You can download the audit logs that record user activities for samples, analyses and workflow presets in Ion Reporter™ Software.
This feature allows you to meet Title 21 CFR Part 11 of Federal Regulations that establishes the United States Food and Drug Administration regulations on electronic records and signatures, password policies, and user activity auditing.
In the Samples or Analyses tabs, click Overview.
Select the row of the Sample or Analysis that you want to audit.
Click Actions > Audit Log.
The audit log opens.
Click Export > PDF.
The downloaded filename is sample_name.pdf or analysis_name.pdf.
