pharma-industry-production
Measuring instruments and all-in-one solutions for pharmaceutical production
If pharmaceuticals are produced and stored under the wrong climatic conditions, the stability and therefore the efficacy of the drugs can suffer as a result. Possible consequences: commercial losses or even extensive compensation claims.
Don’t let it come to that: Testo can support you in a GMP-regulated environment with reliable measuring technology and all-in-one solutions that are audit-safe.
IAQ monitoring: Stationary monitoring of environmental parameters
From simple hygrometers and data loggers through to automated IAQ monitoring systems: Testo’s measurement solutions offer you reliable and continuous measurement of the relevant ambient conditions. This enables you to reliably comply with external and internal quality requirements in GMP-regulated environments.
The all-in-one solution: The testo Saveris Pharma environmental monitoring system
Uninterrupted monitoring during pharmaceutical production – using one system
• Integrated system comprising sensors, software and services
• Seamless recording and documentation of all audit-relevant IAQ parameters in pharmaceutical production
• Compliant with GxP and 21 CFR Part 11
Flexible environmental monitoring with data loggers
testo 175 H1 data logger
Your data logger for the long-term measurement and documentation of temperature, relative humidity and dewpoint.
testo 176 P1 data logger
Ideal for high-precision and reliable documentation of pressure, temperature and humidity in pharmaceutical production.
Which data logger is best for your application? Download the comparison brochure now.