S.C. Code Regs. § § 61-4.300.303
Current through Register Vol. 48, 12, December 27, 2024
The Bureau Director shall coordinate applications for bulk manufacture of schedules I and II controlled substances with the DEA of the U.S. Department of Justice. Applications may be received by the Bureau Director for such bulk manufacture, but shall not be acted upon until tentative or conditional approval is made by the appropriate federal agency, and after such notifications, publications, and other actions required by Chapter II, Title 21, Code of Federal Regulations [ 21 CFR §1301, ff.] are effected by the applicant.
S.C. Code Regs. § 61-4.300.303