(a) If an authorized provider is authorized to dispense or conduct research under State law, the Department shall register the authorized provider to dispense a controlled dangerous substance or to conduct research with a controlled dangerous substance listed in Schedule II through Schedule V.
(b) An authorized provider who prescribes a controlled dangerous substance listed in Schedule II through Schedule V shall be registered with the Prescription Drug Monitoring Program described in Title 21, Subtitle 2A of the Health – General Article before obtaining a new or renewal registration with the Department under subsection (a) of this section.
(c) The Department need not require separate registration under this section for an authorized provider who is:
(1) engaged in research with a nonnarcotic controlled dangerous substance in Schedule II through Schedule V; and
(2) already registered under this subtitle in another capacity.
(d) An authorized provider may conduct research in the State with a controlled dangerous substance listed in Schedule I if the authorized provider is registered under federal law to conduct research with a controlled dangerous substance listed in Schedule I and gives evidence of the registration to the Department.
Structure Maryland Statutes
Title 5 - Controlled Dangerous Substances, Prescriptions, and Other Substances
Subtitle 3 - Registration of Manufacturers, Distributors, and Dispensers
Section 5-301 - Registration Required
Section 5-302 - Term of Registration
Section 5-303 - Manufacturers and Distributors
Section 5-304 - Authorized Providers
Section 5-306 - Required Record Keeping
Section 5-307 - Suspensions, Revocations, and Denials -- Grounds
Section 5-308 - Suspensions, Revocations, and Denials -- Notice and Hearing
Section 5-309 - Placing Under Seal and Disposing of Controlled Dangerous Substances