The Evolution of Clinical Trial Monitoring through the eISF

2020-01-06T12:12:42-05:00

Clinical Trial Monitoring is an essential element of the clinical trial process and a vital connection between the sponsor/CRO and the Research Site. Monitoring is the sponsor/CRO’s obligation to ensure that the Research Site conducts the trial per the protocol, SOPs, GCP, and any other regulatory requirements. Ultimately, when conducting an IND trial, regulations [...]