Following the guide lines of the Food
and Drug Association (FDA), the software includes an audit trail for
all objects, that can be modified, according
to the CFR
21 part 11 guide lines. An audit trail is a list of all modifications
of an object. It shows the complete history of an object from the point
of creation until now and all things happened meanwhile. Every modification
will cause an entry in the audit trail of the object, containing detailed
information about modification properties, respectively. The audit trail
of an object can be reviewed in the audit
trail tab.
