Importer of Controlled Substances Application: Fisher Clinical Services, Inc.
Published Date: 11/26/2025
Notice
Summary
Fisher Clinical Services, Inc. wants to become an official importer of certain controlled substances like marijuana and its extracts. This affects companies involved in drug manufacturing and importation, who can comment or request a hearing by December 26, 2025. No direct costs are mentioned, but the decision could impact how these substances enter the U.S. market.
Analyzed Economic Effects
3 provisions identified: 2 benefits, 1 costs, 0 mixed.
No Commercial Finished Dosage Imports Allowed
The registration, if approved, will not authorize importation of Food and Drug Administration‑approved or non‑approved finished dosage forms for commercial sale; approval is limited to activities consistent with 21 U.S.C. 952(a)(2).
Deadline to Comment or Request Hearing
If you are a registered bulk manufacturer or an applicant, you may submit electronic comments or objections, or file a written request for a hearing, by December 26, 2025. Comments must be submitted through https://www.regulations.gov and hearing requests must also be mailed to the Drug Enforcement Administration addresses listed in the notice.
Application to Import Specific Controlled Substances
Fisher Clinical Services, Inc. applied on August 26, 2025 to be registered to import specific Schedule I and II substances — including marihuana, marihuana extract, tetrahydrocannabinols, 5‑MeO‑DMT, DMT, psilocybin, methylphenidate, levorphanol, noroxymorphone, and tapentadol — and says it plans to import them for use in clinical trials only.
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