You can view an audit log for samples in Ion Reporter™ Software. The sample audit log allows you to see who has accessed a specific sample and changes that are associated with the sample. Sample audit logs are not available for the preinstalled demo data samples.
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 tab, click Overview.
Select the row of the sample that you want to report on.
Click (Actions) > Audit Log.
The audit log opens.
(Optional) Click Export PDF. The downloaded filename is sample_name.pdf, where sample_name is the name of the sample.
