Unparalleled high performance range

User safety, product quality and data integrity are ICOS PHARMA core values. The washing and drying solutions for the pharmaceutical field are precisely addressed to the critical/validated cleaning, disinfection and drying of components used in manufacturing drugs: Glassware; filling line components and tools; tubing; TC fittings; valve and pump bodies, filter housings; reactor vessels and diverse equipment; bulk containers, tanks and carboys

ICOS PHARMA "know-how" allows the client's to benefit from optimal solutions for their individual requirements, in order to perform effectively and reproducibility cleaning and validation of pharma production components.

Only the best available "Non-Proprietary" components such as valves are sourced. Components are selected for their reliability and availability to reduce running costs and down time. ICOS PHARMA can use customer preferred parts provided that these meet performance and reliability requirements.

Our respected engineering experience in the medical, laboratory, pharmaceutical and biotech fields allows us to develop a proven approach that prioritizes the pharma manufacturing process and safety bearing in mind life cycle costs of the equipment. Furthermore, all the processes are optimized to minimize the waste of energy and detergents and we can also offer solutions to reduce consumptions and cycle time.

LB Series, Bin washer equipement

For the perfect cleaning of large items as bins, drums, tanks, IBC, IBC...

ML Series, Pharma Grade Parts and glassware washer

Optimal performance in a compact size and footprint solution. Chamber volume from 4.65 cu.m./16 cu.ft to 3.8 cu.m./134 cu.ft.

Trolleys and washing carts: maximum flexibility customized solutions

Quality details, modular elements for flexible and specific solutions for the most challenging requests.

Control system and integrated architecture

Safe reliable communication. ICOS PHARMA automation systems are developed according to stringent GAMP (Good Automated Manufacturing Practice) guidelines of the pharmaceutical industry, and are FDA 21 CFR part 11 capable.


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