PharmEquip is proud to be your source for Behringer hygienic hangers and support systems.
Our range includes Weir-style, Radial Diaphragms and Fasteners from Diaphragms Direct®.
PharmEquip supplies high-quality pharmaceutical and bioprocess equipment designed for manufacturing environments.
Our range brings together UltraPure hygienic strainers for process protection and advanced microfiltration systems for critical filtration applications.
Our selection of fittings is meticulously curated to synergise with plastic, rubber tubing and hose systems.
At PharmEquip, we are proud to partner with Alfa Laval and Exergy LLC, both leaders in high-quality heat transfer products.
We supply a focused range of NewAge Industries Inc., and AdvantaPure hose solutions for pharmaceutical, high-purity and industrial process environments.
Newman Gaskets meet strict sanitary standards to support product integrity and minimise contamination risk.
The NovAseptic® range is a complete portfolio of aseptic fluid handling hardware designed for high-purity pharmaceutical and biotechnology processing.
Newman O-rings are designed to protect product integrity, prevent contamination, and deliver reliable sealing performance across critical applications.
PharmEquip supplies Alfa Laval UltraPure pumps, engineered specifically for high-purity and ultra-hygienic pharmaceutical processes.
PharmEquip supplies a comprehensive range of single-use technologies designed to support safe, efficient, and flexible manufacturing.
Discover PharmEquip’s range of Alfa Laval tank cleaning equipment, designed to deliver efficient, reliable and validated cleaning performance.
Explore our range of tubing solutions from NewAge Industries Inc., and AdvantaPure, supporting a wide variety of industrial and hygienic process applications
Alfa Laval valve sensing and control units are designed to monitor and regulate flow in fluid handling systems.
The UltraPure valve range includes butterfly, control and check, diaphragm, double seat, regulating, safety, sampling, and shutter valves.
Advanced WFI Systems for Pharmaceutical Manufacturing
Water for Injection (WFI) is a critical pharmaceutical utility used in the manufacture of parenteral drugs, biologics, and other high-purity applications where product safety, sterility, and regulatory compliance are essential.
Stilmas WFI generation systems are engineered to produce high-purity water in accordance with global pharmacopoeia standards, including EP, USP, and JP. Designed for GMP-compliant environments, these systems support consistent, validated production of WFI for use across sterile manufacturing processes.
Utilising proven technologies, Stilmas solutions are configured to meet specific production requirements, facility constraints, and energy efficiency targets.
WFI Generation Technologies
Stilmas offers a range of WFI generation technologies to suit different production scales and operational requirements.
Multiple Effect Distillation (MED)
A widely used thermal process for WFI generation, MED systems provide reliable, high-capacity production with excellent energy efficiency through multi-stage heat recovery.
Vapor Compression (VC)
VC systems deliver efficient WFI generation by compressing and reusing steam energy, reducing overall utility consumption while maintaining high purity and consistent output.
Membrane-Based WFI Systems
Modern membrane technologies enable WFI production through advanced filtration processes, offering a compact, energy-efficient alternative aligned with updated regulatory acceptance in certain regions.
Designed for GMP Compliance & Validation
WFI systems are designed to meet stringent pharmaceutical requirements, supporting validated operation, consistent water quality, and full traceability. Hygienic design principles, high-grade materials, and controlled process parameters ensure compliance with global regulatory standards.
Integration with advanced automation platforms enables precise monitoring and control of critical parameters, supporting validation activities and long-term system reliability within regulated manufacturing environments.
As part of the Masco Group, Stilmas systems are supported by specialised validation expertise, enabling alignment with IQ, OQ, and PQ requirements and ensuring readiness for compliant operation within pharmaceutical production.
Our Products