Proper site management adds positive momentum to successful patient recruitment, which secures the success of clinical trial deliverables. EPS's site management services contract with the trial sites (hospitals and medical institutions) and assist with complex trial work so that trials can be properly conducted per GCP guidelines without interruption.
In usual practice, site management activities depend on the clinical research associate's capabilities. However, in complex studies, EPS has extended its site management services through a site management organization. EPS collaborates with medical institutions (hospitals and/or clinical research institutions) to enhance the site's performance at the site level. The benefit of this practice is that it ensures robust patient recruitment and retention. With input from both the CRA and the site's services (via SMO), we can ensure optimal use of clinical trial time and resources.
A full range of site management organization services that are your assurance of successful clinical trials.