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    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.

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    Ensure quality and compliance

    Measuring Instruments and All-in-One Solutions for Pharmaceutical Production

    IAQ Monitoring: Continuous Monitoring of Environmental Parameters

    From basic hygrometers and data loggers to advanced automated IAQ monitoring systems, Testo provides reliable measurement solutions for continuous monitoring of essential ambient conditions. Our technology ensures consistent compliance with both internal and external quality standards 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

    Laboratory staff take samples from a refrigerator
    Tips

    GxP Dictionary

    This GxP Dictionary provides clear explanations for the majority of terms related to GxP, qualification, validation, and quality assurance.

    Download here
    GxP Dictionary

    Flexible environmental monitoring with data loggers

    testo 175 H1 data logger in pharmaceutical production

    Humidity

    testo 175 H1

    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 in pharmaceutical production

    Pressure

    testo 176 P1

    testo 176 P1 data logger

    Ideal for high-precision and reliable documentation of pressure, temperature and humidity in pharmaceutical production.

    Data logger Comparison brochure

    Which data logger is best for your application?

    Download the comparison brochure now.

    Go to download
    Comparison brochure data loggers

    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.

    Laboratory

    Laboratory

    Find out more

    Cleanroom

    Cleanroom

    Find out more

    Pharmaceutical logistics

    Pharmaceutical logistics

    Find out more

    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

    Didn’t find what you were looking for? Tell us your measurement job, we’re happy to help!

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