The need for pharmaceutical laboratories to comply with Title 21 of the Code of Federal Regulations Part 11 is an increasingly important issue. Labindia Analytical now offers a special FDA 21 CFR Part 11 compliant version of its titration software.

Titration is the fundamental chemical analysis procedure whereby concentration of chemical substance in solution is determined by reacting it with measured amount of another chemical. TITRA SMART performs this analysis using motor driven dispenser, stirred reaction vessel and electrodes which sense the completion of reaction by measuring the potential difference between two electrodes. Making use of this instrument, it is possible to increases the accuracy, repeatability, reproducibility and minimize the error in calculation and documentation.

The instrument is supplied with high speed vortex stirrer with digital speed indication. This specially designed stirrer provides excellent homogenous mixing of samples. An optional magnetic stirrer is also available. A wide selection of Titra SMART Titrator is available from process or quality control in production to research and development works in laboratory.

Send Enquiry
Contact Labindia
Standard Features of TITRA SMART Titrator
  • User interactive for ease of operation with protection against invalid entries.
  • Vortex stirrer for vigorous and homogenous stirring with specially designed glass propeller for total chemical inertness.
  • Quick interchangeable imported burette assemblies with intelligent recognition for its volume size. Burette factor for dispensing corrections is available for true end point calculations.
  • System recognises proper connectivity of other peripherals like Burette, Stirrer, Electrode etc. gives indication in case of improper connectivity.
  • Composite Differential Electrode Amplifier unit for Potentiometric and Voltametric / KF Titrations, having connectivity to various Electrodes. Temperature Sensor with 4-line measurement technique ensures correct temperature indication.
  • Large memory capacity for method storage with suitable scientific parameters having GLP compliance.
  • Standardised modes of titration, namely incremental, equilibrium of titration.
  • By selecting titration method, instrument prints the type of appropriate electrode.
  • During titration, the measured variable i.e. electrode potential (mV) or the pH value is shown on the display together with dispensed volume and number of End Points (EP) detected.
  • User selectable End Point (EP) evaluation up to 9 EP during the run, and calculation by first, last, largest, all or selected EP with display of results and printout.
  • Audit Trail for all activities with search facility, report generation and printing.
  • 200 User IDs with alphanumeric entries of user name, password and role based privileges selection.
  • Multi-level roles with password protection and complexity.
  • User authentication is per formed for each and every operation done.
  • Customizable PDF report file can be created through print.
  • USB Printing eliminates the need of serial port to connect with instrument. The user can take printout on any local or network printer as well.
  • Electronic signature functionality.
  • Manual Archive and Data Backup facility available.