E+E Elektronik Ges.m.b.H.
E+E Elektronik Ges.m.b.H.
22.02.2026 01:02
Reliable, GMP-compliant measurements — with sensors that withstand sterilisation, high temperatures and dust-laden environments
In pharmaceutical machinery, measurement accuracy isn't optional — it's regulated. Whether it's differential pressure in laminar-flow hoods, monitoring critical laminar airflow in isolators, humidity measurement in drying systems, or monitoring process gases in packaging machines: E+E Elektronik sensors are designed to support compliance with GMP guidelines and, where required, ATEX/IECEx standards. At the same time, this equipment must withstand harsh sterilisation conditions such as hydrogen peroxide (H₂O₂) decontamination. High temperatures, solvent cleaning, and dusty or potentially explosive atmospheres are not uncommon.
Your Advantages
Reliable Measurement for Compliance, Quality, and Safety
In the pharmaceutical industry, measurement accuracy underpins product safety and regulatory compliance. Whether in sterile filling lines, drying systems, cleanrooms, or storage facilities, all relevant parameters must be controlled, verified, and documented. GMP, ISO 14644 and FDA require continuous monitoring, traceable calibration, and certified devices in ATEX/IECEx-classified zones. E+E Elektronik provides cleanroom-ready sensors for humidity, temperature, differential pressure, air velocity, dew point, and CO₂ all designed with robust, sterilisation-resistant construction. This ensures precise, regulation-compliant measurements across the entire pharmaceutical value chain.
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