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.
Supporting Australian GMP Manufacturers
In Australia’s regulated pharmaceutical and life sciences environment, validation plays a critical role in ensuring equipment, processes and controlled manufacturing environments consistently meet Good Manufacturing Practice (GMP) requirements.
PharmEquip supports Australian manufacturers with structured validation services aligned with Therapeutic Goods Administration (TGA) and PIC/S GMP expectations.
Through our partnership with MascoLab , we provide access to internationally recognised expertise across process, laboratory and equipment validation.
Working alongside your engineering, validation and quality teams, PharmEquip and MascoLab support validation activities across manufacturing equipment, utilities, packaging systems and laboratory processes to ensure systems are properly tested, documented and prepared for regulatory inspection.
Why Validation Matters for Australian Manufacturers
From new installations to facility expansions and system upgrades, structured validation is essential to demonstrating that manufacturing systems operate reliably and within defined GMP parameters.
Without a clear validation strategy and properly executed qualification activities, commissioning delays, compliance risks and audit findings can quickly arise.
Together with MascoLab and the broader DOC validation framework, PharmEquip helps manufacturers move efficiently from equipment installation to compliant operation, ensuring systems:
Are installed in accordance with approved specifications and operate within validated, controlled parameters.
Perform consistently and reproducibly during routine use
Are supported by controlled, inspection-ready validation documentation
Discover MascoLab
MascoLab is a specialist validation laboratory developed by DOC, Masco Group’s Commissioning, Qualification and Validation (CQV) division with more than 25 years of industry experience.
Our Approach
Our Validation Support Includes
Want to find out more?
Contact our team today to discuss your needs and how PharmEquip can help you
FAQs
Yes. Under TGA and PIC/S GMP guidelines, manufacturers must demonstrate that equipment and processes operate as intended. Installation and Operational Qualification are standard requirements for compliance.
Yes. PharmEquip supplies hygienic process equipment and coordinates validation services through our partnership with MascoLab, providing a streamlined approach from installation through to compliant operation.
Yes. Validation activities are supported by controlled documentation aligned with GMP requirements and suitable for regulatory inspection.
We can assist with PQ planning and execution can be supported in collaboration with MascoLab and your internal QA and validation teams to ensure full lifecycle coverage.
Accelerate Your Path to Compliant Operation.
Reduce risk. Protect timelines. Strengthen audit confidence.