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.
Automated Cleaning & Sterilisation for GMP Manufacturing
Pharmaceutical cleaning systems, including CIP (Clean-in-Place) and SIP (Sterilise-in-Place) are critical to maintaining hygiene, sterility, and compliance in pharmaceutical and biopharmaceutical manufacturing. These automated systems clean and sterilise process equipment, vessels, and pipelines without disassembly, reducing downtime while ensuring consistent, validated results.
Olsa CIP/SIP systems are engineered to deliver reliable, repeatable, and validated cleaning and sterilisation across liquid, semi-solid, and solid processing applications. Drawing on extensive experience in complex process systems, Olsa designs fully automated units that support efficient operation, compliance, and consistent process outcomes.
Applications Across Pharmaceutical Processing
Olsa CIP and SIP systems are designed to support a wide range of equipment and manufacturing environments, ensuring effective cleaning and sterilisation across critical process stages.
Typical applications include bioreactors, process vessels, and transfer lines, as well as API and fine chemical production equipment. Systems are also widely used across pharmaceutical and biotechnology manufacturing facilities where sterility, repeatability, and validation are essential.
Pharmaceutical Cleaning System Design & Integration
Olsa systems are engineered for seamless integration into existing process equipment and facility layouts. Configurations can be tailored to specific cleaning requirements, process flows, and plant constraints, supporting flexible and scalable implementation.
Each system is designed to deliver repeatable, validated cleaning cycles, ensuring consistent removal of residues and preparation of equipment for sterile processing.
Monitoring, Control & Cleaning Performance
Integrated heating systems, chemical dosing, and in-line monitoring technologies support controlled and verifiable cleaning performance. Parameters such as conductivity, pH, and TOC are monitored throughout the cleaning cycle to confirm effectiveness and support validation.
Advanced PLC- and SCADA-based automation platforms enable fully automated operation, aligned with 21 CFR Part 11 requirements for data integrity and process control. Optimised system design also improves water and chemical efficiency, supporting reliable performance while reducing operational impact.
