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Idaho Code § 37-2717

Registration

Known as the Uniform Controlled Substances Act

The act spans §§ 37–37 (65 sections).

I.C., § 37-2717, as added by 1971, ch. 215, § 1, p. 939; am. 2015, ch. 25, § 3, p. 30.

The board shall register an applicant to manufacture, prescribe, administer, dispense, distribute or conduct research with controlled substances included in sections 37-2705, 37-2707, 37-2709, 37-2711 and 37-2713, Idaho Code, unless it determines that the issuance of that registration would be inconsistent with the public interest. In determining the public interest, the board shall consider the following factors:

(1) Maintenance of effective controls against diversion of controlled substances into other than legitimate medical, scientific, or industrial channels;

(2) Compliance with applicable state and local law;

(3) Any convictions of the applicant under any federal and state laws relating to any controlled substance;

(4) Past experience in the manufacture, dispensing, prescribing, administering, research or distribution of controlled substances, and the existence in the applicant’s establishment of effective controls against diversions;

(5) Furnishing by the applicant of false or fraudulent material in any application filed under this chapter;

(6) Restriction, suspension or revocation of the applicant’s federal registration; and

(7) Any other factors relevant to and consistent with the public health and safety.

Current official text: Idaho Statutes (Idaho Legislature). Digitized from the UniCourt Code Improvement Commission public-domain capture. Reproduced from public-domain Idaho statutes; confirm against the official source for the current text. Not legal advice.