How does LabChart's GLP Module fulfill FDA requirements for electronic records?

The GLP Module for LabChart fulfills the FDA requirements for electronic records by: 

  1. Ensuring data integrity by preventing modifications of the data (i.e. raw data cannot be deleted or modified)
  2. Maintaining audit logs of all the LabChart settings and actions used to record the data ensuring the data can be reproduced and analyzed (and complete logs can be quickly provided for auditing purposes).
  3. Enabling data files to be validated with electronic signatures


For further technical assistance with this or any other issue, please contact ADInstruments Technical Support by clicking HERE.