Metrohm^® Titrando^® Family

Compatibility and security

GLP, GMP, and 21 CFR Part 11 are becoming increasingly important in day-to-day laboratory life. Titrando is entirely oriented toward quality management in the laboratory and offers the following possibilities:

• Each time Titrando is switched on, it carries out a self-diagnosis
• If Titrando has been programmed accordingly, it will remind you about any validation or service work that is due
• The titer of the titrant can be monitored as a function of time in both tabular form or as a graph, similar to a control card
• The «calibration history» of the sensors can be called up; alterations to the sensor caused by aging can be recognized before they affect the results
• All changes to the methods are documented; traceability is ensured

Titrando allows strict control of rights of access using login and password. The requirements defined in FDA regulation 21 CFR Part 11 regarding electronic signature and electronic record are fulfilled. This also applies to the other points contained in this regulation, namely the protection of electronic records against accidental or intentional alteration as well as complete traceability. For long-term archiving, a machine-readable PC/LIMS report is available.