Testo: your reliable service partner
When it comes to the testo 190 CFR data loggers, our experts can implement your requirements in the areas of calibration, qualification, validation and cGxP compliance as needed, and in a cost-effective manner. Additionally, we offer quality assurance support for the introduction, maintenance, and optimization of the validation service. We can provide the necessary support and knowledge at peak times or for more comprehensive or customizable projects.
The exact scope of our services is customizable and can be determined by interaction with Testo and the customer. You can either let us carry out the complete validation, or call on us for partial aspects, such as calibration or training.
Hardware, software, service: Your building blocks for achieving efficient validation
The testo 190 CFR data loggers
Robust, durable, and airtight
The multifunction case
Fast programming and readout while safely storing and transporting the data loggers
The testo 190 CFR software
Efficient user friendly interface and full, audit-proof documentation in just one click.
Calibration
Data loggers and stationary systems, DAkkS or ISO; traceable.
Validation
Processes and software according to FDA 21 CFR Part 11 and EU Annex 11.
Qualification
cGxP-compliant and risk-based (DQ, IQ, OQ, PQ)
Seminars and training
From experts in the field, find out what it takes to ensure professional calibration, validation and qualification.
How can the testo 190 CFR data logger system help you specifically?
