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Hemp Processing

High-Volume Cannabinoid Isolation for Hemp Processors

Pharmaceutical-grade CBD, CBG, and minor cannabinoid isolate production at commercial scale.

The hemp-derived cannabinoid market is undergoing a fundamental shift. As the FDA moves toward a regulatory framework for hemp-derived CBD and other cannabinoids in food, dietary supplements, and pharmaceutical applications, the quality and documentation standards required to access premium markets are rising sharply.

Prodigy systems give hemp processors the pharmaceutical-grade infrastructure needed to supply the highest-value market segments — pharmaceutical APIs, dietary supplement manufacturers, and international markets requiring CE/PED and EU GMP documentation. The MPS 30 Multi-Processing System is specifically designed for the post-processing workflow that produces ~99%+ pure cannabis isolate (e.g., THCA) from hemp-derived crude extract.

Why Move Beyond Commodity CBD? The commodity CBD market is crowded and margin-compressed. Processors who invest in pharmaceutical-grade infrastructure can access higher-value market segments: pharmaceutical API supply chains, dietary supplement manufacturers requiring cGMP documentation, and international markets with CE/PED and EU GMP requirements. The result is higher margins, longer-term customer relationships, and a defensible market position built on quality and documentation rather than price alone.

Note: Prodigy equipment and documentation support these regulatory pathways. Market access ultimately depends on the customer's facility, quality management system, procedures, personnel, and regulatory approvals.

Common Applications

CBD isolate production for pharmaceutical and supplement markets
CBG, CBN, and minor cannabinoid isolation
Hemp-derived API manufacturing for international markets
Winterization-free cannabinoid isolation
Terpene capture and separation with HTE system
Scale-up from pilot to commercial production

Applicable Standards & Project Considerations

ASME BPE

Pharmaceutical-grade fabrication for premium market access

FDA cGMP

GMP documentation for dietary supplement and pharma supply

EU GMP EudraLex Vol. 4

EU market access documentation

CE/PED

EU Pressure Equipment Directive for European operations

ICH Q7

API manufacturing standard for pharmaceutical supply chain

Made in USA

Manufactured in Ohio by Mitchell Fabricators

Ready to Get Started?

Contact our engineering team to discuss your application, throughput requirements, and compliance pathway.

Standards & Project Considerations:FDA cGMP*EU GMP EudraLex Vol. 4*ICH Q7*ASME BPE*CRN*CE/PED*C1D1IQ/OQ/PQ*

Product specifications, performance, throughput, purity, recovery rates, temperature ranges, pressure ratings, and final product characteristics are process-, configuration-, and application-dependent. References to FDA cGMP, EU GMP, ICH Q7, ASME BPE, C1D1, CRN, CE/PED, IQ/OQ/PQ, and other standards, certifications, or regulatory frameworks describe applicable design considerations, available configurations, or documentation support and do not constitute regulatory approval or certification unless expressly stated for a specific system or build. Equipment and documentation are designed to support customer qualification, validation, and GMP compliance activities; final regulatory compliance, process validation, product purity, and API status depend on the customer's facility, process, operating procedures, quality systems, validation program, and applicable jurisdictional requirements. Certifications, ratings, specifications, and documentation packages are build-specific and should be confirmed in the final quotation and engineering documentation.

Prodigy Processing Solutions

Engineering pharmaceutical-grade cannabinoid extraction and API manufacturing systems for cannabis operators, hemp processors, and pharmaceutical manufacturers worldwide.

800-710-0815info@prodigyusa.com
Manufactured in Hartville, Ohio, USA
by Mitchell Fabricators in partnership with Prodigy Processing Solutions

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Prodigy™ is a trademark of Prodigy USA LC.