Page:United States Statutes at Large Volume 84 Part 1.djvu/1312

 1254

PUBLIC LAW 91-513-OCT. 27, 1970

[84 STAT.

petitive conditions for legitimate medical, scientific, research, and industrial purposes; Compliance. (2) compliance with applicable State and local law; Technology. ^3) promotion of technical advances in the art of manufacturing these substances and the development of new substances; Applicants, (4) prior conviction record of applicant under Federal and ^e" o^rd.°"^*'°" State laws relating to the manufacture, distribution, or dispensing of such substances; Experience. (5) past experience in the manufacture of controlled substances, and the existence in the establishment of effective control against diversion; and (6) such other factors as may be relevant to and consistent with the public health and safety. sirten\°with°"ubiic (^) '^^^ Attomey General shall register an applicant to distribute interest. a coutrolled substance in schedule I or II unless he determines that the issuance of such registration is inconsistent with the public interest. I n determining the public interest, the following factors shall be considered: (1) maintenance of effective control against diversion of particular controlled substances into other than legitimate medical, scientific, and industrial channels; (2) compliance with applicable State and local law; (3) prior conviction record of applicant under Federal or State laws relating to the manufacture, distribution, or dispensing of such substances; (4) past experience in the distribution of controlled substances; and (5) such other factors as may be relevant to and consistent with the public health and safety. Prohibition. ^^^ Registration granted under subsections (a) and (b) of this section shall not entitle a registrant to (1) manufacture or distribute controlled substances in schedule I or II other than those specified in the registration, or (2) manufacture any quantity of those controlled Post, p. 1257. substances in excess of the quota assigned pursuant to section 306. (d) The Attorney General shall register an applicant to manufacture controlled substances in schedule III, IV, or V, unless he determines that the issuance of such registration is inconsistent with the public interest. I n determining the public interest, the following factors shall be considered: (1) maintenance of effective controls against diversion of particular controlled substances and any controlled substance in schedule III, IV, or V compounded therefrom into other than legitimate medical, scientific, or industrial channels; (2) compliance with applicable State and local law; (3) promotion of technical advances in the art of manufacturing these substances and the development of new substances; (4) prior conviction record of applicant under Federal or State laws relating to the manufacture, distribution, or dispensing of such substances; (5) past experience in the manufacture, distribution, and dispensing of controlled substances, and the existence in the establishment of effective controls against diversion; and (6) such other factors as may be relevant to and consistent with the public health and safety. (e) The Attorney General shall register an applicant to distribute controlled substances in schedule III, IV, or V, unless he determines that the issuance of such registration is inconsistent with the public interest. In determining the public interest, the following factors shall be considered:

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