ProX Pharmaceutical Extraction System
Pharmaceutical-Grade Cannabinoid Manufacturing

The Regulatory
Landscape Changed.
Your Equipment
Should Too.

Schedule III rescheduling has created a more defined federal pathway for qualifying medical marijuana activity. Prodigy builds systems for pharmaceutical-grade cannabinoid API (Active Pharmaceutical Ingredient) projects, with design and documentation considerations informed by FDA cGMP, EU GMP, ASME BPE, and ICH Q7.

FDA cGMPEU GMP EudraLex Vol. 4ICH Q7ASME BPECRNCE/PEDC1D1IQ/OQ/PQ
$15B → $96B
Cannabinoid pharmaceutical market (industry analyst projections) — the Schedule III opportunity
The April 28, 2026 DEA final rule placed qualifying medical marijuana activity in Schedule III, creating an important planning opportunity for pharmaceutical-grade cannabinoid API projects.
Read the Schedule III Brief
$15B
Cannabinoid pharma market today*
Industry analyst estimates
$96B
Projected market size*
Industry analyst projections
~99%+
Cannabis isolate purity*
e.g., THCA · Achievable with MPS
50 States
PSI certified for use*
Plus CRN & CE/PED

The Complete
Crude-to-API Pipeline

Integrated cannabinoid extraction, isolation, and separation systems — one validated pathway from raw biomass to active pharmaceutical ingredients.

Raw InputBiomassCultivated hemp or cannabis biomass
01 · ExtractionProXClosed-loop hydrocarbon extraction to crude cannabis oil
02 · Post-ProcessingMPSTHCa isolation, HTE separation & distillate refining
OutputPure Cannabinoid API~99%+ Cannabis Isolate (e.g., THCA)
~95%+ THC Delta-9 Distillate
ProX
Step 01
Extraction

ProX

Hydrocarbon Extraction System

The only closed-loop hydrocarbon extractor engineered to full ASME BPE pharmaceutical standards.

Pharmaceutical-grade closed-loop hydrocarbon extraction engineered to ASME BPE standards. The ProX is the foundation of Prodigy's crude-to-API pharmaceutical-grade cannabinoid pipeline.

316L SS
Material
250 PSIG
Pressure
C1D1
Rating
View Full Specifications
MPS
Step 02
Post-Processing

MPS

Multi-Processing System

THCa isolation, High Terpene Extract separation, and cannabinoid distillate refining — one integrated post-processing platform.

The MPS refines crude or decarboxylated cannabis extract into high-purity concentrated cannabinoid distillate without a separate wiped-film or short-path system. Its integrated workflow also supports THCa isolation and High Terpene Extract (HTE) separation.

~99%+
Cannabis Isolate (e.g., THCA)
30L
Vessels
ASME
Standard
View Full Specifications
inTEST
Step 03
Thermal Control

inTEST

Precision Thermal Management

Cryogenic-to-heated precision in a single unit — the thermal backbone every extraction system requires.

Industrial-grade chilling systems engineered for precise temperature control in pharmaceutical extraction and post-processing environments. Every extraction stage — from initial winterization to final crystallization — depends on precision thermal management.

Cryo→Heat
Range
±0.1°C
Control
Redundant
Safety
View Full Specifications

PROCHILL™ LC-5.000.170 · In Stock, Ready to Ship

One process chiller: 5 kW at −80°C and 11 kW at −60°C. Confirm availability and application fit.

Explore PROCHILL
Custom Builds
Step 04
Custom Scale-Up

Custom Builds

ASME BPE Custom Engineering

From pilot to commercial scale — every system engineered, validated, and documented to your exact specification.

Bespoke pharmaceutical-grade processing systems engineered to your exact specifications. Whether you're scaling from pilot to commercial production or integrating into an existing GMP facility, Prodigy engineers the system around your process — not the other way around.

Any
Scale
ASME BPE
Standard
IQ/OQ/PQ
Docs
View Full Specifications

What Sets Us Apart

Built better.
Documented to prove it.

