Notice2025-17650

Importer of Controlled Substance Application: Fisher Clinical Services, Inc.

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
September 12, 2025

Issuing agencies

Justice DepartmentDrug Enforcement Administration

Abstract

Fisher Clinical Services, Inc. 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.

Full Text

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<title>Federal Register, Volume 90 Issue 175 (Friday, September 12, 2025)</title>
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[Federal Register Volume 90, Number 175 (Friday, September 12, 2025)]
[Notices]
[Pages 44238-44239]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-17650]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1595]


Importer of Controlled Substance Application: Fisher Clinical 
Services, Inc.

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Fisher Clinical Services, Inc. has applied to be registered as 
an importer of basic class(es) of controlled substance(s). Refer to 
Supplementary

[[Page 44239]]

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 14, 2025. Such persons may also file a written request for a 
hearing on the application on or before October 14, 2025.

ADDRESSES: 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 of the web page or attach a file for lengthier 
comments. Please go to <a href="https://www.regulations.gov">https://www.regulations.gov</a> and follow the 
online instructions at that sit for submitting comments. Upon 
submission of your comment, you will receive a Comment Tracking Number, 
your comment has been successfully submitted and there is no need to 
resubmit the same comment. All request 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 request 
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 August 22, 2025, Fisher Clinical Services, Inc., 7554 
Schantz Road, Allentown, Pennsylvania 18106-9032, applied to be 
registered as an importer of the following basic class(es) of 
controlled substance(s):

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        Controlled substance            Drug code          Schedule
------------------------------------------------------------------------
Marihuana Extract..................            7350  I
Marihuana..........................            7360  I
Tetrahydrocannabinols..............            7370  I
5-Methoxy-N-N-Dimethyltryptamine...            7431  I
Dimethyltryptamine.................            7435  I
Psilocybin.........................            7437  I
Methylphenidate....................            1724  II
Levorphanol........................            9220  II
Noroxymorphone.....................            9668  II
Tapentadol.........................            9780  II
------------------------------------------------------------------------

    The company plans to import the listed controlled substances for 
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-approved finished 
dosage forms for commercial sale.

Justin Wood,
Acting Deputy Assistant Administrator.
[FR Doc. 2025-17650 Filed 9-11-25; 8:45 am]
BILLING CODE P


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Indexed from Federal Register on September 12, 2025.

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.