Prior Agency decisions have repeatedly
determined that it is appropriate to consider a provision of 21
U.S.C. 824(a) when determining whether to grant a practitioner
registration application. Robert Wayne Locklear, M.D., 86 FR 33,738,
33,744-33,745 (2021) (collecting cases); see also Dinorah Drug
Store, Inc., 61 FR 15,972, 15,973-15,974 (1996).
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A hearing was held before DEA Chief Administrative Law Judge John
J. Mulrooney, II (the Chief ALJ), who, on November 16, 2023, issued his
Recommended Rulings, Findings of Fact, Conclusions of Law, and Decision
(Recommended Decision or RD), which recommended denial of Applicant's
application. RD, at 19. Following the issuance of the RD, Applicant
filed Exceptions.\2\ Having reviewed the entire record, the Agency
adopts and hereby incorporates by reference the entirety of the Chief
ALJ's rulings, credibility findings,\3\ findings of fact, conclusions
of law, sanctions analysis, and recommended sanction as found in the
RD.
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\2\ In Applicant's Exceptions document, dated November 22, 2023,
Applicant does not put forward any particular arguments contesting
the Chief ALJ's Recommended Decision, but simply requests an appeal
of the Decision. Applicant's Exceptions, at 1-2.
\3\ The Agency adopts the Chief ALJ's summary of each of the
witnesses' testimonies as well as the Chief ALJ's assessment of each
of the witnesses' credibility. See RD, at 3-10. The Agency agrees
with the Chief ALJ that the testimony from the DEA Diversion
Investigator (DI), which was primarily focused on the non-
controversial introduction of documentary evidence and the DI's
contact with the case, was sufficiently detailed, plausible, and
internally consistent without indication of any motive to fabricate
or exaggerate and thus warranted full credibility. Id. at 4. The
Agency also agrees with the Chief ALJ that the testimony from
Applicant, which was focused on Applicant's criminal conviction, the
underlying facts of Applicant's criminal conviction, and the
mandatory exclusion resulting from Applicant's criminal conviction,
was ``ubiquitously inconsistent, frequently lacking in detail, and
commonly bereft of even a modest level of basic plausibility.'' Id.
at 9. The Chief ALJ also noted, and the Agency agrees, that
Applicant was ``unwilling to acknowledge his own misconduct on any
level.'' Id. Based on these factors, the Chief ALJ found, and the
Agency agrees, that Applicant's testimony was lacking in credibility
and warranted reduced weight. Id. at 9-10.
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I. Findings of Fact
1. Applicant's Criminal Conviction and Exclusion
In 2021, Applicant was convicted of two felony counts of healthcare
fraud in violation of 18 U.S.C. 1347. RD, at 4; Government Exhibit (GX)
3. As a result of Applicant's conviction, the U.S. Department of Health
and Human Services, Office of Inspector General (HHS/OIG) excluded
Applicant, effective July 20, 2022, from participation in Medicare,
Medicaid, and all federal health care programs pursuant to 42 U.S.C.
1320a-7(a) for a period of twenty-seven years. RD, at 4; GX 4; Tr. 26-
28.
2. Applicant's Argument
Regarding the allegations underlying his criminal conviction,
Applicant testified that he started implementing in his practice a
cardiovascular therapy called ``external counter pulsation therapy''
(ECP) designed to help patients with heart failure. Tr. 59. Applicant
testified that he offered this therapy with 25 certified physicians in
Pennsylvania. Id. According to Applicant, ``[t]he mistake was the
billing of this therapy.'' RD; at 7; Tr. 59-60. Applicant testified
that he is ``not trained as a biller'' and he ``had a private company
who prepared all the codes and billing forms.'' RD, at 7; Tr. at 60.
Applicant asserted that he ``did not realize that the billing was not
done correctly,'' but also that he ``did everything by the book and the
law.'' RD, at 7; Tr. 60, 90. Nonetheless, Applicant stated, ``the
biller is responsible for what happened . . . my name was used, but
he's liable.'' RD, at 7; Tr. 104.