Made in USA
Manufactured in Hartville, Ohio by Mitchell Fabricators — ASME-certified
ASME BPE
Every system built to the pharmaceutical bioprocessing equipment standard
IQ/OQ/PQ
Full validation documentation package included with every system
April 28, 2026DEA Final Order

Schedule III Is Here.
Prodigy Was Already Ready.

The U.S. Department of Justice issued its final rule placing FDA-approved drug products containing marijuana and qualifying marijuana activity conducted under a state medical-marijuana license in Schedule III of the Controlled Substances Act. The rule creates a more defined federal controlled-substance framework, while product approvals and site requirements remain specific to each project.

Tax Considerations
Qualifying operators should evaluate the rule's potential tax implications with qualified tax counsel.
Controlled-Substance Planning
Applicable DEA, state, recordkeeping, security, and documentation requirements depend on the product and activity.
Pharma Project Readiness
Equipment, documentation, and quality planning can support projects that meet their applicable FDA, DEA, state, and customer requirements.

Built to the Highest Standards

Every Prodigy system is engineered and documented to meet the most demanding pharmaceutical and regulatory requirements in the world.

ASME BPE Certified*

Built to ASME Bioprocessing Equipment standards for pharmaceutical-grade fabrication

FDA cGMP & EU GMP*

Designed to support FDA 21 CFR and EU GMP EudraLex Volume 4 manufacturing standards

Made in USA

Manufactured in Hartville, Ohio by Mitchell Fabricators — ASME-certified fabrication partner

Full Documentation*

IQ/OQ/PQ validation packages, SOPs, and compliance documentation included with every system

Stainless ASME-stamped pressure vessels on the MITCO shop floor
Manufacturing Partner · Est. 1981

Built by MITCO — Mitchell Fabricators

Every Prodigy vessel is fabricated in Hartville, Ohio by MITCO (Mitchell Companies) — a 90,000 sq ft ASME code shop with 45+ years of pressure-vessel and process-piping experience. MITCO holds the ASME U, S, and PP Code Stamps and NBIC R certification. When we say our builds meet ASME and GMP requirements, it is because MITCO engineers and welds them to exactly those specifications.

Visit MITCO Fabrication & Welding
45+
Years in Operation
90,000
Sq Ft Shop Floor
U · S · PP
ASME Code Stamps
R
NBIC Certified
CRYOLOOP
A Prodigy Thermal Solutions Platform

CRYOLOOP™

Built for pharma. Applied to everything.

CRYOLOOP is a patent-pending cryogenic cooling platform designed to replace the conventional chiller-plant function upstream of a data center’s existing facility-water system. Its closed nitrogen circuit and skid-confined SYLTHERM XLT loop chill the water supply without an HFC refrigerant circuit or cooling-tower evaporative water use.

Born from Prodigy’s pharmaceutical thermal engineering, CRYOLOOP now targets the single largest non-compute slice of data center energy: the 40% consumed by cooling. One patent-pending platform — no compressors, no HFC refrigerants, zero evaporative cooling-water use by design. Colder tech for a cooler planet.

−196°C
Liquid nitrogen source
0
HFC refrigerant charge
0
Evaporative cooling-water use
19
PCT claims found novel & inventive
Patent-pending in US, Canada, China, EU, UK & India — Favorable ISR/Written Opinion — Prototype built by MITCO
Klever Brands

“Our custom ProX 80 is processing over 1,000 lbs of biomass per 8-hour shift. After upgrading with Prodigy’s GC Max gas compressor to run active recovery, we’re seeing processing speeds that are unheard of in this industry — while maintaining incredible yields and purity. The build quality, the documentation, and the ongoing engineering support have been exactly what we needed to operate at this scale.”

Robert SemaanKlever Brands — Lindenhurst, Long Island, NY
1,000+
lbs / 8-hr shift
ProX 80
Custom Build
NY
Licensed & Operating

Ready to Build Your
Pharmaceutical-Grade Pipeline?

Talk to a Prodigy engineer about your specific application, throughput requirements, and compliance pathway. We'll help you design the right system.

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

© 2026 Prodigy Processing Solutions. All rights reserved.

Prodigy™ is a trademark of Prodigy USA LC.