By using a Super-Cryo Ethanol (-90 degrees Celsius) Extraction method, we can efficiently and consistently remove the cannabinoids from the hemp flower. This allows for the cleanest distillate oil on the market.

Rather than using the most oversized equipment available, we chose to scale to a size allowing for the most control, then scaled out with redundancy.

To ensure we stay on the mark with our parameters, we invested in analytical equipment and experts with years of experience to test the material throughout each process stage.

The FDA defines current good manufacturing practices (cGMPs) as systems to assure proper design, monitoring, and control over manufacturing processes and facilities in pharmaceutical and other FDA-regulated industries.

cGMP certification ensures procedures, technologies, and systems are up-to-date to comply with the regulation and that the correct methods and equipment are in place to prevent contamination and errors that affect consumers.

cGMP systems include a series of controls for quality-focused operations, including:

Management systems
Quality raw materials
Standard operating procedures
Detecting and investigating deviations
Reliable analytical testing

This is achieved by utilizing high-performance liquid chromatography (HPLC) and flash chromatography within our facility to ensure materials' identity, strength, purity, and quality at every step of the extraction process.

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