Pharmaceutical

Pharmaceutical manufacturing uses water as both a raw ingredient and a critical cleaning agent. USP Purified Water and Water for Injection (WFI) standards exist because water quality directly affects drug safety and efficacy — trace endotoxins, dissolved ions, or microbial contamination in process water can compromise an entire production batch.

AMPAC USA designs and manufactures ultrapure water purification systems that meet Reagent Grade Laboratory Water Type I, II, and III specifications, as well as USP Purified Water and WFI quality standards. Our pharmaceutical-grade systems combine reverse osmosis, electrodeionization (EDI), and UV sterilization in validated, documented configurations suitable for FDA-regulated environments.

Systems are built on passivated stainless steel skids, use pharmaceutical-grade fittings and tubing, and are engineered to support IQ/OQ/PQ validation protocols. Every system ships with full documentation, including material certificates, pressure test records, and factory acceptance test reports.

Call (909) 548-4900 to discuss water purity specifications for your pharmaceutical manufacturing application.