The objective of Transval is to allow the user to apply easily the statistical methodology for the transfer of any quantitative analytical methods.
The main features of Transval are:

  • Transfer design: Transval allows the evaluation of the transfer towards up to 5 laboratories and can evaluate different concentration levels.
  • Transfer Profile: For every receiving laboratories, the corresponding transfer profile based on total error is calculated (graphical representation) and serves as decision tool.
  • Estimation of trueness, precision and accuracy: The optimal estimation of the main criteria required for the transfer in accordance with regulatory documents such as ICH Q2R1 and ISO.
  • Risk estimation: The risk of having OOS results at each receiving lab is known.
  • Reporting: A transfer report containing whole the information required and necessary to judge the acceptability of the method transfer.

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TRANSVAL 2.0 DEMO  Last Update: November 6 2017  © Pharmalex 2019.