Medical research clean room

for the pharmaceutical industrymedicalfor airborne infection isolation

Applications
A cleanroom is designed to minimise airborne particles and control biological and molecular contamination. Common applications include semiconductor and LCD manufacturing, electronics and precision component production, hospitals, pharmaceutical manufacturing, university research laboratories, and food production facilities.

Product overview
According to JIS (Japanese Industrial Standards), a cleanroom is a controlled area where airborne particles, airborne microorganisms and molecular contaminants are maintained below specified cleanliness levels. Materials, fluids and utilities supplied to the room are controlled for cleanliness, and environmental parameters such as temperature, humidity and pressure are regulated as required.

Environmental control capabilities

• Airborne particle reduction and classification (cleanliness class).
• Microbial control and sterilisation options for medical and aseptic environments.
• Control of temperature, relative humidity and differential pressure.
• Optional control of trace gases, static electricity, micro‑vibrations and electromagnetic interference.

BSL‑3 and CPF specifics
BSL‑3 rooms are airtight, negatively pressurised containment spaces for handling pathogens and genetically modified organisms to prevent release to surrounding areas. CPF (Cell Processing Facility) rooms are configured for cell therapy processes (for example iPS cell processing) and require aseptic workflow design and validation.

Key points of our offering

• Requirements analysis and tailored design proposals
• Integrated delivery: design, construction, commissioning and validation
• After‑sales support including scheduled inspections and maintenance

Cleanroom class explained
Airborne particles are invisible to the eye; cleanliness classes standardise the allowable particle counts per unit volume of air. Class selection depends on the product or process requirements and regulatory constraints.

Product examples

• C30CR (CR‑compatible robot vacuum)
• Cleanroom (various classes and configurations)
• Biohazard containment room (BSL-3)
• CPF (Cell Processing Facility)
• Aseptic processing room
• Aseptic operating theatre

Technical characteristics / specifications

• Category: Cleanrooms / BSL-3 / CPF
• Standards reference: JIS definition for cleanrooms
• Controlled factors: airborne particles, airborne microorganisms, molecular contamination, temperature, humidity, pressure
• Additional controllable parameters: trace gas components, static electricity, micro‑vibrations, electromagnetic interference
• BSL‑3: airtight negative‑pressure containment for pathogen and GMO handling
• CPF: facilities and workflow for cell processing (e.g., iPS cells)
• Services: requirements analysis, tailored design, integrated construction and commissioning, validation and periodic post‑installation inspections