cGMP Cleanroom
At Arizone, manufacturing is an exact science of stability and scale. We operate as a high-capacity extension of your brand, providing the technical infrastructure required to transform raw concepts into shelf-ready reality. Our facility is engineered for zero-defect production, utilizing fully automated lines and pharmaceutical-grade cleanroom protocols to ensure every batch is a benchmark for purity and potency. We don’t just manufacture; we validate your brand’s promise to the consumer.
Talk to Our TeamHigh-speed filling for Gelatin and Vegan shells with precise dosage control.
Advanced phospholipid delivery for maximum nutrient bioavailability.
High-potency botanical processing that preserves molecular integrity.
Homogenized infusions and specialty oils optimized for shelf-stability.
Our facility is equipped with the latest generation of semi and fully-automated encapsulation lines, capable of producing over 500 million units annually. By eliminating manual touchpoints, we significantly reduce cross-contamination risks and ensure that your brand can scale from pilot runs to multi-million unit orders without the bottleneck of manufacturing delays.
As a leader in liposomal technology, we specialize in “protecting the active.” Our proprietary cold-process emulsification ensures that sensitive nutrients are shielded within lipid bilayers, bypassing digestive degradation. This results in a product that isn’t just manufactured — it’s molecularly optimized for superior consumer results.
Every batch undergoes a rigorous 3-stage validation process within our dedicated laboratory. From raw material identity testing to final microbial clearance, we provide full batch transparency. Our “Technical Standard” ensures that every bottle leaving our facility meets the strictest pharmaceutical-grade safety requirements.
We can help you with all types of manufacturing, whichever is suitable for your brand needs.
Scale-Up LogicWhether you are a startup or an enterprise, our facility adapts. We provide the agility for small-batch market testing and the industrial power for global launches.
Formula StabilityWe specialize in "difficult" formulas — ensuring bitter botanicals are palatable and unstable compounds remain potent throughout their shelf-life.
Global ComplianceOur manufacturing protocols meet cGMP, ISO 22000 and FSSAI standards, providing the documentation and safety rigor required for international markets.