Health

DEA Notice: Research Triangle Institute Application to Import Schedule I and II Controlled Substances for NIDA-Funded Research

🇺🇸United States··Notice·Medium Impact·View source ↗

AI-generated summary for informational purposes only. Not legal advice. See the original source for the authoritative text.

🇬🇧 English

The U.S. Drug Enforcement Administration (DEA) has published a notice that Research Triangle Institute (RTI), located in Durham, North Carolina, filed an application on March 3, 2026 to become a registered importer of a broad range of Schedule I and Schedule II controlled substances. The application covers over 200 distinct drug codes spanning stimulants, opioids, hallucinogens, synthetic cannabinoids, benzodiazepine analogs, cathinones, fentanyl analogs, and dissociative drugs. The purpose of this registration is to support small-quantity importation exclusively for research activities funded by the National Institute on Drug Abuse (NIDA). No commercial sale, distribution, or importation of FDA-approved or non-approved finished dosage forms is authorized under this application. Registered bulk manufacturers of the affected substance classes, as well as other applicants, may submit electronic comments or objections through the federal rulemaking portal at regulations.gov, or file a written request for a hearing, on or before May 1, 2026. All hearing requests must be directed to the DEA Hearing Clerk/OALJ and the DEA Federal Register Representative at 8701 Morrissette Drive, Springfield, Virginia. Approval of the permit will only be granted if RTI's business activities remain consistent with the authorization under 21 U.S.C. 952(a)(2), which governs the importation of controlled substances for legitimate scientific and research purposes.

AI-generated summary. May contain errors. Refer to official sources for legal decisions.

Key Changes

  • Research Triangle Institute applied on March 3, 2026 to register as a DEA-authorized importer of controlled substances under 21 CFR 1301.34(a)
  • Application covers 200+ Schedule I and Schedule II controlled substances including fentanyl analogs, synthetic cannabinoids, opioid derivatives, cathinones, hallucinogens, and dissociatives
  • Importation is strictly limited to small quantities for NIDA-funded research — no commercial sale or finished dosage form importation permitted

+ 3 more changes with Pro

Obligations

What this law requires

high

Research Triangle Institute must limit importation of Schedule I and II controlled substances to small quantities exclusively for NIDA-funded research activities only

Research Triangle Institute
operational
high

Research Triangle Institute is prohibited from engaging in commercial sale, distribution, or importation of FDA-approved or non-approved finished dosage forms of controlled substances

Research Triangle Institute
prohibition
medium

Registered bulk manufacturers of affected Schedule I and II controlled substance classes may submit electronic comments or written objections through regulations.gov on or before May 1, 2026

Registered bulk manufacturers of affected controlled substance classes
disclosure
medium

Any party seeking a hearing on the RTI registration application must file a written request with the DEA Hearing Clerk/OALJ and DEA Federal Register Representative at 8701 Morrissette Drive, Springfield, Virginia on or before May 1, 2026

Registered bulk manufacturers and other applicants
reporting
medium

All hearing requests must be sent to three addresses: (1) DEA Hearing Clerk/OALJ, (2) DEA Federal Register Representative/DPW, and (3) DEA Administrator, all at 8701 Morrissette Drive, Springfield, Virginia 22152

Any party filing a hearing request
operational

Affected Parties

Research Triangle Institute (RTI) — the applicant seeking importer registrationRegistered bulk manufacturers of Schedule I and II controlled substances who may object+4 more…

Tags

controlled substances,DEA registration,drug importation