Notably, when Applicant appealed his criminal conviction, the
United States Court of Appeals for the Third Circuit (Court of Appeals)
found that the ECP therapy that Applicant was prescribing and billing
for was unnecessary. RD, at 7 (citing United States v. Shah, 43 F.4th
356, 366-367 (3d Cir. 2022)). Even so, Applicant testified that every
patient to whom he prescribed ECP therapy needed it. RD, at 7; Tr. 77,
85-86. The Court of Appeals also found that Applicant had advertised
his ECP therapy to accomplish unrealistic goals, such as that it would
make patients ``younger and smarter'' and could help with a plethora of
conditions including obesity, erectile disfunction, restless leg
syndrome, and blood pressure issues. RD, at 7 (citing United States v.
Shah, 43 F.4th at 361). According to Applicant, ``[t]hose comments were
made by a couple of [his] office employees without [his] knowledge.''
RD, at 7; Tr. 89. As for the finding by the Court of Appeals that
Applicant was often not present to supervise the ECP treatments, see
United States v. Shah, 43 F.4th at 361, Applicant testified that this
finding was ``bogus'' because other physicians were present. RD, at 7;
Tr. 89-90.
As highlighted by the Chief ALJ, Applicant also repeatedly
emphasized that he had ``hired a very awful attorney in Western
Pennsylvania as [his] attorney to defend [his] case.'' RD, at 7-8; Tr.
60. Specifically, Applicant took issue with his attorney's legal
strategy (which led to the attorney firing Applicant as a client) as
well as the fact that the attorney went on to accept an appointment as
a federal prosecutor, which Applicant characterized as creating a
conflict of interest regarding his case. RD, at 8; Tr. 61. As noted by
the Chief ALJ, Applicant's latter complaint was raised with the Court
of Appeals and found to be without merit. RD, at 8 (citing United
States v. Shah, 43 F.4th at 363-365). Furthermore, Applicant claimed he
was forced to go to trial without access to relevant medical files and
also was unable to have these files reviewed by a potential expert
witness. RD, at 8; Tr. 77, 81-82, 84. Again, the Court of Appeals found
this contention to be without merit. RD, at 8 (citing United States v.
Shah, 43 F.4th at 364-365). Finally, Applicant made claims as to the
Court of Appeals itself. Specifically, Applicant claimed incorrectly
that the panel of the Court of Appeals that affirmed his conviction was
split. RD, at 8 (citing United States v. Shah, 43 F.4th at 360); Tr.
83. Applicant also claimed that his request for an en banc
reconsideration of his case was denied ``because they're busy, they're
on vacations and everything, they denied my ten-judge panel appeal.''
RD, at 8; Tr. 83. Overall, Applicant characterized his conviction as a
``complete miscarriage of justice.'' RD, at 8; Tr. 88. Regarding the
findings of HHS/OIG, Applicant testified that HHS/OIG ``just had a
summary judgment'' without providing Applicant with a trial or hearing.
RD, at 9; Tr. 93.
Applicant testified that the criminal court had ordered $1.2
million in restitution and that he was paying $300 per month. RD, at 9;
Tr. 70. As for any potential remedial measures, Applicant testified
that when he restarts his practice, he will not need Medicare patients
and he plans to focus on weight loss and cosmetic procedures for
``cash-paying patients.'' RD, at 9; Tr. 70-71.
[[Page 71933]]
II. Discussion
1. The Five Public Interest Factors
Pursuant to Section 303(g)(1) of the Controlled Substances Act
(CSA), ``[t]he Attorney General shall register practitioners . . . to
dispense . . . controlled substances . . . if the applicant is
authorized to dispense . . . controlled substances under the laws of
the State in which he practices.'' 21 U.S.C. 823(g)(1). Section
303(g)(1) further provides that an application for a practitioner's
registration may be denied upon a determination that ``the issuance of
such registration . . . would be inconsistent with the public
interest.'' Id. In making the public interest determination, the CSA
requires consideration of the following factors:
(A) The recommendation of the appropriate State licensing board
or professional disciplinary authority.
