Life Sciences and Pharma
Instrumentation, calibration and monitoring for pharmaceutical, biotechnology and medical device operations: precision and compliance at every stage of the GMP- and GDP-regulated lifecycle.
From the R&D lab to the warehouse, every data point must be traceable
In a regulated environment, every environmental measurement is evidence. From the research lab to production, packaging and storage areas, AKRIBIS integrates high-accuracy instrumentation, SI-traceable calibration and continuous monitoring to sustain GMP and GDP compliance across the entire product lifecycle.
We don't sell an isolated sensor: we bring measurement, calibration, validation and regulatory consulting together on a single risk-mitigation platform, so that every audit finds complete, defensible records.
Environmental monitoring for GxP-regulated environments
Continuous logging of temperature, humidity and other critical variables with documented traceability, out-of-range alerts and audit-ready data. Built for the areas where a single out-of-specification excursion puts the product or compliance at risk.
- Production and packaging areas
- Cleanrooms and classified areas
- Warehouses and distribution centers
- Cold rooms, freezers and ultra-freezers (−80 °C)
- Quality control and R&D laboratories
- Pharmacies, distributors and hospitals
- Biobanks and sample storage
- Incubators, stability chambers and isolators
What we measure in life science processes
Temperature
Cold chain, stability chambers, incubators and −80 °C storage.
Ver más →Humidity
Cleanrooms, test chambers and warehouses, with sensors tolerant to chemical decontamination.
Ver más →Hydrogen peroxide
Validation of VHP bio-decontamination cycles in isolators and cRABS.
Ver más →CO₂
Cell-culture incubators and controlled laboratory atmospheres.
Ver más →Dew point
Compressed air and process gases, drying and low-humidity areas.
Ver más →Pressure
Differential pressure between cleanrooms and containment cascades.
Ver más →Where we apply these solutions
Cleanrooms
Continuous monitoring and qualification under ISO 14644.
Ver más →Bio-decontamination (VHP)
Validation of vaporized hydrogen peroxide cycles.
Ver más →Warehouse monitoring
Cold-chain traceability and out-of-range alerts.
Ver más →Cold chain
Cold rooms, freezers and ultra-freezers for GDP preservation.
Ver más →Laboratory equipment
Analytical instruments and full lifecycle support.
Ver más →An integrated platform, not just another supplier
In regulated operations, an instrument's accuracy means little without traceable calibration, documented validation and regulatory support behind it. That is why AKRIBIS One brings the ecosystem's units together around a single goal: reducing the risk of every stage of the pharmaceutical lifecycle.
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AKRIMET
Metrology, calibration, qualifications and validations (HVAC, ISO 14644 clean areas) with SI traceability and OAA Level I recognition (RE-016).
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SOLFARMA
GMP/FDA/EMA regulatory consulting, URS and validation support for processes and areas.
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AKIoT
Continuous monitoring with telemetry, dashboards and alerts, with cryptographically traceable calibration.
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AKUTEMP
Cold chain and thermal equipment: cold rooms, freezers and ultra-freezers (−80 °C) under GMP/GDP.
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AKZOTEC
Engineering, automation and installation of the solutions on the plant floor and on site.
Adding one unit means integrating with AKRIBIS One, the ecosystem's holistic risk-mitigation platform. Explore our metrology, qualification and validation capability.
Related application notes
Humidity in Pharmaceutical and Life Science Cleanrooms
Why regulators require continuous humidity and temperature logging, and how to withstand hydrogen peroxide decontamination.
Ver más →
Vaporized Hydrogen Peroxide (VHP) Bio-Decontamination
The four phases of the bio-decontamination cycle, and why relative humidity stops being a reliable indicator with VHP.
Ver más →
CO₂ Measurement in Incubators
Why CO₂ control is critical in cell culture, and how to measure it in a stable, traceable way.
Ver más →
Humidity in Climatic and Test Chambers
Why sealing materials and samples under test skew the reading, and how chemical purge solves the condensation risk.
Ver más →Want to know how we apply this to your process?
An AKRIBIS ecosystem specialist can advise you on instrumentation, calibration or validation specific to your regulated operation.