Qualification, and Initiation
The GLOBAL CRO Approach
The success of a clinical trial hinges on the quality of sites that are selected for participation. You must be able to properly identify, select and begin trial start-up within the clinical trial timelines. This can be a challenge without an experienced management team and access to high-performing sites.
GLOBAL CRO leverages a robust clinical trial network of collaborative investigators. Our clinical team brings strong relationships that have been built over years working in the medical device and pharmaceutical industries in multiple therapeutic areas. These relationships include private sites, academic institutions, consortiums and individuals and cover early stage to pivotal and post market trials.
Under our program, sites are initially contacted to gauge their interest in the trial. Sites are assessed in depth to ensure they can meet all protocol specific requirements and have committed staff that will adhere to all regulatory requirements. Our team will provide you with data so you can choose sites and investigators appropriate for your clinical trial needs.
Sites that are chosen to participate as clinical sites will go through the site initiation process. Our team works one on one with each site to ensure regulatory submissions are submitted to the appropriate local regulatory body for approval, and sites are prepared, trained and ready to conduct the clinical trial within your timelines.
Our Consulting Services Include:
Comprehensive Site Selection Process
Integrated Approach to Site Selection
Why Choose GLOBAL CRO?
GLOBAL CRO nurtures strong relationships and partners with highly qualified investigators that can potentially participate in your trial. We have extensive experience in assessing sites to gauge their interest levels, trial competence and staffing levels so that the potential site list is of the highest quality. Our network of sites provides optimization across site selection, qualification, initiation, management, and monitoring.