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Cannabinoid R&D

Extraction Systems for Cannabinoid Research

For research institutions, universities, and pilot-scale API development labs.

Cannabinoid research is accelerating rapidly in the wake of Schedule III rescheduling. Research institutions, universities, and pharmaceutical R&D labs require validated, GMP-documented extraction and isolation systems that can support IND-enabling studies, clinical trial material production, and the analytical method development required for regulatory submissions.

Prodigy's pilot-scale systems are designed specifically for research applications — delivering the same pharmaceutical-grade construction, documentation, and validation infrastructure as commercial systems, in configurations optimized for R&D throughput and flexibility. Every system supports the analytical traceability and process documentation required for FDA and EU regulatory submissions.

Technology Transfer

Designed to support seamless technology transfer from laboratory-scale development to commercial manufacturing. Successful processes developed on Prodigy pilot systems can transition into full-scale commercial production using the same engineering philosophy, documentation standards, and validation approach — reducing tech-transfer risk and accelerating time to market.

Common Applications

IND-enabling study material production
Clinical trial material (CTM) manufacturing
Analytical method development and validation
Process development and scale-up studies
University and research institution cannabinoid programs
Pilot-scale API development for NDA/ANDA pathways

Applicable Standards & Project Considerations

ICH Q7

API manufacturing GMP for research and development

FDA cGMP

21 CFR compliance for IND and NDA support

IQ/OQ/PQ

Equipment qualification for regulatory submissions

ASME BPE

Pharmaceutical-grade fabrication standard

EU GMP EudraLex Vol. 4

EU regulatory submission support

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.