(B) The applicant's experience in dispensing, or conducting
research with respect to controlled substances.
(C) The applicant's conviction record under Federal or State
laws relating to the manufacture, distribution, or dispensing of
controlled substances.
(D) Compliance with applicable State, Federal, or local laws
relating to controlled substances.
(E) Such other conduct which may threaten the public health and
safety.
21 U.S.C. 823(g)(1).
In the current matter, it is undisputed that Applicant holds a
valid state medical license and is authorized to dispense controlled
substances in the Commonwealth of Pennsylvania where he practices.
Moreover, because the Government has not alleged that Applicant's
registration is inconsistent with the public interest under section
823, and although the Agency has considered section 823, the Agency
will not analyze Applicant's application under the public interest
factors. Therefore, in accordance with prior agency decisions, the
Agency will move to assess whether the Government has proven by
substantial evidence that a ground for suspension exists under 21
U.S.C. 824(a). See supra n.1.
2. Mandatory Exclusion From Federal Health Care Programs
Under Section 824(a) of the CSA, a registration ``may be suspended
or revoked'' upon a finding of one or more of five grounds. 21 U.S.C.
824(a). The ground in 21 U.S.C. 824(a)(5) requires that the registrant
``has been excluded (or directed to be excluded) from participation in
a program pursuant to section 1320a-7(a) of Title 42.'' Id. at Sec.
824(a)(5). Here, there is no dispute in the record that Applicant is
mandatorily excluded from federal health care programs under 42 U.S.C.
1320a-7(a). The Government has presented substantial evidence of
Applicant's exclusion and the underlying criminal conviction that led
to that exclusion, and Applicant has admitted to the same. GX 2-8;
Applicant's Post-Hearing Brief, at 4-5. Accordingly, the Agency will
sustain the Government's allegation that Applicant has been excluded
from participation in a program pursuant to section 1320a-7(a) of Title
42 and find that the Government has established that a ground exists
upon which a registration could be revoked pursuant to 21 U.S.C.
824(a)(5).
Further, although the language of 21 U.S.C. 824(a)(5) discusses
suspension and revocation of a registration, for the reasons discussed
above, see supra n.1, it may also serve as the basis for the denial of
a DEA registration application. Dinorah Drug Store, Inc., 61 FR at
15,973. Applicant's exclusion from participation in a program under 42
U.S.C. 1320a-7(a), therefore, serves as an independent basis for
denying his application for DEA registration. 21 U.S.C. 824(a)(5).\4\
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\4\ The underlying conviction forming the basis for a
registrant's mandatory exclusion from participation in federal
health care programs need not involve controlled substances to
provide the grounds for revocation or denial pursuant to section
824(a)(5). Jeffrey Stein, M.D., 84 FR 46,968, 46,971-46,972 (2019);
see also Narciso Reyes, M.D., 83 FR 61,678, 61,681 (2018); KK
Pharmacy, 64 FR 49,507, 49,510 (1999) (collecting cases); Melvin N.
Seglin, M.D., 63 FR 70,431, 70,433 (1998); Stanley Dubin, D.D.S., 61
FR 60,727, 60,728 (1996).
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III. Sanction
Where, as here, the Government has established sufficient grounds
for revocation or denial, the burden shifts to the registrant to show
why he can be entrusted with the responsibility carried by a
registration. Garret Howard Smith, M.D., 83 FR 18,882, 18,910 (2018).
To establish that he can be entrusted with registration, a registrant
must both accept responsibility and demonstrate that he has undertaken
corrective measures. Holiday CVS, L.L.C., dba CVS Pharmacy Nos 219 and
5195, 77 FR 62,316, 62,339 (2012) (internal quotations omitted). Trust
is necessarily a fact-dependent determination based on individual
circumstances; therefore, the Agency looks at factors such as the
acceptance of responsibility, the credibility of that acceptance as it
relates to the probability of repeat violations or behavior, the nature
of the misconduct that forms the basis for sanction, and the Agency's
interest in deterring similar acts. See, e.g., Robert Wayne Locklear,
M.D., 86 FR 33,738, 33,746 (2021).
