Mitigating the Challenges of Clinical Trial Monitoring: A Technology- | Page 7

eight weeks, to an event-driven paradigm, such as after the first and

Reasons for a Site Visit:
•  he site is prepared to
T
conduct a study
•  he site needs more training
T
in the e-monitoring system
or the protocol
•  he site has a higher number
T
of adverse events than
expected
•  he site is a quick enroller
T

every third subject is enrolled or in the event of a protocol deviation.
The reduced