MN Cannabis Sample

Submit a Minnesota Cannabis Testing Sample

01

Step 1

Create an Order

Complete the new customer form online! You’ll receive a confirmation email with submission instructions, required paperwork, and a direct line of communication to our Client Experience Specialist!

02

Step 2

Create a sample package

Create a lab sample package online using the METRC system.

03

Step 3

Ship Your Samples

Package up the sample and send it via an approved transport method to:

2224 26th St S,
Moorhead, MN 56560

04

Step 4

Testing & Payment

Once samples are received, you’ll receive a welcome email with access to our payment portal (Connect Booster) and a copy of your invoice. Payments can be made by ACH, or by including a check with your samples.

MN licensed cannabis lab

Cannabis testing

Who Can Submit Samples?

Cannabis samples may be submitted to AIT by licensed Minnesota cannabis businesses operating within the state’s regulated market. This includes operators involved in cultivation, manufacturing, and product development.

Submit a Cannabis Sample

Cannabis Sample Requirements

To ensure accurate and representative results, please follow these basic guidelines when submitting your sample.

guideline img 1

Sample Guidelines

  • Use leak-proof, sealed containers

  • Clearly label each sample
  • Package samples securely to prevent damage
  • Follow all applicable state regulations for sample transport
  • Samples must be transferred using licensed transport
  • Transfers must be recorded in METRC
  • We are notified through METRC and maintain chain of custody upon receipt

If you have questions about sample size, packaging, or testing requirements, our team is happy to help.

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New Customer Form

Fill out New Customer Form below to send in samples

MN Cannabis testing FAQs

MN Cannabis Testing Questions

Below are answers to some of the most common questions we receive. If you don’t see what you’re looking for, contact our team and we’ll be happy to help guide you through the process.

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 (retail): microbial, mycotoxins, heavy metals, pesticides, foreign matter, potency, stability  
  • Concentrates: microbial, mycotoxins, heavy metals, pesticides, residual solvents, potency, stability  
  • Final products (edibles, infused products): microbial, potency, homogeneity, stability  
In some cases, testing may not need to be repeated if upstream materials already passed and no new risk is introduced during manufacturing. 
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. 

Submit a MN Cannabis Sample

Sample Submission Forms and Resources

Tell us the tests you need and what information you want on your COA.

Should always accompany mailed in samples showing your product is a legal substance.

Tell us the tests you need, the weight of the beverage, and how many servings to show potency reported as mg per serving!

Questions about sample sizes? We’ve got it all broken down for you!

Use ConfidentLIMS to create your test request. Instructions also include how to ensure that your potency results are reported as mg/serving and how to communicate that you want potency tested before other tests.

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