Pharmaceutical Reverse Osmosis (RO) systems are critical for producing high-purity water that meets stringent global standards such as USP, EP, and BP. Our advanced water purification systems ensure the removal of dissolved salts, organics, and microbiological contaminants, providing a reliable source for drug manufacturing and laboratory applications.
At Fenton Technologies, we design turnkey Pharma RO solutions that integrate cutting-edge membrane technology with automated controls. Our systems are engineered for consistency, ensuring that your production processes stay compliant and efficient 24/7.
What we offer
We provide comprehensive purified water systems (PWS) that include pre-treatment, double-pass RO, and Electrodeionization (EDI). Our solutions are built with sanitary-grade components and feature full validation documentation support (DQ/IQ/OQ/PQ) to meet regulatory requirements.
- High-efficiency Double Pass RO Technology
- Continuous Electrodeionization (CEDI) for Ultra-Purity
- PLC-based Automation with SCADA Connectivity
- Thermal or Hot Water Sanitizable Systems
Our key benefits
Our Pharma RO solutions are designed to deliver water of unmatched quality while optimizing operational costs. By focusing on sanitary design and robust performance, we help you mitigate risks and ensure product safety.
Regulatory Compliance (GMP/USP/EP)
Our systems are designed to meet all international pharmacopeia purity standards.
Total Microbiological Control
Advanced sanitization protocols prevent biofilm and maintain aseptic conditions.
Frequently Asked Questions
Find answers to common questions about our pharmaceutical grade water purification and RO systems.
Our systems are engineered to exceed USP (United States Pharmacopeia), EP (European Pharmacopoeia), and BP (British Pharmacopoeia) standards for Purified Water (PW) and Water for Injection (WFI) pretreatment.
Prevention is achieved through sanitary design (dead-leg free piping, high-velocity circulation) and regular sanitization cycles using either ozone, UV radiation, or thermal/hot water methods.
Yes, we provide full validation documentation packages including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) support.
Our Pharm RO systems are modular and can be customized to fit your existing infrastructure, often coming skid-mounted for easy installation and integration with existing storage tanks and distribution loops.
EDI is an electrochemical purification process that removes ionizable species from water using ion-exchange membranes. It is highly recommended for pharmaceutical water as it produces ultra-pure water continuously without the need for chemical regeneration.