Frequently Asked Questions

The ProX is manufactured for maximum operational efficiencies and the utmost safety of its operators and the end consumer. Prodigy uses only 316L pharmaceutical grade stainless steel in our extraction equipment, guaranteeing the highest level of durability, corrosion resistance, and heat resistance, which is also FDA cGMP and EU GMP compliant, ensuring the safety and purity of your end product.

The ProX system is designed to perform extraction at extremely low temperatures, at -100°F / -73°C and colder. This is significantly colder than the temperature at which most fats, waxes, and lipids — the undesirables that winterization removes — can stay dissolved in the solvent. By operating at these low temperatures, the ProX system ensures these substances don't get extracted in the first place, rendering the winterization process unnecessary. Thus, you can streamline your workflow and enjoy a more efficient extraction process with high-purity results.

When you see "Made in the USA" on Prodigy's equipment, it signifies our commitment to the highest quality and safety standards worldwide. International suppliers often lack stringent quality control measures, which can pose risks, particularly in the highly regulated cannabis industry. Given the combustible nature of hydrocarbon solvents, any compromise on the quality or reliability of the extraction equipment could pose a significant danger to operators. Additionally, if inferior materials are used, they may leech harmful substances into the extract, creating potential health risks for end consumers. By manufacturing our products in the USA, we can ensure close oversight of the entire production process, from material selection to the final product. This allows us to minimize any risks, ensuring the safety of both operators and consumers.

If not in stock, your ProX system can be ready to ship in as little as 4 weeks. Ancillary equipment (e.g., temperature control devices) may take as much as 8–12 weeks. We'll make every effort to get you your equipment in a timeframe that meets your business requirements.

Absolutely! We offer customization options to tailor our extraction systems to your specific requirements, whether it's for scale, automation, or unique processing needs, including ASME pressure vessel and ASME BPE certification. Prodigy will also manufacture stainless steel vessels to meet worldwide standards for food, dietary supplements, nutraceuticals, and pharmaceutical manufacturing. Contact us to discuss our capabilities for your unique project!

Yes! Each Prodigy extraction system comes with a third-party technical report from Pressure Safety Inspectors (PSI), a reputable independent engineering firm. This report is a rigorous evaluation of our equipment's design, safety measures, and operational parameters under various conditions. The PSI technical report signifies to jurisdictional compliance regulators that our ProX extraction systems meet or exceed safety standards and operational guidelines necessary for use in the cannabis extraction industry. Importantly, it also demonstrates compliance with regulations for use across all 50 US states. Please note that you should always check with the AHJ (Authority Having Jurisdiction) in your locale (often the fire marshal), to determine any specific requirements for use where your cannabis processing business is located.

Prodigy's cannabis extraction systems have been designed and manufactured with CRN (Canadian Registration Number) readiness in mind. This means that while they meet the design and manufacturing requirements necessary for certification in Canada, they must still be registered in the specific province where the customer intends to use the equipment. Please note that the process and timeframe for obtaining a CRN can vary from province to province, so it's recommended to start this process as soon as possible. Prodigy's extraction systems also meet the standards set forth by Health Canada under the Cannabis Act and the Cannabis Regulations, for Canadian GMP compliance.

Yes, our extraction systems are designed to meet FDA regulations and are equipped with the necessary documentation to demonstrate compliance for cGMP facilities.

Yes, our extraction systems are designed to comply with EU regulations, including those set forth by the European Medicines Agency (EMA) and European Union Good Manufacturing Practice (EU GMP) standards.

Prodigy's extraction systems comply with EU GMP guidelines, CE marking requirements, and the ATEX Directive for equipment used in explosive atmospheres.

The ATEX Directive (ATmosphères EXplosibles) applies to equipment used in potentially explosive environments. Prodigy's extraction systems are designed and certified to meet ATEX requirements, ensuring safe operation in environments where flammable hydrocarbon solvents are present. This includes proper electrical classification, explosion-proof components, and ventilation systems that meet the directive's stringent safety standards.

ASME BPE (Bioprocessing Equipment) is an ASME standard for equipment used in bioprocessing, pharmaceutical, and other high-hygiene applications. It addresses areas such as materials, design, fabrication, inspection, testing, and certification — the details that help a manufacturer establish a cleanable, well-documented product-contact system. For cannabinoid manufacturers planning for pharmaceutical-grade operations, ASME BPE provides a disciplined engineering baseline for evaluating product-contact materials, fabrication quality, sanitary design, and supporting documentation. It is not, by itself, a certification of a finished facility or automatic proof of cGMP compliance; it is one important component of a broader quality and validation strategy.

The April 2026 federal rule placed FDA-approved drug products containing marijuana and marijuana handled under a state medical marijuana license in Schedule III, effective April 28, 2026. The change creates a more defined federal controlled-substance pathway for qualifying medical marijuana activity, but it does not automatically make a facility cGMP-compliant, convert a product into an FDA-approved drug, or replace state, FDA, DEA, and other applicable requirements. For capital planning, the practical implication is that medical operators should evaluate whether their facility, equipment, documentation, and quality systems can support a pharmaceutical-oriented regulatory path. Prodigy can help define the equipment and documentation scope; your qualified regulatory counsel and quality team should determine the requirements that apply to your specific products and operation.

