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2. Date and time of sample starting and ending; 3. Name, licensed premises address and license number of the distributor or microbusiness from which the sample was obtained; 4. Batch number of the batch from which the representative sample was obtained and the assigned unique sample identifier; 5. Sample matrix; 6. Total batch size, by weight, or unit count; 7. Total weight, or unit count of the representative sample; 8. Sampling conditions or problems encountered during the sampling process, if any; 9. Printed name and signature of the sampler; Each time a sample changes custody between licensees, is transported, or is destroyed, the date, time and names and signatures of persons involved in these activities shall be recorded on the chain of custody form. Testing Methods and Procedures: To the furthest extent practicable, the facility shall develop, implement and validate testing methods for analyses of samples that comport with the following: 1. USDA Bacterial Analytical Manual, 2016 2. AOAC International's Official Methods of Analysis for Containment Testing of AOAC International, 20' Edition, 2016; and 3. U.S. Pharmpacopeia and the National Formulary's Methods of Analysis for Containment Testing, 2016 The Facility shall test each representative sample for the following: 1. Cannabinoids; 2. Foreign Material; 3. Heavy metals; 4. Microbial impurities;