65-4117.Registration.(a) The board shall register an applicant to manufacture, dispense ordistribute controlled substances included in K.S.A. 65-4105, 65-4107, 65-4109,65-4111 and 65-4113, and amendments to these sections, unless itdetermines that the issuance of that registration would be inconsistentwith the public interest. In determining the public interest, the boardshall consider the following factors:
(1) Maintenance of effective controls against diversion of controlledsubstances into other than legitimate medical, scientific or industrial channels;
(2) compliance with applicable state and local law;
(3) any conviction of the applicant under any federal and state lawsrelating to any controlled substance;
(4) past experience in the manufacture, dispensing or distributionof controlled substances and the existence in the applicant'sestablishment of effective controls against diversion;
(5) furnishing by the applicant of false or fraudulent material inany application filed under this act;
(6) suspension or revocation of the applicant's federal registrationto manufacture, distribute or dispense controlled substances asauthorized by federal law; and
(7) any other factors relevant to and consistent with the publichealth and safety.
(b) Registration under subsection (a) does not entitle a registrantto manufacture and distribute controlled substances in schedule I or IIother than those specified in the registration.
(c) Practitioners shall be registered to dispense any controlledsubstances or to conduct research with controlled substances inschedules II through V if they are authorized to prescribe or to conductresearch under the laws of this state.
(d) Pharmacists shall be registered to dispense schedule I designatedprescription substances and controlled substances in schedules II throughV if none of the grounds for revocation, suspension or refusal to renew aregistration exist at the time of application.
(e) The board need not require separate registration under this actfor practitioners or pharmacists engaging in research with nonnarcoticcontrolled substances in schedules II through V where the registrant isalready registered under this act in another capacity. Practitioners orpharmacists registered under federal law to conduct research withschedule I substances may conduct research with schedule I substanceswithin this state upon furnishing the board evidence of that federalregistration.
(f) Compliance by manufacturers and distributors with the provisionsof the federal law respecting registration (excluding fees) entitlesthem to be registered under this act.
History: L. 1972, ch. 234, § 17;L. 1986, ch. 242, § 1; May 1.
65-4117.Registration.(a) The board shall register an applicant to manufacture, dispense ordistribute controlled substances included in K.S.A. 65-4105, 65-4107, 65-4109,65-4111 and 65-4113, and amendments to these sections, unless itdetermines that the issuance of that registration would be inconsistentwith the public interest. In determining the public interest, the boardshall consider the following factors:
(1) Maintenance of effective controls against diversion of controlledsubstances into other than legitimate medical, scientific or industrial channels;
(2) compliance with applicable state and local law;
(3) any conviction of the applicant under any federal and state lawsrelating to any controlled substance;
(4) past experience in the manufacture, dispensing or distributionof controlled substances and the existence in the applicant'sestablishment of effective controls against diversion;
(5) furnishing by the applicant of false or fraudulent material inany application filed under this act;
(6) suspension or revocation of the applicant's federal registrationto manufacture, distribute or dispense controlled substances asauthorized by federal law; and
(7) any other factors relevant to and consistent with the publichealth and safety.
(b) Registration under subsection (a) does not entitle a registrantto manufacture and distribute controlled substances in schedule I or IIother than those specified in the registration.
(c) Practitioners shall be registered to dispense any controlledsubstances or to conduct research with controlled substances inschedules II through V if they are authorized to prescribe or to conductresearch under the laws of this state.
(d) Pharmacists shall be registered to dispense schedule I designatedprescription substances and controlled substances in schedules II throughV if none of the grounds for revocation, suspension or refusal to renew aregistration exist at the time of application.
(e) The board need not require separate registration under this actfor practitioners or pharmacists engaging in research with nonnarcoticcontrolled substances in schedules II through V where the registrant isalready registered under this act in another capacity. Practitioners orpharmacists registered under federal law to conduct research withschedule I substances may conduct research with schedule I substanceswithin this state upon furnishing the board evidence of that federalregistration.
(f) Compliance by manufacturers and distributors with the provisionsof the federal law respecting registration (excluding fees) entitlesthem to be registered under this act.
History: L. 1972, ch. 234, § 17;L. 1986, ch. 242, § 1; May 1.
65-4117.Registration.(a) The board shall register an applicant to manufacture, dispense ordistribute controlled substances included in K.S.A. 65-4105, 65-4107, 65-4109,65-4111 and 65-4113, and amendments to these sections, unless itdetermines that the issuance of that registration would be inconsistentwith the public interest. In determining the public interest, the boardshall consider the following factors:
(1) Maintenance of effective controls against diversion of controlledsubstances into other than legitimate medical, scientific or industrial channels;
(2) compliance with applicable state and local law;
(3) any conviction of the applicant under any federal and state lawsrelating to any controlled substance;
(4) past experience in the manufacture, dispensing or distributionof controlled substances and the existence in the applicant'sestablishment of effective controls against diversion;
(5) furnishing by the applicant of false or fraudulent material inany application filed under this act;
(6) suspension or revocation of the applicant's federal registrationto manufacture, distribute or dispense controlled substances asauthorized by federal law; and
(7) any other factors relevant to and consistent with the publichealth and safety.
(b) Registration under subsection (a) does not entitle a registrantto manufacture and distribute controlled substances in schedule I or IIother than those specified in the registration.
(c) Practitioners shall be registered to dispense any controlledsubstances or to conduct research with controlled substances inschedules II through V if they are authorized to prescribe or to conductresearch under the laws of this state.
(d) Pharmacists shall be registered to dispense schedule I designatedprescription substances and controlled substances in schedules II throughV if none of the grounds for revocation, suspension or refusal to renew aregistration exist at the time of application.
(e) The board need not require separate registration under this actfor practitioners or pharmacists engaging in research with nonnarcoticcontrolled substances in schedules II through V where the registrant isalready registered under this act in another capacity. Practitioners orpharmacists registered under federal law to conduct research withschedule I substances may conduct research with schedule I substanceswithin this state upon furnishing the board evidence of that federalregistration.
(f) Compliance by manufacturers and distributors with the provisionsof the federal law respecting registration (excluding fees) entitlesthem to be registered under this act.
History: L. 1972, ch. 234, § 17;L. 1986, ch. 242, § 1; May 1.
