Thermal and humidity mapping for stability chambers, warehouses, cold rooms, and GMP spaces. ICH Q1A and USP 1079 compliant studies.
Complete thermal and humidity mapping studies for every type of pharmaceutical space — from small stability chambers to full warehouse facilities.
Thermal and humidity mapping of pharmaceutical stability chambers to ICH Q1A guidelines. We map VWR, Thermo, Binder, Lunaire, and all major chamber brands.
Full warehouse temperature mapping studies for pharmaceutical storage and distribution facilities. We map ambient, refrigerated, and controlled temperature areas to GDP and USP 1079 standards.
Mapping of cold rooms, walk-in refrigerators, and ultra-low freezers for pharmaceutical and biotech product storage. Full compliance documentation for cryogenic and refrigerated areas.
Temperature and CO2 mapping of incubators used in pharmaceutical microbiological and cell culture applications. Uniformity studies at operating conditions.
Environmental mapping of pharmaceutical clean rooms, aseptic suites, and controlled manufacturing areas. Temperature, humidity, and pressure differential profiling.
Ambient condition mapping for pharmaceutical manufacturing suites, granulation rooms, and packaging areas. Supports HVAC qualification and ongoing environmental monitoring programs.
We design a sensor placement map based on space dimensions, ICH requirements, and your protocol.
Calibrated data loggers placed per protocol. All loggers are NIST traceable with current calibration certs.
Continuous data collection through the full study period — typically 24–72 hours at steady state.
Full statistical analysis of temperature and humidity data. Hot/cold spots identified, MKT calculated where required.
Complete mapping report with graphical analysis, statistical summaries, and pass/fail determination per protocol.
Contact us for a free quote or to schedule on-site service.
We respond within one business day.