Here, and as noted by the ALJ, ``[Applicant's] consistent
minimization and flat out denial of his wrongdoing supports the
proposition that he has not credibly and unequivocally accepted
responsibility for his actions.'' RD, at 14. Further, Applicant
repeatedly placed the blame on others, including his practice's third-
party billers, his office employees, his attorney, the Court of
Appeals, and HHS/OIG itself. Id. at 14-15. Ultimately, the ALJ
concluded, and the Agency agrees, that Applicant has not demonstrated
unequivocal acceptance of responsibility for his actions. Id. at 16.\5\
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\5\ When a registrant fails to make the threshold showing of
acceptance of responsibility, the Agency need not address the
registrant's remedial measures. Ajay S. Ahuja, M.D., 84 FR 5,479,
5,498 n.33 (2019) (citing Jones Total Health Care Pharmacy, L.L.C. &
SND Health Care, L.L.C., 81 FR 79,188, 79,202-03 (2016)); Daniel A.
Glick, D.D.S., 80 FR 74,800, 74,801, 74,810 (2015). Even so, in the
current matter, the Agency has considered Applicant's testimony that
when he restarts his practice, he intends to avoid Medicare patients
and instead focus on weight loss and cosmetic procedures for ``cash-
paying patients.'' Tr. 70-71.
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In addition to acceptance of responsibility, the Agency considers
both specific and general deterrence when determining an appropriate
sanction. Daniel A. Glick, D.D.S., 80 FR at 74,810. In this case, the
Agency agrees with the ALJ that, regarding specific deterrence,
``[w]ithout understanding the nature of his misconduct and his own
culpability in it, there is no rational reason [to] believe that
[Applicant] would make different choices in the face of the same
circumstances in the future.'' RD, at 17. Further, the Agency agrees
with the ALJ that the interests of general deterrence also support
revocation, as a lack of sanction in the current matter would send a
message to the registrant community that a registrant can commit
similar misconduct without consequences. Id. at 18. The Agency also
agrees with the ALJ that Applicant's actions were egregious, as
```defrauding federal health care programs is egregious.'' RD, at 18
(quoting Gilbert Y. Kim, D.D.S., 87 FR 21,139, 21,145 (2022)). As noted
by the ALJ, Applicant was convicted of two felony counts of healthcare
fraud, with the Court of Appeals itself highlighting that Applicant
``billed insurers for millions of dollars in ECP treatments where they
were either not medical necessary for the patient or delivered without
the required physician supervision or both.'' RD, at 18 (quoting United
States v. Shah, 43 F.4th at 367).
In sum, Applicant has not offered any credible evidence on the
record to rebut the Government's case for denial of his
[[Page 71934]]
application and Applicant has not demonstrated that he can be entrusted
with the responsibility of registration. Id. at 19. Accordingly, the
Agency will order that Applicant's application be denied.
Order
Pursuant to 28 CFR 0.100(b) and the authority vested in me by 21
U.S.C. 823, I hereby deny the pending application for a DEA Certificate
of Registration, Control No. W21057811C, submitted by Samirkumar Shah,
M.D., as well as any other pending application of Samirkumar Shah,
M.D., for additional registration in Pennsylvania. This Order is
effective October 4, 2024.
Signing Authority
This document of the Drug Enforcement Administration was signed on
August 19, 2024, by Administrator Anne Milgram. That document with the
original signature and date is maintained by DEA. For administrative
purposes only, and in compliance with requirements of the Office of the
Federal Register, the undersigned DEA Federal Register Liaison Officer
has been authorized to sign and submit the document in electronic
format for publication, as an official document of DEA. This
administrative process in no way alters the legal effect of this
document upon publication in the Federal Register.
Heather Achbach,
Federal Register Liaison Officer, Drug Enforcement Administration.
[FR Doc. 2024-19731 Filed 9-3-24; 8:45 am]
BILLING CODE 4410-09-P