Alabama Administrative Code
Title 538 - ALABAMA MEDICAL CANNABIS COMMISSION
Chapter 538-X-6 - Regulation of Processors
Section 538-X-6-.02 - Definitions
Current through Register Vol. 43, No. 02, November 27, 2024
As used in this Chapter, the following terms have the following meanings:
(1) "Attractive to or Targets Children"; "Attractive to Minors." Forms, designs, packaging, receptacles, devices, labeling, or branding that contains, features, resembles, or includes:
(2) "Excipients." Inactive (as opposed to active) ingredients in medical cannabis, such as coloring agents, preservatives, and fillers, that serve as the inert vehicle or medium for the medical cannabis product.
(3) "Good Quality Practices." Application of quality control and quality assurance practices in processing medical cannabis, requiring Processors to use a scientific approach and consider factors such as risk assessment, life cycle, and patient protection in all facets of the manufacturing process, using ISO 17025 and/or ISO 9001 Testing and Calibration Laboratories quality standards.
(4) "Pharmaceutical Grade." Manufactured to the same standard or grade as any active or inactive drug, biologic, reagent or other pharmaceutical, in accordance with Good Manufacturing Practices (GMP) and approved, conditionally approved or indexed by the Food and Drug Administration (FDA) or for which a chemical purity standard has been established by recognized compendia.
Author: William H. Webster
Statutory Authority: Code of Ala. 1975, §§ 20-2A-22, as amended.