MN Hemp Sample

Submit a Minnesota Hemp Testing Sample

01

Step 1

Create an Order

Complete the new customer form online. You’ll receive a confirmation email with submission instructions, required documentation, and next steps. You will also receive an invite to Qbench, our LIMS system in MN.

02

Step 2

Create your testing request.

Create your order in Qbench. Click here for further instructions.

03

Step 3

Ship Your Samples

Package up the samples and send with your Chain of Title and Affirmation form via an approved transport method to:


224 26th St S,
Moorhead, MN 56560

04

Step 4

Testing & Payment

Once samples are received, you’ll receive a confirmation email with access to your payment portal and an invoice. Payments may be made via ACH or by including a check with your samples.

Fargo Hemp Testing Lab

Cannabis testing

Who Can Submit Minnesota Hemp Samples?

Hemp businesses operating in Minnesota must submit required compliance samples to a Minnesota-licensed laboratory. AIT, located in Moorhead, Minnesota, is authorized to perform hemp compliance testing in accordance with state regulatory requirements.

Submit MN Hemp Sample

MN Hemp Sample Requirements

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

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Sample Guidelines

  • Use leak-proof, sealed containers
  • Clearly label each sample

  • Include an empty sample bag/container with your samples so we can verify the weight upon arrival
  • Package samples securely to prevent damage
  • Follow all applicable state regulations for sample transport

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

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Accepted Containers

Samples should be packaged securely to prevent leaks or contamination during transit.

Recommended containers include:

  • Double bagged Ziploc bags for wet or dry hemp
  • Centrifuge tubes or containers with secure screw caps
  • Original packaging for finished products, if sealed and leak proof

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New Customer Form

Fill out New Customer Form below to send in samples

MN Hemp testing FAQs

MN Hemp Testing Questions

Have questions about MN Hemp testing at AIT? 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.

How much product should I send in for testing?

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Testing requirements depend on your product type and intended use. Minnesota OCM outlines a risk-based testing approach: 
  • Flower: Potency, Heavy Metals, Pesticides, Mycotoxins, Microbial, Water Activity, Foreign Matter
  • Resin: Potency, Heavy Metals, Pesticides, Mycotoxins, Residual Solvents, Microbial
  • Rosin: Potency, Heavy Metals, Pesticides, Mycotoxins, Microbial
  • Resin (Artificially Derived): Potency, Heavy Metals, Pesticides, Mycotoxins, Residual Solvents, Microbial, Foreign Matter
  • Final Products: Potency, Microbial, (vapes/cartridges also require Heavy Metals)
  • Final Products (non-liquid): Potency, Microbial, Water Activity 
We recommend reviewing the Required Testing Flow Chart on page 6 in the Minnesota OCM Technical Authority for a full breakdown. 
Not always. 
Under a 2026 Minnesota legislative update, lower-potency hemp-derived consumer products may be tested by any ISO/IEC 17025-accredited cannabis-testing laboratory until May 31, 2027. 
 

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.

Hemp samples that need to be Minnesota compliant need to be sent to our Minnesota lab. 

Not at this time.

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. 
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!  
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.  

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. 

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

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.

News and Resources

Minnesota Testing Resources

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Why ISO-IEC 17025-2017 is Necessary for Hemp and Cannabis Labs

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Cannabis and Hemp Lab Testing…what’s the point

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How to tell if your COA is Fraudulent

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