FAQs

Hemp and Cannabis Testing Questions

How much sample should I send in?
The more sample you send in, the more representative it will be of the lot you are testing. The minimum amounts we require to get an accurate result are as follows: 
Data table hemp test img 1

Samples should be securely packaged to prevent leaks or cross-contamination. Recommended options include:

  • Ziploc bags for wet or dry hemp, double bagged when possible
  • Centrifuge tubes or containers with screw caps or secure lids
  • Finished products in sealed containers or original packaging

Pre-sterilized tubes, available from suppliers such as Amazon, can help reduce contamination risk but are not required.

AIT Labs accepts checks, credit cards, and ACH payments.

  • Checks may be included with your sample shipment
  • Credit card and ACH payments are available through our QuickBooks invoice portal
  • A 3.9% processing fee applies to credit card or ACH payments when a check is not included with the samples

All COA information is pulled directly from the Request for Analysis form. This includes sample name, company name, and address. Additional details such as batch number, strain, or batch size can be included if listed on the form.

If you have special reporting needs, contact our office and we will work with you.

AIT Labs accepts hemp samples from anywhere in the United States. Because hemp is federally legal, samples can be shipped across state lines. Many of our clients are located outside of North Dakota.

Most customers use USPS, UPS, FedEx, or Speedee. We recommend including the Chain of Title and Affirmation form inside the shipment so it is clear the material is legal hemp if inspected.

No. Marijuana is federally illegal and cannot be shipped across state lines. Do not send any samples that fall outside the legal definition of hemp.

Promo codes should be entered in the Promo Code section of the Request for Analysis form. If you forget, contact our team and we can update and resend your invoice. Printable coupons can also be included in your shipment.

What tests do I actually need for my product?
Testing requirements depend on your product type and intended use. Minnesota OCM outlines a risk-based testing approach that varies between: 
  • Flower: microbial, mycotoxins, heavy metals, pesticides, foreign matter, water activity, potency  
  • Resins: microbial, mycotoxins, heavy metals, pesticides, residual solvents, potency
  • Rosins: microbial, mycotoxins, heavy metals, pesticides, potency
  • Resins (Artificallay Derived): microbial, mycotoxins, heavy metals, residual solvents, pesticides, foreign matter, potency
  • Final Products (Non-Liquid): microbial, potency, water activity
  • Final Products: microbial, potency, (vapes/cartridges also require heavy metals)
We recommend reviewing the Required Testing Flow Chart on page 6 in the Minnesota OCM Technical Authority for a full breakdown. 
To ensure compliance, you are responsible for providing accurate information about your product, including: 
  • Pesticides applied during cultivation  
  • Solvents or catalysts used during extraction or manufacturing  
  • Complete and accurate batch information in METRC/statewide monitoring system  
This information must be provided to the laboratory when requesting testing, as it directly impacts required analyses and compliance reporting. 
This requirement is defined in the OCM Technical Authority on Page 15  under Test Scheduling and Reporting responsibilities. 
If a batch fails: 
  • You may request a reanalysis (same sample, same lab) within 7 days  
  • If it passes reanalysis → it must be retested by a different lab  
  • If it fails again → the batch must be remediated or destroyed  
Important limitations: 
  • Only one reanalysis and one retest are allowed  
  • The batch must remain intact (no splitting or combining)  
Full requirements are outlined in the OCM Technical Authority on Page under Failed Test Samples. 
Per Minnesota OCM requirements: 
  • Microbial testing must be initiated within 5 days  
  • Testing is generally expected to be completed within 10 days  
  • Results must be reported within 2 business days of completion  
These timelines are defined in the Technical Authority under Testing Timeline on Page 19. 

Our commitment:
 
During initial market rollout and early licensing phases, timelines across the industry may be extended. However, we prioritize fast, predictable turnaround times and actively optimize workflows to keep your product moving to market as quickly as possible. 
Yes. You may submit samples for R&D testing at any time. 
Important notes: 
  • R&D testing does not replace compliance testing  
  • Samples must be designated as R&D in the statewide monitoring system  
  • Results are labeled accordingly and cannot be used for product release  
Defined under Testing for Research and Development in the Technical Authority on Page 16. 
Each testing category includes specific analytes defined by OCM, such as: 
  • Microbial: total yeast/mold, pathogens (Salmonella, E. coli, Aspergillus, etc.)  
  • Heavy metals: arsenic, cadmium, lead, mercury  
  • Pesticides: extensive list of regulated compounds  
  • Residual solvents: e.g., butane, propane, benzene, etc.  
  • Cannabinoids (potency): THC, THCA, CBD, CBDA, CBN, CBG, and others  
Full analyte lists and limits are defined in Sections I–VII of the Technical Authority starting on Page 7.
We also provide a detailed breakdown in our blog: 
[Link to “Complete Guide to Cannabis Test Panels”] – will give 
Yes—we believe your COA should be easy to understand and actionable! 
Your COA includes: 
  • Pass/fail status for all required tests  
  • Cannabinoid potency and profiles  
  • Contaminant results and limits  
  • Supporting data like LOQs and method details  
For a full walkthrough of every section of your COA: 
[Link to “How to Read a Cannabis COA”]– will give 
For products with label claims: 
  • Measured cannabinoid content must be within ±15% of the labeled value  
  • Exception: certain low-level cannabinoids may allow ±25% variance under specific conditions  
These requirements are defined under Potency Testing – Testing Variance starting on Page 13 in the Technical Authority. 
Homogeneity testing ensures that each serving contains consistent cannabinoid content. 
It is required for: 
  • Products with multiple servings or units (e.g., gummies, chocolates, beverages)  
Key requirements: 
  • Typically tested on 10 individual units  
  • Must fall within ±15% of the label claim  
Homogeneity must be demonstrated: 
  • On the first batch  
  • Whenever the manufacturing process changes  
See Section VIII – Homogeneity Testing in the Technical Authority on Page 14. 
Stability testing determines your product’s expiration date and ensures it remains compliant over time. 
Requirements: 
  • Conducted on the final packaged product  
  • Evaluates:  
  • Microbial stability  
  • Cannabinoid potency over time  
  • Potential contamination from packaging  
If no data is available: 
  • Products default to a 6-month expiration date  
For further guidelines and requirements, see Section IX – Stability Testing in the Technical Authority on Page 14. 
Do hemp products in Minnesota have to be tested before they can be sold? 