Start with a risk-based gap assessment that connects your intended product, process, and regulatory pathway to your equipment and quality-system requirements. For product-contact equipment, that commonly includes materials of construction, cleanability, sanitary fabrication, pressure and hazardous-location requirements, instrumentation and calibration, process controls, and batch traceability. The documentation package should be considered alongside the hardware. Depending on your project, the planning set may include a user requirements specification (URS), process and instrumentation documentation, material and weld records, factory and site acceptance testing, operating and maintenance manuals, calibration information, and qualification support. Cleaning validation, SOPs, training, change control, and facility controls remain site-level responsibilities. Prodigy can help scope the equipment-side package around your process and quality objectives.

No. ASME BPE-aligned equipment can be a strong engineering foundation for a high-purity manufacturing operation, but cGMP compliance is a complete operating system — not a single equipment attribute. It also depends on the facility, quality management system, procedures, personnel, process controls, data integrity, cleaning strategy, maintenance, calibration, and documented evidence that the process remains in control. A practical approach is to begin with your intended product and regulatory pathway, then define the user requirements, equipment documentation, site controls, and qualification plan needed to support that objective. Prodigy can support the equipment and documentation discussion, while your quality and regulatory teams retain responsibility for the full compliance program.

There is no responsible one-size-fits-all timeline. The duration depends on the complexity of the system, the maturity of your user requirements and process design, documentation scope, site readiness, utility availability, commissioning results, the number of operating ranges to challenge, and how quickly deviations can be resolved. IQ, OQ, and PQ are commonly planned as part of the equipment qualification and process-validation lifecycle: IQ confirms correct installation against approved specifications; OQ demonstrates operation across intended ranges; and PQ establishes consistent performance in the intended operating environment. The strongest way to reduce avoidable delay is to define requirements, acceptance criteria, roles, and documentation deliverables before fabrication begins. Prodigy can help scope the equipment-side documentation and testing support early in project planning.

Food GMP: Focuses on ensuring the safety and quality of food products. It includes guidelines on equipment, sanitation, proper handling, and manufacturing processes to prevent contamination. Dietary Supplement GMP: Similar to food GMP but includes additional requirements specific to dietary supplements, such as ensuring the identity, purity, strength, and composition of products. Pharmaceutical GMP: More stringent and comprehensive, focusing on the manufacturing of drugs. It includes detailed requirements for facility design, equipment validation, process controls, quality assurance, and documentation to ensure products are safe, effective, and of high quality.

Hydrocarbon extraction offers superior efficiency, higher yields, and the ability to preserve more terpenes and cannabinoids compared to other extraction methods, making it a preferred choice for many processors. And we also supply ethanol extraction systems where that is a better fit for the needs of our customers.

Prodigy specializes in hydrocarbon extraction and post-processing solutions, and we assist customers that are interested ethanol extraction, solventless, supercritical CO2 extraction solutions. Our flagship hydrocarbon cannabis and hemp extraction system, the ProX, is renowned for its efficiency, reliability, speed, and ROI.

Of course! Prodigy works with trusted suppliers of USA made ethanol extraction systems that meet FDA cGMP and EU GMP standards. We'll integrate world class ethanol processing into your facility to maximize your workflow and ROI.

Absolutely! Prodigy's extraction systems are versatile and can be used for both cannabis and hemp extraction, providing high-quality CBD and other cannabinoid isolates.

Yes, we offer professional installation services and comprehensive training programs to ensure your team is fully equipped to operate our extraction systems safely and efficiently.

Prodigy provides ongoing technical support, including remote assistance, on-site visits, and access to our dedicated support team to address any operational issues or questions.

Yes! Through trusted third party financing partners, Prodigy offers a range of flexible financing solutions tailored to fit your business needs. Our goal is to make the transition to the ProX system as smooth and affordable as possible, and our financing options plus product scalability ensure that the latest technology is accessible to processors of all sizes.

Installation timelines vary by system configuration and facility readiness. A standard ProX installation typically takes 2–5 days on-site, including utility connections, system commissioning, and initial operator training. More complex configurations (multi-system installations, custom builds, or facilities requiring utility upgrades) may take 1–3 weeks. Your project engineer will provide a detailed installation timeline during the engineering and procurement phase.

Floor space requirements depend on the specific system configuration and throughput requirements. A standard ProX system typically requires approximately 200–400 sq ft of dedicated extraction space (C1D1-rated for hydrocarbon environments). The MPS 30 requires approximately 100–200 sq ft of post-processing space. Prodigy's Lab Design-Build service includes detailed facility layout planning to optimize your available space for workflow, safety, and compliance.

Utility requirements are build-specific and depend on your system configuration. Common requirements include: 3-phase electrical service (208V or 480V depending on configuration), compressed air (clean, dry, oil-free), chilled water supply (for inTEST integration), adequate HVAC for C1D1-rated spaces, and solvent storage and recovery infrastructure. Your project engineer will provide a detailed utility specification sheet during the engineering phase.

With every Prodigy system, comprehensive operator training programs are available. Basic training is conducted on-site during commissioning and typically runs 3–5 days depending on the customer's extraction experience. Additional advanced training, refresher courses, and process optimization training are available as standalone services.