Vaisala sensors ensure stable humidity and temperature measurements in the most demanding cleanroom environments.
Share:

Humidity and temperature monitoring

 

Vaisala sensors ensure stable humidity and temperature measurements in the most demanding cleanroom environments.

Description

A benchmark in the pharmaceutical and clean room industry for exceptional stability and accuracy. Vaisala’s life science range, backed by its patented HUMICAP technology, also offers high resistance to condensation and chemicals, ensuring reliable long-term measurements, essential to comply with GMP regulations and ensure the integrity of clean rooms.

Enriched content

Vaisala is the global leader in measurement solutions for the life sciences industry, providing technology that ensures compliance with stringent regulations such as GMP (Good Manufacturing Practices) and FDA 21 CFR Part 11. Its ecosystem of equipment is designed to protect the integrity of pharmaceutical and biotech products at every stage of production.

Specialized Solutions for Clean Rooms

In environments where air purity and environmental control are critical, Vaisala offers a high precision integrated range:

  • Humidity and Temperature Transmitters (HMT120, HMW80/90): devices specifically designed for integration into building management systems (BMS). The HMT120 stands out for its optimized design for clean rooms, with chemical cleaning resistant housings and interchangeable probes that facilitate calibration without interrupting the process.
  • Wireless Data Loggers (RFL100): use long-range VaiNet wireless technology to monitor warehouses and cleanrooms without the need for complex cabling, ensuring data continuity even during network failures.
  • HUMICAP® technology: the heart of your humidity sensors. This thin-film sensor offers unmatched long-term stability, resistance to condensation and fast recovery after decontamination processes with vaporized hydrogen peroxide (vH2O2).
  • Continuous Monitoring with viewLinc:

The Vaisala viewLinc Continuous Monitoring System (CMS) acts as the brain of the installation:

  • Centralized Management: Brings together differential pressure, temperature, humidity and CO2 data in a single interface.
  • Regulatory Compliance: Generates protected validation reports and audit trails, essential for passing regulatory inspections.
  • Intelligent Alarms: real-time notifications that allow immediate action to be taken in the event of any deviation from critical parameters, avoiding the loss of valuable batches.

For full integration into modern infrastructures, Vaisala has recently launched viewLinc Cloud, a SaaS version that facilitates scalability and reduces the burden on the IT department.

Other products you may be interested in

  • Hydrogen peroxide is an environmentally friendly way to perform biodecontamination in isolators, hospital rooms, transfer hatches and other applications. H2O2 concentration levels are measured during biodecontamination to ensure that process conditions have been met.
    Peroxide measurement

      Hydrogen peroxide is an environmentally friendly way to perform biodecontamination in isolators, hospital rooms, transfer hatches and other applications. H2O2 concentration levels are measured during biodecontamination to ensure that process conditions have been met.

  • Filter leak testing is a critical technique in cleanroom validation and maintenance, especially in environments where air purity is essential, such as in the pharmaceutical industry, hospitals, biosafety laboratories and semiconductor manufacturing.
    Filter validation

      The filter leakage test (filter leak testing) is a critical technique in the validation and maintenance of clean roomsespecially in environments where air purity is essential, such as in the pharmaceutical industry, hospitals, biosafety laboratories and semiconductor manufacturing.

  • Cleanroom airflow visualization and mapping devices are specialized tools used to perform airflow studies in critical environments such as pharmaceutical laboratories, operating rooms, ISO rooms, and semiconductor manufacturing areas.
    Flow mapping

      Cleanroom airflow visualization and mapping devices are specialized tools used to perform airflow studies in critical environments such as pharmaceutical laboratories, operating rooms, ISO rooms, and semiconductor manufacturing areas.

More information about Humidity and temperature monitoring

Why is thermal validation important?

  • Regulatory compliance: demonstrates compliance with applicable regulations, good manufacturing practices and relevant standards, and provides evidence for regulatory submissions and inspections.
  • Reliable performance and product launch: demonstrates that the process is reproducible and supports sound launch decisions.
  • Quality assurance and product integrity: guarantees microbiological safety while protecting the material, functional and stability properties throughout the product life cycle.
  • Risk mitigation: reduces the likelihood of recalls, deviations, adverse events and costly corrective actions.
  • Audit readiness and data integrity: creates traceable and well-documented records (including raw data and metadata) required for audits and inspections.
  • Life cycle control: defines change control triggers, revalidation criteria and periodic requalification to maintain long-term compliance.
  • Business and reputation protection: helps avoid financial losses and preserves customer and stakeholder confidence.