CleanRoom module : Intelligent monitoring of cleanrooms and controlled atmosphere environments

Environmental monitoring solution (EMS) for critical areas (including ISO 14644) in the pharmaceutical industry, biotechnology laboratories and the electronics industry. GMP Annex 1 and 21 CFR Part 11 compliant. Interface with 0.5/5 µm particle counters, cascade differential pressure transmitters, temperature and humidity transmitters and other ModBus RTU/TCP transmitters…

Explore the world of possibilities with the CleanRoom Module from JRI-MySirius

The CleanRoom module from JRI MySirius revolutionizes cleanroom monitoring and controlled environments through a secure cloud platform and an open architecture. This system combines ease of use with industrial robustness thanks to the OpenBox, a core component that interconnects any hardware with the software, and the CleanBox, its plug-and-play turnkey solution.

This compact electrical cabinet is ready to use and natively integrates 4 to 8 differential pressure transmitters, allowing you to reuse your existing tubing. It also centralizes your airborne particle counters, environmental transmitters (Temperature, Relative Humidity, CO₂…), and critical equipment (IVF incubators, storage freezers, cryogenic tanks) via its Modbus and 4-20 mA inputs.

Designed to protect your on-site teams, the CleanBox features a built-in 3-color beacon with a buzzer, while its offline mode ensures continuous data logging and local alarming even in the event of a network failure.

Engineered to meet the strict requirements of the pharmaceutical, biotechnology, healthcare, cosmetics, and electronics industries, the CleanRoom module guarantees the precise monitoring of your critical parameters: 0.5 µm / 5 µm airborne particles, cascade differential pressure, temperature, and humidity. The solution delivers full 21 CFR Part 11 compliant traceability, which is essential for your regulatory compliance.

Continuous, high-performance, scalable supervision

The CleanRoom module gives you a real-time overview of all the critical parameters in your cleanrooms. This technology controls and secures the compliance of your areas at all times.

  • Fixed or mobile particle counting with PMS , Climet , Lighthouse , Beckman Coulter and other brands:
  • Multisize management: 0.5 µm, 5 µm (ft³/m³, sliding window)
  • Full automation: start/stop + campaign import
  • Universal wired connectivity (ModBus RTU/TCP): ΔP, TH, flow transmitters, existing PLCs
  • Use of existing instruments and guaranteed control of infrastructure costs.

Intelligent alarms for maximum security

To protect your critical processes, you need to be able to react immediately to non-conformities:

  • Real-time deviation detection: visual and audible alarms and instant notifications
  • Control of multi-coloured signal towers for clear signage
  • High-frequency acquisition: fine detection of the smallest variations
  • Stand-alone OpenBox in offline mode: guaranteed process security, zero data loss in the event of a communication breakdown

Centralised, simplified maintenance

JRI has designed the CleanRoom module to take the hassle out of day-to-day management:

  • Full audit trail: interventions/modifications traceable in MySirius
  • Centralised administration: declaration/configuration/monitoring of wired equipment
  • Zero programming required: intuitive interface that can be configured without coding skills
  • Easy maintenance without service interruption or data loss
  • OpenBox industrial: robustness and scalability to support the long-term growth of your business.

Strategic advantages

The CleanRoom module brings immediate benefits:

  • Guaranteed compliance to facilitate your audits and inspections
  • Guaranteed operational continuity thanks to an Off-Line operating mode, with no loss of data even in the event of a network outage.
  • Simplified integration with your existing infrastructure to reduce investment costs: particle counters, samplers, wired sensors, PLCs, light columns and existing equipment.
  • Real time and maximum responsiveness: high-frequency acquisition, instant data processing by the OpenBox and immediate generation of alarms for early detection of non-conformities.
  • Themodular architecture of JRI-MySiriusensures scalability, enabling you to expand your own zones without complex reconfiguration.

By choosing the MySirius CleanRoom JRI module, you can turn a regulatory constraint into a competitive advantage. You reduce your operating costs (less paper, fewer human errors, easier maintenance) while guaranteeing maximum safety for your products and your patients.

More than 15,000 companies trust us for the quality of their measurements and our support.

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Validation & Metrology: Complementary expertise

To meet the requirements of your clean areas, JRI relies on the synergy of the MMS Group: Metrology & Monitoring Solutions. We don’t just monitor your rooms: we validate the compliance of every square metre and every decontamination process.

Two entities, one mission: Guarantee the integrity of your critical environments

Service and field metrology expertise

Its speciality is to ensure that your installations and equipment comply with regulatory requirements through direct technical intervention.

Multi-gauge metrology: Calibration and verification

Qualification of Controlled Atmosphere Zones (CAZ): filtration integrity tests (EMERY/PAO), classification particle counting in accordance with ISO 14644, pressure and air flow measurements.

Heat mapping: Precise characterisation of storage volumes (warehouses, cold rooms) and enclosures (ovens, incubators) in accordance with NF X15-140 / FD V08-601 standards.

Equipment validation (IQ/OQ/PQ): Full support for the regulatory commissioning of your production tools.

The specialist in embedded measurement systems for extreme environments

Design of autonomous measurement systems (Data Loggers) capable of plunging into the heart of the most demanding industrial processes.

Measurements in Extreme Conditions: Expertise in managing high pressure, saturated humidity and thermal shock.

Validation of sterilisation cycles: Measurement of temperature and pressure inside autoclaves and sterilisation tunnels (dry or wet heat) with calculation of lethal values (F0).

Decontamination monitoring (VHP): chemical agent-resistant instrumentation to validate hydrogen peroxide vapour disinfection cycles.

Lyophilisation processes: Specific sensors operating under vacuum and at very low temperatures (-90°C) to ensure safe drying of biological products.

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Need to talk to a JRI expert about your measurement project?

Find the best solution for your business. Contact a JRI Expert today.

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