Yes. OCM’s technical standard states that each batch of cannabis or hemp product must be sampled and analyzed to confirm it meets contaminant limits and potency requirements before entering the retail market.

OCM requires hemp flower for smoking (including flower to be infused) to be tested for:

  • Microbial contaminants 
  • Mycotoxins 
  • Heavy metals 
  • Pesticides 
  • Foreign matter 
  • Potency 
  • Water Activity
Not always. 
Under a 2026 Minnesota legislative update, lower-potency hemp edibles and certain hemp-derived consumer products may be tested by any ISO/IEC 17025-accredited cannabis-testing laboratory until May 31, 2027. 
Because eligibility depends on product type, we recommend confirming your product category prior to submission. hello@aitlabgroup.com
Testing requirements depend on your product type and intended use. Minnesota OCM outlines a risk-based testing approach that varies between: 
  • Flower: microbial, mycotoxins, heavy metals, pesticides, foreign matter, water activity, potency  
  • Resins: microbial, mycotoxins, heavy metals, pesticides, residual solvents, potency
  • Rosins: microbial, mycotoxins, heavy metals, pesticides, potency
  • Resins (Artificallay Derived): microbial, mycotoxins, heavy metals, residual solvents, pesticides, foreign matter, potency
  • Final Products (Non-Liquid): microbial, potency, water activity
  • Final Products: microbial, potency, (vapes/cartridges also require heavy metals)
We recommend reviewing the Required Testing Flow Chart on page 6 in the Minnesota OCM Technical Authority for a full breakdown. 

OCM requires testing for (at minimum) the following cannabinoid analytes: 

THC, THCA, CBD, CBDA, CBN, CBG, CBGA, delta-8 THC, THCV, CBC.  

For products with label claims: 
  • Measured cannabinoid content must be within ±15% of the labeled value  
  • Exception: certain low-level cannabinoids may allow ±25% variance under specific conditions  
These requirements are defined under Potency Testing – Testing Variance on page 14 in the Minnesota OCM Technical Authority

Yes. OCM states homogeneity testing is required for products with serving units, including edibles and beverages, and it must be evaluated on the final packaged form.  

If a batch fails: 
  • You may request a reanalysis (same sample, same lab) within 7 days  
  • If it passes reanalysis → it must be retested by a different lab  
  • If it fails again → the batch must be remediated or destroyed  
Important limitations: 
  • Only one reanalysis and one retest are allowed  
  • The batch must remain intact (no splitting or combining)  

Full requirements are outlined in the OCM Technical Authority under Failed Test Samples on page 16.  

Per Minnesota OCM requirements: 
  • Microbial testing must be initiated within 5 days  
  • Testing is generally expected to be completed within 10 days  
  • Results must be reported within 2 business days of completion  
These timelines are defined in the Technical Authority under Testing Timeline on page 19. 
 
Our commitment: 
During initial licensing phases and market rollout, timelines across the industry may be extended. However, we prioritize fast, predictable turnaround times and actively optimize workflows to keep your product moving to market as quickly as possible. 

Yes. OCM states that cultivators/manufacturers may submit samples for research and development, but those results may not satisfy compliance testing requirements, and the sample must be marked as R&D in the statewide monitoring system.  

Yes—we believe your COA should be easy to understand and actionable. 
Your COA includes: 
  • Pass/fail status for all required tests  
  • Cannabinoid potency and profiles  
  • Contaminant results and limits  
  • Supporting data like LOQs and method details  
Requirements are defined under Certificates of Analysis on pages 20–21 in the Minnesota OCM Technical Authority.

All Minnesota hemp and cannabis must be tested at the Moorhead MN lab. 

No

Each testing category includes specific analytes defined by OCM, such as: 
  • Microbial: total yeast/mold, pathogens (Salmonella, E. coli, Aspergillus, etc.)  
  • Heavy metals: arsenic, cadmium, lead, mercury  
  • Pesticides: extensive list of regulated compounds  
  • Residual solvents: e.g., butane, propane, benzene, etc.  
  • Cannabinoids (potency): THC, THCA, CBD, CBDA, CBN, CBG, and others  
We recommend referencing Sections I–VII on pages 7–13 in the Minnesota OCM Technical Authority for the full analyte lists and limits.  
We also provide a detailed breakdown here in our Blog!  

Yes. OCM states stability testing is required for all products and must be evaluated on the final packaged form to establish the expiration date. 

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