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New York · Through 2026-09-11

N.Y. Public Health Law § 3325: Authority to issue licenses; applications

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Where this section sits in the code
  1. Public Health Law
  2. Article 33. Controlled Substances
  3. Title 3. Research, Instructional Activities, and Chemical Analysis Relating to Controlled Substances

§ 3325. Authority to issue licenses; applications. 1. Subject to the

provisions of this title, the commissioner is authorized to license a

person to manufacture, obtain and possess, dispense, and administer

controlled substances for purposes of scientific research, chemical

analysis or instruction.

2. A license or amendment of a license shall be issued by the

department unless the applicant therefor has failed to furnish a

satisfactory protocol pursuant to subdivision three of this section, or

a satisfactory statement pursuant to section 3326, and proof that the

applicant:

(a) and its managing officers are of good moral character;

(b) possesses or is capable of acquiring facilities, staff and

equipment sufficient to carry on properly the proposed project detailed

in the protocol or statement accompanying the application;

(c) is able to maintain effective control against diversion of the

controlled substances for which the license is sought;

(d) is able to comply with all applicable state and federal laws and

regulations relating to the controlled substances for which the license

is sought.

3. An application for a license or for an amendment to a license shall

be accompanied by a detailed protocol setting forth:

(a) the nature of the proposed project;

(b) the proposed quantity or quantities of each controlled substance

involved;

(c) the qualifications and competence of the applicant to engage in

such project;

(d) specific provisions for the safe administration or dispensing of

controlled substances to humans, if such is contemplated, and the

proposed method of selecting humans;

(e) such other additional information as the commissioner may require.

4. The application for a license pursuant to this title shall include

copies of all papers filed with the Bureau, the Federal Food and Drug

Administration and any other governmental agency, whether state or

federal, in connection with the applicant's proposed project.

Collected 2026-09-14T19:32:45Z. Source file · JSON

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