一、Industry Standards
Southeast Asian Standards: United States Pharmacopeia（USP-NF 2025）, European Pharmacopoeia (EP 12.0), International Pharmacopoeia 2025, Japanese Pharmacopoeia (JP18)
European and American Standards: United States Pharmacopeia（USP-NF 2025）, European Pharmacopoeia (EP 12.0)
Middle East Standards: EU GMP, U.S. Food and Drug Administration (FDA), USP-NF 2025, European Pharmacopoeia (EP 12.0)
Africa Standards: United States Pharmacopeia（USP-NF 2025）, European Pharmacopoeia (EP 12.0) or EU GMP
二、Basic Parameters
The distribution system delivers stored pharmaceutical water to process points, ensuring its pressure, flow rate and temperature meet the requirements of the process points. It conducts online detection and control of the flow rate, pressure, temperature, total organic carbon (TOC), conductivity, ozone, etc., of pharmaceutical water, and effectively controls the microbial load in water through periodic sterilization.
三、Technical Features
Modular design with a small footprint.
Reduces on-site construction and saves costs.
Excellent automatic control for easy operation.
Integrated online detection and recording of key parameters, ensuring system data traceability.
Compliant with GMP/ISPE design concepts.
No dead ends in the system, complying with GMP and FDA requirements.
Meets the validation requirements of WHO/EU GMP/FDA/cGMP.
Price：As it is a non-standard product, the price needs to be quoted based on specific requirements.
