Pharmaceutical production
99 % certainty is not enough.
Measuring instruments and all-in-one solutions for pharmaceutical production
IAQ (Indoor Air Quality) 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 (Indoor Air Quality) parameters in pharmaceutical production
Compliant with GxP and 21 CFR Part 11
GxP Dictionary
This GxP Dictionary explains the majority of terms relating to GxP, qualification, validation and quality assurance.
Flexible environmental monitoring with data loggers
Humidity
testo 175 H1 data logger
Your data logger for the long-term measurement and documentation of temperature, relative humidity and dew point.
Pressure
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.
Qualification and validation of processes
With the testo 190 CFR data loggers, which have been specifically developed for the pharmaceutical industry, you can validate your sterilisation and freeze-drying processes in a highly efficient and simple way.
Freeze-drying
The testo 190 T3/T4 CFR temperature data logger monitors the temperature profile during freeze-drying processes in the pharmaceutical industry
Qualification of the plate temperature with five measuring points per plate
Steam in Place (SIP): Subsequent sterilisation of the system with superheated steam
Sterilisation
The testo 190 T3/T4 CFR temperature data logger enables independent routine checks and validations of steam sterilisers
Physical and biological evidence that the sterilisation method is suitable for the product
Placement of the data logger’s probe tip in the core of the item being sterilised
Other areas of application
Find out more about the measuring solutions that can support you in your laboratory and cleanroom processes and in pharmaceutical logistics.
Services, measuring technology and know-how
Full service
Testo Industrial Services guarantees the first-class quality of your processes and products
Qualification & re-qualification
Measuring instrument calibration & validation
Staff training
Customised probes
Do the standard probes match your requirements? We can develop customised probes
Measuring range & accuracy
Probe tube length
Connection cable