In pharmaceutical manufacturing, even a 0.5°C deviation can compromise drug stability or process validity. Temperature dry well calibrators play a critical role in meeting GMP (Good Manufacturing Practice) standards by ensuring sensors in ovens, refrigerators, and autoclaves are calibrated accurately. This article explains:
How dry wells verify temperature probes used in cleanrooms, where liquid baths risk contamination.
The importance of traceable calibration records (simplified by dry wells with built-in data logging) during FDA audits.
Why dry wells’ ability to calibrate small, delicate sensors (e.g., those in vial filling lines) makes them irreplaceable in sterile environments. For quality managers, a reliable dry well isn’t just a tool—it’s a compliance lifeline.