Controlled Substance Importer Application - Fisher Clinical Services

FR: Drug Enforcement Administration

Published April 1st, 2026

Detected April 1st, 2026

Summary

The DEA published a notice that Fisher Clinical Services, Inc. has applied to be registered as an importer of controlled substances. The application covers 3,4-Methylenedioxy-methamphetamine (MDMA, Schedule I, Drug Code 7405) for clinical trials only. The public comment period closes May 1, 2026.

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What changed

This is a routine DEA notice announcing that Fisher Clinical Services, Inc. (Allentown, PA) has applied for importer registration to bring in 3,4-Methylenedioxy-methamphetamine (MDMA, Schedule I, Drug Code 7405). The application is pursuant to 21 CFR 1301.34(a) and is limited to clinical trials only—authorization will not extend to commercial sale of FDA-approved or non-approved finished dosage forms. The registration would be governed by 21 U.S.C. 952(a)(2).

No immediate action is required by regulated entities. However, registered bulk manufacturers of controlled substances and interested parties may submit electronic comments or written hearing requests to DEA by May 1, 2026 through Regulations.gov or by mail to the Springfield, Virginia address. Any party wishing to oppose this application should file objections before the comment deadline.

Source document (simplified)

Notice

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

A Notice by the Drug Enforcement Administration on 04/01/2026

This document has a comment period that ends in 30 days.
(05/01/2026) View Comment Instructions
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Public Inspection Published Document: 2026-06257 (91 FR 16243) Document Headings ###### Department of Justice

Drug Enforcement Administration

[Docket No. DEA-1695]

AGENCY:

Drug Enforcement Administration, Justice.

ACTION:

Notice of application.

SUMMARY:

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.

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 May 1, 2026. Such persons may also file a written request for a hearing on the application on or before May 1, 2026.

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 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 ( printed page 16244) 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 March 11, 2026, 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):

| Controlled substance | Drug code | Schedule |
| --- | --- | --- |
| 3,4-Methylenedioxy-methamphetamine | 7405 | I |
The company plans to import the listed controlled substance(s) for clinical trials only. No other activity for this drug code is 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.

Thomas Prevoznik,

Deputy Assistant Administrator.

[FR Doc. 2026-06257 Filed 3-31-26; 8:45 am]

BILLING CODE P

Published Document: 2026-06257 (91 FR 16243)