1. (1) Conduct testing on the product in its final form within 12 months of registration for:

   1. (a) the cannabinoid profile by percentage of mass, performed by the Department's analytical laboratory;
   2. (b) solvents;
   3. (c) pesticides;
   4. (d) microbials;
   5. (e) heavy metals; and
   6. (f) mycotoxins.
2. (2) Report test results required in Subsection R66-35-4(1) in accordance with Rule R66-31, including the specified units of measure.

3. (3) The COA shall include the following information:

   1. (a) the batch identification number;
   2. (b) the date the laboratory received the sample;
   3. (c) the date of test completion;
   4. (d) the method of analysis for each test conducted; and
   5. (e) proof that the COA connects to the product.

KEY: CBD labeling, CBD products, cannabinoid product registration; cannabinoid product labeling; cannabinoid testing, cannabinoid COA; violations

Date of Last Change: October 10, 2025

Authorizing, and Implemented or Interpreted Law: 4-41-403(1); 4-41-402(2); 4-41-103(4)