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Navigation

 
The sign in page give access to the main functions of QuBAS through the different modes/rooms.
 
Users will only be able to see and select the tabs for which they have access.
 
 
1

Development Mode

  • Select, create or edit a Data Map to tell QuBAS what the data values are (i.e. Reference Standard, Quality Control sample, Controls, and Test samples) and the doses (concentrations or dilutions) used.
  • Explore and select the analysis options.
  • Create an Analysis Definition, select system and sample suitability criteria.
  • Analyse data in Development mode.
  • Submit a Method as an MCF for sign off for Routine (regulatory) use.
2

Routine Mode

  • Run a previously approved analysis Method in full GLP and GMP mode on a single Data File or batch of Data Files.
3

Audit and second sign off access

  • Examine audit records for a Method, or across Methods, filtered by staff and type of action.
  • Electronically sign reports  and MCF's as a second signatory.
  • Authorise (approve) and lock a Method (which includes the Data Map, Data File and all analysis settings) for routine / regulatory use.
4

Admin

  • Set system and user administrative functions.