Pharmaceutical Production
Improper climatic conditions during production and storage can compromise the stability and efficacy of pharmaceuticals. Avoid these risks with Testo’s reliable measurement technology and all-in-one, audit-safe solutions, designed to support your operations in a GMP-regulated environment.
Measuring instruments and all-in-one solutions for pharmaceutical production
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 complete solution: the testo Saveris 1 environmental monitoring system
Seamless control in pharmaceutical production - with a single system
Holistic system consisting of sensors, software and services
Seamless recording and documentation of all audit-relevant climate 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 dewpoint.
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 sterilization 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 sterilization of the system with superheated steam
Sterilization
The testo 190 T3/T4 CFR temperature data logger enables independent routine checks and validations of steam sterilizers
Physical and biological evidence that the sterilization method is suitable for the product
Placement of the data logger’s probe tip in the core of the item being sterilized
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 standard probes not match your requirements? We can develop customized probes for you
Measuring range & accuracy
Probe tube length
Connection cable