Surprisingly simple: the testo 190 CFR software.

The 21 CFR Part 11-compliant testo 190 CFR software provides you with effective support in your validation and qualification tasks. From fast simultaneous configuration and readout of up to eight data loggers, via comprehensive data analysis to easy, audit-relevant reporting. The clear software structure guides you intuitively through the process step by step and helps you at critical points in the input process through warnings. The range of functions was deliberately restricted to the features which you really need for successful validation.

You will be impressed by these advantages:

  • Full, audit-relevant documentation with just the click of a mouse (1-click report).
  • Whether you are an expert or a novice: testo 190 CFR software provides every user with optimum support during the measuring process. 
  • Fast and reliable overview of the measurement results.
  • No data export to other systems needed (e.g. to Excel).
  • Readout of up to 254 loggers is possible in one validation process.

How to contact us

Would you like to get to know the testo 190 CFR data logger system?

Then simply send us an e-mail or call us. Our experts will be pleased to assist you at any time.

Six steps to getting the result:

Software analysis in the laboratory

1. Logger configuration

  • Define measuring cycle
  • Determine start criteria
  • Carry out batch configuration

2. Logger readout

  • Read out data
  • Define time period
  • Measurement data confirmation by electronic signature

3. Calculation definition

  • Automatic and manual calculation of the holding phases
  • Automatic FO, AO and CO value calculation
  • Automatic saturated steam pressure calculation

4. Acceptance criteria definition

  • Define accepted holding phase duration
  • Determine tolerated temperature differences
  • Define accepted pressure differences

5. Results analysis

  • Graphic and tabular display of the readings
  • Reading statistics
  • Quick overview of measurement success

6. Report creation

  • Reporting with just one click
  • Get comprehensive audit-relevant data
  • Clear and GMP-compliant