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    Pharmaceutical transport

    When transporting pharmaceuticals, clearly defined temperature and humidity limit values have to be observed. Seamlessly and continuously. If these limits are violated, the active substances or the composition of the drugs may be irreversibly altered.

    The control of the entire cold chain from production through to the delivery is an absolute must for GxP-compliant quality management, in order not only to ensure product quality, but also to avoid potential financial losses and damage to the company’s image.

    Patient safety right from the start. Your partner for quality and compliance in pharmaceutical transport.

    The testo 184 data loggers offer:

    • Green light, red light indicator for easy determination of limit values

    • Simple configuration

    • Uninterrupted cold chain data logging

    • Highest level of data protection

    • Compliance to FDA and USP guidelines

    • Life Sciences expertise for highest level of consultation and support.

    Simply brilliant: the Testo data loggers in use.

    Simply activate the Testo data loggers and place them in the shipping container.

    The right measuring instrument for every requirement.

    testo 184 T3 WHO certificate

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    Additional applications

    Testo is also used in laboratories, clean rooms, or in production when accurate results and reliable technology are required.

    Warehouse

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    Laboratory

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    Cleanroom

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    Production

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